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        "refseq_name": "vomeronasal 2 receptor, 32",
        "refseq_ac": "NP_001406376",
        "gene_names_uniprotkb": "Vom2r32",
        "gene_names_refseq": "Vom2r32",
        "protein_names_uniprotkb": "Vomeronasal 2 receptor, 32",
        "protein_names_refseq": "putative pheromone receptor (Go-VN2); vomeronasal 2 receptor, 32; vomeronasal type-2 receptor 116-like",
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        "protein_name": "Albumin superfamily member 1",
        "gene_name": "Albfm1",
        "organism": "Rat",
        "refseq_name": "alpha-fetoprotein related protein",
        "refseq_ac": "NP_001101826",
        "gene_names_uniprotkb": "Albfm1; LOC360919",
        "gene_names_refseq": "Albfm1; Arg",
        "protein_names_uniprotkb": "Albumin superfamily member 1",
        "protein_names_refseq": "alpha-fetoprotein related protein",
        "tax_id": 10116,
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        "record_id": "F7FAY5-1",
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        "uniprot_canonical_ac": "F7FD47-1",
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        "length": 268,
        "protein_name": "Activating transcription factor 1",
        "gene_name": "Atf1",
        "organism": "Rat",
        "refseq_name": "cyclic AMP-dependent transcription factor ATF-1",
        "refseq_ac": "NP_001094365",
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        "gene_names_refseq": "Atf-1; Atf1",
        "protein_names_uniprotkb": "Activating transcription factor 1",
        "protein_names_refseq": "cyclic AMP-dependent transcription factor ATF-1",
        "tax_id": 10116,
        "disease": "polycystic kidney disease (Disease Ontology:DOID:0080322); alcohol use disorder (Disease Ontology:DOID:1574)",
        "pathway": " (rno:315305);  (R-RNO-199920)",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005667 transcription regulator complex;GO:0090575 RNA polymerase II transcription regulator complex;GO:1990590 ATF1-ATF4 transcription factor complex",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0010976 positive regulation of neuron projection development;GO:0014074 response to purine-containing compound;GO:0045944 positive regulation of transcription by RNA polymerase II",
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        "protein_name": "POTE ankyrin domain family, member G",
        "gene_name": "Poteg",
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        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Poteg",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "POTE ankyrin domain family, member G",
        "protein_names_refseq": "",
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        "biomarker_type": "",
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        "hit_score": 0.1,
        "record_id": "F7FH89-1",
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    },
    {
        "uniprot_canonical_ac": "F7FMK8-1",
        "uniprot_id": "F7FMK8_RAT",
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        "length": 966,
        "protein_name": "Mitogen-activated protein kinase kinase kinase 13",
        "gene_name": "Map3k13",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Map3k13",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Mitogen-activated protein kinase kinase kinase 13; 2.7.11.25",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:303823)",
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        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Activates the JUN N-terminal pathway through activation of the MAP kinase kinase MAP2K7., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "2.7.11.1;2.7.12.1;2.7.1.153;2.7.1.137;2.7.11.24;2.7.11.25;2.7.11.22;2.7.11.23;2.7.4.6;2.7.1.154;2.7.11.38;2.7.11.17;2.7.11.21;2.7.12.2;2.7.1.40;2.7.11.12;2.7.11.26;2.7.11.34;2.7.10.2;2.7.1.150;2.7.11.13;4.1.1.32;2.7.11.19;2.7.2.3;2.7.11.11;2.7.11.31;3.1.3.16;2.7.11.4;2.3.1.48;3.1.11.-;2.7.13.3;2.7.4.18;3.1.24.-;3.4.19.12;2.7.11.39;2.4.99.18;2.7.11.10",
        "go_molecular_function": "GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding;GO:0019899 enzyme binding;GO:0042802 identical protein binding;GO:0042803 protein homodimerization activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0016020 membrane",
        "go_biological_process": "GO:1905492 positive regulation of branching morphogenesis of a nerve;GO:0006468 protein phosphorylation;GO:0007254 JNK cascade;GO:0043123 positive regulation of canonical NF-kappaB signal transduction;GO:0046777 protein autophosphorylation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F7FMK8-1",
        "record_type": "protein"
    },
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        "uniprot_canonical_ac": "F7FNC4-1",
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        "length": 164,
        "protein_name": "Interleukin 36, gamma",
        "gene_name": "Il36g",
        "organism": "Rat",
        "refseq_name": "interleukin-36 gamma isoform X1",
        "refseq_ac": "XP_063140406",
        "gene_names_uniprotkb": "Il36g",
        "gene_names_refseq": "Il1f9; Il36g; RGD1563019",
        "protein_names_uniprotkb": "Interleukin 36, gamma",
        "protein_names_refseq": "interleukin-36 gamma isoform X1",
        "tax_id": 10116,
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        "pathway": " (R-RNO-9014826)",
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        "go_molecular_function": "GO:0005125 cytokine activity",
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        "go_biological_process": "GO:1901740 negative regulation of myoblast fusion;GO:0006954 inflammatory response;GO:0006955 immune response;GO:0032755 positive regulation of interleukin-6 production;GO:0071222 cellular response to lipopolysaccharide",
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        "record_type": "protein"
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        "protein_name": "Biogenesis of lysosomal organelles complex 1 subunit 4",
        "gene_name": "Bloc1s4",
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        "refseq_name": "biogenesis of lysosome-related organelles complex 1 subunit 4",
        "refseq_ac": "NP_001094236",
        "gene_names_uniprotkb": "Bloc1s4",
        "gene_names_refseq": "Bloc1s4; Cno; RGD1306037",
        "protein_names_uniprotkb": "Biogenesis of lysosomal organelles complex 1 subunit 4",
        "protein_names_refseq": "biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino; biogenesis of lysosome-related organelles complex 1 subunit 4",
        "tax_id": 10116,
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:1904115 axon cytoplasm;GO:0031083 BLOC-1 complex",
        "go_biological_process": "GO:0050885 neuromuscular process controlling balance;GO:0070527 platelet aggregation;GO:0008089 anterograde axonal transport;GO:0032438 melanosome organization;GO:0048490 anterograde synaptic vesicle transport",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "G3V6R9-1",
        "record_type": "protein"
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        "uniprot_canonical_ac": "G3V6Y3-1",
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        "length": 648,
        "protein_name": "Kinesin-like protein",
        "gene_name": "Kif12",
        "organism": "Rat",
        "refseq_name": "kinesin-like protein KIF12 isoform X1",
        "refseq_ac": "XP_006238315",
        "gene_names_uniprotkb": "Kif12",
        "gene_names_refseq": "Kif12",
        "protein_names_uniprotkb": "Kinesin-like protein",
        "protein_names_refseq": "kinesin-like protein KIF12 isoform X1",
        "tax_id": 10116,
        "disease": "progressive familial intrahepatic cholestasis (Disease Ontology:DOID:0070221); metabolic dysfunction-associated steatohepatitis (Disease Ontology:DOID:0080547)",
        "pathway": " (R-RNO-6811434);  (R-RNO-983189)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Involved in the negative regulation of fatty acid biosynthesis, probably acting as an adapter that allows ubiquitination of acetyl-CoA carboxylase 1 (ACACA) by E3 ubiquitin-protein ligase COP1, and promotes ACACA degradation. The adapter function requires the C-terminal proline-rich domain and may be apart from the kinesin motor activity., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "mined_c_glycosites": 0,
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        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "reported_phosphosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 2,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005524 ATP binding;GO:0008017 microtubule binding;GO:0016887 ATP hydrolysis activity;GO:0003777 microtubule motor activity;GO:1990756 ubiquitin-like ligase-substrate adaptor activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005874 microtubule;GO:0005929 cilium;GO:0070062 extracellular exosome;GO:0005871 kinesin complex",
        "go_biological_process": "GO:0045717 negative regulation of fatty acid biosynthetic process;GO:0007018 microtubule-based movement;GO:0006511 ubiquitin-dependent protein catabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "G3V6Y3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V6Z0-1",
        "uniprot_id": "G3V6Z0_RAT",
        "mass": 34483.0,
        "length": 313,
        "protein_name": "Homeobox A11",
        "gene_name": "Hoxa11",
        "organism": "Rat",
        "refseq_name": "homeobox protein Hox-A11",
        "refseq_ac": "NP_001123350",
        "gene_names_uniprotkb": "Hoxa11; LOC100909443; NEWGENE_1564605",
        "gene_names_refseq": "Hoxa10; Hoxa11; RGD1564605; RGD1566402",
        "protein_names_uniprotkb": "Homeobox A11",
        "protein_names_refseq": "homeo box A10; homeobox protein A10; homeobox protein Hox-A11-like; homeobox protein Hox-A11",
        "tax_id": 10116,
        "disease": "radioulnar synostosis (Disease Ontology:DOID:9827)",
        "pathway": " (rno:103692131)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "18701816",
        "class_list": "",
        "function": "Sequence-specific transcription factor which is part of a developmental regulatory system that provides cells with specific positional identities on the anterior-posterior axis., [UniProtKB, UniProtKB]; This study shows selective association of HOXA10, MSX2, DLX3 and DLX5 homeodomain transcription factors on Runx2 and OC genes at stages of osteoblast maturation and participation of these factors with RUNX2 in chromatin remodeling of bone-specific genes., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 1,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:1990837 sequence-specific double-stranded DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005667 transcription regulator complex;GO:0032993 protein-DNA complex;GO:0032991 protein-containing complex",
        "go_biological_process": "GO:0001759 organ induction;GO:0007501 mesodermal cell fate specification;GO:0010720 positive regulation of cell development;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "G3V6Z0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V7V2-1",
        "uniprot_id": "G3V7V2_RAT",
        "mass": 46939.0,
        "length": 435,
        "protein_name": "Angio-associated migratory cell protein",
        "gene_name": "Aamp",
        "organism": "Rat",
        "refseq_name": "angio-associated migratory cell protein",
        "refseq_ac": "NP_001100390",
        "gene_names_uniprotkb": "Aamp",
        "gene_names_refseq": "Aamp",
        "protein_names_uniprotkb": "Angio-associated migratory cell protein",
        "protein_names_refseq": "angio-associated migratory cell protein; angio-associated migratory protein",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:301512);  (R-RNO-168638);  (R-RNO-177929);  (R-RNO-428930)",
        "pathway_count": 4,
        "publication_count": 1,
        "publication_id_list": "26350504",
        "class_list": "",
        "function": "AAMP Regulates Endothelial Cell Migration and Angiogenesis Through RhoA/Rho Kinase Signaling. Erratum:[Ann Biomed Eng. 2016 Mar;44(3):830-2. PMID: 26715208], [RefSeq, PubMed]; Plays a role in angiogenesis and cell migration. In smooth muscle cell migration, may act through the RhoA pathway., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
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        "reported_c_glycosites": 0,
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        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008201 heparin binding",
        "go_cellular_component": "GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0009986 cell surface;GO:0015630 microtubule cytoskeleton",
        "go_biological_process": "GO:0014909 smooth muscle cell migration",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "G3V7V2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V824-1",
        "uniprot_id": "G3V824_RAT",
        "mass": 273595.0,
        "length": 2481,
        "protein_name": "Cation-independent mannose-6-phosphate receptor",
        "gene_name": "Igf2r",
        "organism": "Rat",
        "refseq_name": "cation-independent mannose-6-phosphate receptor precursor",
        "refseq_ac": "NP_036888",
        "gene_names_uniprotkb": "Igf2r",
        "gene_names_refseq": "IGF-IIR; Igf2r; Igfr2",
        "protein_names_uniprotkb": "Cation-independent mannose-6-phosphate receptor; 300 kDa mannose 6-phosphate receptor; Insulin-like growth factor 2 receptor; Insulin-like growth factor II receptor; M6P/IGF2 receptor",
        "protein_names_refseq": "cation-independent mannose-6-phosphate receptor precursor; cation-independent mannose-6-phosphate receptor",
        "tax_id": 10116,
        "disease": "non-Hodgkin lymphoma (Disease Ontology:DOID:0060060); colon carcinoma (Disease Ontology:DOID:1520); nephroblastoma (Disease Ontology:DOID:2154); amyotrophic lateral sclerosis (Disease Ontology:DOID:332); breast carcinoma (Disease Ontology:DOID:3459); lung adenocarcinoma (Disease Ontology:DOID:3910); hepatocellular carcinoma (Disease Ontology:DOID:684); in situ carcinoma (Disease Ontology:DOID:8719); breast carcinoma in situ (Disease Ontology:DOID:8791); type 2 diabetes mellitus (Disease Ontology:DOID:9352); multiple myeloma (Disease Ontology:DOID:9538); type 1 diabetes mellitus (Disease Ontology:DOID:9744)",
        "pathway": " (rno:25151);  (R-RNO-432722);  (R-RNO-6798695);  (R-RNO-6811440);  (R-RNO-8856825);  (R-RNO-8856828)",
        "pathway_count": 6,
        "publication_count": 7,
        "publication_id_list": "22673903;31584202;34145441;34586566;36462176;36928640;38843836",
        "class_list": "",
        "function": "Cardiac-specific overexpression of insulin-like growth factor II receptor-alpha interferes with the regulation of calcium homeostasis in the heart under hyperglycemic conditions., [RefSeq, PubMed]; Expression of IGF-2 Receptor in the Auditory Cortex Improves the Precision of Recent Fear Memories and Maintains Detailed Remote Fear Memories Over Time., [RefSeq, PubMed]; Insulin-like growth factor II receptor alpha overexpression in heart aggravates hyperglycemia-induced cardiac inflammation and myocardial necrosis., [RefSeq, PubMed]; Mediates the transport of phosphorylated lysosomal enzymes from the Golgi complex and the cell surface to lysosomes. Lysosomal enzymes bearing phosphomannosyl residues bind specifically to mannose-6-phosphate receptors in the Golgi apparatus and the resulting receptor-ligand complex is transported to an acidic prelysosomal compartment where the low pH mediates the dissociation of the complex. The receptor is then recycled back to the Golgi for another round of trafficking through its binding to the retromer. This receptor also binds IGF2. Acts as a positive regulator of T-cell coactivation by binding DPP4., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Perturbed ER homeostasis by IGF-IIRalpha promotes cardiac damage under stresses., [RefSeq, PubMed]; The combined inhibition of the CaMKIIdelta and calcineurin signaling cascade attenuates IGF-IIR-induced cardiac hypertrophy., [RefSeq, PubMed]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "total_reported_n_glycosites": 0,
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        "biomarker_type": "",
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        "disease_count": 12,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0019899 enzyme binding;GO:0042802 identical protein binding;GO:0051219 phosphoprotein binding;GO:0001965 G-protein alpha-subunit binding;GO:0005520 insulin-like growth factor binding",
        "go_cellular_component": "GO:0030118 clathrin coat;GO:0000139 Golgi membrane;GO:0005615 extracellular space;GO:0005634 nucleus;GO:0005641 nuclear envelope lumen",
        "go_biological_process": "GO:0001889 liver development;GO:0007186 G protein-coupled receptor signaling pathway;GO:0007283 spermatogenesis;GO:0043065 positive regulation of apoptotic process;GO:0032526 response to retinoic acid",
        "synthesized_glycan_count": 0,
        "hit_score": 1.0,
        "record_id": "G3V824-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V9V4-1",
        "uniprot_id": "G3V9V4_RAT",
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        "length": 132,
        "protein_name": "Ig-like domain-containing protein",
        "gene_name": "AABR07017902.1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "AABR07017902.1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ig-like domain-containing protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "predicted_s_glycosites": 0,
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        "reported_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0042101 T cell receptor complex",
        "go_biological_process": "GO:0002250 adaptive immune response",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "G3V9V4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "M0R3P1-1",
        "uniprot_id": "M0R3P1_RAT",
        "mass": 34451.0,
        "length": 308,
        "protein_name": "Olfactory receptor family 52 subfamily AC member 1",
        "gene_name": "Or52ac1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Or52ac1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Olfactory receptor family 52 subfamily AC member 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Odorant receptor., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "M0R3P1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "M0R3X1-1",
        "uniprot_id": "M0R3X1_RAT",
        "mass": 57715.0,
        "length": 527,
        "protein_name": "Proactivator polypeptide-like 1",
        "gene_name": "Psapl1",
        "organism": "Rat",
        "refseq_name": "proactivator polypeptide-like 1 precursor",
        "refseq_ac": "NP_001138322",
        "gene_names_uniprotkb": "Psapl1",
        "gene_names_refseq": "Psapl1; RGD1307368",
        "protein_names_uniprotkb": "Proactivator polypeptide-like 1",
        "protein_names_refseq": "Prosaposin (sphingolipid activator protein-1); proactivator polypeptide-like 1 precursor; proactivator polypeptide-like 1",
        "tax_id": 10116,
        "disease": "combined saposin deficiency (Disease Ontology:DOID:0111330)",
        "pathway": " (rno:289720)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "May activate the lysosomal degradation of sphingolipids., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005829 cytosol;GO:0016020 membrane;GO:0005764 lysosome",
        "go_biological_process": "GO:0007193 adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway;GO:0006665 sphingolipid metabolic process;GO:0019216 regulation of lipid metabolic process;GO:0060736 prostate gland growth;GO:0060742 epithelial cell differentiation involved in prostate gland development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "M0R3X1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "M0R3X7-1",
        "uniprot_id": "M0R3X7_RAT",
        "mass": 102204.0,
        "length": 915,
        "protein_name": "hexokinase",
        "gene_name": "Hkdc1",
        "organism": "Rat",
        "refseq_name": "hexokinase domain containing 1 isoform 1",
        "refseq_ac": "NP_001419083",
        "gene_names_uniprotkb": "Hkdc1",
        "gene_names_refseq": "AABR07045032.1; Hkdc1",
        "protein_names_uniprotkb": "hexokinase; 2.7.1.1",
        "protein_names_refseq": "hexokinase 1-like; hexokinase domain containing 1 isoform 1; putative hexokinase HKDC1",
        "tax_id": 10116,
        "disease": "retinitis pigmentosa 92 (Disease Ontology:DOID:0061107); glucose metabolism disease (Disease Ontology:DOID:4194)",
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        "publication_id_list": "33309778",
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        "function": "Integrated Multiomics Reveals Glucose Use Reprogramming and Identifies a Novel Hexokinase in Alcoholic Hepatitis. Erratum:[Gastroenterology. 2021 Sep;161(3):1075. doi: 10.1053/j.gastro.2021.06.068. PMID: 34332936], [RefSeq, PubMed]",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "go_molecular_function": "GO:0042834 peptidoglycan binding;GO:0008745 N-acetylmuramoyl-L-alanine amidase activity;GO:0008270 zinc ion binding;GO:0016019 peptidoglycan immune receptor activity;GO:0140693 molecular condensate scaffold activity",
        "go_cellular_component": "GO:0005615 extracellular space",
        "go_biological_process": "GO:0032827 negative regulation of natural killer cell differentiation involved in immune response;GO:0006955 immune response;GO:0050830 defense response to Gram-positive bacterium;GO:0016045 detection of bacterium;GO:0032689 negative regulation of type II interferon production",
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        "uniprot_canonical_ac": "M0R4U8-1",
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        "protein_name": "Photoreceptor-specific nuclear receptor",
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        "organism": "Rat",
        "refseq_name": "photoreceptor-specific nuclear receptor",
        "refseq_ac": "NP_001414589",
        "gene_names_uniprotkb": "Nr2e3; LOC100365683",
        "gene_names_refseq": "Nr2e3",
        "protein_names_uniprotkb": "Photoreceptor-specific nuclear receptor; Nuclear receptor subfamily 2 group E member 3; Retina-specific nuclear receptor",
        "protein_names_refseq": "photoreceptor-specific nuclear receptor",
        "tax_id": 10116,
        "disease": "enhanced S-cone syndrome 1 (Disease Ontology:DOID:0061231); enhanced S-cone syndrome (Disease Ontology:DOID:0090059); retinitis pigmentosa 37 (Disease Ontology:DOID:0110399)",
        "pathway": " (rno:100365683);  (R-RNO-383280)",
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        "function": "Orphan nuclear receptor of retinal photoreceptor cells. Transcriptional factor that is an activator of rod development and repressor of cone development. Binds the promoter region of a number of rod- and cone-specific genes, including rhodopsin, M- and S-opsin and rod-specific phosphodiesterase beta subunit. Enhances rhodopsin expression. Represses M- and S-cone opsin expression., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0003700 DNA-binding transcription factor activity;GO:0008270 zinc ion binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0043565 sequence-specific DNA binding;GO:0004879 nuclear receptor activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005667 transcription regulator complex",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0008285 negative regulation of cell population proliferation;GO:0010628 positive regulation of gene expression;GO:0045944 positive regulation of transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
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        "protein_name": "Keratin-associated protein",
        "gene_name": "LOC100912272",
        "organism": "Rat",
        "refseq_name": "keratin-associated protein 26-1-like",
        "refseq_ac": "XP_038944657",
        "gene_names_uniprotkb": "LOC100912272",
        "gene_names_refseq": "LOC100912272",
        "protein_names_uniprotkb": "Keratin-associated protein",
        "protein_names_refseq": "keratin-associated protein 26-1-like",
        "tax_id": 10116,
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        "pathway": " (rno:100912272)",
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        "function": "In the hair cortex, hair keratin intermediate filaments are embedded in an interfilamentous matrix, consisting of hair keratin-associated proteins (KRTAP), which are essential for the formation of a rigid and resistant hair shaft through their extensive disulfide bond cross-linking with abundant cysteine residues of hair keratins. The matrix proteins include the high-sulfur and high-glycine-tyrosine keratins., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0005198 structural molecule activity",
        "go_cellular_component": "GO:0005829 cytosol;GO:0045095 keratin filament",
        "go_biological_process": "",
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    {
        "uniprot_canonical_ac": "M0R529-1",
        "uniprot_id": "M0R529_RAT",
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        "length": 314,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or5p69b",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr267",
        "refseq_ac": "NP_001000228",
        "gene_names_uniprotkb": "Or5p69b",
        "gene_names_refseq": "Olr267; Or5p69b; ratchr1-166045849-166046793_ORF",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 267; olfactory receptor Olr267; olfactory receptor gene Olr267",
        "tax_id": 10116,
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        "pathway": " (rno:293435)",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
        "predicted_glycosites": 0,
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        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Pdss1; LOC100364990",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "All trans-polyprenyl-diphosphate synthase PDSS1; 2.5.1.91; All-trans-decaprenyl-diphosphate synthase subunit 1; Decaprenyl-diphosphate synthase subunit 1; Solanesyl-diphosphate synthase subunit 1; Trans-prenyltransferase 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "primary coenzyme Q10 deficiency 2 (Disease Ontology:DOID:0070239)",
        "pathway": " (R-RNO-2142789)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Heterotetrameric enzyme that catalyzes the condensation of farnesyl diphosphate (FPP), which acts as a primer, and isopentenyl diphosphate (IPP) to produce prenyl diphosphates of varying chain lengths and participates in the determination of the side chain of ubiquinone. Supplies nona and decaprenyl diphosphate, the precursors for the side chain of the isoprenoid quinones ubiquinone-9 (Q9)and ubiquinone-10 (Q10) respectively. The enzyme adds isopentenyl diphosphate molecules sequentially to farnesyl diphosphate with trans stereochemistry., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "2.5.1.91",
        "go_molecular_function": "GO:0046872 metal ion binding;GO:0046982 protein heterodimerization activity;GO:0004659 prenyltransferase activity;GO:0097269 all-trans-decaprenyl-diphosphate synthase activity",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005759 mitochondrial matrix;GO:0032991 protein-containing complex;GO:0032478 heterotetrameric polyprenyl diphosphate synthase complex;GO:0032476 polyprenyl diphosphate synthase complex",
        "go_biological_process": "GO:0006744 ubiquinone biosynthetic process;GO:0008299 isoprenoid biosynthetic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "M0R6Q9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "M0R7K9-1",
        "uniprot_id": "M0R7K9_RAT",
        "mass": 18359.0,
        "length": 165,
        "protein_name": "Common salivary protein 1",
        "gene_name": "Csap1",
        "organism": "Rat",
        "refseq_name": "common salivary protein 1 precursor",
        "refseq_ac": "NP_598306",
        "gene_names_uniprotkb": "Csap1; LOC171161",
        "gene_names_refseq": "CSP1; Csap1",
        "protein_names_uniprotkb": "Common salivary protein 1",
        "protein_names_refseq": "common salivary protein 1 precursor",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:171161)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0030246 carbohydrate binding",
        "go_cellular_component": "GO:0005615 extracellular space",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "M0R7K9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "M0R835-1",
        "uniprot_id": "M0R835_RAT",
        "mass": 14783.0,
        "length": 126,
        "protein_name": "Splicing factor 3B subunit 6",
        "gene_name": "Sf3b6",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Sf3b6",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Splicing factor 3B subunit 6; Pre-mRNA branch site protein p14; SF3b 14 kDa subunit",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:100365504)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003729 mRNA binding;GO:0003723 RNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005681 spliceosomal complex;GO:0071011 precatalytic spliceosome;GO:0071006 U2-type catalytic step 1 spliceosome",
        "go_biological_process": "GO:0000398 mRNA splicing, via spliceosome;GO:0001825 blastocyst formation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "M0R835-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "M0R8A3-1",
        "uniprot_id": "M0R8A3_RAT",
        "mass": 35022.0,
        "length": 315,
        "protein_name": "Glycoprotein VI",
        "gene_name": "Gp6",
        "organism": "Rat",
        "refseq_name": "platelet glycoprotein VI isoform 1 precursor",
        "refseq_ac": "NP_001425624",
        "gene_names_uniprotkb": "Gp6",
        "gene_names_refseq": "Gp6",
        "protein_names_uniprotkb": "Glycoprotein VI",
        "protein_names_refseq": "glycoprotein 6 (platelet); platelet glycoprotein VI isoform 1 precursor; platelet glycoprotein VI",
        "tax_id": 10116,
        "disease": "atrial fibrillation (Disease Ontology:DOID:0060224); platelet-type bleeding disorder 11 (Disease Ontology:DOID:0111057); disseminated intravascular coagulation (Disease Ontology:DOID:11247); coronary thrombosis (Disease Ontology:DOID:11847); blood platelet disease (Disease Ontology:DOID:2218); coronary artery disease (Disease Ontology:DOID:3393); myocardial infarction (Disease Ontology:DOID:5844); congestive heart failure (Disease Ontology:DOID:6000); type 2 diabetes mellitus (Disease Ontology:DOID:9352); acute myocardial infarction (Disease Ontology:DOID:9408)",
        "pathway": " (R-RNO-114604);  (R-RNO-75892)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 10,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004888 transmembrane signaling receptor activity;GO:0005518 collagen binding;GO:1990782 protein tyrosine kinase binding;GO:0038064 collagen receptor activity;GO:0140375 immune receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0009986 cell surface;GO:0031012 extracellular matrix;GO:0045121 membrane raft;GO:0097197 tetraspanin-enriched microdomain",
        "go_biological_process": "GO:0002767 immune response-inhibiting cell surface receptor signaling pathway;GO:0018108 peptidyl-tyrosine phosphorylation;GO:0070527 platelet aggregation;GO:0038063 collagen-activated tyrosine kinase receptor signaling pathway;GO:0038065 collagen-activated signaling pathway",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "M0R8A3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "M0R8E0-1",
        "uniprot_id": "M0R8E0_RAT",
        "mass": 32873.0,
        "length": 302,
        "protein_name": "EEF1A lysine methyltransferase 3",
        "gene_name": "Eef1akmt3",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Eef1akmt3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "EEF1A lysine methyltransferase 3; Methyltransferase-like protein 21B; Protein-lysine methyltransferase METTL21B",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Protein-lysine methyltransferase that selectively mono-, di- and trimethylates 'Lys-165' of the translation elongation factors EEF1A1 and EEF1A2 in an aminoacyl-tRNA and GTP-dependent manner. EEF1A1 methylation by EEF1AKMT3 is dynamic as well as inducible by stress conditions, such as ER-stress, and plays a regulatory role on mRNA translation., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "2.1.1.-;2.1.1.361;2.1.1.359;2.1.1.372;2.1.1.355;2.1.1.354;2.1.1.362",
        "go_molecular_function": "GO:0031072 heat shock protein binding;GO:0008168 methyltransferase activity;GO:0016279 protein-lysine N-methyltransferase activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005813 centrosome;GO:0005829 cytosol;GO:0032991 protein-containing complex",
        "go_biological_process": "GO:0018022 peptidyl-lysine methylation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "M0R8E0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "M0R8G4-1",
        "uniprot_id": "M0R8G4_RAT",
        "mass": 64732.0,
        "length": 565,
        "protein_name": "Zinc finger protein 273 like, pseudogene 1",
        "gene_name": "Zfp273l-ps1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Zfp273l-ps1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger protein 273 like, pseudogene 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-212436)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0003677 DNA binding",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006355 regulation of DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0022603 regulation of anatomical structure morphogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "M0R8G4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "M0R8H7-1",
        "uniprot_id": "M0R8H7_RAT",
        "mass": 57918.0,
        "length": 516,
        "protein_name": "Interferon alpha/beta receptor 2",
        "gene_name": "Ifnar2",
        "organism": "Rat",
        "refseq_name": "interferon alpha/beta receptor 2 isoform 1 precursor",
        "refseq_ac": "NP_001413919",
        "gene_names_uniprotkb": "Ifnar2",
        "gene_names_refseq": "Ifnar2",
        "protein_names_uniprotkb": "Interferon alpha/beta receptor 2; Type I interferon receptor 2",
        "protein_names_refseq": "interferon (alpha, beta and omega) receptor 2; interferon alpha/beta receptor 2 isoform 1 precursor; interferon alpha/beta receptor 2",
        "tax_id": 10116,
        "disease": "immunodeficiency 45 (Disease Ontology:DOID:0111994); hepatitis B (Disease Ontology:DOID:2043)",
        "pathway": " (rno:686326);  (R-RNO-909733);  (R-RNO-912694)",
        "pathway_count": 3,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Together with IFNAR1, forms the heterodimeric receptor for type I interferons (including interferons alpha, beta, epsilon, omega and kappa). Type I interferon binding activates the JAK-STAT signaling cascade, resulting in transcriptional activation or repression of interferon-regulated genes that encode the effectors of the interferon response. Mechanistically, type I interferon-binding brings the IFNAR1 and IFNAR2 subunits into close proximity with one another, driving their associated Janus kinases (JAKs) (TYK2 bound to IFNAR1 and JAK1 bound to IFNAR2) to cross-phosphorylate one another. The activated kinases phosphorylate specific tyrosine residues on the intracellular domains of IFNAR1 and IFNAR2, forming docking sites for the STAT transcription factors (STAT1, STAT2 and STAT). STAT proteins are then phosphorylated by the JAKs, promoting their translocation into the nucleus to regulate expression of interferon-regulated genes., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 2,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0019901 protein kinase binding;GO:0019955 cytokine binding;GO:0004905 type I interferon receptor activity;GO:0019962 type I interferon binding",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005886 plasma membrane;GO:0043235 receptor complex",
        "go_biological_process": "GO:0006357 regulation of transcription by RNA polymerase II;GO:0008283 cell population proliferation;GO:0051607 defense response to virus;GO:0060337 type I interferon-mediated signaling pathway;GO:0035458 cellular response to interferon-beta",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "M0R8H7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "M0R926-1",
        "uniprot_id": "M0R926_RAT",
        "mass": 18104.0,
        "length": 156,
        "protein_name": "Ig-like domain-containing protein",
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        "function": "SP-G is a potential new cerebrospinal fluid (CSF) biomarker, possibly not only reflecting aspects of CNS innate immune responses, but also rheo-dynamically relevant changes of CSF composition., [RefSeq, PubMed]",
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        "gene_names_uniprotkb": "Igkv2-112l2",
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        "protein_names_uniprotkb": "Immunoglobulin kappa variable 2-112 like 2",
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        "gene_names_refseq": "Iqcc",
        "protein_names_uniprotkb": "IQ motif containing C",
        "protein_names_refseq": "IQ domain-containing protein C",
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        "gene_name": "Zfp300",
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        "gene_names_refseq": "Zfp300",
        "protein_names_uniprotkb": "Zinc finger protein 300",
        "protein_names_refseq": "rCG42947-like; zinc finger protein 300 isoform 1; zinc finger protein 84",
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        "protein_name": "Ephrin type-B receptor 4",
        "gene_name": "Ephb4",
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        "disease": "central conducting lymphatic anomaly (Disease Ontology:DOID:0081030); hemangiopericytoma (Disease Ontology:DOID:264); cystic kidney disease (Disease Ontology:DOID:2975); esophagus squamous cell carcinoma (Disease Ontology:DOID:3748); lymphatic system disease (Disease Ontology:DOID:75)",
        "pathway": " (rno:686310);  (R-RNO-2682334);  (R-RNO-3928662);  (R-RNO-3928664);  (R-RNO-3928665)",
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        "function": "Receptor tyrosine kinase which binds promiscuously transmembrane ephrin-B family ligands residing on adjacent cells, leading to contact-dependent bidirectional signaling into neighboring cells. The signaling pathway downstream of the receptor is referred to as forward signaling while the signaling pathway downstream of the ephrin ligand is referred to as reverse signaling. Together with its cognate ligand/functional ligand EFNB2 it is involved in the regulation of cell adhesion and migration, and plays a central role in heart morphogenesis, angiogenesis and blood vessel remodeling and permeability. EPHB4-mediated forward signaling controls cellular repulsion and segregation from EFNB2-expressing cells., [UniProtKB, UniProtKB]",
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        "protein_names_refseq": "odorant binding protein 2A; odorant-binding protein 2a precursor; odorant-binding protein 2a",
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        "protein_names_refseq": "N-acetyltransferase family 8 member 2-like",
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        "function": "CD151 and Tspan8 coordinately promote metastasis, where Tspan8 overrides the adhesive features of CD151 by recruiting integrins out of adhesion into motility promoting complexes., [RefSeq, PubMed]; Findings show the presence of Tspan8 in breast cancer primary lesion and metastases and indicate its role as a regulator of cell behaviour and extracellular vesicle release in breast cancer. Tspan8 and p120-catenin were co-immunoprecipitated, indicating that they may interact with each other., [RefSeq, PubMed]; Pubertal down-regulation of Tetraspanin 8 in testicular Sertoli cells is crucial for male fertility., [RefSeq, PubMed]; Regional expression differences of SERT and TSPAN8 in hippocampus, cerebellum and cortex of wild-type young, adult and middle-aged rats., [RefSeq, PubMed]; The molecular interactions of D6.1A with multiple proteins in rat tumor cell lines are reported., [RefSeq, PubMed]; Tspan8 contributes to molecular pathways of exosome-induced endothelial cell activation. Erratum:[Cancer Res.2010 Aug 15;70(16):6683], [RefSeq, PubMed]; Tspan8-Tumor Extracellular Vesicle-Induced Endothelial Cell and Fibroblast Remodeling Relies on the Target Cell-Selective Response. Publication Status: Online-Only, [RefSeq, PubMed]",
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        "protein_names_refseq": "skeletal troponin C; troponin C type 2 (fast); troponin C, skeletal muscle",
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        "go_molecular_function": "GO:0003779 actin binding;GO:0005509 calcium ion binding",
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        "gene_names_uniprotkb": "Defa3; Defa11",
        "gene_names_refseq": "Defa11; Defa3",
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        "protein_names_refseq": "alpha-defensin 11; defensin alpha 11; neutrophil defensin 4 precursor; neutrophil defensin 4",
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        "protein_names_refseq": "SRY (sex determining region Y)-box 18; SRY box 18; SRY-box containing gene 18; transcription factor SOX-18",
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        "disease": "hypotrichosis-lymphedema-telangiectasia-renal defect syndrome (Disease Ontology:DOID:0111360); hypotrichosis-lymphedema-telangiectasia syndrome (Disease Ontology:DOID:0111361)",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0003700 DNA-binding transcription factor activity;GO:0000976 transcription cis-regulatory region binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005667 transcription regulator complex;GO:0000785 chromatin",
        "go_biological_process": "GO:0060214 endocardium formation;GO:0061028 establishment of endothelial barrier;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0001525 angiogenesis;GO:0001570 vasculogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "Q4V7E4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q4Z8P1-1",
        "uniprot_id": "Q4Z8P1_RAT",
        "mass": 50967.0,
        "length": 452,
        "protein_name": "Fli-1 proto-oncogene, ETS transcription factor",
        "gene_name": "Fli1",
        "organism": "Rat",
        "refseq_name": "Friend leukemia integration 1 transcription factor",
        "refseq_ac": "NP_001017381",
        "gene_names_uniprotkb": "Fli1",
        "gene_names_refseq": "Fli1",
        "protein_names_uniprotkb": "Fli-1 proto-oncogene, ETS transcription factor",
        "protein_names_refseq": "Friend leukemia integration 1 transcription factor-like; Friend leukemia integration 1 transcription factor; Friend leukemia virus integration 1",
        "tax_id": 10116,
        "disease": "thrombocytopenia (Disease Ontology:DOID:1588); blood platelet disease (Disease Ontology:DOID:2218); systemic scleroderma (Disease Ontology:DOID:418)",
        "pathway": " (rno:315532)",
        "pathway_count": 1,
        "publication_count": 2,
        "publication_id_list": "22673903;29393594",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 3,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003682 chromatin binding;GO:0000976 transcription cis-regulatory region binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0043565 sequence-specific DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0016604 nuclear body",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0030154 cell differentiation;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0006355 regulation of DNA-templated transcription",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "Q4Z8P1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q5BJN3-1",
        "uniprot_id": "Q5BJN3_RAT",
        "mass": 43389.0,
        "length": 392,
        "protein_name": "Nucleolysin TIAR",
        "gene_name": "Tial1",
        "organism": "Rat",
        "refseq_name": "nucleolysin TIAR isoform 1",
        "refseq_ac": "NP_001013211",
        "gene_names_uniprotkb": "Tial1",
        "gene_names_refseq": "Tial1",
        "protein_names_uniprotkb": "Nucleolysin TIAR; TIA-1-related protein",
        "protein_names_refseq": "RNA binding protein TIAR (TIA-1 related); Tial 1 cytotoxic granule-associated RNA- binding protein-like 1; Tial1 cytotoxic granule-associated RNA binding protein-like 1; nucleolysin TIAR isoform 1; nucleolysin TIAR",
        "tax_id": 10116,
        "disease": "transient cerebral ischemia (Disease Ontology:DOID:224)",
        "pathway": " (rno:361655);  (R-RNO-6803529)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "RNA-binding protein involved in alternative pre-RNA splicing and in cytoplasmic stress granules formation. Shows a preference for uridine-rich RNAs. Activates splicing of alternative exons with weak 5' splice sites followed by a U-rich stretch on its own pre-mRNA and on TIA1 mRNA. Promotes the inclusion of TIA1 exon 5 to give rise to the long isoform (isoform a) of TIA1. Acts downstream of the stress-induced phosphorylation of EIF2S1/EIF2A to promote the recruitment of untranslated mRNAs to cytoplasmic stress granules (SG). Possesses nucleolytic activity against cytotoxic lymphocyte target cells. May be involved in apoptosis., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "F1LQ36",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0003730 mRNA 3'-UTR binding;GO:0035925 mRNA 3'-UTR AU-rich region binding;GO:0140517 protein-RNA adaptor activity;GO:0003723 RNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0010494 cytoplasmic stress granule",
        "go_biological_process": "GO:0008284 positive regulation of cell population proliferation;GO:0008285 negative regulation of cell population proliferation;GO:0006915 apoptotic process;GO:0007281 germ cell development;GO:2000637 positive regulation of miRNA-mediated gene silencing",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "Q5BJN3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q5J3G4-1",
        "uniprot_id": "Q5J3G4_RAT",
        "mass": 34850.0,
        "length": 305,
        "protein_name": "Vomeronasal type-1 receptor",
        "gene_name": "Vom1r29",
        "organism": "Rat",
        "refseq_name": "vomeronasal 1 receptor 29",
        "refseq_ac": "NP_001008946",
        "gene_names_uniprotkb": "Vom1r29",
        "gene_names_refseq": "V1re10; Vom1r29",
        "protein_names_uniprotkb": "Vomeronasal type-1 receptor",
        "protein_names_refseq": "vomernasal 1 receptor Vom1r29; vomeronasal 1 receptor 29; vomeronasal 1 receptor, E10; vomeronasal V1r-type receptor V1re10; vomeronasal type-1 receptor 4",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:494292)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Putative pheromone receptor implicated in the regulation of social as well as reproductive behavior., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005550 pheromone binding;GO:0016503 pheromone receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0019236 response to pheromone;GO:0007606 sensory perception of chemical stimulus",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "Q5J3G4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q5J3I4-1",
        "uniprot_id": "Q5J3I4_RAT",
        "mass": 34419.0,
        "length": 300,
        "protein_name": "Vomeronasal type-1 receptor",
        "gene_name": "Vom1r71",
        "organism": "Rat",
        "refseq_name": "vomeronasal 1 receptor 71",
        "refseq_ac": "NP_001009523",
        "gene_names_uniprotkb": "Vom1r71",
        "gene_names_refseq": "V1rc5; Vom1r71",
        "protein_names_uniprotkb": "Vomeronasal type-1 receptor",
        "protein_names_refseq": "vomernasal 1 receptor Vom1r71; vomeronasal 1 receptor 71; vomeronasal 1 receptor, C5; vomeronasal V1r-type receptor V1rc5; vomeronasal type-1 receptor 100",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:494243)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Putative pheromone receptor implicated in the regulation of social as well as reproductive behavior., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "F1LTU6",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005550 pheromone binding;GO:0016503 pheromone receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0019236 response to pheromone;GO:0007606 sensory perception of chemical stimulus",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "Q5J3I4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q5Q0U0-1",
        "uniprot_id": "S17A5_RAT",
        "mass": 54323.0,
        "length": 495,
        "protein_name": "Sialin",
        "gene_name": "Slc17a5",
        "organism": "Rat",
        "refseq_name": "sialin",
        "refseq_ac": "NP_001009713",
        "gene_names_uniprotkb": "Slc17a5",
        "gene_names_refseq": "AST; Slc17a5; VEAT",
        "protein_names_uniprotkb": "Sialin; AST; H(+)/nitrate cotransporter; H(+)/sialic acid cotransporter; Solute carrier family 17 (Anion/sugar transporter), member 5; VEAT; Vesicular excitatory amino acid transporter",
        "protein_names_refseq": "H(+)/nitrate cotransporter; H(+)/sialic acid cotransporter; proton-coupled sialic acid transporter; sialin; solute carrier family 17 (acidic sugar transporter), member 5; solute carrier family 17 (anion/sugar transporter), member 5; vesicular excitatory amino acid transporter",
        "tax_id": 10116,
        "disease": "sialuria (Disease Ontology:DOID:3659)",
        "pathway": " (rno:363103);  (R-RNO-2160916);  (R-RNO-4085001);  (R-RNO-428643)",
        "pathway_count": 4,
        "publication_count": 6,
        "publication_id_list": "15516337;18695252;20424173;22673903;23221336;35593110",
        "class_list": "",
        "function": "Analysis of crucial residues and substrate-induced conformational changes in SLC17 transporter sialin, [RefSeq, PubMed]; L-aspartate is exocytotically released from nerve terminals after vesicular accumulation by a transporter other than sialin., [RefSeq, PubMed]; Multifunctional anion transporter that operates via two distinct transport mechanisms, namely proton-coupled anion cotransport and membrane potential-dependent anion transport (By similarity). Electroneutral proton-coupled acidic monosaccharide symporter, with a sugar to proton stoichiometry of 1:1. Exports glucuronic acid and free sialic acid derived from sialoglycoconjugate degradation out of lysosomes, driven by outwardly directed lysosomal pH gradient. May regulate lysosome function and metabolism of sialylated conjugates that impact oligodendrocyte lineage differentiation and myelinogenesis in the central nervous system (By similarity) (PubMed:15516337, PubMed:20424173). Electrogenic proton-coupled nitrate symporter that transports nitrate ions across the basolateral membrane of salivary gland acinar cells, with nitrate to proton stoichiometry of 2:1. May contribute to nitrate clearance from serum by salivary glands, where it is further concentrated and secreted in the saliva (By similarity). Uses membrane potential to drive the uptake of acidic amino acids and peptides into synaptic vesicles. Responsible for synaptic vesicular storage of L-aspartate and L-glutamate in pinealocytes as well as vesicular uptake of N-acetyl-L-aspartyl-L-glutamate neuropeptide, relevant to aspartegic-associated glutamatergic neurotransmission and activation of metabotropic receptors that inhibit subsequent transmitter release (By similarity)., [UniProtKB, PubMed, PubMed, UniProtKB, UniProtKB]; Receptor for CM101, a polysaccharide produced by group B Streptococcus with antipathoangiogenic properties., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Sialin mediates submandibular gland regeneration ability by affecting polysialic acid synthesis., [RefSeq, PubMed]; Sialin possesses dual physiological functions and acts as a vesicular aspartate/glutamate transporter, [RefSeq, PubMed]",
        "predicted_glycosites": 3,
        "predicted_n_glycosites": 3,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 15,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 3,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0015136 sialic acid transmembrane transporter activity;GO:0015293 symporter activity;GO:0042880 D-glucuronate transmembrane transporter activity",
        "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005886 plasma membrane;GO:0016323 basolateral plasma membrane;GO:0005764 lysosome;GO:0005765 lysosomal membrane",
        "go_biological_process": "GO:0015739 sialic acid transport;GO:0009617 response to bacterium;GO:0098700 neurotransmitter loading into synaptic vesicle",
        "synthesized_glycan_count": 0,
        "hit_score": 0.7,
        "record_id": "Q5Q0U0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q5QJV4-1",
        "uniprot_id": "Q5QJV4_RAT",
        "mass": 21334.0,
        "length": 182,
        "protein_name": "Inactive ribonuclease-like protein 9",
        "gene_name": "Rnase9",
        "organism": "Rat",
        "refseq_name": "inactive ribonuclease-like protein 9 precursor",
        "refseq_ac": "NP_001008561",
        "gene_names_uniprotkb": "Rnase9",
        "gene_names_refseq": "Rnase9",
        "protein_names_uniprotkb": "Inactive ribonuclease-like protein 9",
        "protein_names_refseq": "inactive ribonuclease-like protein 9 precursor; inactive ribonuclease-like protein 9; ribonuclease 9; ribonuclease, RNase A family, 9 (non-active)",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:364301)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "17005942",
        "class_list": "",
        "function": "Does not exhibit any ribonuclease activity., [UniProtKB, UniProtKB]; The rat RNase9 mRNA was specifically expressed in the epididymis, especially in the caput and corpus, and exhibited an androgen-dependent expression pattern but was downregulated in an epididymitis animal model., [RefSeq, PubMed]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "A6KEC9",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003676 nucleic acid binding",
        "go_cellular_component": "GO:0005576 extracellular region",
        "go_biological_process": "GO:0050830 defense response to Gram-positive bacterium;GO:0060474 positive regulation of flagellated sperm motility involved in capacitation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "Q5QJV4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q5U214-1",
        "uniprot_id": "Q5U214_RAT",
        "mass": 31176.0,
        "length": 281,
        "protein_name": "U1 small nuclear ribonucleoprotein A",
        "gene_name": "Snrpa",
        "organism": "Rat",
        "refseq_name": "U1 small nuclear ribonucleoprotein A",
        "refseq_ac": "NP_001008304",
        "gene_names_uniprotkb": "Snrpa",
        "gene_names_refseq": "Snrpa",
        "protein_names_uniprotkb": "U1 small nuclear ribonucleoprotein A",
        "protein_names_refseq": "U1 small nuclear ribonucleoprotein A",
        "tax_id": 10116,
        "disease": "Alzheimer's disease (Disease Ontology:DOID:10652); germ cell cancer (Disease Ontology:DOID:2994); connective tissue disease (Disease Ontology:DOID:65)",
        "pathway": " (rno:292729);  (R-RNO-9770562)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "ec_number_list": "3.6.5.2;3.6.1.1;3.6.5.-;3.6.5.3;2.3.2.27;2.7.11.1;3.6.5.5;3.6.1.5;3.6.1.-;3.6.5.4",
        "go_molecular_function": "GO:0003924 GTPase activity;GO:0005525 GTP binding;GO:0003747 translation release factor activity",
        "go_cellular_component": "GO:0018444 translation release factor complex;GO:0005829 cytosol",
        "go_biological_process": "GO:0006415 translational termination;GO:0000184 nuclear-transcribed mRNA catabolic process, nonsense-mediated decay;GO:0006412 translation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A096MJE3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A096MJJ4-1",
        "uniprot_id": "A0A096MJJ4_RAT",
        "mass": 103745.0,
        "length": 873,
        "protein_name": "Cilia and flagella associated protein 58",
        "gene_name": "Cfap58",
        "organism": "Rat",
        "refseq_name": "cilia- and flagella-associated protein 58",
        "refseq_ac": "NP_001407019",
        "gene_names_uniprotkb": "Cfap58; Cfap58l1",
        "gene_names_refseq": "Ccdc147; Cfap58l1; Cfap58; RGD1307961",
        "protein_names_uniprotkb": "Cilia and flagella associated protein 58",
        "protein_names_refseq": "cilia and flagella associated protein 58-like 1; cilia- and flagella-associated protein 58; coiled-coil domain containing 147; coiled-coil domain-containing protein 147-like",
        "tax_id": 10116,
        "disease": "oligoasthenoteratozoospermia (Disease Ontology:DOID:0070311); spermatogenic failure 49 (Disease Ontology:DOID:0112271)",
        "pathway": " (rno:102553148)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
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        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
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        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 2,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005813 centrosome;GO:0005856 cytoskeleton;GO:0036126 sperm flagellum;GO:0097228 sperm principal piece;GO:0097225 sperm midpiece",
        "go_biological_process": "GO:0007219 Notch signaling pathway;GO:0030317 flagellated sperm motility;GO:0060271 cilium assembly;GO:0007288 sperm axoneme assembly;GO:0120229 protein localization to motile cilium",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A096MJJ4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A096MJU6-1",
        "uniprot_id": "A0A096MJU6_RAT",
        "mass": 95906.0,
        "length": 857,
        "protein_name": "PR domain zinc finger protein 1",
        "gene_name": "Prdm1",
        "organism": "Rat",
        "refseq_name": "PR domain zinc finger protein 1 isoform X2",
        "refseq_ac": "XP_063135249",
        "gene_names_uniprotkb": "Prdm1",
        "gene_names_refseq": "Prdm1",
        "protein_names_uniprotkb": "PR domain zinc finger protein 1; 2.1.1.-",
        "protein_names_refseq": "PR domain zinc finger protein 1 isoform X2",
        "tax_id": 10116,
        "disease": "diffuse large B-cell lymphoma (Disease Ontology:DOID:0050745); nasal type extranodal NK/T-cell lymphoma (Disease Ontology:DOID:0080797); lung cancer (Disease Ontology:DOID:1324); lung adenocarcinoma (Disease Ontology:DOID:3910); hepatocellular carcinoma (Disease Ontology:DOID:684); systemic lupus erythematosus (Disease Ontology:DOID:9074); colorectal cancer (Disease Ontology:DOID:9256)",
        "pathway": " (rno:309871)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Transcription factor that mediates a transcriptional program in various innate and adaptive immune tissue-resident lymphocyte T cell types such as tissue-resident memory T (Trm), natural killer (trNK) and natural killer T (NKT) cells and negatively regulates gene expression of proteins that promote the egress of tissue-resident T-cell populations from non-lymphoid organs. Plays a role in the development, retention and long-term establishment of adaptive and innate tissue-resident lymphocyte T cell types in non-lymphoid organs, such as the skin and gut, but also in other nonbarrier tissues like liver and kidney, and therefore may provide immediate immunological protection against reactivating infections or viral reinfection. Binds specifically to the PRDI element in the promoter of the beta-interferon gene. Drives the maturation of B-lymphocytes into Ig secreting cells. Associates with the transcriptional repressor ZNF683 to chromatin at gene promoter regions., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 7,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0042826 histone deacetylase binding;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific;GO:0000976 transcription cis-regulatory region binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0003170 heart valve development;GO:0032823 regulation of natural killer cell differentiation;GO:0033082 regulation of extrathymic T cell differentiation;GO:0051136 regulation of NK T cell differentiation;GO:1990654 sebum secreting cell proliferation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A096MJU6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A096MJX5-1",
        "uniprot_id": "A0A096MJX5_RAT",
        "mass": 33544.0,
        "length": 289,
        "protein_name": "Similar to human chromosome 9 open reading frame 78",
        "gene_name": "C3h9orf78",
        "organism": "Rat",
        "refseq_name": "telomere length and silencing protein 1 homolog",
        "refseq_ac": "NP_001386510",
        "gene_names_uniprotkb": "C3h9orf78; RGD1305178",
        "gene_names_refseq": "C3h9orf78; RGD1305178",
        "protein_names_uniprotkb": "Similar to human chromosome 9 open reading frame 78",
        "protein_names_refseq": "telomere length and silencing protein 1 homolog; uncharacterized protein C9orf78 homolog",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:311855);  (R-RNO-72163)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
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        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "glyco_site_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0030623 U5 snRNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005681 spliceosomal complex;GO:0000775 chromosome, centromeric region",
        "go_biological_process": "GO:0060629 regulation of homologous chromosome segregation;GO:0000398 mRNA splicing, via spliceosome;GO:0045292 mRNA cis splicing, via spliceosome",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A096MJX5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A0G2JSL0-1",
        "uniprot_id": "A0A0G2JSL0_RAT",
        "mass": 25304.0,
        "length": 238,
        "protein_name": "Proteasome subunit beta",
        "gene_name": "Psmb6l1",
        "organism": "Rat",
        "refseq_name": "proteasome 20S subunit beta 6 like 1",
        "refseq_ac": "NP_001316812",
        "gene_names_uniprotkb": "Psmb6l1; LOC100360846",
        "gene_names_refseq": "Psmb6l1",
        "protein_names_uniprotkb": "Proteasome subunit beta",
        "protein_names_refseq": "Proteasome subunit beta type-6-like; proteasome 20S subunit beta 6 like 1; proteasome subunit beta type-6",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:100360846);  (R-RNO-1169091);  (R-RNO-1234176);  (R-RNO-1236974);  (R-RNO-1236978);  (R-RNO-174084);  (R-RNO-174113);  (R-RNO-174154);  (R-RNO-174178);  (R-RNO-174184);  (R-RNO-187577);  (R-RNO-195253);  (R-RNO-202424);  (R-RNO-2467813);  (R-RNO-2871837);  (R-RNO-349425);  (R-RNO-350562);  (R-RNO-382556);  (R-RNO-450408);  (R-RNO-4608870);  (R-RNO-4641257);  (R-RNO-4641258);  (R-RNO-5358346);  (R-RNO-5607761);  (R-RNO-5607764);  (R-RNO-5610780);  (R-RNO-5610785);  (R-RNO-5632684);  (R-RNO-5658442);  (R-RNO-5668541);  (R-RNO-5676590);  (R-RNO-5687128);  (R-RNO-5689603);  (R-RNO-5689880);  (R-RNO-68867);  (R-RNO-68949);  (R-RNO-69017);  (R-RNO-69481);  (R-RNO-69601);  (R-RNO-75815);  (R-RNO-8852276);  (R-RNO-8854050);  (R-RNO-8939236);  (R-RNO-8941858);  (R-RNO-8948751);  (R-RNO-8951664);  (R-RNO-9020702);  (R-RNO-9755511);  (R-RNO-9762114);  (R-RNO-9766229);  (R-RNO-983168);  (R-RNO-9907900);  (R-RNO-9912633);  (R-RNO-9929356);  (R-RNO-9929491);  (R-RNO-9931269);  (R-RNO-9932298);  (R-RNO-9954709)",
        "pathway_count": 58,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Component of the proteasome, a multicatalytic proteinase complex which is characterized by its ability to cleave peptides with Arg, Phe, Tyr, Leu, and Glu adjacent to the leaving group at neutral or slightly basic pH. The proteasome has an ATP-dependent proteolytic activity., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "reported_c_glycosites": 0,
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        "reported_c_glycosites_with_glycan": 0,
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        "reported_mutagensis": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004175 endopeptidase activity;GO:0004298 threonine-type endopeptidase activity",
        "go_cellular_component": "GO:0019774 proteasome core complex, beta-subunit complex;GO:0005634 nucleus;GO:0005829 cytosol;GO:0005737 cytoplasm;GO:0005839 proteasome core complex",
        "go_biological_process": "GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process;GO:0051603 proteolysis involved in protein catabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A0G2JSL0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A0G2JTY4-1",
        "uniprot_id": "NFAC3_RAT",
        "mass": 115656.0,
        "length": 1076,
        "protein_name": "Nuclear factor of activated T-cells, cytoplasmic 3",
        "gene_name": "Nfatc3",
        "organism": "Rat",
        "refseq_name": "nuclear factor of activated T-cells, cytoplasmic 3 isoform 2",
        "refseq_ac": "NP_001421511",
        "gene_names_uniprotkb": "Nfatc3; Nfat4",
        "gene_names_refseq": "NFAT4; NFATx; Nfatc3",
        "protein_names_uniprotkb": "Nuclear factor of activated T-cells, cytoplasmic 3; NFATc3; NFATx; T-cell transcription factor NFAT4",
        "protein_names_refseq": "T cell transcription factor NFAT4; nuclear factor of activated T-cells, cytoplasmic 3 isoform 2; nuclear factor of activated T-cells, cytoplasmic 3; nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 3",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:361400);  (R-RNO-2025928);  (R-RNO-2871809);  (R-RNO-5607763)",
        "pathway_count": 4,
        "publication_count": 8,
        "publication_id_list": "19538478;22673903;30980393;33495839;34845564;36373478;36825443;38242872",
        "class_list": "",
        "function": "Acts as a regulator of transcriptional activation. Binds to the TNFSF11/RANKL promoter region and promotes TNFSF11 transcription (By similarity). Binding to the TNFSF11 promoter region is increased by high levels of Ca(2+) which induce NFATC3 expression and may lead to regulation of TNFSF11 expression in osteoblasts (By similarity). Plays a role in promoting mesenteric arterial wall remodeling in response to the intermittent hypoxia-induced increase in EDN1 and ROCK signaling (By similarity). As a result NFATC3 colocalizes with F-actin filaments, translocates to the nucleus and promotes transcription of the smooth muscle hypertrophy and differentiation marker ACTA2 (By similarity). Promotes lipopolysaccharide-induced apoptosis and hypertrophy in cardiomyocytes (PubMed:30980393). Following JAK/STAT signaling activation and as part of a complex with NFATC4 and STAT3, binds to the alpha-beta E4 promoter region of CRYAB and activates transcription in cardiomyocytes (PubMed:19538478). In conjunction with NFATC4, involved in embryonic heart development via maintenance of cardiomyocyte survival, proliferation and differentiation (By similarity). Plays a role in the inducible expression of cytokine genes in T-cells, especially in the induction of the IL-2 (By similarity). Required for thymocyte maturation during DN3 to DN4 transition and during positive selection (By similarity). Positively regulates macrophage-derived polymicrobial clearance, via binding to the promoter region and promoting transcription of NOS2 resulting in subsequent generation of nitric oxide (By similarity). Involved in Ca(2+)-mediated transcriptional responses upon Ca(2+) influx via ORAI1 CRAC channels., [UniProtKB, UniProtKB, PubMed, UniProtKB, PubMed]; Induction of cardiomyocyte calcification is dependent on FoxO1/NFATc3/Runx2 signaling., [RefSeq, PubMed]; MiR-339-3p promotes AT1-AA-induced vascular inflammation by upregulating NFATc3 protein expression in vascular smooth muscle cells., [RefSeq, PubMed]; MicroRNA153 attenuates hypoxiainduced excessive proliferation and migration of pulmonary arterial smooth muscle cells by targeting ROCK1 and NFATc3. Erratum:[Mol Med Rep. 2022 Nov;26(5):332. doi: 10.3892/mmr.2022.12848. PMID: 36082819], [RefSeq, PubMed]; MicroRNA153 induces apoptosis by targeting NFATc3 to improve vascular remodeling in pulmonary hypertension., [RefSeq, PubMed]; The transplant rejection response involves neutrophil and macrophage adhesion-mediated trogocytosis and is regulated by NFATc3. Publication Status: Online-Only, [RefSeq, PubMed]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
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        "reported_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "total_n_glycosites": 0,
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        "total_c_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 3,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0003682 chromatin binding;GO:0003700 DNA-binding transcription factor activity;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific;GO:0000976 transcription cis-regulatory region binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005667 transcription regulator complex",
        "go_biological_process": "GO:0014904 myotube cell development;GO:1905064 negative regulation of vascular associated smooth muscle cell differentiation;GO:0006351 DNA-templated transcription;GO:0007507 heart development;GO:0043065 positive regulation of apoptotic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.9,
        "record_id": "A0A0G2JTY4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A0G2JUK9-1",
        "uniprot_id": "A0A0G2JUK9_RAT",
        "mass": 35325.0,
        "length": 315,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or5m10b",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr465",
        "refseq_ac": "NP_001000297",
        "gene_names_uniprotkb": "Or5m10b",
        "gene_names_refseq": "Olr465; Or5m10b",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 465; olfactory receptor Olr465; olfactory receptor gene Olr465",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:295735)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Odorant receptor., [UniProtKB, UniProtKB]; Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
        "predicted_glycosites": 0,
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        "go_cellular_component": "GO:0005737 cytoplasm;GO:0048471 perinuclear region of cytoplasm;GO:0005764 lysosome",
        "go_biological_process": "GO:0097352 autophagosome maturation;GO:0048877 homeostasis of number of retina cells;GO:0006954 inflammatory response;GO:0045087 innate immune response;GO:0051402 neuron apoptotic process",
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    },
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        "refseq_name": "uncharacterized protein LOC691468",
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        "gene_names_uniprotkb": "Zfpl; RGD1561277",
        "gene_names_refseq": "RGD1561277; Zfpl",
        "protein_names_uniprotkb": "Zinc finger protein like",
        "protein_names_refseq": "uncharacterized protein LOC691468; zinc finger protein 300; zinc finger protein 383",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus",
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        "length": 517,
        "protein_name": "LSM family member 14B",
        "gene_name": "Lsm14b",
        "organism": "Rat",
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        "gene_names_uniprotkb": "Lsm14b",
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        "go_molecular_function": "GO:0003723 RNA binding;GO:0003729 mRNA binding",
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        "go_biological_process": "GO:0006417 regulation of translation;GO:0001541 ovarian follicle development;GO:0048477 oogenesis;GO:0140694 membraneless organelle assembly;GO:1903537 meiotic cell cycle process involved in oocyte maturation",
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    },
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        "length": 683,
        "protein_name": "Acyl-CoA synthetase short-chain family member 3, mitochondrial",
        "gene_name": "Acss3",
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        "refseq_name": "acyl-CoA synthetase short-chain family member 3, mitochondrial isoform 1",
        "refseq_ac": "NP_001401870",
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        "gene_names_refseq": "Acss3; RGD1307051",
        "protein_names_uniprotkb": "Acyl-CoA synthetase short-chain family member 3, mitochondrial; 6.2.1.17; 6.2.1.1; Acetate--CoA ligase 3; Acyl-CoA synthetase short-chain family member 3; Propionate--CoA ligase",
        "protein_names_refseq": "acetate--CoA ligase 3; acyl-CoA synthetase short-chain family member 3, mitochondrial isoform 1; acyl-CoA synthetase short-chain family member 3, mitochondrial; propionate--CoA ligase",
        "tax_id": 10116,
        "disease": "",
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        "function": "Catalyzes the synthesis of acetyl-CoA from short-chain fatty acids (PubMed:28003429). Propionate is the preferred substrate but can also utilize acetate and butyrate with a much lower affinity (PubMed:28003429)., [UniProtKB, PubMed]; Catalyzes the synthesis of acetyl-CoA from short-chain fatty acids. Propionate is the preferred substrate but can also utilize acetate and butyrate with a much lower affinity., [UniProtKB, UniProtKB, UniProtKB]; The results suggested that ACSS3 is a liver mitochondrial matrix enzyme with high affinity to propionic acid, and its expression level is upregulated under ketogenic conditions., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0005524 ATP binding;GO:0003987 acetate-CoA ligase activity;GO:0050218 propionate-CoA ligase activity;GO:0031956 medium-chain fatty acid-CoA ligase activity",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005759 mitochondrial matrix",
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        "protein_names_refseq": "ADAM metallopeptidase domain 20; ADAM metallopeptidase domain 21 precursor; ADAM metallopeptidase domain 21; disintegrin and metalloproteinase domain-containing protein 20; disintegrin and metalloproteinase domain-containing protein 21-like; disintegrin and metalloproteinase domain-containing protein 29",
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        "go_molecular_function": "GO:0004222 metalloendopeptidase activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0030424 axon;GO:0043025 neuronal cell body;GO:0009897 external side of plasma membrane;GO:0043005 neuron projection",
        "go_biological_process": "GO:0006508 proteolysis;GO:0008584 male gonad development",
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        "protein_name": "Insulin-like growth factor 2 mRNA binding protein 3",
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        "refseq_ac": "NP_001359041",
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        "protein_names_uniprotkb": "Insulin-like growth factor 2 mRNA binding protein 3",
        "protein_names_refseq": "insulin-like growth factor 2 mRNA-binding protein 3; insulin-like growth factor 2, binding protein 3",
        "tax_id": 10116,
        "disease": "acquired metabolic disease (Disease Ontology:DOID:0060158)",
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        "publication_id_list": "22673903;23621518",
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        "function": "The overexpression of CD146 and/or IMP3 was proportionally correlated with shortened survival., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0003730 mRNA 3'-UTR binding;GO:0048027 mRNA 5'-UTR binding;GO:1990247 N6-methyladenosine-containing RNA reader activity;GO:0003723 RNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0000932 P-body;GO:0010494 cytoplasmic stress granule",
        "go_biological_process": "GO:0070934 CRD-mediated mRNA stabilization;GO:0006417 regulation of translation;GO:0007399 nervous system development;GO:0051028 mRNA transport",
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    },
    {
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        "length": 851,
        "protein_name": "NOP14 nucleolar protein",
        "gene_name": "Nop14",
        "organism": "Rat",
        "refseq_name": "",
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        "gene_names_uniprotkb": "Nop14",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "NOP14 nucleolar protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (rno:289724);  (R-RNO-6791226)",
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        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Involved in nucleolar processing of pre-18S ribosomal RNA. Has a role in the nuclear export of 40S pre-ribosomal subunit to the cytoplasm., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0019899 enzyme binding",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0030692 Noc4p-Nop14p complex;GO:0032040 small-subunit processome",
        "go_biological_process": "GO:0030490 maturation of SSU-rRNA;GO:0006364 rRNA processing",
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    {
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        "length": 164,
        "protein_name": "Ig-like domain-containing protein",
        "gene_name": "AABR07065813.1",
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        "gene_names_uniprotkb": "AABR07065813.1",
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        "pathway": " (R-RNO-173623);  (R-RNO-198933);  (R-RNO-202733);  (R-RNO-2029481);  (R-RNO-2029482);  (R-RNO-2029485);  (R-RNO-2168880);  (R-RNO-2454202);  (R-RNO-2730905);  (R-RNO-2871796);  (R-RNO-2871809);  (R-RNO-2871837);  (R-RNO-5690714);  (R-RNO-977606);  (R-RNO-983695)",
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        "go_molecular_function": "GO:0003823 antigen binding",
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        "uniprot_id": "A0A0G2K1A1_RAT",
        "mass": 8498.0,
        "length": 76,
        "protein_name": "Zinc finger protein 706",
        "gene_name": "Zfp706",
        "organism": "Rat",
        "refseq_name": "zinc finger protein 706",
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        "gene_names_refseq": "Zfp706; Znf706",
        "protein_names_uniprotkb": "Zinc finger protein 706",
        "protein_names_refseq": "zinc finger protein 706",
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        "pathway": " (R-RNO-212436)",
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        "function": "Transcription repressor involved in the exit of embryonic stem cells (ESCs) from self-renewal. Acts by repressing expression of KLF4., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm",
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    {
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        "length": 439,
        "protein_name": "Proline rich 33",
        "gene_name": "Prr33",
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        "refseq_name": "proline rich 33 isoform a",
        "refseq_ac": "NP_001419493",
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        "gene_names_refseq": "Prr33",
        "protein_names_uniprotkb": "Proline rich 33",
        "protein_names_refseq": "proline rich 33 isoform a; proline-rich protein 33",
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    },
    {
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        "protein_name": "Protein p13 MTCP-1",
        "gene_name": "Cmc4",
        "organism": "Rat",
        "refseq_name": "protein p13 MTCP-1",
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        "gene_names_uniprotkb": "Cmc4; LOC102546764; Mtcp1",
        "gene_names_refseq": "Mtcp1",
        "protein_names_uniprotkb": "Protein p13 MTCP-1; Mature T-cell proliferation-1 type B1",
        "protein_names_refseq": "protein p13 MTCP-1",
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        "function": "Enhances the phosphorylation and activation of AKT1 and AKT2., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0019901 protein kinase binding;GO:0043539 protein serine/threonine kinase activator activity",
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    },
    {
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        "length": 410,
        "protein_name": "G protein-coupled receptor, class C, group 5, member B",
        "gene_name": "Gprc5b",
        "organism": "Rat",
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        "gene_names_uniprotkb": "Gprc5b",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "G protein-coupled receptor, class C, group 5, member B",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0019901 protein kinase binding;GO:0030295 protein kinase activator activity;GO:0004860 protein kinase inhibitor activity;GO:1990782 protein tyrosine kinase binding",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0009986 cell surface;GO:0045121 membrane raft;GO:0070062 extracellular exosome;GO:0043235 receptor complex",
        "go_biological_process": "GO:0001934 positive regulation of protein phosphorylation;GO:0007626 locomotory behavior;GO:0010976 positive regulation of neuron projection development;GO:0035556 intracellular signal transduction;GO:0045860 positive regulation of protein kinase activity",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A0G2K620-1",
        "uniprot_id": "A0A0G2K620_RAT",
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        "length": 312,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or9g4",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr450",
        "refseq_ac": "NP_001000288",
        "gene_names_uniprotkb": "Or9g4",
        "gene_names_refseq": "Olr450; Or9g4; ratchr3-68788895-68787957_ORF",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 450; olfactory receptor Olr450; olfactory receptor gene Olr450",
        "tax_id": 10116,
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        "pathway": " (rno:295721)",
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        "class_list": "",
        "function": "Odorant receptor., [UniProtKB, UniProtKB]; Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "secondary_ac_list": "D4AA86",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A0G2K6W4-1",
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        "length": 257,
        "protein_name": "Transcription cofactor HES-6",
        "gene_name": "Hes6",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Hes6",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Transcription cofactor HES-6; Hairy and enhancer of split 6",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "coronary artery disease (Disease Ontology:DOID:3393); central nervous system cancer (Disease Ontology:DOID:3620)",
        "pathway": " (rno:316626)",
        "pathway_count": 1,
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        "publication_id_list": "",
        "class_list": "",
        "function": "Does not bind DNA itself but suppresses both HES1-mediated N box-dependent transcriptional repression and binding of HES1 to E box sequences. Also suppresses HES1-mediated inhibition of the heterodimer formed by ASCL1/MASH1 and TCF3/E47, allowing ASCL1 and TCF3 to up-regulate transcription in its presence. Promotes cell differentiation., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0003700 DNA-binding transcription factor activity;GO:0046983 protein dimerization activity;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005667 transcription regulator complex",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0007399 nervous system development;GO:0030154 cell differentiation",
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        "record_id": "A0A0G2K6W4-1",
        "record_type": "protein"
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        "length": 87,
        "protein_name": "RIKEN cDNA 1700020N01 gene like",
        "gene_name": "1700020N01Rikl",
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        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "1700020N01Rikl; LOC108349468",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "RIKEN cDNA 1700020N01 gene like",
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        "go_biological_process": "GO:0006355 regulation of DNA-templated transcription",
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        "record_id": "A0A0G2K861-1",
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        "length": 271,
        "protein_name": "Ubiquitin-conjugating enzyme E2 J2",
        "gene_name": "Ube2j2",
        "organism": "Rat",
        "refseq_name": "ubiquitin-conjugating enzyme E2 J2",
        "refseq_ac": "NP_001007656",
        "gene_names_uniprotkb": "Ube2j2",
        "gene_names_refseq": "Ube2j2",
        "protein_names_uniprotkb": "Ubiquitin-conjugating enzyme E2 J2; 2.3.2.23; Non-canonical ubiquitin-conjugating enzyme 2",
        "protein_names_refseq": "ubiquitin-conjugating enzyme E2 J2; ubiquitin-conjugating enzyme E2, J2 (UBC6 homolog, yeast)",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:298689);  (R-RNO-9609523);  (R-RNO-983168)",
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        "class_list": "",
        "function": "Catalyzes the covalent attachment of ubiquitin to other proteins. Seems to function in the selective degradation of misfolded membrane proteins from the endoplasmic reticulum (ERAD). In cooperation with the GATOR2 complex, catalyzes 'Lys-6'-linked ubiquitination of NPRL2., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005509 calcium ion binding;GO:0005112 Notch binding",
        "go_cellular_component": "GO:0005769 early endosome;GO:0005886 plasma membrane;GO:0030425 dendrite;GO:0043025 neuronal cell body",
        "go_biological_process": "GO:0007219 Notch signaling pathway;GO:0007220 Notch receptor processing;GO:0007417 central nervous system development;GO:0048741 skeletal muscle fiber development;GO:0010001 glial cell differentiation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A1W2Q656-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0MV40-1",
        "uniprot_id": "A0MV40_RAT",
        "mass": 21467.0,
        "length": 197,
        "protein_name": "Shisa family member 4",
        "gene_name": "Shisa4",
        "organism": "Rat",
        "refseq_name": "protein shisa-4 precursor",
        "refseq_ac": "NP_001071294",
        "gene_names_uniprotkb": "Shisa4",
        "gene_names_refseq": "Prmp; RGD1312041; Shisa4; Tmem58",
        "protein_names_uniprotkb": "Shisa family member 4",
        "protein_names_refseq": "proline rich membrane protein; protein shisa-4 precursor; protein shisa-4; shisa homolog 4; transmembrane protein 58",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:360848)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "17005852",
        "class_list": "",
        "function": "At the O4+ oligodendrocyte differentiation stage, a new proline-rich transmembrane protein, Prmp, is expressed. At the plasma membrane, Prmp displays adhesive properties that may link the extracellular matrix to the actin cytoskeleton., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "secondary_ac_list": "A6ICF0",
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        "go_cellular_component": "GO:0016020 membrane",
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        "record_id": "A0MV40-1",
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    },
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        "uniprot_canonical_ac": "A1L133-1",
        "uniprot_id": "A1L133_RAT",
        "mass": 18035.0,
        "length": 161,
        "protein_name": "Protein BTG1",
        "gene_name": "Btg1b",
        "organism": "Rat",
        "refseq_name": "Protein BTG1-like",
        "refseq_ac": "NP_001073365",
        "gene_names_uniprotkb": "Btg1b; LOC367975",
        "gene_names_refseq": "Btg1b",
        "protein_names_uniprotkb": "Protein BTG1; B-cell translocation gene 1 protein",
        "protein_names_refseq": "Protein BTG1-like",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:367975)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Anti-proliferative protein., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "biomarker_type": "",
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0008285 negative regulation of cell population proliferation",
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        "hit_score": 0.1,
        "record_id": "A1L133-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A5HKJ1-1",
        "uniprot_id": "A5HKJ1_RAT",
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        "length": 143,
        "protein_name": "Potassium voltage-gated channel subfamily E regulatory subunit 5",
        "gene_name": "Kcne5",
        "organism": "Rat",
        "refseq_name": "potassium voltage-gated channel subfamily E regulatory beta subunit 5",
        "refseq_ac": "NP_001094473",
        "gene_names_uniprotkb": "Kcne5; Kcne1l",
        "gene_names_refseq": "Kcne1l; Kcne5",
        "protein_names_uniprotkb": "Potassium voltage-gated channel subfamily E regulatory subunit 5",
        "protein_names_refseq": "KCNE1-like; potassium channel, voltage gated subfamily E regulatory beta subunit 5; potassium channel, voltage-gated Isk-related subfamily E regulatory beta subunit 5; potassium voltage-gated channel subfamily E member 1-like protein; potassium voltage-gated channel subfamily E regulatory beta subunit 5; potassium voltage-gated channel, Isk-related family, member 1-like; voltage-gated potassium channel accessory subunit 5",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:681190);  (R-RNO-5576890);  (R-RNO-5576893)",
        "pathway_count": 3,
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        "class_list": "",
        "function": "",
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0015459 potassium channel regulator activity;GO:0044325 transmembrane transporter binding;GO:0005249 voltage-gated potassium channel activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0008076 voltage-gated potassium channel complex",
        "go_biological_process": "GO:1901379 regulation of potassium ion transmembrane transport;GO:1901380 negative regulation of potassium ion transmembrane transport;GO:0086011 membrane repolarization during action potential;GO:0098915 membrane repolarization during ventricular cardiac muscle cell action potential;GO:1903765 negative regulation of potassium ion export across plasma membrane",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A5HKJ1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A7UJ12-1",
        "uniprot_id": "A7UJ12_RAT",
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        "length": 224,
        "protein_name": "Retinoschisin",
        "gene_name": "Rs1",
        "organism": "Rat",
        "refseq_name": "retinoschisin precursor",
        "refseq_ac": "NP_001098113",
        "gene_names_uniprotkb": "Rs1",
        "gene_names_refseq": "Rs1",
        "protein_names_uniprotkb": "Retinoschisin",
        "protein_names_refseq": "retinoschisin precursor",
        "tax_id": 10116,
        "disease": "X-linked juvenile retinoschisis 1 (Disease Ontology:DOID:0060763); retinoschisis (Disease Ontology:DOID:8465)",
        "pathway": " (rno:100125595)",
        "pathway_count": 1,
        "publication_count": 3,
        "publication_id_list": "34548657;36360232;38797343",
        "class_list": "",
        "function": "Binds negatively charged membrane lipids, such as phosphatidylserine and phosphoinositides. May play a role in cell-cell adhesion processes in the retina, via homomeric interaction between octamers present on the surface of two neighboring cells. Required for normal structure and function of the retina., [UniProtKB, UniProtKB, UniProtKB]; Retinoschisin Is Required for Pineal Gland Calcification and Cellular Communication in Pinealocytes of Rats and Mice., [RefSeq, PubMed]; Rs1h(-/y) exon 3-del rat model of X-linked retinoschisis with early onset and rapid phenotype is rescued by RS1 supplementation., [RefSeq, PubMed]; XLRS Rat with Rs1[-/Y] Exon-1-Del Shows Failure of Early Postnatal Outer Retina Development. Publication Status: Online-Only, [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "biomarker_type": "",
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        "binding_glycan_count": 0,
        "secondary_ac_list": "F1LSP1",
        "ec_number_list": "",
        "go_molecular_function": "GO:0010314 phosphatidylinositol-5-phosphate binding;GO:0005546 phosphatidylinositol-4,5-bisphosphate binding;GO:0005547 phosphatidylinositol-3,4,5-trisphosphate binding;GO:0043325 phosphatidylinositol-3,4-bisphosphate binding;GO:0044877 protein-containing complex binding",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0005615 extracellular space;GO:0009986 cell surface;GO:0009897 external side of plasma membrane;GO:0001917 photoreceptor inner segment",
        "go_biological_process": "GO:0007155 cell adhesion;GO:0051260 protein homooligomerization;GO:0007601 visual perception;GO:0010842 retina layer formation;GO:0001654 eye development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "A7UJ12-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "B0BMS9-1",
        "uniprot_id": "B0BMS9_RAT",
        "mass": 21481.0,
        "length": 186,
        "protein_name": "PRKR interacting protein 1",
        "gene_name": "Prkrip1",
        "organism": "Rat",
        "refseq_name": "PRKR-interacting protein 1",
        "refseq_ac": "NP_001092263",
        "gene_names_uniprotkb": "Prkrip1",
        "gene_names_refseq": "Prkrip1",
        "protein_names_uniprotkb": "PRKR interacting protein 1",
        "protein_names_refseq": "PRKR-interacting protein 1; Prkr interacting protein 1 (IL11 inducible)",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:498171);  (R-RNO-72163)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "29393594",
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        "function": "",
        "predicted_glycosites": 0,
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        "reported_c_glycosites_with_glycan": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0019901 protein kinase binding;GO:0004860 protein kinase inhibitor activity;GO:0003725 double-stranded RNA binding",
        "go_cellular_component": "GO:0005730 nucleolus;GO:0005829 cytosol;GO:0015629 actin cytoskeleton;GO:0005681 spliceosomal complex;GO:0071006 U2-type catalytic step 1 spliceosome",
        "go_biological_process": "GO:0006469 negative regulation of protein kinase activity;GO:0003014 renal system process;GO:0042326 negative regulation of phosphorylation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "B0BMS9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "B1H220-1",
        "uniprot_id": "B1H220_RAT",
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        "length": 517,
        "protein_name": "Zinc finger and BTB domain containing 3",
        "gene_name": "Zbtb3",
        "organism": "Rat",
        "refseq_name": "zinc finger and BTB domain-containing protein 3",
        "refseq_ac": "NP_001102632",
        "gene_names_uniprotkb": "Zbtb3",
        "gene_names_refseq": "RGD1561140; Zbtb3",
        "protein_names_uniprotkb": "Zinc finger and BTB domain containing 3",
        "protein_names_refseq": "zinc finger and BTB domain-containing protein 3",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:499313)",
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        "publication_count": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0008270 zinc ion binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
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        "record_id": "B1H220-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "B1WBQ1-1",
        "uniprot_id": "B1WBQ1_RAT",
        "mass": 53201.0,
        "length": 494,
        "protein_name": "Insulin receptor substrate 3",
        "gene_name": "Irs3",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Irs3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Insulin receptor substrate 3",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "intellectual disability (Disease Ontology:DOID:1059); amnestic disorder (Disease Ontology:DOID:10914); glucose metabolism disease (Disease Ontology:DOID:4194); type 2 diabetes mellitus (Disease Ontology:DOID:9352)",
        "pathway": "",
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005158 insulin receptor binding;GO:0043548 phosphatidylinositol 3-kinase binding;GO:0141038 phosphatidylinositol 3-kinase activator activity",
        "go_cellular_component": "GO:0005829 cytosol;GO:0005886 plasma membrane",
        "go_biological_process": "GO:0051897 positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction;GO:0008286 insulin receptor signaling pathway",
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        "hit_score": 0.1,
        "record_id": "B1WBQ1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "B1WBT3-1",
        "uniprot_id": "B1WBT3_RAT",
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        "protein_name": "BICD family-like cargo adapter 2",
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        "gene_names_uniprotkb": "Bicdl2",
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        "protein_names_uniprotkb": "BICD family-like cargo adapter 2; Bicaudal D-related protein 2; Coiled-coil domain-containing protein 64B",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (rno:302964)",
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        "go_molecular_function": "GO:0031267 small GTPase binding",
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        "length": 533,
        "protein_name": "Sodium-dependent lysophosphatidylcholine symporter 1",
        "gene_name": "Mfsd2a",
        "organism": "Rat",
        "refseq_name": "sodium-dependent lysophosphatidylcholine symporter 1 isoform X1",
        "refseq_ac": "XP_006238854",
        "gene_names_uniprotkb": "Mfsd2a",
        "gene_names_refseq": "Mfsd2a; Mfsd2; RGD1310174",
        "protein_names_uniprotkb": "Sodium-dependent lysophosphatidylcholine symporter 1; Major facilitator superfamily domain-containing protein 2A",
        "protein_names_refseq": "sodium-dependent lysophosphatidylcholine symporter 1 isoform X1",
        "tax_id": 10116,
        "disease": "primary autosomal recessive microcephaly 15 (Disease Ontology:DOID:0070277); microcephaly (Disease Ontology:DOID:10907)",
        "pathway": " (rno:298504);  (R-RNO-1483191)",
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        "go_molecular_function": "GO:0015245 fatty acid transmembrane transporter activity;GO:0051978 lysophospholipid:sodium symporter activity;GO:0005324 long-chain fatty acid transmembrane transporter activity;GO:0015293 symporter activity;GO:0140348 lysophosphatidylcholine flippase activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0005764 lysosome;GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0060042 retina morphogenesis in camera-type eye;GO:0051977 lysophospholipid transport;GO:1990379 lipid transport across blood-brain barrier;GO:0060856 establishment of blood-brain barrier;GO:0030307 positive regulation of cell growth",
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        "record_id": "B1WBW6-1",
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        "length": 291,
        "protein_name": "NKAP domain containing 1",
        "gene_name": "Nkapd1",
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        "refseq_name": "uncharacterized protein NKAPD1 isoform 4",
        "refseq_ac": "NP_001120975",
        "gene_names_uniprotkb": "Nkapd1; LOC100151767",
        "gene_names_refseq": "Nkapd1",
        "protein_names_uniprotkb": "NKAP domain containing 1",
        "protein_names_refseq": "uncharacterized protein C11orf57 homolog; uncharacterized protein NKAPD1 isoform 4",
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        "pathway": " (rno:100151767)",
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        "go_molecular_function": "GO:0042802 identical protein binding",
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        "record_id": "B1WC13-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "B1WC33-1",
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        "length": 350,
        "protein_name": "CDC42 effector protein 4",
        "gene_name": "Cdc42ep4",
        "organism": "Rat",
        "refseq_name": "cdc42 effector protein 4",
        "refseq_ac": "NP_001100533",
        "gene_names_uniprotkb": "Cdc42ep4",
        "gene_names_refseq": "Cdc42ep4",
        "protein_names_uniprotkb": "CDC42 effector protein 4",
        "protein_names_refseq": "CDC42 effector protein (Rho GTPase binding) 4; cdc42 effector protein 4",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:303653);  (R-RNO-9013149);  (R-RNO-9013404);  (R-RNO-9013406)",
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        "go_molecular_function": "GO:0031267 small GTPase binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005856 cytoskeleton;GO:0005886 plasma membrane;GO:0005912 adherens junction;GO:0015629 actin cytoskeleton",
        "go_biological_process": "GO:0007266 Rho protein signal transduction;GO:0008360 regulation of cell shape;GO:0031274 positive regulation of pseudopodium assembly;GO:0071346 cellular response to type II interferon;GO:0030838 positive regulation of actin filament polymerization",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "B1WC33-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "B1WCA0-1",
        "uniprot_id": "B1WCA0_RAT",
        "mass": 65683.0,
        "length": 598,
        "protein_name": "Protein phosphatase, Mg2+/Mn2+ dependent, 1D",
        "gene_name": "Ppm1d",
        "organism": "Rat",
        "refseq_name": "protein phosphatase 1D",
        "refseq_ac": "NP_001099295",
        "gene_names_uniprotkb": "Ppm1d",
        "gene_names_refseq": "Ppm1d; Wip1",
        "protein_names_uniprotkb": "Protein phosphatase, Mg2+/Mn2+ dependent, 1D",
        "protein_names_refseq": "p53-induced protein phosphatase 1; protein phosphatase 1D",
        "tax_id": 10116,
        "disease": "pre-malignant neoplasm (Disease Ontology:DOID:0060071); breast cancer (Disease Ontology:DOID:1612)",
        "pathway": " (rno:287585)",
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        "publication_id_list": "25791630;27207279;28780681;33417178",
        "class_list": "",
        "function": "Double immunofluorescence showed colocalization of Wip1 with NF-kappaB in LPS-stimulated primary astrocytes, which indicating a potential interaction between Wip1 with NF-kappaB signaling., [RefSeq, PubMed]; Suggest that downregulated Wip1 expression plays an important role in Mn-induced neuronal death in the brain striatum via the modulation of p53 signaling., [RefSeq, PubMed]; Wip1 Aggravates the Cerulein-Induced Cell Autophagy and Inflammatory Injury by Targeting STING/TBK1/IRF3 in Acute Pancreatitis., [RefSeq, PubMed]; Wip1 might participate in astrocyte activation in optic nerve (ON) injury-induced retinal neuroinflammation via regulating NF-kappaB signaling, which may be closely associated with ON injury, [RefSeq, PubMed]",
        "predicted_glycosites": 2,
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        "go_molecular_function": "GO:0046872 metal ion binding;GO:0051019 mitogen-activated protein kinase binding;GO:0004722 protein serine/threonine phosphatase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005829 cytosol",
        "go_biological_process": "GO:0000086 G2/M transition of mitotic cell cycle;GO:0009617 response to bacterium;GO:1902531 regulation of intracellular signal transduction;GO:0009267 cellular response to starvation;GO:0045814 negative regulation of gene expression, epigenetic",
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        "record_id": "B1WCA0-1",
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    },
    {
        "uniprot_canonical_ac": "B2GUZ7-1",
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        "length": 329,
        "protein_name": "Tubulin-specific chaperone C",
        "gene_name": "Tbcc",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Tbcc",
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        "protein_names_uniprotkb": "Tubulin-specific chaperone C; Tubulin-folding cofactor C",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:316221)",
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        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Tubulin-folding protein; involved in the final step of the tubulin folding pathway., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0003924 GTPase activity;GO:0005096 GTPase activator activity;GO:0015631 tubulin binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0032391 photoreceptor connecting cilium",
        "go_biological_process": "GO:0006457 protein folding;GO:0007021 tubulin complex assembly;GO:0007023 post-chaperonin tubulin folding pathway",
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        "record_id": "B2GUZ7-1",
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    {
        "uniprot_canonical_ac": "B2RZ65-1",
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        "length": 140,
        "protein_name": "NTF2-related export protein",
        "gene_name": "Nxt1",
        "organism": "Rat",
        "refseq_name": "NTF2-related export protein 1",
        "refseq_ac": "NP_001099991",
        "gene_names_uniprotkb": "Nxt1",
        "gene_names_refseq": "Nxt1",
        "protein_names_uniprotkb": "NTF2-related export protein",
        "protein_names_refseq": "NTF2-like export factor 1; NTF2-related export protein 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:296219);  (R-RNO-159236)",
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        "publication_count": 1,
        "publication_id_list": "35219094",
        "class_list": "",
        "function": "Genetic characterization of nuclear export factor NXT1 and its paralog NXT2 in primates and murine rodents., [RefSeq, PubMed]; Has a role in nuclear-cytoplasmic transport of proteins and mRNAs., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "go_molecular_function": "GO:0031267 small GTPase binding",
        "go_cellular_component": "GO:0042272 nuclear RNA export factor complex;GO:0005634 nucleus;GO:0005643 nuclear pore;GO:0005654 nucleoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0016973 poly(A)+ mRNA export from nucleus;GO:0006406 mRNA export from nucleus;GO:0006611 protein export from nucleus;GO:0006405 RNA export from nucleus",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "B2RZ65-1",
        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "B2RZ66-1",
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        "length": 144,
        "protein_name": "Signal recognition particle 19 kDa protein",
        "gene_name": "Srp19",
        "organism": "Rat",
        "refseq_name": "signal recognition particle 19 kDa protein",
        "refseq_ac": "NP_001099627",
        "gene_names_uniprotkb": "Srp19",
        "gene_names_refseq": "Srp19",
        "protein_names_uniprotkb": "Signal recognition particle 19 kDa protein",
        "protein_names_refseq": "signal recognition particle 19 kDa protein",
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        "class_list": "",
        "function": "Component of the signal recognition particle (SRP) complex, a ribonucleoprotein complex that mediates the cotranslational targeting of secretory and membrane proteins to the endoplasmic reticulum (ER). Binds directly to 7SL RNA. Mediates binding of SRP54 to the SRP complex., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0003723 RNA binding;GO:0043022 ribosome binding;GO:0008312 7S RNA binding",
        "go_cellular_component": "GO:0005786 signal recognition particle, endoplasmic reticulum targeting;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005829 cytosol;GO:0048500 signal recognition particle",
        "go_biological_process": "GO:0006617 SRP-dependent cotranslational protein targeting to membrane, signal sequence recognition;GO:0006614 SRP-dependent cotranslational protein targeting to membrane",
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    },
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        "uniprot_canonical_ac": "B3EY82-1",
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        "length": 175,
        "protein_name": "Lipocalin 8",
        "gene_name": "Lcn8",
        "organism": "Rat",
        "refseq_name": "epididymal-specific lipocalin-8 precursor",
        "refseq_ac": "NP_001121655",
        "gene_names_uniprotkb": "Lcn8",
        "gene_names_refseq": "Lcn8; RGD1306747",
        "protein_names_uniprotkb": "Lipocalin 8",
        "protein_names_refseq": "epididymal 17 kDa protein; epididymal-specific lipocalin-8 precursor; epididymal-specific lipocalin-8",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:366008)",
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        "biomarker_type": "",
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        "secondary_ac_list": "",
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        "go_molecular_function": "GO:0036094 small molecule binding",
        "go_cellular_component": "GO:0005576 extracellular region",
        "go_biological_process": "GO:0009725 response to hormone",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "B3EY82-1",
        "record_type": "protein"
    },
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        "mass": 105487.0,
        "length": 973,
        "protein_name": "Splicing regulator ARVCF",
        "gene_name": "Arvcf",
        "organism": "Rat",
        "refseq_name": "splicing regulator ARVCF",
        "refseq_ac": "NP_001124485",
        "gene_names_uniprotkb": "Arvcf",
        "gene_names_refseq": "Arvcf",
        "protein_names_uniprotkb": "Splicing regulator ARVCF; Armadillo repeat protein deleted in velo-cardio-facial syndrome homolog",
        "protein_names_refseq": "armadillo repeat gene deleted in velo-cardio-facial syndrome; armadillo repeat protein deleted in velo-cardio-facial syndrome homolog; armadillo repeat protein deleted in velo-cardio-facial syndrome; splicing regulator ARVCF",
        "tax_id": 10116,
        "disease": "autism spectrum disorder (Disease Ontology:DOID:0060041); DiGeorge syndrome (Disease Ontology:DOID:11198)",
        "pathway": " (rno:303798)",
        "pathway_count": 1,
        "publication_count": 3,
        "publication_id_list": "22673903;29445566;31384490",
        "class_list": "",
        "function": "Contributes to the regulation of alternative splicing of pre-mRNAs., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "biomarker_type": "",
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        "go_molecular_function": "GO:0045296 cadherin binding",
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        "go_biological_process": "GO:0006397 mRNA processing;GO:0098609 cell-cell adhesion;GO:0008380 RNA splicing",
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        "hit_score": 0.4,
        "record_id": "B4F7F3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "B5DEH9-1",
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        "length": 713,
        "protein_name": "Ankyrin repeat domain-containing protein 6",
        "gene_name": "Ankrd6",
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        "refseq_name": "ankyrin repeat domain-containing protein 6",
        "refseq_ac": "NP_001128441",
        "gene_names_uniprotkb": "Ankrd6",
        "gene_names_refseq": "Ankrd6",
        "protein_names_uniprotkb": "Ankyrin repeat domain-containing protein 6; Diversin",
        "protein_names_refseq": "ankyrin repeat domain-containing protein 6",
        "tax_id": 10116,
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        "pathway": " (rno:500430)",
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        "function": "Recruits CKI-epsilon to the beta-catenin degradation complex that consists of AXN1 or AXN2 and GSK3-beta and allows efficient phosphorylation of beta-catenin, thereby inhibiting beta-catenin/Tcf signals., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0090090 negative regulation of canonical Wnt signaling pathway;GO:2000096 positive regulation of Wnt signaling pathway, planar cell polarity pathway;GO:0030111 regulation of Wnt signaling pathway;GO:0007163 establishment or maintenance of cell polarity",
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    },
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        "length": 106,
        "protein_name": "NADH dehydrogenase [ubiquinone] iron-sulfur protein 5",
        "gene_name": "Ndufs5",
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        "refseq_name": "NADH dehydrogenase [ubiquinone] iron-sulfur protein 5",
        "refseq_ac": "NP_001025223",
        "gene_names_uniprotkb": "Ndufs5; LOC100363268; Ndufs5-ps2",
        "gene_names_refseq": "Ndufs5b; Ndufs5",
        "protein_names_uniprotkb": "NADH dehydrogenase [ubiquinone] iron-sulfur protein 5; Complex I-15 kDa; NADH-ubiquinone oxidoreductase 15 kDa subunit",
        "protein_names_refseq": "NADH dehydrogenase (ubiquinone) Fe-S protein 5b, 15kDa (NADH-coenzyme Q reductase); NADH dehydrogenase [ubiquinone] iron-sulfur protein 5",
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        "disease": "",
        "pathway": " (rno:362588);  (R-RNO-611105);  (R-RNO-6799198)",
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        "publication_id_list": "26446791;27213235",
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        "function": "Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone., [UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005743 mitochondrial inner membrane;GO:0005758 mitochondrial intermembrane space;GO:0045271 respiratory chain complex I",
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        "length": 225,
        "protein_name": "Small nuclear ribonucleoprotein polypeptide B2",
        "gene_name": "Snrpb2",
        "organism": "Rat",
        "refseq_name": "U2 small nuclear ribonucleoprotein B''",
        "refseq_ac": "NP_001102062",
        "gene_names_uniprotkb": "Snrpb2",
        "gene_names_refseq": "Snrpb2",
        "protein_names_uniprotkb": "Small nuclear ribonucleoprotein polypeptide B2",
        "protein_names_refseq": "U2 small nuclear ribonucleoprotein B''; U2 small nuclear ribonucleoprotein B; small nuclear ribonucleoprotein polypeptide B''",
        "tax_id": 10116,
        "disease": "disease of cellular proliferation (Disease Ontology:DOID:14566); germ cell cancer (Disease Ontology:DOID:2994); connective tissue disease (Disease Ontology:DOID:65)",
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    },
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        "length": 681,
        "protein_name": "F-box protein 34",
        "gene_name": "Fbxo34",
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        "refseq_name": "F-box only protein 34 isoform X1",
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        "gene_names_refseq": "Fbxo34",
        "protein_names_uniprotkb": "F-box protein 34",
        "protein_names_refseq": "F-box only protein 34 isoform X1",
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        "length": 280,
        "protein_name": "E2F-associated phosphoprotein",
        "gene_name": "Eapp",
        "organism": "Rat",
        "refseq_name": "E2F-associated phosphoprotein isoform 1",
        "refseq_ac": "NP_001128459",
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        "gene_names_refseq": "Eapp; RGD1309624",
        "protein_names_uniprotkb": "E2F-associated phosphoprotein",
        "protein_names_refseq": "E2F-associated phosphoprotein isoform 1",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0016607 nuclear speck",
        "go_biological_process": "GO:0008284 positive regulation of cell population proliferation;GO:0032968 positive regulation of transcription elongation by RNA polymerase II;GO:0034244 negative regulation of transcription elongation by RNA polymerase II",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "B5DF09-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "B5DF13-1",
        "uniprot_id": "B5DF13_RAT",
        "mass": 47357.0,
        "length": 403,
        "protein_name": "Tripartite motif-containing protein 59",
        "gene_name": "Trim59",
        "organism": "Rat",
        "refseq_name": "tripartite motif-containing protein 59",
        "refseq_ac": "NP_001102415",
        "gene_names_uniprotkb": "Trim59",
        "gene_names_refseq": "RGD1311956; Trim59",
        "protein_names_uniprotkb": "Tripartite motif-containing protein 59",
        "protein_names_refseq": "tripartite motif-containing protein 59",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:365813)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "37978515",
        "class_list": "",
        "function": "A role of TRIM59 in pulmonary hypertension: modulating the protein ubiquitylation modification. Publication Status: Online-Only, [RefSeq, PubMed]; E3 ubiquitin ligase involved in different processes such as development and immune response. Serves as a negative regulator for innate immune signaling pathways by suppressing RLR-induced activation of IRF3/7 and NF-kappa-B via interaction with adapter ECSIT. Regulates autophagy through modulating both the transcription and the ubiquitination of BECN1. On the one hand, regulates the transcription of BECN1 through negatively modulating the NF-kappa-B pathway. On the other hand, regulates TRAF6-mediated 'Lys-63'-linked ubiquitination of BECN1, thus affecting the formation of the BECN1-PIK3C3 complex. In addition, mediates 'Lys-48'-linked ubiquitination of TRAF6 and thereby promotes TRAF6 proteasomal degradation. Also acts as a critical regulator for early embryo development from blastocyst stage to gastrula through modulating F-actin assembly and WASH1 'Lys-63'-linked ubiquitination., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
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        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0061630 ubiquitin protein ligase activity",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0045087 innate immune response;GO:0043124 negative regulation of canonical NF-kappaB signal transduction;GO:0046597 host-mediated suppression of symbiont invasion",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "B5DF13-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "B5DF37-1",
        "uniprot_id": "B5DF37_RAT",
        "mass": 68038.0,
        "length": 623,
        "protein_name": "TAF6-like RNA polymerase II p300/CBP-associated factor-associated factor 65 kDa subunit 6L",
        "gene_name": "Taf6l",
        "organism": "Rat",
        "refseq_name": "TAF6-like RNA polymerase II p300/CBP-associated factor-associated factor 65 kDa subunit 6L",
        "refseq_ac": "NP_001101045",
        "gene_names_uniprotkb": "Taf6l",
        "gene_names_refseq": "Taf6l",
        "protein_names_uniprotkb": "TAF6-like RNA polymerase II p300/CBP-associated factor-associated factor 65 kDa subunit 6L; PCAF-associated factor 65-alpha",
        "protein_names_refseq": "TAF6-like RNA polymerase II p300/CBP-associated factor-associated factor 65 kDa subunit 6L; TAF6-like RNA polymerase II, p300/CBP-associated factor (PCAF)-associated factor",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:309194)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Functions as a component of the PCAF complex. The PCAF complex is capable of efficiently acetylating histones in a nucleosomal context. The PCAF complex could be considered as the human version of the yeast SAGA complex. With TAF5L, acts as an epigenetic regulator essential for somatic reprogramming. Regulates target genes through H3K9ac deposition and MYC recruitment which trigger MYC regulatory network to orchestrate gene expression programs to control embryonic stem cell state. Functions with MYC to activate target gene expression through RNA polymerase II pause release., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
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        "reported_phosphosites": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "F7F938",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003713 transcription coactivator activity;GO:0046982 protein heterodimerization activity;GO:0016251 RNA polymerase II general transcription initiation factor activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005669 transcription factor TFIID complex;GO:0000124 SAGA complex;GO:0046695 SLIK (SAGA-like) complex",
        "go_biological_process": "GO:0006355 regulation of DNA-templated transcription;GO:0051123 RNA polymerase II preinitiation complex assembly;GO:1904672 regulation of somatic stem cell population maintenance;GO:0006367 transcription initiation at RNA polymerase II promoter",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "B5DF37-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "B5DF55-1",
        "uniprot_id": "B5DF55_RAT",
        "mass": 59592.0,
        "length": 547,
        "protein_name": "Signal transducing adaptor molecule",
        "gene_name": "Stam",
        "organism": "Rat",
        "refseq_name": "signal transducing adapter molecule 1",
        "refseq_ac": "NP_001102591",
        "gene_names_uniprotkb": "Stam",
        "gene_names_refseq": "RGD1564499; Stam",
        "protein_names_uniprotkb": "Signal transducing adaptor molecule",
        "protein_names_refseq": "signal transducing adapter molecule 1; signal transducing adaptor molecule (SH3 domain and ITAM motif) 1",
        "tax_id": 10116,
        "disease": "polycystic kidney disease (Disease Ontology:DOID:0080322)",
        "pathway": " (rno:498798);  (R-RNO-182971);  (R-RNO-5689901);  (R-RNO-6807004);  (R-RNO-8856825);  (R-RNO-8856828);  (R-RNO-9013420);  (R-RNO-917729)",
        "pathway_count": 8,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Involved in intracellular signal transduction mediated by cytokines and growth factors. Upon IL-2 and GM-CSL stimulation, it plays a role in signaling leading to DNA synthesis and MYC induction. May also play a role in T-cell development. Involved in down-regulation of receptor tyrosine kinase via multivesicular body (MVBs) when complexed with HGS (ESCRT-0 complex). The ESCRT-0 complex binds ubiquitin and acts as a sorting machinery that recognizes ubiquitinated receptors and transfers them to further sequential lysosomal sorting/trafficking processes., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
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        "reported_phosphosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0035091 phosphatidylinositol binding;GO:0043130 ubiquitin binding;GO:0044389 ubiquitin-like protein ligase binding",
        "go_cellular_component": "GO:0033565 ESCRT-0 complex;GO:0031901 early endosome membrane",
        "go_biological_process": "GO:0036258 multivesicular body assembly;GO:0043328 protein transport to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway;GO:0016236 macroautophagy;GO:1903543 positive regulation of exosomal secretion;GO:1903551 regulation of extracellular exosome assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "B5DF55-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "B5DFF2-1",
        "uniprot_id": "RBPS2_RAT",
        "mass": 22701.0,
        "length": 210,
        "protein_name": "RNA binding protein, mRNA processing factor 2",
        "gene_name": "Rbpms2",
        "organism": "Rat",
        "refseq_name": "RNA binding protein, mRNA processing factor 2",
        "refseq_ac": "NP_001166897",
        "gene_names_uniprotkb": "Rbpms2",
        "gene_names_refseq": "RGD1561222; Rbpms2",
        "protein_names_uniprotkb": "RNA binding protein, mRNA processing factor 2; Rbpms2 protein",
        "protein_names_refseq": "RNA binding protein with multiple splicing 2; RNA binding protein, mRNA processing factor 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:503214)",
        "pathway_count": 1,
        "publication_count": 2,
        "publication_id_list": "16870336;31283468",
        "class_list": "",
        "function": "RNA-binding protein involved in the regulation of smooth muscle cell differentiation and proliferation in the gastrointestinal system (By similarity). Binds NOG mRNA, the major inhibitor of the bone morphogenetic protein (BMP) pathway. Mediates an increase of NOG mRNA levels, thereby contributing to the negative regulation of BMP signaling pathway and promoting reversible dedifferentiation and proliferation of smooth muscle cells (By similarity). Acts as a pre-mRNA alternative splicing regulator (PubMed:31283468). Mediates ACTN1 and FLNB alternative splicing (PubMed:31283468). Likely binds to mRNA tandem CAC trinucleotide or CA dinucleotide motifs (By similarity)., [UniProtKB, PubMed, UniProtKB, UniProtKB]; Specific expression of hermes in retinal ganglion cells qualifies this gene as a potential RGC marker in the retina., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_s_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
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        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "binding_glycan_count": 0,
        "secondary_ac_list": "F1M9N3",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003729 mRNA binding;GO:0042802 identical protein binding;GO:0042803 protein homodimerization activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0010494 cytoplasmic stress granule",
        "go_biological_process": "GO:0051151 negative regulation of smooth muscle cell differentiation;GO:0000381 regulation of alternative mRNA splicing, via spliceosome",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "B5DFF2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "B5DFG0-1",
        "uniprot_id": "B5DFG0_RAT",
        "mass": 27586.0,
        "length": 223,
        "protein_name": "Coiled-coil domain containing 70",
        "gene_name": "Ccdc70",
        "organism": "Rat",
        "refseq_name": "coiled-coil domain-containing protein 70",
        "refseq_ac": "NP_001407861",
        "gene_names_uniprotkb": "Ccdc70",
        "gene_names_refseq": "Ccdc70; RGD1559811",
        "protein_names_uniprotkb": "Coiled-coil domain containing 70",
        "protein_names_refseq": "coiled-coil domain-containing protein 70",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:498657)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
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        "total_n_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "B5DFG0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "B5DFG1-1",
        "uniprot_id": "PINK1_RAT",
        "mass": 63219.0,
        "length": 580,
        "protein_name": "Serine/threonine-protein kinase PINK1, mitochondrial",
        "gene_name": "Pink1",
        "organism": "Rat",
        "refseq_name": "serine/threonine-protein kinase PINK1, mitochondrial",
        "refseq_ac": "NP_001425048",
        "gene_names_uniprotkb": "Pink1",
        "gene_names_refseq": "Pink1",
        "protein_names_uniprotkb": "Serine/threonine-protein kinase PINK1, mitochondrial; 2.7.11.1; PTEN-induced putative kinase 1",
        "protein_names_refseq": "PTEN induced putative kinase 1; serine/threonine-protein kinase PINK1, mitochondrial",
        "tax_id": 10116,
        "disease": "Parkinson's disease 6 (Disease Ontology:DOID:0060369); early-onset Parkinson's disease (Disease Ontology:DOID:0060894); metabolic dysfunction-associated steatohepatitis (Disease Ontology:DOID:0080547); Parkinsonism (Disease Ontology:DOID:0080855); Hirschsprung's disease (Disease Ontology:DOID:10487); Parkinson's disease (Disease Ontology:DOID:14330); testicular cancer (Disease Ontology:DOID:2998)",
        "pathway": " (rno:298575);  (R-RNO-5205685)",
        "pathway_count": 2,
        "publication_count": 9,
        "publication_id_list": "29934347;31536960;36647045;38438964;38580154;38685371;38788061;39097918;40380818",
        "class_list": "",
        "function": "Activation of Pink1/Parkin-mediated mitochondrial autophagy alleviates exertional heat stroke-induced acute lung injury in rats., [RefSeq, PubMed]; Aging accelerates locomotor decline in PINK1 knockout rats in association with decreased nigral, but not striatal, dopamine and tyrosine hydroxylase expression., [RefSeq, PubMed]; Deciphering the neuroprotective mechanisms of RACK1 in cerebral ischemia-reperfusion injury: Pioneering insights into mitochondrial autophagy and the PINK1/Parkin axis., [RefSeq, PubMed]; Prodromal Parkinson disease signs are predicted by a whole-blood inflammatory transcriptional signature in young Pink1[-/-] rats. Publication Status: Online-Only, [RefSeq, PubMed]; Serine/threonine-protein kinase which acts as a sensor of mitochondrial damage and protects against mitochondrial dysfunction during cellular stress (By similarity). It phosphorylates mitochondrial proteins to coordinate mitochondrial quality control mechanisms that remove and replace dysfunctional mitochondrial components (By similarity). In healthy mitochondria, PINK1 is translocated across the mitochondrial outer membrane (MOM) via the translocase of the outer membrane (TOM) complex, and inserted into the mitochondrial inner membrane (MIM) via the translocase of the inner membrane (TIM23) complex where it is cleaved and released into the cytosol (By similarity). Depending on the severity of mitochondrial damage, activity ranges from preventing apoptosis and stimulating mitochondrial biogenesis to eliminating severely damaged mitochondria via PINK1-PRKN-dependent mitophagy (By similarity). When cellular stress results in irreversible mitochondrial damage, PINK1 accumulates at the outer mitochondrial membrane (OMM) where it phosphorylates pre-existing polyubiquitin chains at 'Ser-65', recruits PRKN from the cytosol to the OMM and activates PRKN by phosphorylation at 'Ser-65' (By similarity). Activated PRKN then ubiquitinates VDAC1 and other OMM proteins to initiate mitophagy (By similarity). The PINK1-PRKN pathway also promotes fission of damaged mitochondria by phosphorylating and thus promoting the PRKN-dependent degradation of mitochondrial proteins involved in fission such as MFN2 (By similarity). This prevents the refusion of unhealthy mitochondria with the mitochondrial network or initiates mitochondrial fragmentation facilitating their later engulfment by autophagosomes (By similarity). Also promotes mitochondrial fission independently of PRKN and ATG7-mediated mitophagy, via the phosphorylation and activation of DNM1L (By similarity). Regulates motility of damaged mitochondria by promoting the ubiquitination and subsequent degradation of MIRO1 and MIRO2; in motor neurons, this likely inhibits mitochondrial intracellular anterograde transport along the axons which probably increases the chance of the mitochondria undergoing mitophagy in the soma (By similarity). Required for ubiquinone reduction by mitochondrial complex I by mediating phosphorylation of complex I subunit NDUFA10 (By similarity). Phosphorylates LETM1, positively regulating its mitochondrial calcium transport activity (By similarity)., [UniProtKB, UniProtKB, UniProtKB]; Vocal and tongue exercise in early to mid-stage Parkinson disease using the Pink1-/- rat., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 1,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 1,
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        "total_n_glycosites": 0,
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        "reported_fully_resolved_glycans": 1,
        "reported_phosphosites": 2,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 0,
        "biomarker_type": "",
        "glycan_count": 1,
        "disease_count": 7,
        "glyco_site_count": 1,
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        "secondary_ac_list": "",
        "ec_number_list": "2.7.11.1;2.7.12.1;2.7.1.153;2.7.1.137;2.7.11.24;2.7.11.25;2.7.11.22;2.7.11.23;2.7.4.6;2.7.1.154;2.7.11.38;2.7.11.17;2.7.11.21;2.7.12.2;2.7.1.40;2.7.11.12;2.7.11.26;2.7.11.34;2.7.10.2;2.7.1.150;2.7.11.13;4.1.1.32;2.7.11.19;2.7.2.3;2.7.11.11;2.7.11.31;3.1.3.16;2.7.11.4;2.3.1.48;3.1.11.-;2.7.13.3;2.7.4.18;3.1.24.-;3.4.19.12;2.7.11.39;3.6.5.-;2.4.99.18;2.3.2.31;2.7.11.10",
        "go_molecular_function": "GO:0055131 C3HC4-type RING finger domain binding;GO:0000287 magnesium ion binding;GO:0002020 protease binding;GO:0004672 protein kinase activity;GO:0004674 protein serine/threonine kinase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005739 mitochondrion;GO:0005741 mitochondrial outer membrane;GO:0005743 mitochondrial inner membrane",
        "go_biological_process": "GO:1901525 negative regulation of mitophagy;GO:1902902 negative regulation of autophagosome assembly;GO:1903751 negative regulation of intrinsic apoptotic signaling pathway in response to hydrogen peroxide;GO:0001934 positive regulation of protein phosphorylation;GO:0002931 response to ischemia",
        "synthesized_glycan_count": 0,
        "hit_score": 1.2,
        "record_id": "B5DFG1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "B5DFI7-1",
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        "length": 383,
        "protein_name": "Glutaminyl-peptide cyclotransferase-like protein",
        "gene_name": "Qpctl",
        "organism": "Rat",
        "refseq_name": "glutaminyl-peptide cyclotransferase-like protein",
        "refseq_ac": "NP_001099700",
        "gene_names_uniprotkb": "Qpctl",
        "gene_names_refseq": "Qpctl; RGD1308128",
        "protein_names_uniprotkb": "Glutaminyl-peptide cyclotransferase-like protein; 2.3.2.5; Golgi-resident glutaminyl-peptide cyclotransferase; isoQC",
        "protein_names_refseq": "glutaminyl-peptide cyclotransferase-like protein",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:292687)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Responsible for the biosynthesis of pyroglutamyl peptides., [UniProtKB, UniProtKB]",
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        "secondary_ac_list": "",
        "ec_number_list": "2.3.2.5",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0016603 glutaminyl-peptide cyclotransferase activity",
        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005794 Golgi apparatus",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "B5DFI7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "B5DFK6-1",
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        "length": 1204,
        "protein_name": "AP-3 complex subunit delta-1",
        "gene_name": "Ap3d1",
        "organism": "Rat",
        "refseq_name": "AP-3 complex subunit delta-1",
        "refseq_ac": "NP_001094189",
        "gene_names_uniprotkb": "Ap3d1",
        "gene_names_refseq": "Ap3d1; Ap3d",
        "protein_names_uniprotkb": "AP-3 complex subunit delta-1; AP-3 complex subunit delta; Adaptor-related protein complex 3 subunit delta-1; Delta-adaptin",
        "protein_names_refseq": "AP-3 complex subunit delta-1; adaptor-related protein complex 3, delta 1 subunit; adaptor-related protein complex 3, delta subunit",
        "tax_id": 10116,
        "disease": "Hermansky-Pudlak syndrome 1 (Disease Ontology:DOID:0060539); Hermansky-Pudlak syndrome 2 (Disease Ontology:DOID:0060540); platelet storage pool deficiency (Disease Ontology:DOID:2223); Hermansky-Pudlak syndrome (Disease Ontology:DOID:3753)",
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        "function": "Part of the AP-3 complex, an adaptor-related complex which is not clathrin-associated. The complex is associated with the Golgi region as well as more peripheral structures. It facilitates the budding of vesicles from the Golgi membrane and may be directly involved in trafficking to lysosomes. Involved in process of CD8+ T-cell and NK cell degranulation. In concert with the BLOC-1 complex, AP-3 is required to target cargos into vesicles assembled at cell bodies for delivery into neurites and nerve terminals., [UniProtKB, UniProtKB, UniProtKB]",
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        "record_id": "B5DFK6-1",
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    },
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        "gene_name": "Bcas2",
        "organism": "Rat",
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        "refseq_ac": "NP_001099928",
        "gene_names_uniprotkb": "Bcas2",
        "gene_names_refseq": "Bcas2",
        "protein_names_uniprotkb": "Pre-mRNA-splicing factor SPF27",
        "protein_names_refseq": "breast carcinoma amplified sequence 2; pre-mRNA-splicing factor SPF27",
        "tax_id": 10116,
        "disease": "breast cancer (Disease Ontology:DOID:1612)",
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    },
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        "length": 305,
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        "refseq_name": "GS homeobox 2",
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        "gene_names_refseq": "Gsh2; Gsx2",
        "protein_names_uniprotkb": "GS homeobox 2",
        "protein_names_refseq": "GS homeobox 2; genomic screened homeo box 2 protein",
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:1990837 sequence-specific double-stranded DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0021544 subpallium development;GO:0006351 DNA-templated transcription;GO:0048714 positive regulation of oligodendrocyte differentiation;GO:0002087 regulation of respiratory gaseous exchange by nervous system process;GO:0007417 central nervous system development",
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    },
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        "length": 240,
        "protein_name": "SRY-box transcription factor 14",
        "gene_name": "Sox14",
        "organism": "Rat",
        "refseq_name": "transcription factor SOX-14",
        "refseq_ac": "NP_001100320",
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        "gene_names_refseq": "Sox14",
        "protein_names_uniprotkb": "SRY-box transcription factor 14",
        "protein_names_refseq": "SRY (sex determining region Y)-box 14; SRY box 14; SRY-box containing gene 14; transcription factor SOX-14",
        "tax_id": 10116,
        "disease": "intestinal cancer (Disease Ontology:DOID:10155)",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005667 transcription regulator complex",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0007420 brain development;GO:0007601 visual perception",
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        "record_id": "B7SZV3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3Z826-1",
        "uniprot_id": "D3Z826_RAT",
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        "length": 540,
        "protein_name": "G protein-coupled receptor 75",
        "gene_name": "Gpr75",
        "organism": "Rat",
        "refseq_name": "probable G-protein coupled receptor 75",
        "refseq_ac": "NP_001102566",
        "gene_names_uniprotkb": "Gpr75",
        "gene_names_refseq": "Gpr75",
        "protein_names_uniprotkb": "G protein-coupled receptor 75",
        "protein_names_refseq": "G protein-coupled receptor GPR75; probable G-protein coupled receptor 75",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0016493 C-C chemokine receptor activity",
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        "uniprot_canonical_ac": "D3Z8I4-1",
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        "length": 833,
        "protein_name": "Mitogen-activated protein kinase kinase kinase kinase",
        "gene_name": "Map4k1",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Map4k1",
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        "protein_names_uniprotkb": "Mitogen-activated protein kinase kinase kinase kinase; 2.7.11.1",
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        "tax_id": 10116,
        "disease": "ciliopathy (Disease Ontology:DOID:0060340); alcohol use disorder (Disease Ontology:DOID:1574); transient cerebral ischemia (Disease Ontology:DOID:224)",
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        "ec_number_list": "2.7.11.1;2.7.12.1;2.7.1.153;2.7.1.137;2.7.11.24;2.7.11.25;2.7.11.22;2.7.11.23;2.7.4.6;2.7.1.154;2.7.11.38;2.7.11.17;2.7.11.21;2.7.12.2;2.7.1.40;2.7.11.12;2.7.11.26;2.7.11.34;2.7.10.2;2.7.1.150;2.7.11.13;4.1.1.32;2.7.11.19;2.7.2.3;2.7.11.11;2.7.11.31;3.1.3.16;2.7.11.4;2.3.1.48;3.1.11.-;2.7.13.3;2.7.4.18;3.1.24.-;3.4.19.12;2.7.11.39;2.4.99.18;2.7.11.10",
        "go_molecular_function": "GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding;GO:0008349 MAP kinase kinase kinase kinase activity",
        "go_cellular_component": "GO:0005737 cytoplasm",
        "go_biological_process": "GO:0006468 protein phosphorylation;GO:0008283 cell population proliferation;GO:0035556 intracellular signal transduction;GO:0043410 positive regulation of MAPK cascade;GO:0007254 JNK cascade",
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        "record_type": "protein"
    },
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        "length": 65,
        "protein_name": "Stress-associated endoplasmic reticulum protein",
        "gene_name": "Serp2",
        "organism": "Rat",
        "refseq_name": "stress-associated endoplasmic reticulum protein 2",
        "refseq_ac": "NP_001381721",
        "gene_names_uniprotkb": "Serp2",
        "gene_names_refseq": "RGD1566076; Serp2",
        "protein_names_uniprotkb": "Stress-associated endoplasmic reticulum protein",
        "protein_names_refseq": "stress-associated endoplasmic reticulum protein 2",
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        "publication_id_list": "",
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        "function": "Interacts with target proteins during their translocation into the lumen of the endoplasmic reticulum. Protects unfolded target proteins against degradation during ER stress. May facilitate glycosylation of target proteins after termination of ER stress. May modulate the use of N-glycosylation sites on target proteins., [UniProtKB, UniProtKB, UniProtKB]; Interacts with target proteins during translocation into the lumen of the endoplasmic reticulum. Protects unfolded target proteins against degradation and facilitate correct glycosylation., [UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0006986 response to unfolded protein",
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        "hit_score": 0.1,
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    },
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        "uniprot_id": "D3Z916_RAT",
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        "length": 444,
        "protein_name": "Ubiquitin carboxyl-terminal hydrolase MINDY",
        "gene_name": "Mindy3",
        "organism": "Rat",
        "refseq_name": "ubiquitin carboxyl-terminal hydrolase MINDY-3",
        "refseq_ac": "NP_001099592",
        "gene_names_uniprotkb": "Mindy3; Fam188a",
        "gene_names_refseq": "Fam188a; Mindy3; RGD1309605",
        "protein_names_uniprotkb": "Ubiquitin carboxyl-terminal hydrolase MINDY; 3.4.19.12",
        "protein_names_refseq": "family with sequence similarity 188, member A; protein FAM188A; ubiquitin carboxyl-terminal hydrolase MINDY-3",
        "tax_id": 10116,
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        "pathway": " (rno:291320)",
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        "class_list": "",
        "function": "Hydrolase that can remove 'Lys-48'-linked conjugated ubiquitin from proteins., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0004843 cysteine-type deubiquitinase activity;GO:1990380 K48-linked deubiquitinase activity",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0031965 nuclear membrane",
        "go_biological_process": "GO:0006508 proteolysis;GO:0006915 apoptotic process;GO:0071108 protein K48-linked deubiquitination",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3Z916-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3Z939-1",
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        "length": 722,
        "protein_name": "Dpy-19 like 4",
        "gene_name": "Dpy19l4",
        "organism": "Rat",
        "refseq_name": "probable C-mannosyltransferase DPY19L4",
        "refseq_ac": "NP_001292209",
        "gene_names_uniprotkb": "Dpy19l4",
        "gene_names_refseq": "Dpy19l4; RGD1305828",
        "protein_names_uniprotkb": "Dpy-19 like 4",
        "protein_names_refseq": "probable C-mannosyltransferase DPY19L4; protein dpy-19 homolog 4",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:297824)",
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        "record_id": "D3Z939-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3Z952-1",
        "uniprot_id": "D3Z952_RAT",
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        "length": 185,
        "protein_name": "Microfibril associated protein 2",
        "gene_name": "Mfap2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Mfap2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Microfibril associated protein 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (rno:313662);  (R-RNO-1566948);  (R-RNO-2129379)",
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        "go_molecular_function": "GO:0001968 fibronectin binding;GO:0070051 fibrinogen binding",
        "go_cellular_component": "GO:0001527 microfibril",
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        "record_id": "D3Z952-1",
        "record_type": "protein"
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        "uniprot_id": "D3Z955_RAT",
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        "length": 621,
        "protein_name": "Phosphoglucomutase 2-like 1",
        "gene_name": "Pgm2l1",
        "organism": "Rat",
        "refseq_name": "glucose 1,6-bisphosphate synthase",
        "refseq_ac": "NP_001102924",
        "gene_names_uniprotkb": "Pgm2l1",
        "gene_names_refseq": "Pgm2l1",
        "protein_names_uniprotkb": "Phosphoglucomutase 2-like 1",
        "protein_names_refseq": "glucose 1,6-bisphosphate synthase",
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        "pathway": " (rno:685076);  (R-RNO-70171)",
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        "go_molecular_function": "GO:0046872 metal ion binding;GO:0004614 phosphoglucomutase activity;GO:0047933 glucose-1,6-bisphosphate synthase activity",
        "go_cellular_component": "GO:0005829 cytosol",
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        "record_id": "D3Z955-1",
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    },
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        "uniprot_canonical_ac": "D3Z9C2-1",
        "uniprot_id": "D3Z9C2_RAT",
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        "length": 335,
        "protein_name": "Family with sequence similarity 50, member B",
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        "organism": "Rat",
        "refseq_name": "protein FAM50B",
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        "gene_names_refseq": "Fam50b; RGD1563458",
        "protein_names_uniprotkb": "Family with sequence similarity 50, member B",
        "protein_names_refseq": "protein FAM50B",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0045171 intercellular bridge;GO:0030496 midbody",
        "go_biological_process": "GO:0006325 chromatin organization",
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        "hit_score": 0.1,
        "record_id": "D3Z9C2-1",
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    },
    {
        "uniprot_canonical_ac": "D3Z9F3-1",
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        "length": 312,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or5aq1",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr540",
        "refseq_ac": "NP_001000321",
        "gene_names_uniprotkb": "Or5aq1",
        "gene_names_refseq": "Olr540; Or5aq1",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 540; olfactory receptor Olr540; olfactory receptor gene Olr540",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:295792)",
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        "function": "Odorant receptor., [UniProtKB, UniProtKB]; Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding",
        "go_cellular_component": "GO:0005886 plasma membrane",
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        "hit_score": 0.1,
        "record_id": "D3Z9F3-1",
        "record_type": "protein"
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    {
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        "length": 197,
        "protein_name": "Cerebellin 3 precursor",
        "gene_name": "Cbln3",
        "organism": "Rat",
        "refseq_name": "cerebellin-3 precursor",
        "refseq_ac": "NP_001102800",
        "gene_names_uniprotkb": "Cbln3",
        "gene_names_refseq": "Cbln3; RGD1563731",
        "protein_names_uniprotkb": "Cerebellin 3 precursor",
        "protein_names_refseq": "cerebellin 3 precursor protein; cerebellin-3 precursor; cerebellin-3",
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        "pathway": " (rno:501998)",
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        "go_cellular_component": "GO:0005615 extracellular space;GO:0045202 synapse;GO:0043083 synaptic cleft;GO:0098688 parallel fiber to Purkinje cell synapse",
        "go_biological_process": "GO:0099558 maintenance of synapse structure;GO:0099550 trans-synaptic signaling, modulating synaptic transmission",
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    },
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        "length": 108,
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        "gene_name": "Coa3",
        "organism": "Rat",
        "refseq_name": "coiled-coil domain-containing protein 56",
        "refseq_ac": "NP_001102517",
        "gene_names_uniprotkb": "Coa3",
        "gene_names_refseq": "Ccdc56; Coa3; RGD1564337",
        "protein_names_uniprotkb": "Cytochrome c oxidase assembly factor 3",
        "protein_names_refseq": "coiled-coil domain containing 56; coiled-coil domain-containing protein 56",
        "tax_id": 10116,
        "disease": "mitochondrial complex IV deficiency nuclear type 14 (Disease Ontology:DOID:0070499)",
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        "publication_id_list": "29393594",
        "class_list": "",
        "function": "Core component of the MITRAC (mitochondrial translation regulation assembly intermediate of cytochrome c oxidase complex) complex, that regulates cytochrome c oxidase assembly. MITRAC complexes regulate both translation of mitochondrial encoded components and assembly of nuclear-encoded components imported in mitochondrion. Required for efficient translation of MT-CO1 and mitochondrial respiratory chain complex IV assembly., [UniProtKB, UniProtKB]; Required for assembly of cytochrome c oxidase (complex IV)., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0044183 protein folding chaperone",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005743 mitochondrial inner membrane",
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    },
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        "protein_name": "Solute carrier family 26 member 6",
        "gene_name": "Slc26a6",
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        "refseq_name": "solute carrier family 26 member 6 isoform X1",
        "refseq_ac": "XP_006243817",
        "gene_names_uniprotkb": "Slc26a6",
        "gene_names_refseq": "Slc26a6",
        "protein_names_uniprotkb": "Solute carrier family 26 member 6",
        "protein_names_refseq": "solute carrier family 26 member 6 isoform X1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:301010);  (R-RNO-427601)",
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        "go_molecular_function": "GO:0015499 formate transmembrane transporter activity;GO:0042802 identical protein binding;GO:0030165 PDZ domain binding;GO:0015562 efflux transmembrane transporter activity;GO:0005452 solute:inorganic anion antiporter activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane;GO:0016323 basolateral plasma membrane;GO:0016324 apical plasma membrane;GO:0031982 vesicle",
        "go_biological_process": "GO:0042045 epithelial fluid transport;GO:0015724 formate transport;GO:0015797 mannitol transmembrane transport;GO:0019532 oxalate transport;GO:0046724 oxalic acid secretion",
        "synthesized_glycan_count": 0,
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        "record_type": "protein"
    },
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        "protein_name": "Large ribosomal subunit protein mL54",
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        "organism": "Rat",
        "refseq_name": "large ribosomal subunit protein mL54",
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        "gene_names_refseq": "Mrpl54",
        "protein_names_uniprotkb": "Large ribosomal subunit protein mL54",
        "protein_names_refseq": "39S ribosomal protein L54, mitochondrial; large ribosomal subunit protein mL54",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:299628);  (R-RNO-5389840);  (R-RNO-5419276);  (R-RNO-9937383)",
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        "record_type": "protein"
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        "protein_name": "Glycerophosphodiester phosphodiesterase domain containing 2",
        "gene_name": "Gdpd2",
        "organism": "Rat",
        "refseq_name": "glycerophosphoinositol inositolphosphodiesterase GDPD2",
        "refseq_ac": "NP_001100414",
        "gene_names_uniprotkb": "Gdpd2",
        "gene_names_refseq": "Gdpd2; RGD1560780",
        "protein_names_uniprotkb": "Glycerophosphodiester phosphodiesterase domain containing 2",
        "protein_names_refseq": "glycerophosphoinositol inositolphosphodiesterase GDPD2",
        "tax_id": 10116,
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        "pathway": " (rno:302421)",
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        "go_molecular_function": "GO:0008889 glycerophosphodiester phosphodiesterase activity;GO:0004629 phospholipase C activity;GO:0008081 phosphoric diester hydrolase activity",
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        "go_biological_process": "GO:0006629 lipid metabolic process;GO:0045597 positive regulation of cell differentiation;GO:0070446 negative regulation of oligodendrocyte progenitor proliferation;GO:0007015 actin filament organization;GO:0009306 protein secretion",
        "synthesized_glycan_count": 0,
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        "record_id": "D3Z9K9-1",
        "record_type": "protein"
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        "length": 499,
        "protein_name": "Stabilizer of axonemal microtubules 5",
        "gene_name": "Saxo5",
        "organism": "Rat",
        "refseq_name": "stabilizer of axonemal microtubules 5",
        "refseq_ac": "NP_001102529",
        "gene_names_uniprotkb": "Saxo5; RGD1563425; Tex45",
        "gene_names_refseq": "RGD1563425; Saxo5; Tex45",
        "protein_names_uniprotkb": "Stabilizer of axonemal microtubules 5",
        "protein_names_refseq": "stabilizer of axonemal microtubules 5; testis expressed 45; testis-expressed protein 45; uncharacterized protein C19orf45 homolog",
        "tax_id": 10116,
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        "length": 435,
        "protein_name": "Transmembrane protease serine 4",
        "gene_name": "Tmprss4",
        "organism": "Rat",
        "refseq_name": "transmembrane protease serine 4",
        "refseq_ac": "NP_001102468",
        "gene_names_uniprotkb": "Tmprss4",
        "gene_names_refseq": "Tmprss4",
        "protein_names_uniprotkb": "Transmembrane protease serine 4",
        "protein_names_refseq": "transmembrane protease serine 4; transmembrane protease, serine 4",
        "tax_id": 10116,
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        "pathway": " (rno:367074)",
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        "function": "Plasma membrane-anchored serine protease that directly induces processing of pro-uPA/PLAU into the active form through proteolytic activity. Seems to be capable of activating ENaC., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0004252 serine-type endopeptidase activity;GO:0008236 serine-type peptidase activity",
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        "go_biological_process": "GO:0006508 proteolysis;GO:0016485 protein processing;GO:0009611 response to wounding;GO:0046598 positive regulation of viral entry into host cell;GO:0010468 regulation of gene expression",
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    {
        "uniprot_canonical_ac": "D3ZA02-1",
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        "length": 698,
        "protein_name": "Family with sequence similarity 13, member A",
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        "gene_names_uniprotkb": "Fam13a",
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        "protein_names_uniprotkb": "Family with sequence similarity 13, member A",
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        "disease": "chronic obstructive pulmonary disease (Disease Ontology:DOID:3083)",
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        "function": "Iron-sulfur cluster scaffold protein which can assemble [4Fe-4S] clusters and deliver them to target proteins., [UniProtKB, UniProtKB]",
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        "protein_name": "Olfactory receptor",
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        "gene_names_refseq": "Olr731; Or4c3e",
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        "protein_name": "Transcriptional regulator Kaiso",
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        "protein_names_uniprotkb": "Transcriptional regulator Kaiso; Zinc finger and BTB domain-containing protein 33",
        "protein_names_refseq": "transcriptional regulator Kaiso-like; transcriptional regulator Kaiso",
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        "protein_names_refseq": "dual specificity protein phosphatase 21",
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        "protein_names_refseq": "male specific lethal 1 homolog; male-specific lethal 1 homolog isoform 2",
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        "protein_name": "Ephrin type-A receptor 2",
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        "refseq_name": "ephrin type-A receptor 2 precursor",
        "refseq_ac": "NP_001102447",
        "gene_names_uniprotkb": "Epha2",
        "gene_names_refseq": "Epha2",
        "protein_names_uniprotkb": "Ephrin type-A receptor 2; 2.7.10.1",
        "protein_names_refseq": "ephrin receptor EphA2; ephrin type-A receptor 2 precursor; ephrin type-A receptor 2",
        "tax_id": 10116,
        "disease": "cataract 6 multiple types (Disease Ontology:DOID:0110229)",
        "pathway": " (rno:366492);  (R-RNO-2682334);  (R-RNO-3928663);  (R-RNO-3928665);  (R-RNO-9013149);  (R-RNO-9013404);  (R-RNO-9013408);  (R-RNO-9013420);  (R-RNO-9013423);  (R-RNO-9013424);  (R-RNO-9696264);  (R-RNO-9696270);  (R-RNO-9696273)",
        "pathway_count": 13,
        "publication_count": 5,
        "publication_id_list": "22673903;29901110;30986645;32721428;37904187",
        "class_list": "",
        "function": "High expression of EphA2 led to secondary injury by destruction of BBB integrity though the ROCK pathway after diffuse axonal injury., [RefSeq, PubMed]; MiR-141 inhibits glioma neovascularization by controlling EphA2 expression., [RefSeq, PubMed]; MiR-210 promotes bone formation in ovariectomized rats by regulating osteogenic/adipogenic differentiation of bone marrow mesenchymal stem cells through downregulation of EPHA2. Publication Status: Online-Only, [RefSeq, PubMed]; Our data indicate that EphA2 receptor plays an essential role in LPS-induced acute lung injury (ALI) and EphA2 antagonism has protective effects against LPS-induced ALI via Nrf2/HO-1, TLR4/MyD88 and RhoA/ROCK pathways.  These results suggest that antagonism of EphA2 may be an effective therapeutic strategy for the treatment of ALI., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
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        "mined_o_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "2.7.12.1;2.7.10.1;3.4.19.12;2.7.11.1;2.7.1.153;2.7.1.137;2.7.10.2;2.7.12.2;2.7.1.40;2.3.2.26;3.6.5.2;3.1.3.48;2.7.11.13;2.7.3.2;1.2.1.3;1.2.1.94;2.7.10.4;3.1.4.4;2.7.1.32;2.7.1.82;2.7.11.23;2.7.11.39;3.6.4.13;2.7.11.25;1.6.3.-;2.3.2.27;3.4.17.22",
        "go_molecular_function": "GO:0005524 ATP binding;GO:0019838 growth factor binding;GO:0004714 transmembrane receptor protein tyrosine kinase activity;GO:0005003 ephrin receptor activity;GO:0140677 molecular function activator activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0005925 focal adhesion;GO:0009986 cell surface;GO:0030027 lamellipodium;GO:0030054 cell junction",
        "go_biological_process": "GO:0030316 osteoclast differentiation;GO:0048570 notochord morphogenesis;GO:0046058 cAMP metabolic process;GO:0060035 notochord cell development;GO:1901491 negative regulation of lymphangiogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.6,
        "record_id": "D3ZBN3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZBP3-1",
        "uniprot_id": "D3ZBP3_RAT",
        "mass": 32690.0,
        "length": 293,
        "protein_name": "Exosome complex component RRP4",
        "gene_name": "Exosc2",
        "organism": "Rat",
        "refseq_name": "exosome complex component RRP4",
        "refseq_ac": "NP_001102422",
        "gene_names_uniprotkb": "Exosc2",
        "gene_names_refseq": "Exosc2",
        "protein_names_uniprotkb": "Exosome complex component RRP4; Exosome component 2; Ribosomal RNA-processing protein 4",
        "protein_names_refseq": "exosome complex component RRP4; exosome complex exonuclease RRP4",
        "tax_id": 10116,
        "disease": "short stature, hearing loss, retinitis pigmentosa, and distinctive facies (Disease Ontology:DOID:0081175); multiple myeloma (Disease Ontology:DOID:9538)",
        "pathway": " (rno:366017);  (R-RNO-429958);  (R-RNO-450385);  (R-RNO-450513);  (R-RNO-450604);  (R-RNO-6791226);  (R-RNO-9930044)",
        "pathway_count": 7,
        "publication_count": 1,
        "publication_id_list": "29393594",
        "class_list": "",
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        "predicted_glycosites": 1,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003723 RNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0006396 RNA processing;GO:0030307 positive regulation of cell growth;GO:0000956 nuclear-transcribed mRNA catabolic process;GO:0006401 RNA catabolic process;GO:0000467 exonucleolytic trimming to generate mature 3'-end of 5.8S rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA)",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D3ZBP3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZBQ1-1",
        "uniprot_id": "D3ZBQ1_RAT",
        "mass": 71198.0,
        "length": 672,
        "protein_name": "Forkhead box O3",
        "gene_name": "Foxo3",
        "organism": "Rat",
        "refseq_name": "forkhead box protein O3",
        "refseq_ac": "NP_001099865",
        "gene_names_uniprotkb": "Foxo3",
        "gene_names_refseq": "Fkhrl1; Foxo3a; Foxo3",
        "protein_names_uniprotkb": "Forkhead box O3",
        "protein_names_refseq": "forkhead box O3a; forkhead box protein O3",
        "tax_id": 10116,
        "disease": "prostate cancer (Disease Ontology:DOID:10283); Alzheimer's disease (Disease Ontology:DOID:10652); Parkinson's disease (Disease Ontology:DOID:14330); endometrial adenocarcinoma (Disease Ontology:DOID:2870); temporal lobe epilepsy (Disease Ontology:DOID:3328); dermoid cyst of ovary (Disease Ontology:DOID:5117); rheumatoid arthritis (Disease Ontology:DOID:7148); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (rno:294515);  (R-RNO-1181150);  (R-RNO-198693);  (R-RNO-5687128);  (R-RNO-9607240);  (R-RNO-9614399);  (R-RNO-9617629);  (R-RNO-9617828);  (R-RNO-9634638);  (R-RNO-9841251)",
        "pathway_count": 10,
        "publication_count": 9,
        "publication_id_list": "11875118;11964479;12027802;22673903;36922709;37018819;37267686;37534549;37585996",
        "class_list": "",
        "function": "As a target of FSH, E2 and IGF-I signaling in granulosa cells, FKHR likely coordinates numerous cell survival mechanisms., [RefSeq, PubMed]; Association of FOXO3A with right ventricular myocardial fibrosis and its detection by speckle-tracking echocardiography in pulmonary hypertension., [RefSeq, PubMed]; Decreased growth differentiation factor 9, bone morphogenetic protein 15, and forkhead box O3a expressions in the ovary via ulipristal acetate. Publication Status: Online-Only, [RefSeq, PubMed]; Energy stress modulation of AMPK/FoxO3 signaling inhibits mitochondria-associated ferroptosis., [RefSeq, PubMed]; FKHRL1 role in downregulation of HMG-CoA synthase., [RefSeq, PubMed]; Hippocampus mitochondrial MnSOD activation by a SIRT3 activator, honokiol, correlates with its deacetylation and upregulation of FoxO3a and PGC1alpha in a rat model of ammonia neurotoxicity., [RefSeq, PubMed]; Mechanism of myocardial fibrosis regulation by IGF-1R in atrial fibrillation through the PI3K/Akt/FoxO3a pathway., [RefSeq, PubMed]; Role for FOXO3a in inducing a delay in the G2-M phase in response to stress stimuli during which it contributes to the repair of damaged DNA by a Gadd45a-dependent mechanism., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "missing_score": 10000,
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        "ec_number_list": "",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0003700 DNA-binding transcription factor activity;GO:0019901 protein kinase binding;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific;GO:0000976 transcription cis-regulatory region binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005739 mitochondrion;GO:0005741 mitochondrial outer membrane",
        "go_biological_process": "GO:0001547 antral ovarian follicle growth;GO:0001544 initiation of primordial ovarian follicle growth;GO:1901300 positive regulation of hydrogen peroxide-mediated programmed cell death;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006357 regulation of transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
        "hit_score": 1.0,
        "record_id": "D3ZBQ1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZBS9-1",
        "uniprot_id": "D3ZBS9_RAT",
        "mass": 65924.0,
        "length": 590,
        "protein_name": "SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1",
        "gene_name": "Smarcd1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Smarcd1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "Coffin-Siris syndrome 11 (Disease Ontology:DOID:0112372); familial hyperlipidemia (Disease Ontology:DOID:1168); alcohol use disorder (Disease Ontology:DOID:1574); Coffin-Siris syndrome (Disease Ontology:DOID:1925)",
        "pathway": " (R-RNO-3214858);  (R-RNO-8939243);  (R-RNO-9933937);  (R-RNO-9933939);  (R-RNO-9933946);  (R-RNO-9933947);  (R-RNO-9934037)",
        "pathway_count": 7,
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        "predicted_glycosites": 1,
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        "go_molecular_function": "GO:0060090 molecular adaptor activity;GO:0003682 chromatin binding;GO:0005102 signaling receptor binding;GO:0003712 transcription coregulator activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0016514 SWI/SNF complex;GO:0071564 npBAF complex;GO:0071565 nBAF complex",
        "go_biological_process": "GO:0006338 chromatin remodeling;GO:0006357 regulation of transcription by RNA polymerase II;GO:0045815 transcription initiation-coupled chromatin remodeling;GO:0006337 nucleosome disassembly;GO:0071398 cellular response to fatty acid",
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    },
    {
        "uniprot_canonical_ac": "D3ZBX1-1",
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        "length": 314,
        "protein_name": "Galectin",
        "gene_name": "Lgals12",
        "organism": "Rat",
        "refseq_name": "galectin-12",
        "refseq_ac": "NP_001099803",
        "gene_names_uniprotkb": "Lgals12",
        "gene_names_refseq": "Lgals12",
        "protein_names_uniprotkb": "Galectin",
        "protein_names_refseq": "galectin-12; lectin, galactose binding, soluble 12; lectin, galactoside-binding, soluble, 12",
        "tax_id": 10116,
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        "pathway": " (rno:293710)",
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        "function": "Binds lactose. May participate in the apoptosis of adipocytes., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0030395 lactose binding;GO:0030246 carbohydrate binding",
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    {
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        "protein_name": "Protein dispatched homolog 2",
        "gene_name": "Disp2",
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        "refseq_name": "protein dispatched homolog 2",
        "refseq_ac": "NP_001101229",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane",
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    },
    {
        "uniprot_canonical_ac": "D3ZC01-1",
        "uniprot_id": "D3ZC01_RAT",
        "mass": 59050.0,
        "length": 538,
        "protein_name": "Retinoblastoma-binding protein 5",
        "gene_name": "Rbbp5",
        "organism": "Rat",
        "refseq_name": "retinoblastoma-binding protein 5 isoform 1",
        "refseq_ac": "NP_001100644",
        "gene_names_uniprotkb": "Rbbp5",
        "gene_names_refseq": "Rbbp5",
        "protein_names_uniprotkb": "Retinoblastoma-binding protein 5",
        "protein_names_refseq": "retinoblastoma-binding protein 5 isoform 1; retinoblastoma-binding protein 5",
        "tax_id": 10116,
        "disease": "congenital heart disease (Disease Ontology:DOID:1682)",
        "pathway": " (rno:304794);  (R-RNO-201722);  (R-RNO-3214841);  (R-RNO-3769402);  (R-RNO-8936459);  (R-RNO-8951664);  (R-RNO-9772755);  (R-RNO-9909649)",
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        "function": "In embryonic stem (ES) cells, plays a crucial role in the differentiation potential, particularly along the neural lineage, regulating gene induction and H3 'Lys-4' methylation at key developmental loci, including that mediated by retinoic acid. Does not affect ES cell self-renewal. Component or associated component of some histone methyltransferase complexes which regulates transcription through recruitment of those complexes to gene promoters. As part of the MLL1/MLL complex, involved in mono-, di- and trimethylation at 'Lys-4' of histone H3. Histone H3 'Lys-4' methylation represents a specific tag for epigenetic transcriptional activation. In association with ASH2L and WDR5, stimulates the histone methyltransferase activities of KMT2A, KMT2B, KMT2C, KMT2D, SETD1A and SETD1B., [UniProtKB, UniProtKB]",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0000976 transcription cis-regulatory region binding;GO:0042393 histone binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0035097 histone methyltransferase complex;GO:0044666 MLL3/4 complex",
        "go_biological_process": "GO:0006974 DNA damage response;GO:0045815 transcription initiation-coupled chromatin remodeling;GO:0043627 response to estrogen;GO:0010467 gene expression",
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        "record_type": "protein"
    },
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        "length": 740,
        "protein_name": "G2/M-phase specific E3 ubiquitin protein ligase",
        "gene_name": "G2e3",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "G2e3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "G2/M-phase specific E3 ubiquitin protein ligase",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0061630 ubiquitin protein ligase activity;GO:0140851 histone H3K14 ubiquitin ligase activity;GO:0004842 ubiquitin-protein transferase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005829 cytosol;GO:0005721 pericentric heterochromatin",
        "go_biological_process": "GO:0031508 pericentric heterochromatin formation;GO:0000209 protein polyubiquitination;GO:2001243 negative regulation of intrinsic apoptotic signaling pathway;GO:0034502 protein localization to chromosome;GO:0031507 heterochromatin formation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
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        "record_type": "protein"
    },
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        "protein_name": "Olfactory receptor",
        "gene_name": "Or5an9",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr329",
        "refseq_ac": "NP_001000251",
        "gene_names_uniprotkb": "Or5an9",
        "gene_names_refseq": "Olr329; Or5an9; ratchr1-215287476-215288417_ORF",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 329; olfactory receptor Olr329; olfactory receptor gene Olr329",
        "tax_id": 10116,
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        "pathway": " (rno:293773)",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding",
        "go_cellular_component": "GO:0005886 plasma membrane",
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        "gene_name": "B3gnt6",
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        "refseq_name": "acetylgalactosaminyl-O-glycosyl-glycoprotein beta-1,3-N-acetylglucosaminyltransferase",
        "refseq_ac": "NP_001099681",
        "gene_names_uniprotkb": "B3gnt6",
        "gene_names_refseq": "B3gnt6; RGD1310926",
        "protein_names_uniprotkb": "Hexosyltransferase; 2.4.1.-",
        "protein_names_refseq": "UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 (core 3 synthase); acetylgalactosaminyl-O-glycosyl-glycoprotein beta-1,3-N-acetylglucosaminyltransferase",
        "tax_id": 10116,
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        "ec_number_list": "2.4.1.-;2.4.1.206",
        "go_molecular_function": "GO:0008194 UDP-glycosyltransferase activity;GO:0008378 galactosyltransferase activity;GO:0008499 N-acetyl-beta-D-glucosaminide beta-(1,3)-galactosyltransferase activity",
        "go_cellular_component": "GO:0000139 Golgi membrane",
        "go_biological_process": "GO:0016266 protein O-linked glycosylation via N-acetyl-galactosamine;GO:0030311 poly-N-acetyllactosamine biosynthetic process",
        "synthesized_glycan_count": 897,
        "hit_score": 0.1,
        "record_id": "D3ZC66-1",
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    {
        "uniprot_canonical_ac": "D3ZC81-1",
        "uniprot_id": "D3ZC81_RAT",
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        "length": 324,
        "protein_name": "Peroxisome biogenesis factor 10",
        "gene_name": "Pex10",
        "organism": "Rat",
        "refseq_name": "peroxisome biogenesis factor 10",
        "refseq_ac": "NP_001102875",
        "gene_names_uniprotkb": "Pex10",
        "gene_names_refseq": "Pex10",
        "protein_names_uniprotkb": "Peroxisome biogenesis factor 10; 2.3.2.27; Peroxin-10; Peroxisomal biogenesis factor 10; Peroxisome assembly protein 10",
        "protein_names_refseq": "peroxisome biogenesis factor 10",
        "tax_id": 10116,
        "disease": "peroxisome biogenesis disorder 6A (Disease Ontology:DOID:0080481); Peroxisome biogenesis disorder 6B (Disease Ontology:DOID:0081435); peroxisomal disease (Disease Ontology:DOID:906)",
        "pathway": " (rno:680424);  (R-RNO-8866654);  (R-RNO-9033241)",
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        "function": "E3 ubiquitin-protein ligase component of a retrotranslocation channel required for peroxisome organization by mediating export of the PEX5 receptor from peroxisomes to the cytosol, thereby promoting PEX5 recycling. The retrotranslocation channel is composed of PEX2, PEX10 and PEX12; each subunit contributing transmembrane segments that coassemble into an open channel that specifically allows the passage of PEX5 through the peroxisomal membrane. PEX10 also regulates PEX5 recycling by acting as a E3 ubiquitin-protein ligase. When PEX5 recycling is compromised, PEX10 catalyzes polyubiquitination of PEX5 during its passage through the retrotranslocation channel, leading to its degradation., [UniProtKB, UniProtKB]",
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        "ec_number_list": "1.1.3.15;1.2.3.5;3.4.21.-;2.3.2.27;2.3.2.24;2.3.2.23;1.4.3.1;1.4.3.3;3.1.2.2;3.1.2.-;1.11.1.6;2.3.1.16;2.3.1.9;2.3.1.155;1.3.3.6;2.6.1.51;2.6.1.44;2.3.1.137;2.3.1.176;2.3.2.36;2.5.1.18;3.4.24.56;1.1.1.42;3.6.4.-;1.14.11.18;5.1.99.4;4.1.3.4;6.2.1.3;6.2.1.-;6.2.1.7;6.2.1.24;6.2.1.15;1.14.13.39;3.4.21.53;5.3.3.8;5.3.3.21;3.1.2.27;2.3.1.65;3.6.1.-;3.6.1.77;2.3.1.7;4.1.2.63;3.1.2.1;3.1.2.11;3.1.2.3;3.1.2.5;1.1.1.300;1.1.1.184;4.1.1.9;2.5.1.26;2.3.1.42;1.3.1.38;2.7.4.6;1.3.1.124",
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        "go_cellular_component": "GO:0005777 peroxisome;GO:0005778 peroxisomal membrane;GO:0000151 ubiquitin ligase complex",
        "go_biological_process": "GO:0007031 peroxisome organization;GO:0000209 protein polyubiquitination;GO:0034614 cellular response to reactive oxygen species;GO:0016558 protein import into peroxisome matrix;GO:0016562 protein import into peroxisome matrix, receptor recycling",
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        "protein_name": "Olfactory receptor",
        "gene_name": "Or4c120",
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        "refseq_name": "olfactory receptor Olr686",
        "refseq_ac": "NP_001000355",
        "gene_names_uniprotkb": "Or4c120",
        "gene_names_refseq": "Olr686; Or4c120",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "organism": "Rat",
        "refseq_name": "CD209 antigen-like protein E",
        "refseq_ac": "NP_001178934",
        "gene_names_uniprotkb": "Cd209e",
        "gene_names_refseq": "Cd209e; RGD1563333",
        "protein_names_uniprotkb": "CD209e molecule",
        "protein_names_refseq": "CD209 antigen-like protein E; CD209e antigen",
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        "disease": "extrapulmonary tuberculosis (Disease Ontology:DOID:0050598); rheumatic heart disease (Disease Ontology:DOID:0050827); Coronavirus infectious disease (Disease Ontology:DOID:0080599); bronchopulmonary dysplasia (Disease Ontology:DOID:11650); dengue disease (Disease Ontology:DOID:12205); dengue hemorrhagic fever (Disease Ontology:DOID:12206); aspergillosis (Disease Ontology:DOID:13564); asthma (Disease Ontology:DOID:2841); severe acute respiratory syndrome (Disease Ontology:DOID:2945); pulmonary tuberculosis (Disease Ontology:DOID:2957); tuberculosis (Disease Ontology:DOID:399); human immunodeficiency virus infectious disease (Disease Ontology:DOID:526); acquired immunodeficiency syndrome (Disease Ontology:DOID:635); pulmonary hypertension (Disease Ontology:DOID:6432)",
        "pathway": " (rno:501797)",
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        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0015252 proton channel activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:1902600 proton transmembrane transport",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZCS6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZCS9-1",
        "uniprot_id": "D3ZCS9_RAT",
        "mass": 16010.0,
        "length": 141,
        "protein_name": "5-hydroxyisourate hydrolase",
        "gene_name": "Urah",
        "organism": "Rat",
        "refseq_name": "5-hydroxyisourate hydrolase",
        "refseq_ac": "NP_001127979",
        "gene_names_uniprotkb": "Urah; RGD1309350",
        "gene_names_refseq": "RGD1309350; Urah",
        "protein_names_uniprotkb": "5-hydroxyisourate hydrolase; 3.5.2.17; HIU hydrolase; HIUHase",
        "protein_names_refseq": "5-hydroxyisourate hydrolase",
        "tax_id": 10116,
        "disease": "hyperuricemia (Disease Ontology:DOID:1920)",
        "pathway": " (rno:293613)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Catalyzes the hydrolysis of 5-hydroxyisourate (HIU) to 2-oxo-4-hydroxy-4-carboxy-5-ureidoimidazoline (OHCU)., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
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        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "3.5.2.17",
        "go_molecular_function": "GO:0033971 hydroxyisourate hydrolase activity",
        "go_cellular_component": "GO:0005777 peroxisome",
        "go_biological_process": "GO:0019628 urate catabolic process;GO:0006154 adenosine catabolic process;GO:0006157 deoxyadenosine catabolic process;GO:0006196 AMP catabolic process;GO:0009115 xanthine catabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZCS9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZCV6-1",
        "uniprot_id": "D3ZCV6_RAT",
        "mass": 312834.0,
        "length": 2902,
        "protein_name": "Otogelin",
        "gene_name": "Otog",
        "organism": "Rat",
        "refseq_name": "otogelin precursor",
        "refseq_ac": "NP_001099732",
        "gene_names_uniprotkb": "Otog",
        "gene_names_refseq": "Otog",
        "protein_names_uniprotkb": "Otogelin",
        "protein_names_refseq": "otogelin precursor",
        "tax_id": 10116,
        "disease": "autosomal recessive nonsyndromic deafness 18B (Disease Ontology:DOID:0110474)",
        "pathway": " (rno:292918)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Glycoprotein specific to acellular membranes of the inner ear. May be required for the anchoring of the otoconial membranes and cupulae to the underlying neuroepithelia in the vestibule. May be involved in the organization and/or stabilization of the fibrillar network that compose the tectorial membrane in the cochlea. May play a role in mechanotransduction processes., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 5,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 5,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 5,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005198 structural molecule activity;GO:0005201 extracellular matrix structural constituent;GO:0046556 alpha-L-arabinofuranosidase activity",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005829 cytosol;GO:0031012 extracellular matrix;GO:0016324 apical plasma membrane",
        "go_biological_process": "GO:0008344 adult locomotory behavior;GO:0007605 sensory perception of sound;GO:0008104 intracellular protein localization;GO:0060122 inner ear receptor cell stereocilium organization;GO:0046373 L-arabinose metabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZCV6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZD22-1",
        "uniprot_id": "D3ZD22_RAT",
        "mass": 27036.0,
        "length": 247,
        "protein_name": "Kallikrein related-peptidase 12",
        "gene_name": "Klk12",
        "organism": "Rat",
        "refseq_name": "kallikrein-12 precursor",
        "refseq_ac": "NP_001100978",
        "gene_names_uniprotkb": "Klk12",
        "gene_names_refseq": "Klk12; Klnk",
        "protein_names_uniprotkb": "Kallikrein related-peptidase 12",
        "protein_names_refseq": "kallikrein 12; kallikrein k; kallikrein-12 precursor",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:308564);  (R-RNO-6809371)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 0,
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        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "A0A1R3UCK1",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004252 serine-type endopeptidase activity;GO:0008233 peptidase activity;GO:0008236 serine-type peptidase activity",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0030141 secretory granule",
        "go_biological_process": "GO:0006508 proteolysis;GO:0051604 protein maturation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZD22-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZD44-1",
        "uniprot_id": "D3ZD44_RAT",
        "mass": 34836.0,
        "length": 310,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or5ar1",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr462",
        "refseq_ac": "NP_001000295",
        "gene_names_uniprotkb": "Or5ar1",
        "gene_names_refseq": "Olr462; Or5ar1",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 462; olfactory receptor Olr462; olfactory receptor gene Olr462",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:295732)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Odorant receptor., [UniProtKB, UniProtKB]; Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "reported_mutagensis": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0005507 copper ion binding;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0050907 detection of chemical stimulus involved in sensory perception",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZD44-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZDC2-1",
        "uniprot_id": "D3ZDC2_RAT",
        "mass": 62501.0,
        "length": 568,
        "protein_name": "Large neutral amino acids transporter small subunit 4",
        "gene_name": "Slc43a2",
        "organism": "Rat",
        "refseq_name": "large neutral amino acids transporter small subunit 4",
        "refseq_ac": "NP_001099282",
        "gene_names_uniprotkb": "Slc43a2",
        "gene_names_refseq": "RGD1305819; Slc43a2",
        "protein_names_uniprotkb": "Large neutral amino acids transporter small subunit 4; L-type amino acid transporter 4; Solute carrier family 43 member 2",
        "protein_names_refseq": "large neutral amino acids transporter small subunit 4; solute carrier family 43 (amino acid system L transporter), member 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:287532);  (R-RNO-352230)",
        "pathway_count": 2,
        "publication_count": 2,
        "publication_id_list": "16641100;22673903",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0015188 L-isoleucine transmembrane transporter activity;GO:0015179 L-amino acid transmembrane transporter activity;GO:0015175 neutral L-amino acid transmembrane transporter activity;GO:0015190 L-leucine transmembrane transporter activity;GO:0015191 L-methionine transmembrane transporter activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0016323 basolateral plasma membrane",
        "go_biological_process": "GO:0015820 L-leucine transport;GO:0015804 neutral amino acid transport;GO:0015807 L-amino acid transport;GO:0051956 negative regulation of amino acid transport;GO:0015823 phenylalanine transport",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "D3ZDC2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZDD6-1",
        "uniprot_id": "D3ZDD6_RAT",
        "mass": 10495.0,
        "length": 88,
        "protein_name": "Synaptonemal complex central element protein 3",
        "gene_name": "Syce3",
        "organism": "Rat",
        "refseq_name": "synaptonemal complex central element protein 3",
        "refseq_ac": "NP_001128725",
        "gene_names_uniprotkb": "Syce3",
        "gene_names_refseq": "Syce3",
        "protein_names_uniprotkb": "Synaptonemal complex central element protein 3",
        "protein_names_refseq": "synaptonemal complex central element protein 3",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:689933)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
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        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0000801 central element;GO:0005634 nucleus;GO:0005694 chromosome",
        "go_biological_process": "GO:0007283 spermatogenesis;GO:0043065 positive regulation of apoptotic process;GO:0007130 synaptonemal complex assembly;GO:0007131 reciprocal meiotic recombination",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZDD6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZDI7-1",
        "uniprot_id": "D3ZDI7_RAT",
        "mass": 56337.0,
        "length": 486,
        "protein_name": "Serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit",
        "gene_name": "Ppp2r5a",
        "organism": "Rat",
        "refseq_name": "serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit alpha isoform",
        "refseq_ac": "NP_001101361",
        "gene_names_uniprotkb": "Ppp2r5a",
        "gene_names_refseq": "Ppp2r5a",
        "protein_names_uniprotkb": "Serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit",
        "protein_names_refseq": "serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit alpha isoform",
        "tax_id": 10116,
        "disease": "cancer (Disease Ontology:DOID:162)",
        "pathway": " (rno:312754);  (R-RNO-141430);  (R-RNO-141444);  (R-RNO-195253);  (R-RNO-196299);  (R-RNO-2467813);  (R-RNO-2500257);  (R-RNO-389356);  (R-RNO-389513);  (R-RNO-432142);  (R-RNO-4641262);  (R-RNO-5663220);  (R-RNO-5673000);  (R-RNO-5675221);  (R-RNO-6811558);  (R-RNO-68877);  (R-RNO-9648025);  (R-RNO-9833482)",
        "pathway_count": 18,
        "publication_count": 3,
        "publication_id_list": "17700073;22673903;29393594",
        "class_list": "",
        "function": "The B regulatory subunit might modulate substrate selectivity and catalytic activity, and also might direct the localization of the catalytic enzyme to a particular subcellular compartment., [UniProtKB, UniProtKB, UniProtKB]; These findings suggest that activation of a PP2A isoform that contains the B56 alpha regulatory subunit is required for ischemia-induced cell death in kidney epithelial proximal tubule cells., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0019888 protein phosphatase regulator activity;GO:0019900 kinase binding;GO:0072542 protein phosphatase activator activity;GO:0019210 kinase inhibitor activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005813 centrosome;GO:0005829 cytosol;GO:0005886 plasma membrane",
        "go_biological_process": "GO:0007165 signal transduction;GO:1903077 negative regulation of protein localization to plasma membrane",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "D3ZDI7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZDI8-1",
        "uniprot_id": "PDE6B_RAT",
        "mass": 98492.0,
        "length": 856,
        "protein_name": "Rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit beta",
        "gene_name": "Pde6b",
        "organism": "Rat",
        "refseq_name": "rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit beta",
        "refseq_ac": "NP_001099494",
        "gene_names_uniprotkb": "Pde6b",
        "gene_names_refseq": "Pde6b",
        "protein_names_uniprotkb": "Rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit beta; 3.1.4.35",
        "protein_names_refseq": "phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide; phosphodiesterase 6B, cGMP-specific, rod, beta; rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit beta",
        "tax_id": 10116,
        "disease": "retinitis pigmentosa 40 (Disease Ontology:DOID:0110375); congenital stationary night blindness autosomal dominant 2 (Disease Ontology:DOID:0110863); retinitis pigmentosa (Disease Ontology:DOID:10584); retinal degeneration (Disease Ontology:DOID:8466)",
        "pathway": " (rno:289878);  (R-RNO-2485179);  (R-RNO-2514859);  (R-RNO-4086398)",
        "pathway_count": 4,
        "publication_count": 2,
        "publication_id_list": "1309771;31009522",
        "class_list": "",
        "function": "Catalytic beta subunit of the rod-specific cGMP phosphodiesterase (PDE6) complex, which hydrolyzes 3',5'-cyclic GMP in the phototransduction cascade. The PDE6 holoenzyme consists of two catalytic subunits (PDE6A and PDE6B) and two inhibitory gamma subunits (PDE6G). Light-activated GNAT1 relieves gamma subunit-mediated inhibition, enabling the catalytic subunits to hydrolyze cGMP and thereby mediate visual signal transduction and amplification. Decreased cytosolic cGMP levels result in closure of cGMP-gated cation channels at the plasma membrane, leading to rod photoreceptor hyperpolarization (By similarity). Involved in retinal circadian rhythm photoentrainment via modulation of UVA and orange light-induced phase-shift of the retina clock (By similarity)., [UniProtKB, UniProtKB, UniProtKB]; The Pde6b knockout rat exhibits photoreceptor degeneration. It may provide a better model for experimental therapy for retinitis pigmentosa because of its slower progression and larger anatomic architecture than the corresponding mouse model., [RefSeq, PubMed]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 4,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "3.1.4.-;3.1.4.35;3.1.4.17;3.6.1.1;3.6.1.25;3.6.1.14;3.1.4.53",
        "go_molecular_function": "GO:0046872 metal ion binding;GO:0047555 3',5'-cyclic-GMP phosphodiesterase activity;GO:0004115 3',5'-cyclic-AMP phosphodiesterase activity",
        "go_cellular_component": "GO:0001750 photoreceptor outer segment;GO:0042622 photoreceptor outer segment membrane",
        "go_biological_process": "GO:0009583 detection of light stimulus;GO:0007165 signal transduction;GO:0007601 visual perception;GO:0060041 retina development in camera-type eye;GO:1990009 retinal cell apoptotic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "D3ZDI8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZDM7-1",
        "uniprot_id": "OXDD_RAT",
        "mass": 37543.0,
        "length": 341,
        "protein_name": "D-aspartate oxidase",
        "gene_name": "Ddo",
        "organism": "Rat",
        "refseq_name": "D-aspartate oxidase precursor",
        "refseq_ac": "NP_001102935",
        "gene_names_uniprotkb": "Ddo; LOC100911156",
        "gene_names_refseq": "DASOX; DASPO; Ddo",
        "protein_names_uniprotkb": "D-aspartate oxidase; 1.4.3.1; DASOX; DASPO; DDO",
        "protein_names_refseq": "D-aspartate oxidase precursor",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:685325);  (R-RNO-389661);  (R-RNO-9033241)",
        "pathway_count": 3,
        "publication_count": 8,
        "publication_id_list": "12209855;1991137;22673903;25747990;29292239;29393594;32376478;7903300",
        "class_list": "",
        "function": "Selectively catalyzes the oxidative deamination of acidic amino acids (PubMed:1991137, PubMed:25747990, PubMed:29292239, PubMed:32376478). Suppresses the level of D-aspartate in the brain, an amino acid that can act as an agonist for glutamate receptors (By similarity). Protects the organism from the toxicity of D-amino acids (PubMed:7903300). May also function in the intestine (By similarity)., [UniProtKB, PubMed, PubMed, PubMed, PubMed, PubMed, UniProtKB]; Selectively catalyzes the oxidative deamination of acidic amino acids. Suppresses the level of D-aspartate in the brain, an amino acid that can act as an agonist for glutamate receptors. Protects the organism from the toxicity of D-amino acids. May also function in the intestine., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "reported_phosphosites": 0,
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        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "A6KTC0",
        "ec_number_list": "1.1.3.15;1.2.3.5;3.4.21.-;2.3.2.27;1.4.3.1;1.4.3.3;3.1.2.2;3.1.2.-;1.11.1.6;1.3.3.6;2.6.1.51;2.6.1.44;2.3.1.137;2.3.1.176;2.3.1.16;2.3.1.155;2.3.2.36;2.5.1.18;3.4.24.56;1.1.1.42;5.1.99.4;4.1.3.4;6.2.1.3;6.2.1.-;6.2.1.7;6.2.1.24;6.2.1.15;1.14.13.39;3.4.21.53;5.3.3.8;5.3.3.21;3.1.2.27;2.3.1.65;3.6.1.-;3.6.1.77;2.3.1.7;4.1.2.63;3.1.2.1;3.1.2.11;3.1.2.3;3.1.2.5;1.1.1.300;1.1.1.184;4.1.1.9;2.3.1.42;1.3.1.38;2.7.4.6;1.3.1.124",
        "go_molecular_function": "GO:0008445 D-aspartate oxidase activity;GO:0071949 FAD binding",
        "go_cellular_component": "GO:0005777 peroxisome;GO:0005782 peroxisomal matrix;GO:0005829 cytosol",
        "go_biological_process": "GO:0007320 insemination;GO:0019478 D-amino acid catabolic process;GO:0006533 L-aspartate catabolic process;GO:0050877 nervous system process;GO:0006531 aspartate metabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.9,
        "record_id": "D3ZDM7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZDN0-1",
        "uniprot_id": "D3ZDN0_RAT",
        "mass": 18343.0,
        "length": 159,
        "protein_name": "Uncharacterized protein",
        "gene_name": "AABR07040789.1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "AABR07040789.1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Uncharacterized protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
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        "class_list": "",
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        "predicted_n_glycosites": 0,
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        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZDN0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZDN6-1",
        "uniprot_id": "D3ZDN6_RAT",
        "mass": 37239.0,
        "length": 353,
        "protein_name": "Zinc finger protein 787",
        "gene_name": "Zfp787",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Zfp787",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger protein 787",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:365176)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
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        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "total_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0043565 sequence-specific DNA binding;GO:1990837 sequence-specific double-stranded DNA binding",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZDN6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZDP7-1",
        "uniprot_id": "D3ZDP7_RAT",
        "mass": 87837.0,
        "length": 836,
        "protein_name": "Neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adaptor 1",
        "gene_name": "Nyap1",
        "organism": "Rat",
        "refseq_name": "neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 1 isoform X1",
        "refseq_ac": "XP_006249206",
        "gene_names_uniprotkb": "Nyap1",
        "gene_names_refseq": "Nyap1; RGD1310964",
        "protein_names_uniprotkb": "Neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adaptor 1",
        "protein_names_refseq": "neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 1 isoform X1",
        "tax_id": 10116,
        "disease": "",
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        "class_list": "",
        "function": "",
        "predicted_glycosites": 3,
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        "reported_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 3,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "",
        "go_biological_process": "GO:0048812 neuron projection morphogenesis;GO:0043491 phosphatidylinositol 3-kinase/protein kinase B signal transduction",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZDP7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZDP9-1",
        "uniprot_id": "D3ZDP9_RAT",
        "mass": 118709.0,
        "length": 1052,
        "protein_name": "Zinc finger and BTB domain-containing protein 11",
        "gene_name": "Zbtb11",
        "organism": "Rat",
        "refseq_name": "zinc finger and BTB domain-containing protein 11",
        "refseq_ac": "NP_001100567",
        "gene_names_uniprotkb": "Zbtb11",
        "gene_names_refseq": "Zbtb11",
        "protein_names_uniprotkb": "Zinc finger and BTB domain-containing protein 11",
        "protein_names_refseq": "zinc finger and BTB domain-containing protein 11",
        "tax_id": 10116,
        "disease": "autosomal recessive intellectual developmental disorder 69 (Disease Ontology:DOID:0081230)",
        "pathway": " (rno:304010)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005730 nucleolus",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006355 regulation of DNA-templated transcription",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D3ZDP9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZE59-1",
        "uniprot_id": "D3ZE59_RAT",
        "mass": 38054.0,
        "length": 350,
        "protein_name": "Transmembrane protein 115",
        "gene_name": "Tmem115",
        "organism": "Rat",
        "refseq_name": "transmembrane protein 115",
        "refseq_ac": "NP_001102249",
        "gene_names_uniprotkb": "Tmem115",
        "gene_names_refseq": "RGD1310540; Tmem115",
        "protein_names_uniprotkb": "Transmembrane protein 115",
        "protein_names_refseq": "transmembrane protein 115",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:363136);  (R-RNO-6807878)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 1,
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        "biomarker_type": "",
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0042802 identical protein binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005794 Golgi apparatus;GO:0032580 Golgi cisterna membrane;GO:0017119 Golgi transport complex",
        "go_biological_process": "GO:0006890 retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D3ZE59-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZE72-1",
        "uniprot_id": "D3ZE72_RAT",
        "mass": 46803.0,
        "length": 418,
        "protein_name": "Methionine aminopeptidase",
        "gene_name": "Metap1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Metap1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Methionine aminopeptidase; 3.4.11.18",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:295500);  (R-RNO-2514859)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Cotranslationally removes the N-terminal methionine from nascent proteins. The N-terminal methionine is often cleaved when the second residue in the primary sequence is small and uncharged (Met-Ala-, Cys, Gly, Pro, Ser, Thr, or Val)., [UniProtKB, HAMAP, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "3.4.11.18",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0004177 aminopeptidase activity;GO:0070006 metalloaminopeptidase activity;GO:0004239 initiator methionyl aminopeptidase activity",
        "go_cellular_component": "GO:0005829 cytosol;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0006508 proteolysis;GO:0051604 protein maturation",
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        "hit_score": 0.1,
        "record_id": "D3ZE72-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZE94-1",
        "uniprot_id": "D3ZE94_RAT",
        "mass": 27879.0,
        "length": 256,
        "protein_name": "Ciliary microtubule associated protein 1A",
        "gene_name": "Cimap1a",
        "organism": "Rat",
        "refseq_name": "ciliary microtubule associated protein 1A isoform 2",
        "refseq_ac": "NP_001102394",
        "gene_names_uniprotkb": "Cimap1a; Odf3",
        "gene_names_refseq": "Cimap1a; Odf3",
        "protein_names_uniprotkb": "Ciliary microtubule associated protein 1A",
        "protein_names_refseq": "ciliary microtubule associated protein 1A isoform 2; outer dense fiber of sperm tails 3; outer dense fiber protein 3",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:365387)",
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        "go_cellular_component": "GO:0001520 outer dense fiber;GO:0005856 cytoskeleton;GO:0036126 sperm flagellum",
        "go_biological_process": "GO:0030317 flagellated sperm motility",
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        "record_id": "D3ZE94-1",
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    },
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        "length": 1136,
        "protein_name": "ubiquitinyl hydrolase 1",
        "gene_name": "Usp43",
        "organism": "Rat",
        "refseq_name": "ubiquitin carboxyl-terminal hydrolase 43 isoform X1",
        "refseq_ac": "XP_038940907",
        "gene_names_uniprotkb": "Usp43",
        "gene_names_refseq": "Usp43",
        "protein_names_uniprotkb": "ubiquitinyl hydrolase 1; 3.4.19.12",
        "protein_names_refseq": "ubiquitin carboxyl-terminal hydrolase 43 isoform X1",
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        "ec_number_list": "3.4.19.12",
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        "record_id": "D3ZED6-1",
        "record_type": "protein"
    },
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        "uniprot_canonical_ac": "D3ZEE4-1",
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        "length": 577,
        "protein_name": "Plexin domain containing 1",
        "gene_name": "Plxdc1",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Plxdc1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Plexin domain containing 1",
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        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005886 plasma membrane;GO:0030425 dendrite;GO:0043025 neuronal cell body;GO:0043235 receptor complex",
        "go_biological_process": "GO:0021510 spinal cord development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZEE4-1",
        "record_type": "protein"
    },
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        "uniprot_canonical_ac": "D3ZEF1-1",
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        "length": 313,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or14a260",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr14",
        "refseq_ac": "NP_001000695",
        "gene_names_uniprotkb": "Or14a260",
        "gene_names_refseq": "Olr14; Or14a260",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 14A2-like; olfactory receptor Olr14; olfactory receptor gene Olr14",
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        "function": "Odorant receptor., [UniProtKB, UniProtKB]; Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZEF1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZEF9-1",
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        "length": 397,
        "protein_name": "Hexosyltransferase",
        "gene_name": "B3gnt2",
        "organism": "Rat",
        "refseq_name": "N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2",
        "refseq_ac": "NP_001100710",
        "gene_names_uniprotkb": "B3gnt2",
        "gene_names_refseq": "B3gnt1; B3gnt2",
        "protein_names_uniprotkb": "Hexosyltransferase; 2.4.1.-",
        "protein_names_refseq": "N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2; UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:305571);  (R-RNO-2022854);  (R-RNO-913709)",
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "2.4.1.-;2.4.1.206",
        "go_molecular_function": "GO:0008532 N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase activity",
        "go_cellular_component": "GO:0000139 Golgi membrane",
        "go_biological_process": "GO:0009101 glycoprotein biosynthetic process;GO:0030311 poly-N-acetyllactosamine biosynthetic process",
        "synthesized_glycan_count": 1159,
        "hit_score": 0.2,
        "record_id": "D3ZEF9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZEG0-1",
        "uniprot_id": "D3ZEG0_RAT",
        "mass": 26654.0,
        "length": 254,
        "protein_name": "Histone H1.8",
        "gene_name": "H1f8",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "H1f8; H1foo",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Histone H1.8; Histone H1oo; Oocyte-specific histone H1; Oocyte-specific linker histone H1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:502875)",
        "pathway_count": 1,
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        "publication_id_list": "",
        "class_list": "",
        "function": "May play a key role in the control of gene expression during oogenesis and early embryogenesis, presumably through the perturbation of chromatin structure. Essential for meiotic maturation of germinal vesicle-stage oocytes. The somatic type linker histone H1c is rapidly replaced by H1oo in a donor nucleus transplanted into an oocyte. The greater mobility of H1oo as compared to H1c may contribute to this rapid replacement and increased instability of the embryonic chromatin structure. The rapid replacement of H1c with H1oo may play an important role in nuclear remodeling., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003690 double-stranded DNA binding;GO:0031492 nucleosomal DNA binding;GO:0030527 structural constituent of chromatin",
        "go_cellular_component": "GO:0005634 nucleus;GO:0000786 nucleosome",
        "go_biological_process": "GO:0006334 nucleosome assembly;GO:0030261 chromosome condensation;GO:0040029 epigenetic regulation of gene expression;GO:0045910 negative regulation of DNA recombination",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZEG0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZEP2-1",
        "uniprot_id": "D3ZEP2_RAT",
        "mass": 14700.0,
        "length": 131,
        "protein_name": "Norrin",
        "gene_name": "Ndp",
        "organism": "Rat",
        "refseq_name": "norrin precursor",
        "refseq_ac": "NP_001102284",
        "gene_names_uniprotkb": "Ndp",
        "gene_names_refseq": "Ndph; Ndp; RGD1563968",
        "protein_names_uniprotkb": "Norrin",
        "protein_names_refseq": "NDP, norrin cystine knot growth factor; Norrie disease (pseudoglioma); Norrie disease homolog; norrin precursor; norrin-like; norrin",
        "tax_id": 10116,
        "disease": "exudative vitreoretinopathy (Disease Ontology:DOID:0050535); Norrie disease (Disease Ontology:DOID:0060844); X-linked exudative vitreoretinopathy 2 (Disease Ontology:DOID:0111413); retinopathy of prematurity (Disease Ontology:DOID:13025)",
        "pathway": " (rno:363443)",
        "pathway_count": 1,
        "publication_count": 4,
        "publication_id_list": "21899531;25188337;25550365;29933759",
        "class_list": "",
        "function": "Activates the canonical Wnt signaling pathway through FZD4 and LRP5 coreceptor. Plays a central role in retinal vascularization by acting as a ligand for FZD4 that signals via stabilizing beta-catenin (CTNNB1) and activating LEF/TCF-mediated transcriptional programs. Acts in concert with TSPAN12 to activate FZD4 independently of the Wnt-dependent activation of FZD4, suggesting the existence of a Wnt-independent signaling that also promote accumulation the beta-catenin (CTNNB1). May be involved in a pathway that regulates neural cell differentiation and proliferation. Possible role in neuroectodermal cell-cell interaction., [UniProtKB, UniProtKB, UniProtKB]; Norrin might regulate the decidual reaction and the placental angiogenesis along with the survival and the differentiation of luminal and glandular epithelial and decidual cells in rats., [RefSeq, PubMed]; Norrin upregulation protected blood-brain barrier integrity and improved outcome after subarachnoid hemorrhage., [RefSeq, PubMed]; Studied the influence of dendrobium nobile Lindley (DNL) extract and its bibenzyl component moscatilin on the expression of placental growth factor (PLGF) and Norrie disease protein (NDP) in hypoxia model in retinal cells. Found DNL and moscatilin are able to protect against retinal ischemic/hypoxic changes respectively by downregulating PLGF and upregulating NDP. Publication Status: Online-Only, [RefSeq, PubMed]; The endogenously expressed Lgr4 may act as an antagonist molecule that helps to fine-tune the R-spondin/norrin-mediated Lgr4-Wnt signaling during gonadal development. Publication Status: Online-Only, [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
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        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 4,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005109 frizzled binding;GO:0042803 protein homodimerization activity;GO:0005125 cytokine activity",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0009986 cell surface",
        "go_biological_process": "GO:0060042 retina morphogenesis in camera-type eye;GO:0060856 establishment of blood-brain barrier;GO:0000278 mitotic cell cycle;GO:0001525 angiogenesis;GO:0003407 neural retina development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.5,
        "record_id": "D3ZEP2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZES1-1",
        "uniprot_id": "D3ZES1_RAT",
        "mass": 18879.0,
        "length": 168,
        "protein_name": "ADP-ribosylation factor like GTPase 5C",
        "gene_name": "Arl5c",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Arl5c",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "ADP-ribosylation factor like GTPase 5C",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:497990)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003924 GTPase activity;GO:0005525 GTP binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005802 trans-Golgi network",
        "go_biological_process": "GO:0006886 intracellular protein transport;GO:0016192 vesicle-mediated transport;GO:1903292 protein localization to Golgi membrane",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZES1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZF11-1",
        "uniprot_id": "D3ZF11_RAT",
        "mass": 16390.0,
        "length": 156,
        "protein_name": "Ragulator complex protein LAMTOR5",
        "gene_name": "Lamtor5",
        "organism": "Rat",
        "refseq_name": "ragulator complex protein LAMTOR5",
        "refseq_ac": "NP_001099932",
        "gene_names_uniprotkb": "Lamtor5",
        "gene_names_refseq": "Hbxip; Lamtor5",
        "protein_names_uniprotkb": "Ragulator complex protein LAMTOR5; Late endosomal/lysosomal adaptor and MAPK and MTOR activator 5",
        "protein_names_refseq": "hepatitis B virus x interacting protein; ragulator complex protein LAMTOR5",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:295357);  (R-RNO-1632852);  (R-RNO-165159);  (R-RNO-166208);  (R-RNO-380972);  (R-RNO-5628897);  (R-RNO-8943724);  (R-RNO-9639288)",
        "pathway_count": 8,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "As part of the Ragulator complex it is involved in amino acid sensing and activation of mTORC1, a signaling complex promoting cell growth in response to growth factors, energy levels, and amino acids. Activated by amino acids through a mechanism involving the lysosomal V-ATPase, the Ragulator plays a dual role for the small GTPases Rag (RagA/RRAGA, RagB/RRAGB, RagC/RRAGC and/or RagD/RRAGD): it (1) acts as a guanine nucleotide exchange factor (GEF), activating the small GTPases Rag and (2) mediates recruitment of Rag GTPases to the lysosome membrane. Activated Ragulator and Rag GTPases function as a scaffold recruiting mTORC1 to lysosomes where it is in turn activated. When complexed to BIRC5, interferes with apoptosome assembly, preventing recruitment of pro-caspase-9 to oligomerized APAF1, thereby selectively suppressing apoptosis initiated via the mitochondrial/cytochrome c pathway., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005829 cytosol;GO:0005764 lysosome;GO:0005765 lysosomal membrane;GO:0032991 protein-containing complex;GO:0071986 Ragulator complex",
        "go_biological_process": "GO:1904263 positive regulation of TORC1 signaling;GO:0010628 positive regulation of gene expression;GO:0043066 negative regulation of apoptotic process;GO:0043123 positive regulation of canonical NF-kappaB signal transduction;GO:0032008 positive regulation of TOR signaling",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZF11-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZF19-1",
        "uniprot_id": "D3ZF19_RAT",
        "mass": 37796.0,
        "length": 329,
        "protein_name": "Transmembrane protein 68",
        "gene_name": "Tmem68",
        "organism": "Rat",
        "refseq_name": "DGAT1/2-independent enzyme synthesizing storage lipids isoform a",
        "refseq_ac": "NP_001101373",
        "gene_names_uniprotkb": "Tmem68",
        "gene_names_refseq": "RGD1309006; Tmem68",
        "protein_names_uniprotkb": "Transmembrane protein 68",
        "protein_names_refseq": "DGAT1/2-independent enzyme synthesizing storage lipids isoform a; DGAT1/2-independent enzyme synthesizing storage lipids",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:312946)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0046027 phospholipid:diacylglycerol acyltransferase activity",
        "go_cellular_component": "GO:0016020 membrane;GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0019432 triglyceride biosynthetic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZF19-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZF25-1",
        "uniprot_id": "D3ZF25_RAT",
        "mass": 35704.0,
        "length": 330,
        "protein_name": "Ring finger protein 225",
        "gene_name": "Rnf225",
        "organism": "Rat",
        "refseq_name": "RING finger protein 225",
        "refseq_ac": "NP_001102804",
        "gene_names_uniprotkb": "Rnf225; RGD1561909",
        "gene_names_refseq": "RGD1561909; Rnf225",
        "protein_names_uniprotkb": "Ring finger protein 225",
        "protein_names_refseq": "RING finger protein 225",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:502300)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0061630 ubiquitin protein ligase activity",
        "go_cellular_component": "",
        "go_biological_process": "GO:0016567 protein ubiquitination",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZF25-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZF97-1",
        "uniprot_id": "D3ZF97_RAT",
        "mass": 54666.0,
        "length": 482,
        "protein_name": "Endoplasmic reticulum lectin",
        "gene_name": "Erlec1",
        "organism": "Rat",
        "refseq_name": "endoplasmic reticulum lectin 1 precursor",
        "refseq_ac": "NP_001099493",
        "gene_names_uniprotkb": "Erlec1",
        "gene_names_refseq": "Erlec1; RGD1306508",
        "protein_names_uniprotkb": "Endoplasmic reticulum lectin",
        "protein_names_refseq": "endoplasmic reticulum lectin 1 precursor",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:289874);  (R-RNO-382556);  (R-RNO-5358346);  (R-RNO-9931269)",
        "pathway_count": 4,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Lectin involved in the quality control of the secretory pathway. As a member of the endoplasmic reticulum-associated degradation lumenal (ERAD-L) surveillance system, targets misfolded endoplasmic reticulum lumenal glycoproteins for degradation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Probable lectin that binds selectively to improperly folded lumenal proteins. May function in endoplasmic reticulum quality control and endoplasmic reticulum-associated degradation (ERAD) of both non-glycosylated proteins and glycoproteins., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "reported_o_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "total_n_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0051082 unfolded protein binding;GO:0030246 carbohydrate binding",
        "go_cellular_component": "GO:0005788 endoplasmic reticulum lumen",
        "go_biological_process": "GO:0030968 endoplasmic reticulum unfolded protein response;GO:0036503 ERAD pathway;GO:0030970 retrograde protein transport, ER to cytosol;GO:1904153 negative regulation of retrograde protein transport, ER to cytosol",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZF97-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZFD9-1",
        "uniprot_id": "D3ZFD9_RAT",
        "mass": 50324.0,
        "length": 448,
        "protein_name": "Retinoic acid receptor beta",
        "gene_name": "Rarb",
        "organism": "Rat",
        "refseq_name": "retinoic acid receptor beta",
        "refseq_ac": "NP_113717",
        "gene_names_uniprotkb": "Rarb; LOC684994",
        "gene_names_refseq": "Rarb",
        "protein_names_uniprotkb": "Retinoic acid receptor beta; Nuclear receptor subfamily 1 group B member 2",
        "protein_names_refseq": "retinoic acid receptor beta",
        "tax_id": 10116,
        "disease": "stroke (Disease Ontology:DOID:0051061); left ventricular failure (Disease Ontology:DOID:0051064); thrombosis (Disease Ontology:DOID:0060903); COVID-19 (Disease Ontology:DOID:0080600); calcium oxalate nephrolithiasis (Disease Ontology:DOID:0080652); acquired angioedema (Disease Ontology:DOID:0080941); syndromic microphthalmia 12 (Disease Ontology:DOID:0111800); thrombophilia due to thrombin defect (Disease Ontology:DOID:0111907); sensorineural hearing loss (Disease Ontology:DOID:10003); osteonecrosis (Disease Ontology:DOID:10159); pre-eclampsia (Disease Ontology:DOID:10591); celiac disease (Disease Ontology:DOID:10608); sickle cell anemia (Disease Ontology:DOID:10923); urinary bladder cancer (Disease Ontology:DOID:11054); disseminated intravascular coagulation (Disease Ontology:DOID:11247); portal vein thrombosis (Disease Ontology:DOID:11695); factor VIII deficiency (Disease Ontology:DOID:12134); Chagas disease (Disease Ontology:DOID:12140); dengue disease (Disease Ontology:DOID:12205); hemophilia B (Disease Ontology:DOID:12259); hemolytic-uremic syndrome (Disease Ontology:DOID:12554); Huntington's disease (Disease Ontology:DOID:12858); carotid stenosis (Disease Ontology:DOID:13001); toxic shock syndrome (Disease Ontology:DOID:14115); hereditary angioedema (Disease Ontology:DOID:14735); urticaria (Disease Ontology:DOID:1555); retinal vein occlusion (Disease Ontology:DOID:1727); hepatitis C (Disease Ontology:DOID:1883); atherosclerosis (Disease Ontology:DOID:1936); autoimmune hepatitis (Disease Ontology:DOID:2048); prothrombin deficiency (Disease Ontology:DOID:2235); leptospirosis (Disease Ontology:DOID:2297); ovarian cancer (Disease Ontology:DOID:2394); thrombophilia (Disease Ontology:DOID:2452); nephrosis (Disease Ontology:DOID:2527); asthma (Disease Ontology:DOID:2841); glomerulonephritis (Disease Ontology:DOID:2921); familial Mediterranean fever (Disease Ontology:DOID:2987); high grade glioma (Disease Ontology:DOID:3070); chronic obstructive pulmonary disease (Disease Ontology:DOID:3083); atopic dermatitis (Disease Ontology:DOID:3310); coronary artery disease (Disease Ontology:DOID:3393); cerebral infarction (Disease Ontology:DOID:3526); lung non-small cell carcinoma (Disease Ontology:DOID:3908); lung adenocarcinoma (Disease Ontology:DOID:3910); systemic scleroderma (Disease Ontology:DOID:418); hyperglycemia (Disease Ontology:DOID:4195); clear cell renal cell carcinoma (Disease Ontology:DOID:4467); allergic rhinitis (Disease Ontology:DOID:4481); brain edema (Disease Ontology:DOID:4724); liver cirrhosis (Disease Ontology:DOID:5082); lung small cell carcinoma (Disease Ontology:DOID:5409); eye disease (Disease Ontology:DOID:5614); myocardial infarction (Disease Ontology:DOID:5844); hepatocellular carcinoma (Disease Ontology:DOID:684); asbestos-related lung carcinoma (Disease Ontology:DOID:7596); end stage renal disease (Disease Ontology:DOID:783); appendicitis (Disease Ontology:DOID:8337); bullous pemphigoid (Disease Ontology:DOID:8506); herpes zoster (Disease Ontology:DOID:8536); ulcerative colitis (Disease Ontology:DOID:8577); bacterial pneumonia (Disease Ontology:DOID:874); Crohn's disease (Disease Ontology:DOID:8778); systemic lupus erythematosus (Disease Ontology:DOID:9074); hyperhomocysteinemia (Disease Ontology:DOID:9279); type 2 diabetes mellitus (Disease Ontology:DOID:9352); pulmonary embolism (Disease Ontology:DOID:9477); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (rno:24706)",
        "pathway_count": 1,
        "publication_count": 2,
        "publication_id_list": "26923513;33130074",
        "class_list": "",
        "function": "Maternal vitamin A deficiency impairs cholinergic and nitrergic neurons, leading to gastrointestinal dysfunction in rat offspring via RARbeta., [RefSeq, PubMed]; RARbeta in the kidney, which was induced in a retinoic acid-dependent manner, was downregulated by 90% in nonobese Goto-Kakizaki rats., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 68,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0004879 nuclear receptor activity;GO:0003700 DNA-binding transcription factor activity;GO:0044877 protein-containing complex binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0090575 RNA polymerase II transcription regulator complex",
        "go_biological_process": "GO:0002068 glandular epithelial cell development;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0008284 positive regulation of cell population proliferation;GO:0030154 cell differentiation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "D3ZFD9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZFE0-1",
        "uniprot_id": "D3ZFE0_RAT",
        "mass": 35184.0,
        "length": 314,
        "protein_name": "Olfactory receptor family 1 subfamily A member 1B",
        "gene_name": "Or1a1b",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr1514",
        "refseq_ac": "NP_001000036",
        "gene_names_uniprotkb": "Or1a1b",
        "gene_names_refseq": "Olr1514; Or1a1b; ratchr10-61507754-61506810_ORF",
        "protein_names_uniprotkb": "Olfactory receptor family 1 subfamily A member 1B",
        "protein_names_refseq": "olfactory receptor 1514; olfactory receptor Olr1514; olfactory receptor gene Olr1514",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:287514)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Odorant receptor., [UniProtKB, UniProtKB]; Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0007165 signal transduction;GO:0032467 positive regulation of cytokinesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZFE0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZFG3-1",
        "uniprot_id": "D3ZFG3_RAT",
        "mass": 30519.0,
        "length": 283,
        "protein_name": "Chymotrypsin like elastase 3B",
        "gene_name": "Cela3b",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Cela3b",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Chymotrypsin like elastase 3B",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
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        "predicted_glycosites": 0,
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        "reported_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "total_reported_s_glycosites": 0,
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        "reported_phosphosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004252 serine-type endopeptidase activity",
        "go_cellular_component": "GO:0005615 extracellular space",
        "go_biological_process": "GO:0006508 proteolysis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZFG3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZTG3-1",
        "uniprot_id": "D3ZTG3_RAT",
        "mass": 91990.0,
        "length": 823,
        "protein_name": "Family with sequence similarity 171, member B",
        "gene_name": "Fam171b",
        "organism": "Rat",
        "refseq_name": "protein FAM171B precursor",
        "refseq_ac": "NP_001417694",
        "gene_names_uniprotkb": "Fam171b",
        "gene_names_refseq": "Fam171b; RGD1562526",
        "protein_names_uniprotkb": "Family with sequence similarity 171, member B",
        "protein_names_refseq": "protein FAM171B precursor; protein FAM171B",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:499821)",
        "pathway_count": 1,
        "publication_count": 2,
        "publication_id_list": "22673903;38843836",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0016020 membrane;GO:0045202 synapse",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.5,
        "record_id": "D3ZTG3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V828-1",
        "uniprot_id": "G3V828_RAT",
        "mass": 39821.0,
        "length": 361,
        "protein_name": "Protein canopy homolog 3",
        "gene_name": "Cnpy3",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Cnpy3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Protein canopy homolog 3",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "developmental and epileptic encephalopathy 60 (Disease Ontology:DOID:0080432)",
        "pathway": " (R-RNO-1679131)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
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        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0005102 signaling receptor binding",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum",
        "go_biological_process": "GO:0045087 innate immune response",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "G3V828-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZPL7-1",
        "uniprot_id": "D3ZPL7_RAT",
        "mass": 230198.0,
        "length": 2111,
        "protein_name": "Cell adhesion molecule DSCAML1",
        "gene_name": "Dscaml1",
        "organism": "Rat",
        "refseq_name": "cell adhesion molecule DSCAML1",
        "refseq_ac": "NP_001101611",
        "gene_names_uniprotkb": "Dscaml1",
        "gene_names_refseq": "Dscaml1",
        "protein_names_uniprotkb": "Cell adhesion molecule DSCAML1",
        "protein_names_refseq": "Down syndrome cell adhesion molecule-like 1; Down syndrome cell adhesion molecule-like protein 1; cell adhesion molecule DSCAML1",
        "tax_id": 10116,
        "disease": "autism spectrum disorder (Disease Ontology:DOID:0060041); ocular motor apraxia, Cogan type (Disease Ontology:DOID:0080849); ocular motility disease (Disease Ontology:DOID:1279); Down syndrome (Disease Ontology:DOID:14250)",
        "pathway": " (rno:315615);  (R-RNO-376172)",
        "pathway_count": 2,
        "publication_count": 2,
        "publication_id_list": "24084194;33256836",
        "class_list": "",
        "function": "Cell adhesion molecule that plays a role in neuronal self-avoidance. Promotes repulsion between specific neuronal processes of either the same cell or the same subtype of cells. Promotes both isoneuronal self-avoidance for creating an orderly neurite arborization in retinal rod bipolar cells and heteroneuronal self-avoidance to maintain mosaic spacing between AII amacrine cells. Adhesion molecule that promotes lamina-specific synaptic connections in the retina: expressed in specific subsets of interneurons and retinal ganglion cells (RGCs) and promotes synaptic connectivity via homophilic interactions., [UniProtKB, UniProtKB]; DSCAML1 promotes dendritic self-avoidance in cortical neurons, and that phosphorylation at Y1808 is essential in mediating the effects of DSCAML1., [RefSeq, PubMed]; Down syndrome cell adhesion molecule like-1 (DSCAML1) links the GABA system and seizure susceptibility. Publication Status: Online-Only, [RefSeq, PubMed]",
        "predicted_glycosites": 2,
        "predicted_n_glycosites": 0,
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        "reported_c_glycosites_with_glycan": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 2,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0042803 protein homodimerization activity;GO:0098632 cell-cell adhesion mediator activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0045202 synapse;GO:0009986 cell surface;GO:0030424 axon",
        "go_biological_process": "GO:0007155 cell adhesion;GO:0007399 nervous system development;GO:0007162 negative regulation of cell adhesion;GO:0007417 central nervous system development;GO:0007420 brain development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "D3ZPL7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZWF2-1",
        "uniprot_id": "D3ZWF2_RAT",
        "mass": 104050.0,
        "length": 981,
        "protein_name": "Fibrosin",
        "gene_name": "Fbrs",
        "organism": "Rat",
        "refseq_name": "probable fibrosin-1",
        "refseq_ac": "NP_001419617",
        "gene_names_uniprotkb": "Fbrs",
        "gene_names_refseq": "Fbrs",
        "protein_names_uniprotkb": "Fibrosin",
        "protein_names_refseq": "probable fibrosin-1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:691899)",
        "pathway_count": 1,
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        "missing_score": 10000,
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        "go_molecular_function": "GO:0008083 growth factor activity",
        "go_cellular_component": "GO:0005615 extracellular space",
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        "record_id": "D3ZWF2-1",
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    },
    {
        "uniprot_canonical_ac": "D3ZPL1-1",
        "uniprot_id": "D3ZPL1_RAT",
        "mass": 59180.0,
        "length": 551,
        "protein_name": "Cleavage and polyadenylation specificity factor subunit 6",
        "gene_name": "Cpsf6",
        "organism": "Rat",
        "refseq_name": "cleavage and polyadenylation specificity factor subunit 6 isoform 1",
        "refseq_ac": "NP_001100255",
        "gene_names_uniprotkb": "Cpsf6",
        "gene_names_refseq": "Cpsf6",
        "protein_names_uniprotkb": "Cleavage and polyadenylation specificity factor subunit 6",
        "protein_names_refseq": "cleavage and polyadenylation specific factor 6, 68kDa; cleavage and polyadenylation specificity factor subunit 6 isoform 1; cleavage and polyadenylation specificity factor subunit 6",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:299811);  (R-RNO-73856);  (R-RNO-77595);  (R-RNO-9770562)",
        "pathway_count": 4,
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        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Component of the cleavage factor Im (CFIm) complex that functions as an activator of the pre-mRNA 3'-end cleavage and polyadenylation processing required for the maturation of pre-mRNA into functional mRNAs. CFIm contributes to the recruitment of multiprotein complexes on specific sequences on the pre-mRNA 3'-end, so called cleavage and polyadenylation signals (pA signals). Most pre-mRNAs contain multiple pA signals, resulting in alternative cleavage and polyadenylation (APA) producing mRNAs with variable 3'-end formation. The CFIm complex acts as a key regulator of cleavage and polyadenylation site choice during APA through its binding to 5'-UGUA-3' elements localized in the 3'-untranslated region (UTR) for a huge number of pre-mRNAs. CPSF6 enhances NUDT21/CPSF5 binding to 5'-UGUA-3' elements localized upstream of pA signals and promotes RNA looping, and hence activates directly the mRNA 3'-processing machinery. Plays a role in mRNA export., [UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0003729 mRNA binding;GO:0043023 ribosomal large subunit binding;GO:1990448 exon-exon junction complex binding",
        "go_cellular_component": "GO:0005726 perichromatin fibrils;GO:0005737 cytoplasm;GO:0016607 nuclear speck;GO:1990904 ribonucleoprotein complex;GO:0005847 mRNA cleavage and polyadenylation specificity factor complex",
        "go_biological_process": "GO:0046833 positive regulation of RNA export from nucleus;GO:0051290 protein heterotetramerization;GO:0110104 mRNA alternative polyadenylation;GO:0180010 co-transcriptional mRNA 3'-end processing, cleavage and polyadenylation pathway;GO:0006397 mRNA processing",
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        "record_id": "D3ZPL1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F1MAA5-1",
        "uniprot_id": "F1MAA5_RAT",
        "mass": 63143.0,
        "length": 586,
        "protein_name": "Ran GTPase-activating protein 1",
        "gene_name": "Rangap1",
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        "refseq_name": "ran GTPase-activating protein 1",
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        "gene_names_uniprotkb": "Rangap1",
        "gene_names_refseq": "Rangap1",
        "protein_names_uniprotkb": "Ran GTPase-activating protein 1",
        "protein_names_refseq": "ran GTPase-activating protein 1",
        "tax_id": 10116,
        "disease": "sciatic neuropathy (Disease Ontology:DOID:11446)",
        "pathway": " (rno:362965);  (R-RNO-141430);  (R-RNO-141444);  (R-RNO-2467813);  (R-RNO-2500257);  (R-RNO-4615885);  (R-RNO-5663220);  (R-RNO-68877);  (R-RNO-9615933);  (R-RNO-9648025);  (R-RNO-9793242)",
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        "function": "RanGAP1 expression, neointima formation in rat carotid arteries was associated with a significant upregulation of RanGAP1 expression at 3 and 7 days after balloon injury. Publication Status: Online-Only, [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0003723 RNA binding;GO:0005096 GTPase activator activity;GO:0031625 ubiquitin protein ligase binding;GO:0031267 small GTPase binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005635 nuclear envelope;GO:0005643 nuclear pore;GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0007165 signal transduction;GO:0016925 protein sumoylation;GO:1904117 cellular response to vasopressin;GO:0048678 response to axon injury;GO:0071375 cellular response to peptide hormone stimulus",
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        "uniprot_canonical_ac": "D4ADK8-1",
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        "length": 361,
        "protein_name": "Family with sequence similarity 131, member A",
        "gene_name": "Fam131a",
        "organism": "Rat",
        "refseq_name": "protein FAM131A isoform 2",
        "refseq_ac": "NP_001408372",
        "gene_names_uniprotkb": "Fam131a",
        "gene_names_refseq": "Fam131a",
        "protein_names_uniprotkb": "Family with sequence similarity 131, member A",
        "protein_names_refseq": "protein FAM131A isoform 2; protein FAM131A-like; rCG36585-like",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:100360487)",
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        "function": "",
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    {
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        "mass": 22448.0,
        "length": 199,
        "protein_name": "Thioesterase superfamily member 7",
        "gene_name": "Them7",
        "organism": "Rat",
        "refseq_name": "uncharacterized protein LOC691083",
        "refseq_ac": "NP_001138334",
        "gene_names_uniprotkb": "Them7; LOC691083",
        "gene_names_refseq": "RGD1306990; Them7",
        "protein_names_uniprotkb": "Thioesterase superfamily member 7",
        "protein_names_refseq": "uncharacterized protein LOC691083",
        "tax_id": 10116,
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        "go_molecular_function": "GO:0047617 fatty acyl-CoA hydrolase activity;GO:0016787 hydrolase activity",
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        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4AEL0-1",
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    },
    {
        "uniprot_canonical_ac": "D4ABK7-1",
        "uniprot_id": "D4ABK7_RAT",
        "mass": 36869.0,
        "length": 346,
        "protein_name": "Heterogeneous nuclear ribonucleoprotein H3",
        "gene_name": "Hnrnph3",
        "organism": "Rat",
        "refseq_name": "heterogeneous nuclear ribonucleoprotein H3",
        "refseq_ac": "NP_001102002",
        "gene_names_uniprotkb": "Hnrnph3",
        "gene_names_refseq": "Hnrnph3; Hnrph3",
        "protein_names_uniprotkb": "Heterogeneous nuclear ribonucleoprotein H3",
        "protein_names_refseq": "heterogeneous nuclear ribonucleoprotein H3 (2H9); heterogeneous nuclear ribonucleoprotein H3",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:361838)",
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        "class_list": "",
        "function": "These results establish hnRNP H and hnRNP F as being repressors of exon inclusion and suggest that Fox proteins enhance their ability to antagonize ASF/SF2., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0003723 RNA binding;GO:0003676 nucleic acid binding",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:1990904 ribonucleoprotein complex;GO:0005634 nucleus",
        "go_biological_process": "GO:0006397 mRNA processing;GO:0030855 epithelial cell differentiation;GO:0043484 regulation of RNA splicing",
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        "record_id": "D4ABK7-1",
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    },
    {
        "uniprot_canonical_ac": "D3ZYB4-1",
        "uniprot_id": "D3ZYB4_RAT",
        "mass": 99709.0,
        "length": 894,
        "protein_name": "phosphatidate phosphatase",
        "gene_name": "Lpin2",
        "organism": "Rat",
        "refseq_name": "phosphatidate phosphatase LPIN2",
        "refseq_ac": "NP_001101706",
        "gene_names_uniprotkb": "Lpin2",
        "gene_names_refseq": "Lpin2",
        "protein_names_uniprotkb": "phosphatidate phosphatase; 3.1.3.4",
        "protein_names_refseq": "phosphatidate phosphatase LPIN2",
        "tax_id": 10116,
        "disease": "Majeed syndrome (Disease Ontology:DOID:0061224); myoglobinuria (Disease Ontology:DOID:0080108); lipid metabolism disorder (Disease Ontology:DOID:3146); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (rno:316737);  (R-RNO-1483191);  (R-RNO-1483213);  (R-RNO-4419969);  (R-RNO-75109)",
        "pathway_count": 5,
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        "publication_id_list": "22673903;23505321",
        "class_list": "",
        "function": "Novel differences in the regulation of lipins 1,2,3, PPARalpha, and PGC-1alpha splice variants during fasting in heart versus liver, even though the ultimate outcome in both tissues is to increase FA turnover and oxidation., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "3.1.3.4;3.6.1.75;3.1.3.-;3.1.3.106;2.7.11.22;2.7.11.23;3.1.3.16",
        "go_molecular_function": "GO:0008195 phosphatidate phosphatase activity;GO:0003713 transcription coactivator activity",
        "go_cellular_component": "GO:0005829 cytosol;GO:0005789 endoplasmic reticulum membrane;GO:0005634 nucleus",
        "go_biological_process": "GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0019432 triglyceride biosynthetic process;GO:0006629 lipid metabolic process;GO:0009062 fatty acid catabolic process;GO:0032869 cellular response to insulin stimulus",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "D3ZYB4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "E9PU42-1",
        "uniprot_id": "E9PU42_RAT",
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        "length": 297,
        "protein_name": "Vacuolar protein sorting-associated protein 26C",
        "gene_name": "Vps26c",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Vps26c; Dscr3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Vacuolar protein sorting-associated protein 26C",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
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        "pathway_count": 0,
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        "function": "Component of the commander complex that is essential for endosomal recycling of transmembrane cargos; the commander complex is composed of the CCC subcomplex and the retriever subcomplex. Component of the retriever complex, which is a heterotrimeric complex related to retromer cargo-selective complex (CSC) and essential for retromer-independent retrieval and recycling of numerous cargos such as integrin alpha-5/beta-1 (ITGA5:ITGB1). The recruitment of the retriever complex to the endosomal membrane involves CCC and WASH complexes. In the endosomes, drives the retriever and recycling of NxxY-motif-containing cargo proteins by coupling to SNX17, a cargo essential for the homeostatic maintenance of numerous cell surface proteins associated with processes that include cell migration, cell adhesion, nutrient supply and cell signaling., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "length": 284,
        "protein_name": "Receptor expression-enhancing protein",
        "gene_name": "Reep1",
        "organism": "Rat",
        "refseq_name": "receptor expression-enhancing protein 1 isoform 2",
        "refseq_ac": "NP_001416085",
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        "gene_names_refseq": "RGD1305230; Reep1",
        "protein_names_uniprotkb": "Receptor expression-enhancing protein",
        "protein_names_refseq": "receptor expression-enhancing protein 1 isoform 2; receptor expression-enhancing protein 1",
        "tax_id": 10116,
        "disease": "autosomal recessive distal hereditary motor neuronopathy 6 (Disease Ontology:DOID:0081425); hereditary spastic paraplegia 31 (Disease Ontology:DOID:0110782); autosomal dominant distal hereditary motor neuronopathy 12 (Disease Ontology:DOID:0111205)",
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        "go_molecular_function": "GO:0008017 microtubule binding;GO:0031849 olfactory receptor binding",
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        "gene_name": "Magea8",
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        "gene_names_uniprotkb": "Magea8; Magea10-ps3; Magea4",
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        "protein_names_uniprotkb": "MAGE family member A10, pseudogene 3",
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        "refseq_name": "transmembrane protein 256",
        "refseq_ac": "NP_001164020",
        "gene_names_uniprotkb": "Tmem256; RGD1563438",
        "gene_names_refseq": "RGD1563438; Tmem256",
        "protein_names_uniprotkb": "Transmembrane protein 256",
        "protein_names_refseq": "transmembrane protein 256",
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        "go_cellular_component": "GO:0016020 membrane",
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    {
        "uniprot_canonical_ac": "D4A031-1",
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        "mass": 102067.0,
        "length": 929,
        "protein_name": "ATP-dependent RNA helicase DDX42",
        "gene_name": "Ddx42",
        "organism": "Rat",
        "refseq_name": "ATP-dependent RNA helicase DDX42",
        "refseq_ac": "NP_001100529",
        "gene_names_uniprotkb": "Ddx42",
        "gene_names_refseq": "Ddx42",
        "protein_names_uniprotkb": "ATP-dependent RNA helicase DDX42; 3.6.4.13; DEAD box protein 42",
        "protein_names_refseq": "ATP-dependent RNA helicase DDX42; DEAD (Asp-Glu-Ala-Asp) box helicase 42; DEAD (Asp-Glu-Ala-Asp) box polypeptide 42",
        "tax_id": 10116,
        "disease": "myelodysplastic syndrome (Disease Ontology:DOID:0050908)",
        "pathway": " (rno:303607);  (R-RNO-72163);  (R-RNO-72165);  (R-RNO-9770562);  (R-RNO-9943411)",
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        "function": "ATP-dependent RNA helicase that binds to partially double-stranded RNAs (dsRNAs) in order to unwind RNA secondary structures. Unwinding is promoted in the presence of single-strand binding proteins. Also mediates RNA duplex formation thereby displacing the single-strand RNA binding protein. ATP and ADP modulate its activity: ATP binding and hydrolysis by DDX42 triggers RNA strand separation, whereas the ADP-bound form of the protein triggers annealing of complementary RNA strands. Required for assembly of the 17S U2 SnRNP complex of the spliceosome, a large ribonucleoprotein complex that removes introns from transcribed pre-mRNAs: DDX42 associates transiently with the SF3B subcomplex of the 17S U2 SnRNP complex and is released after fulfilling its role in the assembly of 17S U2 SnRNP. Involved in the survival of cells by interacting with TP53BP2 and thereby counteracting the apoptosis-stimulating activity of TP53BP2. Relocalizes TP53BP2 to the cytoplasm., [UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "5.6.2.3;3.6.4.13;3.6.4.12;2.7.11.1;3.6.1.5;3.6.4.10;3.6.4.-;2.3.2.27;2.7.7.19;5.6.2.4;5.2.1.8;3.6.5.-;5.6.2.-;3.1.-.-;2.7.7.6;2.7.7.7;2.7.7.49;3.1.13.1;4.2.99.18;7.6.2.2;7.6.2.3;7.6.2.-;5.6.1.6;7.2.2.-;3.6.1.15;3.6.4.6;3.1.3.1;3.9.1.1;6.1.1.12;3.6.1.-;3.1.3.16;3.1.3.53;2.7.7.52;2.7.4.3;2.7.1.78;3.1.4.-;3.4.24.-;3.6.-.-;3.4.21.53;5.6.2.5",
        "go_molecular_function": "GO:0003723 RNA binding;GO:0005524 ATP binding;GO:0016787 hydrolase activity;GO:0003724 RNA helicase activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0016607 nuclear speck;GO:0071004 U2-type prespliceosome;GO:0005634 nucleus",
        "go_biological_process": "GO:0042981 regulation of apoptotic process;GO:0008104 intracellular protein localization;GO:1903241 U2-type prespliceosome assembly",
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        "protein_name": "Chromobox 1",
        "gene_name": "Cbx1",
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        "refseq_name": "",
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        "protein_names_uniprotkb": "Chromobox 1",
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        "tax_id": 10116,
        "disease": "prostate cancer (Disease Ontology:DOID:10283)",
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        "go_molecular_function": "GO:0003682 chromatin binding;GO:0042802 identical protein binding;GO:1990226 histone methyltransferase binding;GO:0062072 histone H3K9me2/3 reader activity;GO:0160267 histone H1K26me1 reader activity",
        "go_cellular_component": "GO:0005819 spindle;GO:0016604 nuclear body;GO:0001939 female pronucleus;GO:0001940 male pronucleus;GO:1990904 ribonucleoprotein complex",
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        "record_id": "D4A3T3-1",
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        "length": 203,
        "protein_name": "PYM homolog 1, exon junction complex associated factor",
        "gene_name": "Pym1",
        "organism": "Rat",
        "refseq_name": "partner of Y14 and mago",
        "refseq_ac": "NP_001102456",
        "gene_names_uniprotkb": "Pym1",
        "gene_names_refseq": "Pym1; RGD1306096; Wibg",
        "protein_names_uniprotkb": "PYM homolog 1, exon junction complex associated factor",
        "protein_names_refseq": "PYM homolog 1, exon junction complex associated factor; partner of Y14 and mago; within bgcn homolog",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:366790)",
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        "go_molecular_function": "GO:0003723 RNA binding;GO:0043022 ribosome binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0035145 exon-exon junction complex;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005829 cytosol",
        "go_biological_process": "GO:1903259 exon-exon junction complex disassembly;GO:0000184 nuclear-transcribed mRNA catabolic process, nonsense-mediated decay;GO:0045727 positive regulation of translation",
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        "uniprot_canonical_ac": "D4A2L9-1",
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        "length": 674,
        "protein_name": "F-box/LRR-repeat protein 19",
        "gene_name": "Fbxl19",
        "organism": "Rat",
        "refseq_name": "F-box/LRR-repeat protein 19",
        "refseq_ac": "NP_001402857",
        "gene_names_uniprotkb": "Fbxl19",
        "gene_names_refseq": "Fbxl19",
        "protein_names_uniprotkb": "F-box/LRR-repeat protein 19; F-box and leucine-rich repeat protein 19",
        "protein_names_refseq": "F-box/LRR-repeat protein 19",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:308999);  (R-RNO-8951664);  (R-RNO-983168)",
        "pathway_count": 3,
        "publication_count": 0,
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        "class_list": "",
        "function": "Substrate-recognition component of the SCF (SKP1-CUL1-F-box protein)-type E3 ubiquitin ligase complex that plays a role in different processes including cell migration, cell proliferation or cytoskeletal reorganization. Mediates RHOA ubiquitination and degradation in a ERK2-dependent manner. Induces RAC1 and RAC3 degradation by the proteasome system and thereby regulates TGFB1-induced E-cadherin down-regulation and cell migration. Also mediates ubiquitination and degradation of IL-33-induced receptor IL1RL1 and subsequently blocks IL-33-mediated apoptosis. Within the nucleus, binds to DNA containing unmethylated cytidine-phosphate-guanosine (CpG) dinucleotides. Recruits CDK-mediator to chromatin and targets CDK8 to promoters of silent developmental genes leading to induction of these genes during cell differentiation. In addition, plays a critical role in the recruitment of RNF20 to histone H2B leading to H2B mono-ubiquitination., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0003712 transcription coregulator activity;GO:0032452 histone demethylase activity;GO:1990756 ubiquitin-like ligase-substrate adaptor activity;GO:0045322 unmethylated CpG binding",
        "go_cellular_component": "GO:0019005 SCF ubiquitin ligase complex",
        "go_biological_process": "GO:0006338 chromatin remodeling;GO:0006357 regulation of transcription by RNA polymerase II;GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4A2L9-1",
        "record_type": "protein"
    },
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        "uniprot_canonical_ac": "D4A3E7-1",
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        "length": 370,
        "protein_name": "Transmembrane 6 superfamily member 1",
        "gene_name": "Tm6sf1",
        "organism": "Rat",
        "refseq_name": "transmembrane 6 superfamily member 1",
        "refseq_ac": "NP_001382048",
        "gene_names_uniprotkb": "Tm6sf1",
        "gene_names_refseq": "Tm6sf1",
        "protein_names_uniprotkb": "Transmembrane 6 superfamily member 1",
        "protein_names_refseq": "transmembrane 6 superfamily member 1",
        "tax_id": 10116,
        "disease": "steatotic liver disease (Disease Ontology:DOID:9452)",
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        "publication_id_list": "",
        "class_list": "",
        "function": "May function as sterol isomerase., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005765 lysosomal membrane",
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        "record_id": "D4A3E7-1",
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    },
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        "length": 215,
        "protein_name": "Myelin protein zero-like 2",
        "gene_name": "Mpzl2; Mpzl3",
        "organism": "Rat",
        "refseq_name": "myelin protein zero-like protein 2 precursor",
        "refseq_ac": "NP_001100288",
        "gene_names_uniprotkb": "Mpzl2; Mpzl3; Mpzl2",
        "gene_names_refseq": "Eva1; Eva; Mpzl2",
        "protein_names_uniprotkb": "Myelin protein zero-like 2",
        "protein_names_refseq": "epithelial V-like antigen 1; myelin protein zero-like protein 2 precursor; myelin protein zero-like protein 2",
        "tax_id": 10116,
        "disease": "autosomal recessive nonsyndromic deafness 111 (Disease Ontology:DOID:0111640); lung cancer (Disease Ontology:DOID:1324)",
        "pathway": " (rno:300679);  (rno:363054)",
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane",
        "go_biological_process": "GO:0098609 cell-cell adhesion;GO:0033077 T cell differentiation in thymus;GO:0030198 extracellular matrix organization;GO:0042633 hair cycle",
        "synthesized_glycan_count": 0,
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        "record_id": "D4AAE2-1",
        "record_type": "protein"
    },
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        "uniprot_canonical_ac": "F7EXF4-1",
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        "mass": 94070.0,
        "length": 829,
        "protein_name": "Centrosomal protein 85-like",
        "gene_name": "Cep85l",
        "organism": "Rat",
        "refseq_name": "centrosomal protein of 85 kDa-like isoform X1",
        "refseq_ac": "XP_017457013",
        "gene_names_uniprotkb": "Cep85l; LOC100365935",
        "gene_names_refseq": "Cep85l",
        "protein_names_uniprotkb": "Centrosomal protein 85-like",
        "protein_names_refseq": "centrosomal protein of 85 kDa-like isoform X1",
        "tax_id": 10116,
        "disease": "lissencephaly 10 (Disease Ontology:DOID:0112229)",
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        "missing_score": 10000,
        "biomarker_type": "",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005813 centrosome;GO:0000242 pericentriolar material",
        "go_biological_process": "GO:0001764 neuron migration",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F7EXF4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZG18-1",
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        "length": 1098,
        "protein_name": "Protocadherin-19",
        "gene_name": "Pcdh19",
        "organism": "Rat",
        "refseq_name": "protocadherin-19 precursor",
        "refseq_ac": "NP_001162600",
        "gene_names_uniprotkb": "Pcdh19",
        "gene_names_refseq": "Pcdh19; RGD1565392",
        "protein_names_uniprotkb": "Protocadherin-19",
        "protein_names_refseq": "protocadherin-19 precursor",
        "tax_id": 10116,
        "disease": "developmental and epileptic encephalopathy 9 (Disease Ontology:DOID:0060848)",
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        "publication_id_list": "32880860;38843836",
        "class_list": "",
        "function": "Calcium-dependent cell-adhesion protein., [UniProtKB, UniProtKB, UniProtKB]; The Epilepsy-Related Protein PCDH19 Regulates Tonic Inhibition, GABAAR Kinetics, and the Intrinsic Excitability of Hippocampal Neurons., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0005509 calcium ion binding;GO:0050839 cell adhesion molecule binding",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0007155 cell adhesion;GO:0007156 homophilic cell adhesion via plasma membrane adhesion molecules",
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        "hit_score": 0.5,
        "record_id": "D3ZG18-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZV74-1",
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        "length": 295,
        "protein_name": "Nudix hydrolase 7",
        "gene_name": "Nudt7",
        "organism": "Rat",
        "refseq_name": "peroxisomal coenzyme A diphosphatase NUDT7 isoform X2",
        "refseq_ac": "XP_063134210",
        "gene_names_uniprotkb": "Nudt7",
        "gene_names_refseq": "Nudt7",
        "protein_names_uniprotkb": "Nudix hydrolase 7",
        "protein_names_refseq": "peroxisomal coenzyme A diphosphatase NUDT7 isoform X2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-9033241)",
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        "go_molecular_function": "GO:0000287 magnesium ion binding;GO:0030145 manganese ion binding;GO:0010945 coenzyme A diphosphatase activity;GO:0030515 snoRNA binding",
        "go_cellular_component": "GO:0005777 peroxisome",
        "go_biological_process": "GO:0009132 nucleoside diphosphate metabolic process;GO:0050873 brown fat cell differentiation;GO:0036114 medium-chain fatty-acyl-CoA catabolic process;GO:2001294 malonyl-CoA catabolic process;GO:0015938 coenzyme A catabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZV74-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZY73-1",
        "uniprot_id": "D3ZY73_RAT",
        "mass": 26607.0,
        "length": 240,
        "protein_name": "Retinal pigment epithelium derived rhodopsin homolog",
        "gene_name": "Rrh",
        "organism": "Rat",
        "refseq_name": "visual pigment-like receptor peropsin isoform 2",
        "refseq_ac": "NP_001101196",
        "gene_names_uniprotkb": "Rrh",
        "gene_names_refseq": "Rrh",
        "protein_names_uniprotkb": "Retinal pigment epithelium derived rhodopsin homolog",
        "protein_names_refseq": "visual pigment-like receptor peropsin isoform 2; visual pigment-like receptor peropsin",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:310869);  (R-RNO-418594);  (R-RNO-419771)",
        "pathway_count": 3,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "May play a role in rpe physiology either by detecting light directly or by monitoring the concentration of retinoids or other photoreceptor-derived compounds., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "go_molecular_function": "GO:0008020 G protein-coupled photoreceptor activity;GO:0004930 G protein-coupled receptor activity;GO:0009881 photoreceptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane",
        "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007601 visual perception;GO:0007602 phototransduction;GO:0071482 cellular response to light stimulus",
        "synthesized_glycan_count": 0,
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        "record_id": "D3ZY73-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A445-1",
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        "mass": 30213.0,
        "length": 267,
        "protein_name": "Putative transcription factor Ovo-like 1",
        "gene_name": "Ovol1",
        "organism": "Rat",
        "refseq_name": "putative transcription factor Ovo-like 1",
        "refseq_ac": "NP_001101042",
        "gene_names_uniprotkb": "Ovol1",
        "gene_names_refseq": "Ovol1",
        "protein_names_uniprotkb": "Putative transcription factor Ovo-like 1",
        "protein_names_refseq": "OVO homolog-like 1; ovo-like 1(Drosophila); ovo-like zinc finger 1; putative transcription factor Ovo-like 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:309164)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "19882138",
        "class_list": "",
        "function": "OVOL1 may play an important role in regulating the balance between proliferation and differentiation of pancreatic cells., [RefSeq, PubMed]; Putative transcription factor. Involved in hair formation and spermatogenesis. May function in the differentiation and/or maintenance of the urogenital system., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:1990837 sequence-specific double-stranded DNA binding",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:1901994 negative regulation of meiotic cell cycle phase transition;GO:0009913 epidermal cell differentiation;GO:2000647 negative regulation of stem cell proliferation;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006357 regulation of transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D4A445-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F1LV60-1",
        "uniprot_id": "F1LV60_RAT",
        "mass": 93721.0,
        "length": 842,
        "protein_name": "CDKN1A interacting zinc finger protein 1",
        "gene_name": "Ciz1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ciz1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "CDKN1A interacting zinc finger protein 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "alcohol use disorder (Disease Ontology:DOID:1574)",
        "pathway": " (rno:296639)",
        "pathway_count": 1,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0003676 nucleic acid binding;GO:0030332 cyclin binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0060816 random inactivation of X chromosome;GO:0051457 maintenance of protein location in nucleus;GO:0032298 positive regulation of DNA-templated DNA replication initiation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F1LV60-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4ADE8-1",
        "uniprot_id": "D4ADE8_RAT",
        "mass": 73145.0,
        "length": 662,
        "protein_name": "RNA helicase",
        "gene_name": "Ddx3x; Ddx3",
        "organism": "Rat",
        "refseq_name": "ATP-dependent RNA helicase DDX3X isoform 2",
        "refseq_ac": "NP_001385681",
        "gene_names_uniprotkb": "Ddx3x; Ddx3; Ddx3x; RGD1309586",
        "gene_names_refseq": "Ddx3x",
        "protein_names_uniprotkb": "RNA helicase; 3.6.4.13",
        "protein_names_refseq": "ATP-dependent RNA helicase DDX3X isoform 2; ATP-dependent RNA helicase DDX3X; DEAD (Asp-Glu-Ala-Asp) box helicase 3, X-linked; DEAD (Asp-Glu-Ala-Asp) box polypeptide 3, X-linked; DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 3, X-linked",
        "tax_id": 10116,
        "disease": "Sertoli cell-only syndrome (Disease Ontology:DOID:0050457); syndromic X-linked intellectual disability (Disease Ontology:DOID:0060309); childhood medulloblastoma (Disease Ontology:DOID:3869); hepatocellular carcinoma (Disease Ontology:DOID:684); colorectal cancer (Disease Ontology:DOID:9256)",
        "pathway": " (rno:317335);  (rno:364073);  (R-RNO-6798695)",
        "pathway_count": 3,
        "publication_count": 4,
        "publication_id_list": "22673903;34502162;35467791;38843836",
        "class_list": "",
        "function": "DDX3X alleviates doxorubicin-induced cardiotoxicity by regulating Wnt/beta-catenin signaling pathway in an in vitro model., [RefSeq, PubMed]",
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        "ec_number_list": "5.6.2.3;3.6.4.13;3.6.4.12;2.7.11.1;3.6.1.5;3.6.4.10;3.6.4.-;2.3.2.27;5.6.2.4;5.2.1.8;3.6.5.-;5.6.2.-;3.1.-.-;1.1.1.205;3.2.1.23;2.7.7.7;2.7.7.49;3.5.4.5;2.3.2.5;3.1.13.1;2.4.1.25;3.2.1.33;4.2.99.18;4.1.2.4;7.6.2.2;7.6.2.3;7.6.2.-;5.6.1.6;7.2.2.-;3.6.1.15;3.6.4.6;2.4.1.186;3.5.4.6;3.1.1.47;2.7.1.35;3.4.22.1;1.11.1.6;2.5.1.18;4.1.2.13;4.2.1.24;3.2.1.31;3.1.3.1;3.9.1.1;2.4.1.1;2.7.10.2;2.7.1.40;1.13.11.-;1.13.11.34;3.4.19.1;6.1.1.12;2.3.3.8;1.16.3.1;2.7.4.6;2.7.13.3;3.4.23.5;5.4.2.11;5.4.2.4;2.7.1.1;3.6.1.-;3.3.2.6;3.4.11.4;2.7.1.11;5.3.2.1;5.3.3.12;3.4.21.46;3.1.6.4;2.4.2.7;5.4.2.2;1.1.1.42;3.4.24.35;3.1.6.12;2.3.2.26;2.7.11.24;2.4.2.1;3.4.22.52;3.4.22.27;2.7.4.3;2.7.11.39;3.1.4.-;5.3.1.9;5.1.3.-;3.5.1.23;3.5.1.-;3.4.24.-;3.6.-.-;3.6.1.6;3.4.21.53;5.6.2.5;3.4.25.1;3.4.18.1;1.11.1.24",
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        "record_type": "protein"
    },
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        "protein_name": "Nuclear protein, co-activator of histone transcription",
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        "refseq_name": "protein NPAT isoform 2",
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        "protein_names_refseq": "nuclear protein in the AT region; nuclear protein, ataxia-telangiectasia locus; protein NPAT isoform 2; protein NPAT",
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        "record_id": "D4A6Y1-1",
        "record_type": "protein"
    },
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        "uniprot_canonical_ac": "D4A8S0-1",
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        "refseq_name": "transcription factor SOX-13 isoform X3",
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        "gene_names_refseq": "Sox13",
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        "tax_id": 10116,
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0042802 identical protein binding;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific;GO:0000976 transcription cis-regulatory region binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0090090 negative regulation of canonical Wnt signaling pathway;GO:0006355 regulation of DNA-templated transcription;GO:0045892 negative regulation of DNA-templated transcription;GO:0090336 positive regulation of brown fat cell differentiation",
        "synthesized_glycan_count": 0,
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        "record_id": "D4A8S0-1",
        "record_type": "protein"
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        "uniprot_canonical_ac": "D4A2T5-1",
        "uniprot_id": "D4A2T5_RAT",
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        "length": 477,
        "protein_name": "Meis homeobox 2",
        "gene_name": "Meis2",
        "organism": "Rat",
        "refseq_name": "homeobox protein Meis2 isoform X3",
        "refseq_ac": "XP_006234809",
        "gene_names_uniprotkb": "Meis2",
        "gene_names_refseq": "Meis2",
        "protein_names_uniprotkb": "Meis homeobox 2",
        "protein_names_refseq": "homeobox protein Meis2 isoform X3",
        "tax_id": 10116,
        "disease": "restless legs syndrome (Disease Ontology:DOID:0050425); orofacial cleft (Disease Ontology:DOID:0050567); cleft palate, cardiac defects, and intellectual disability (Disease Ontology:DOID:0111697); open-angle glaucoma (Disease Ontology:DOID:1067); leukemia (Disease Ontology:DOID:1240); brain infarction (Disease Ontology:DOID:3454); cleft palate (Disease Ontology:DOID:674); learning disability (Disease Ontology:DOID:8927)",
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0043565 sequence-specific DNA binding;GO:0001228 DNA-binding transcription activator activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus",
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        "record_id": "D4A2T5-1",
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    {
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        "length": 455,
        "protein_name": "Transmembrane protease serine 5",
        "gene_name": "Tmprss5",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Tmprss5",
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        "protein_names_uniprotkb": "Transmembrane protease serine 5; Spinesin",
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        "function": "May play a role in hearing., [UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0004252 serine-type endopeptidase activity;GO:0008233 peptidase activity;GO:0008236 serine-type peptidase activity",
        "go_cellular_component": "GO:0016020 membrane;GO:0005886 plasma membrane;GO:0043025 neuronal cell body",
        "go_biological_process": "GO:0006508 proteolysis;GO:0016485 protein processing",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F1LSP0-1",
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    {
        "uniprot_canonical_ac": "F1LY63-1",
        "uniprot_id": "F1LY63_RAT",
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        "length": 729,
        "protein_name": "RING-type E3 ubiquitin transferase",
        "gene_name": "Trim36",
        "organism": "Rat",
        "refseq_name": "E3 ubiquitin-protein ligase TRIM36 isoform 1",
        "refseq_ac": "NP_001099617",
        "gene_names_uniprotkb": "Trim36",
        "gene_names_refseq": "Trim36",
        "protein_names_uniprotkb": "RING-type E3 ubiquitin transferase; 2.3.2.27; RING-type E3 ubiquitin transferase TRIM36; Tripartite motif-containing protein 36",
        "protein_names_refseq": "E3 ubiquitin-protein ligase TRIM36 isoform 1; E3 ubiquitin-protein ligase TRIM36; tripartite motif protein 36",
        "tax_id": 10116,
        "disease": "anencephaly (Disease Ontology:DOID:0060668)",
        "pathway": " (rno:291597);  (R-RNO-983168)",
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        "function": "E3 ubiquitin-protein ligase which mediates ubiquitination and subsequent proteasomal degradation of target proteins. Involved in chromosome segregation and cell cycle regulation. May play a role in the acrosome reaction and fertilization., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "2.3.2.26;2.3.2.32;2.3.2.31;2.3.2.23;2.3.2.27;2.3.2.34;2.3.2.24;2.3.2.-;2.3.2.25",
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        "length": 108,
        "protein_name": "Protein phosphatase 1, regulatory (inhibitor) subunit 1C",
        "gene_name": "Ppp1r1c",
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        "refseq_name": "protein phosphatase 1 regulatory subunit 1C",
        "refseq_ac": "NP_001102670",
        "gene_names_uniprotkb": "Ppp1r1c",
        "gene_names_refseq": "Ppp1r1c; RGD1562095",
        "protein_names_uniprotkb": "Protein phosphatase 1, regulatory (inhibitor) subunit 1C",
        "protein_names_refseq": "protein phosphatase 1 regulatory subunit 1C",
        "tax_id": 10116,
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        "pathway": " (rno:499818)",
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        "go_molecular_function": "GO:0004864 protein phosphatase inhibitor activity",
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        "record_id": "D3ZSW2-1",
        "record_type": "protein"
    },
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        "length": 385,
        "protein_name": "MARVEL domain containing 3",
        "gene_name": "Marveld3",
        "organism": "Rat",
        "refseq_name": "MARVEL domain-containing protein 3",
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        "gene_names_refseq": "Marveld3; RGD1562056",
        "protein_names_uniprotkb": "MARVEL domain containing 3",
        "protein_names_refseq": "MARVEL domain-containing protein 3",
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        "disease": "",
        "pathway": " (rno:498950)",
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        "class_list": "",
        "function": "Upregulation of PRRX2 by silencing Marveld3 as a protective mechanism against radiation-induced ferroptosis in skin cells. Publication Status: Online-Only, [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0031435 mitogen-activated protein kinase kinase kinase binding",
        "go_cellular_component": "GO:0016020 membrane;GO:0005737 cytoplasm;GO:0005923 bicellular tight junction;GO:0031410 cytoplasmic vesicle",
        "go_biological_process": "GO:0010633 negative regulation of epithelial cell migration;GO:0006970 response to osmotic stress;GO:0050680 negative regulation of epithelial cell proliferation;GO:0070830 bicellular tight junction assembly;GO:0046329 negative regulation of JNK cascade",
        "synthesized_glycan_count": 0,
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        "record_id": "D4A1D5-1",
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    },
    {
        "uniprot_canonical_ac": "D3ZG81-1",
        "uniprot_id": "D3ZG81_RAT",
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        "length": 286,
        "protein_name": "RING-type E3 ubiquitin transferase",
        "gene_name": "Marchf8",
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        "refseq_name": "E3 ubiquitin-protein ligase MARCHF8 isoform 1",
        "refseq_ac": "NP_001101352",
        "gene_names_uniprotkb": "Marchf8; March8",
        "gene_names_refseq": "March8; Marchf8; Mir",
        "protein_names_uniprotkb": "RING-type E3 ubiquitin transferase; 2.3.2.27",
        "protein_names_refseq": "E3 ubiquitin-protein ligase MARCH8; E3 ubiquitin-protein ligase MARCHF8 isoform 1; E3 ubiquitin-protein ligase MARCHF8; c-mir, cellular modulator of immune recognition; membrane-associated ring finger (C3HC4) 8, E3 ubiquitin protein ligase",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0061630 ubiquitin protein ligase activity;GO:0042287 MHC protein binding;GO:0004842 ubiquitin-protein transferase activity;GO:0042289 MHC class II protein binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005764 lysosome;GO:0005765 lysosomal membrane;GO:0031902 late endosome membrane;GO:0031901 early endosome membrane",
        "go_biological_process": "GO:0006955 immune response;GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process;GO:0000209 protein polyubiquitination;GO:0002495 antigen processing and presentation of peptide antigen via MHC class II;GO:0016567 protein ubiquitination",
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        "hit_score": 0.1,
        "record_id": "D3ZG81-1",
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    },
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        "uniprot_canonical_ac": "D3ZGL6-1",
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        "length": 722,
        "protein_name": "Cyclin T2",
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        "refseq_name": "cyclin-T2",
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        "pathway": " (rno:304758);  (R-RNO-112382);  (R-RNO-2173796);  (R-RNO-674695);  (R-RNO-6796648);  (R-RNO-6807505);  (R-RNO-75955)",
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        "publication_id_list": "33600051",
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        "function": "Restoration of NRF2 attenuates myocardial ischemia reperfusion injury through mediating microRNA-29a-3p/CCNT2 axis., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0016538 cyclin-dependent protein serine/threonine kinase regulator activity;GO:0003682 chromatin binding;GO:0019901 protein kinase binding;GO:0070063 RNA polymerase binding;GO:0001223 transcription coactivator binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0048471 perinuclear region of cytoplasm;GO:0008024 cyclin/CDK positive transcription elongation factor complex",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0051301 cell division;GO:0019085 early viral transcription;GO:0019086 late viral transcription",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D3ZGL6-1",
        "record_type": "protein"
    },
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        "length": 550,
        "protein_name": "Serine beta-lactamase-like protein LACTB, mitochondrial",
        "gene_name": "Lactb",
        "organism": "Rat",
        "refseq_name": "serine beta-lactamase-like protein LACTB, mitochondrial",
        "refseq_ac": "NP_001100303",
        "gene_names_uniprotkb": "Lactb",
        "gene_names_refseq": "Lactb",
        "protein_names_uniprotkb": "Serine beta-lactamase-like protein LACTB, mitochondrial",
        "protein_names_refseq": "serine beta-lactamase-like protein LACTB, mitochondrial",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:300803)",
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        "publication_count": 1,
        "publication_id_list": "19858488",
        "class_list": "",
        "function": "LACTB resides in the mitochondrial intermembrane space and forms a soluble high molecular weight homopolymer., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "missing_score": 10000,
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        "go_molecular_function": "GO:0042802 identical protein binding;GO:0008233 peptidase activity",
        "go_cellular_component": "GO:0005739 mitochondrion",
        "go_biological_process": "GO:0006508 proteolysis;GO:0006629 lipid metabolic process;GO:0019216 regulation of lipid metabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D3ZFJ6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZFK5-1",
        "uniprot_id": "D3ZFK5_RAT",
        "mass": 18100.0,
        "length": 162,
        "protein_name": "Signal peptidase complex subunit 1",
        "gene_name": "Spcs1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Spcs1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Signal peptidase complex subunit 1; Microsomal signal peptidase 12 kDa subunit",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-422085);  (R-RNO-9768727)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Component of the signal peptidase complex (SPC) which catalyzes the cleavage of N-terminal signal sequences from nascent proteins as they are translocated into the lumen of the endoplasmic reticulum. Dispensable for SPC enzymatic activity., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "missing_score": 10000,
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        "go_molecular_function": "GO:0043022 ribosome binding",
        "go_cellular_component": "GO:0005789 endoplasmic reticulum membrane;GO:0005787 signal peptidase complex",
        "go_biological_process": "GO:0019082 viral protein processing;GO:0019068 virion assembly;GO:0045047 protein targeting to ER;GO:0006465 signal peptide processing",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZFK5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZFK8-1",
        "uniprot_id": "D3ZFK8_RAT",
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        "length": 1060,
        "protein_name": "FERM, ARHGEF and pleckstrin domain-containing protein 2",
        "gene_name": "Farp2",
        "organism": "Rat",
        "refseq_name": "FERM, ARHGEF and pleckstrin domain-containing protein 2",
        "refseq_ac": "NP_001101703",
        "gene_names_uniprotkb": "Farp2",
        "gene_names_refseq": "Farp2",
        "protein_names_uniprotkb": "FERM, ARHGEF and pleckstrin domain-containing protein 2; FERM, RhoGEF and pleckstrin domain-containing protein 2",
        "protein_names_refseq": "FERM, ARHGEF and pleckstrin domain-containing protein 2; FERM, RhoGEF and pleckstrin domain protein 2; FERM, RhoGEF and pleckstrin domain-containing protein 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:316639);  (R-RNO-399955);  (R-RNO-9013149);  (R-RNO-9958810)",
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        "publication_id_list": "22673903;29393594",
        "class_list": "",
        "function": "Functions as a guanine nucleotide exchange factor that activates RAC1. May have relatively low activity. Plays a role in the response to class 3 semaphorins and remodeling of the actin cytoskeleton. Plays a role in TNFSF11-mediated osteoclast differentiation, especially in podosome rearrangement and reorganization of the actin cytoskeleton. Regulates the activation of ITGB3, integrin signaling and cell adhesion., [UniProtKB, UniProtKB, UniProtKB]",
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        "protein_names_uniprotkb": "Cysteine-rich C-terminal 1",
        "protein_names_refseq": "cysteine-rich C-terminal protein 1",
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        "disease": "",
        "pathway": " (rno:120100590)",
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        "ec_number_list": "",
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        "record_id": "D3ZGI6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZGJ6-1",
        "uniprot_id": "D3ZGJ6_RAT",
        "mass": 37452.0,
        "length": 342,
        "protein_name": "Sulfotransferase",
        "gene_name": "Hs3st6",
        "organism": "Rat",
        "refseq_name": "heparan sulfate glucosamine 3-O-sulfotransferase 6",
        "refseq_ac": "NP_001102920",
        "gene_names_uniprotkb": "Hs3st6",
        "gene_names_refseq": "Hs3st6",
        "protein_names_uniprotkb": "Sulfotransferase; 2.8.2.-",
        "protein_names_refseq": "heparan sulfate (glucosamine) 3-O-sulfotransferase 6; heparan sulfate glucosamine 3-O-sulfotransferase 6",
        "tax_id": 10116,
        "disease": "hereditary angioedema (Disease Ontology:DOID:14735)",
        "pathway": " (rno:684979);  (R-RNO-2022928)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "2.8.2.-;2.8.2.29",
        "go_molecular_function": "GO:0008467 [heparan sulfate]-glucosamine 3-sulfotransferase activity",
        "go_cellular_component": "GO:0005794 Golgi apparatus",
        "go_biological_process": "GO:0015012 heparan sulfate proteoglycan biosynthetic process;GO:0001835 blastocyst hatching",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZGJ6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZGJ9-1",
        "uniprot_id": "D3ZGJ9_RAT",
        "mass": 92563.0,
        "length": 809,
        "protein_name": "DEP domain-containing protein 1A",
        "gene_name": "Depdc1",
        "organism": "Rat",
        "refseq_name": "DEP domain-containing protein 1A",
        "refseq_ac": "NP_001292134",
        "gene_names_uniprotkb": "Depdc1",
        "gene_names_refseq": "Depdc1a; Depdc1",
        "protein_names_uniprotkb": "DEP domain-containing protein 1A",
        "protein_names_refseq": "DEP domain containing 1a; DEP domain-containing protein 1A",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:295538)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "May be involved in transcriptional regulation as a transcriptional corepressor. The DEPDC1A-ZNF224 complex may play a critical role in bladder carcinogenesis by repressing the transcription of the A20 gene, leading to transport of NF-KB protein into the nucleus, resulting in suppression of apoptosis of bladder cancer cells., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005096 GTPase activator activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0001650 fibrillar center;GO:0017053 transcription repressor complex",
        "go_biological_process": "GO:0035556 intracellular signal transduction;GO:0045892 negative regulation of DNA-templated transcription",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZGJ9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZGL5-1",
        "uniprot_id": "D3ZGL5_RAT",
        "mass": 42548.0,
        "length": 362,
        "protein_name": "Pre-mRNA-splicing factor 38B",
        "gene_name": "Prpf38a",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Prpf38a",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Pre-mRNA-splicing factor 38B",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "May be required for pre-mRNA splicing., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0071011 precatalytic spliceosome;GO:0071005 U2-type precatalytic spliceosome",
        "go_biological_process": "GO:0000398 mRNA splicing, via spliceosome",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D3ZGL5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZGQ2-1",
        "uniprot_id": "D3ZGQ2_RAT",
        "mass": 31089.0,
        "length": 270,
        "protein_name": "Thymidine kinase 2, mitochondrial",
        "gene_name": "Tk2",
        "organism": "Rat",
        "refseq_name": "thymidine kinase 2",
        "refseq_ac": "NP_001099636",
        "gene_names_uniprotkb": "Tk2",
        "gene_names_refseq": "Tk2",
        "protein_names_uniprotkb": "Thymidine kinase 2, mitochondrial; 2'-deoxyuridine kinase TK2; 2.7.1.21; 2.7.1.74; Deoxycytidine kinase TK2",
        "protein_names_refseq": "thymidine kinase 2, mitochondrial; thymidine kinase 2",
        "tax_id": 10116,
        "disease": "mitochondrial DNA depletion syndrome 2 (Disease Ontology:DOID:0080120); autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 3 (Disease Ontology:DOID:0111523)",
        "pathway": " (rno:291824);  (R-RNO-73614)",
        "pathway_count": 2,
        "publication_count": 2,
        "publication_id_list": "20544526;32345222",
        "class_list": "",
        "function": "A cytosolic form of TK2 was identified in all tested tissues in addition to mitochondrial TK2. TK1 was detected in liver and spleen cytosolic extracts while dCK was found in liver, spleen and lung cytosolic extracts., [RefSeq, PubMed]; Basic biochemical characterization of cytosolic enzymes in thymidine nucleotide synthesis in adult rat tissues: implications for tissue specific mitochondrial DNA depletion and deoxynucleoside-based therapy for TK2-deficiency. Publication Status: Online-Only, [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "missing_score": 10000,
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        "secondary_ac_list": "",
        "ec_number_list": "2.7.1.21;2.7.1.74",
        "go_molecular_function": "GO:0005524 ATP binding;GO:0004137 deoxycytidine kinase activity;GO:0004797 thymidine kinase activity;GO:0019136 deoxynucleoside kinase activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005739 mitochondrion",
        "go_biological_process": "GO:0071897 DNA biosynthetic process;GO:0046092 deoxycytidine metabolic process;GO:0046104 thymidine metabolic process;GO:0006264 mitochondrial DNA replication;GO:0032042 mitochondrial DNA metabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "D3ZGQ2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZGX2-1",
        "uniprot_id": "D3ZGX2_RAT",
        "mass": 21613.0,
        "length": 185,
        "protein_name": "C-type lectin domain family 2, member M",
        "gene_name": "Clec2m",
        "organism": "Rat",
        "refseq_name": "C-type lectin domain family 2 member M",
        "refseq_ac": "NP_001181914",
        "gene_names_uniprotkb": "Clec2m; Clec2ml1; RGD1564770",
        "gene_names_refseq": "Clec2ml1; Clec2m; RGD1564770",
        "protein_names_uniprotkb": "C-type lectin domain family 2, member M",
        "protein_names_refseq": "C-type lectin domain family 2 member M; C-type lectin domain family 2, member M like 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:500335)",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0030246 carbohydrate binding",
        "go_cellular_component": "GO:0016020 membrane",
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        "hit_score": 0.1,
        "record_id": "D3ZGX2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZH41-1",
        "uniprot_id": "D3ZH41_RAT",
        "mass": 63547.0,
        "length": 575,
        "protein_name": "Cytoskeleton-associated protein 4",
        "gene_name": "Ckap4",
        "organism": "Rat",
        "refseq_name": "cytoskeleton-associated protein 4",
        "refseq_ac": "NP_001102210",
        "gene_names_uniprotkb": "Ckap4",
        "gene_names_refseq": "Ckap4",
        "protein_names_uniprotkb": "Cytoskeleton-associated protein 4",
        "protein_names_refseq": "cytoskeleton-associated protein 4",
        "tax_id": 10116,
        "disease": "hepatocellular carcinoma (Disease Ontology:DOID:684)",
        "pathway": " (R-RNO-381426);  (R-RNO-5683826);  (R-RNO-6798695);  (R-RNO-8957275);  (R-RNO-9696264);  (R-RNO-9696270)",
        "pathway_count": 6,
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        "publication_id_list": "20870746;38843836",
        "class_list": "",
        "function": "Data demonstrate an important role for the PI3-kinase-Akt pathway in intracellular transport of surfactant protein A receptor P63., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "total_reported_n_glycosites": 0,
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005791 rough endoplasmic reticulum;GO:0005811 lipid droplet;GO:0005886 plasma membrane",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.5,
        "record_id": "D3ZH41-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZH66-1",
        "uniprot_id": "D3ZH66_RAT",
        "mass": 86704.0,
        "length": 798,
        "protein_name": "Transcription initiation factor TFIID subunit 5",
        "gene_name": "Taf5",
        "organism": "Rat",
        "refseq_name": "transcription initiation factor TFIID subunit 5",
        "refseq_ac": "NP_001099835",
        "gene_names_uniprotkb": "Taf5",
        "gene_names_refseq": "Taf5",
        "protein_names_uniprotkb": "Transcription initiation factor TFIID subunit 5; Transcription initiation factor TFIID 100 kDa subunit",
        "protein_names_refseq": "TAF5 RNA polymerase II, TATA box binding protein (TBP)-associated factor; transcription initiation factor TFIID subunit 5",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:294018);  (R-RNO-674695);  (R-RNO-6804756);  (R-RNO-6807505);  (R-RNO-73776);  (R-RNO-73779);  (R-RNO-75953);  (R-RNO-76042)",
        "pathway_count": 8,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "The TFIID basal transcription factor complex plays a major role in the initiation of RNA polymerase II (Pol II)-dependent transcription. TFIID recognizes and binds promoters with or without a TATA box via its subunit TBP, a TATA-box-binding protein, and promotes assembly of the pre-initiation complex (PIC). The TFIID complex consists of TBP and TBP-associated factors (TAFs), including TAF1, TAF2, TAF3, TAF4, TAF5, TAF6, TAF7, TAF8, TAF9, TAF10, TAF11, TAF12 and TAF13. The TFIID complex structure can be divided into 3 modules TFIID-A, TFIID-B, and TFIID-C. TAF5 is involved in two modules of TFIID, in TFIID-A together with TAF3 and TBP, and in TFIID-B with TAF8. Involved in contacts between TFIID and TFIIF in the PIC., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "gene_names_uniprotkb": "Rasal1",
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        "protein_names_refseq": "RAS protein activator like 1 (GAP1 like); rasGAP-activating-like protein 1 isoform 1; rasGAP-activating-like protein 1",
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        "pathway": " (rno:360814);  (R-RNO-5658442)",
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        "publication_id_list": "22056649;27396351",
        "class_list": "",
        "function": "Hypermethylation of RASAL1 is associated with the perpetuation of fibroblast activation and fibrogenesis in the liver, [RefSeq, PubMed]; Paridis rhizoma sapoinins attenuate CCl4-induced liver fibrosis through the regulation of RASAL1/ERK1/2 signal pathway., [RefSeq, PubMed]",
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        "protein_names_uniprotkb": "Galactose-3-O-sulfotransferase 4; Beta-galactose-3-O-sulfotransferase 4; Gal-beta-1,3-GalNAc 3'-sulfotransferase",
        "protein_names_refseq": "galactose-3-O-sulfotransferase 4",
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        "length": 312,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or6c33b",
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        "refseq_name": "olfactory receptor Olr1065",
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        "gene_names_uniprotkb": "Or6c33b",
        "gene_names_refseq": "Olr1065; Or6c33b; ratchr7-8119953-8120891_ORF",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 1065; olfactory receptor 2AP1-like; olfactory receptor 6C4-like; olfactory receptor Olr1065; olfactory receptor gene Olr1065",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
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        "length": 258,
        "protein_name": "UBX domain-containing protein 2A",
        "gene_name": "Ubxn2a",
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        "refseq_name": "UBX domain-containing protein 2A",
        "refseq_ac": "NP_001102952",
        "gene_names_uniprotkb": "Ubxn2a",
        "gene_names_refseq": "Ubxd4; Ubxn2a",
        "protein_names_uniprotkb": "UBX domain-containing protein 2A; UBX domain protein 2A",
        "protein_names_refseq": "UBX domain containing 4; UBX domain-containing protein 2A",
        "tax_id": 10116,
        "disease": "",
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        "function": "Acts to repress the ubiquitination and subsequent endoplasmic reticulum-associated degradation of CHRNA3 by the STUB1-VCP-UBXN2A complex in cortical neurons (PubMed:26265139). Also acts to promote the translocation of CHRNA3 to the plasma membrane and subsequently increases plasma membrane acetylcholine-gated ion-channel activation (By similarity). Plays a role in the inhibition of STUB1-mediated TP53 degradation, via its interaction with HSPA9 which acts to inhibit TP53 binding to HSPA9 (By similarity). Positively mediates the ubiquitination and proteosomal degradation of RICTOR, may thereby act as a negative regulator of the mTORC2 pathway (By similarity)., [UniProtKB, PubMed, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; The data of this study suggested that UBXD4 modulates the distribution of alpha3* nAChRs between specialized intracellular compartments and the plasma membrane., [RefSeq, PubMed]",
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        "secondary_ac_list": "A6HAJ7",
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        "go_molecular_function": "GO:0033130 acetylcholine receptor binding;GO:0043130 ubiquitin binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005783 endoplasmic reticulum;GO:0005794 Golgi apparatus;GO:0005829 cytosol",
        "go_biological_process": "GO:0031468 nuclear membrane reassembly;GO:0000045 autophagosome assembly;GO:1990830 cellular response to leukemia inhibitory factor;GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process;GO:0045732 positive regulation of protein catabolic process",
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        "protein_name": "heparosan-N-sulfate-glucuronate 5-epimerase",
        "gene_name": "Glce",
        "organism": "Rat",
        "refseq_name": "D-glucuronyl C5-epimerase",
        "refseq_ac": "NP_001414556",
        "gene_names_uniprotkb": "Glce",
        "gene_names_refseq": "Glce; RGD1565253",
        "protein_names_uniprotkb": "heparosan-N-sulfate-glucuronate 5-epimerase; 5.1.3.17",
        "protein_names_refseq": "D-glucuronyl C5-epimerase; glucuronyl C5-epimerase",
        "tax_id": 10116,
        "disease": "hypertension (Disease Ontology:DOID:10763); cerebrovascular disease (Disease Ontology:DOID:6713)",
        "pathway": " (rno:363073)",
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        "function": "The function of GLCE in neuritogenesis via SMAD/ID3 signalling was studied via mutagenesis and gene silencing studies., [RefSeq, PubMed]",
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        "refseq_name": "zinc transporter ZIP2",
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        "protein_names_refseq": "solute carrier family 39 (zinc transporter), member 2; zinc transporter ZIP2",
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        "uniprot_canonical_ac": "D3ZJ66-1",
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        "length": 595,
        "protein_name": "Neuronal PAS domain-containing protein 1",
        "gene_name": "Npas1",
        "organism": "Rat",
        "refseq_name": "neuronal PAS domain-containing protein 1",
        "refseq_ac": "NP_001100949",
        "gene_names_uniprotkb": "Npas1",
        "gene_names_refseq": "Npas1",
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        "protein_names_refseq": "neuronal PAS domain-containing protein 1",
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        "function": "May control regulatory pathways relevant to schizophrenia and to psychotic illness. May play a role in late central nervous system development by modulating EPO expression in response to cellular oxygen level. Forms a heterodimer that binds core DNA sequence 5'-TACGTG-3' within the hypoxia response element (HRE) leading to transcriptional repression on its target gene TH., [UniProtKB, UniProtKB]",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0046982 protein heterodimerization activity;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0001964 startle response;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0045892 negative regulation of DNA-templated transcription",
        "synthesized_glycan_count": 0,
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    },
    {
        "uniprot_canonical_ac": "D3ZJ84-1",
        "uniprot_id": "D3ZJ84_RAT",
        "mass": 42287.0,
        "length": 372,
        "protein_name": "non-specific serine/threonine protein kinase",
        "gene_name": "Tssk5",
        "organism": "Rat",
        "refseq_name": "testis-specific serine/threonine-protein kinase 5",
        "refseq_ac": "NP_001014108",
        "gene_names_uniprotkb": "Tssk5",
        "gene_names_refseq": "RGD1308613; Tssk5",
        "protein_names_uniprotkb": "non-specific serine/threonine protein kinase; 2.7.11.1",
        "protein_names_refseq": "testis-specific serine/threonine kinase; testis-specific serine/threonine-protein kinase 5",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:315095)",
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        "ec_number_list": "2.7.11.1;2.7.12.1;2.7.1.153;2.7.1.137;2.7.11.24;2.7.11.25;2.7.11.22;2.7.11.23;2.7.4.6;2.7.1.154;2.7.11.38;2.7.11.17;2.7.11.21;2.7.12.2;2.7.1.40;2.7.11.12;2.7.11.26;2.7.11.34;2.7.10.2;2.7.1.150;2.7.11.13;4.1.1.32;2.7.11.19;2.7.2.3;2.7.11.11;2.7.11.31;3.1.3.16;2.7.11.4;2.3.1.48;3.1.11.-;2.7.13.3;2.7.4.18;3.1.24.-;3.4.19.12;2.7.11.39;2.4.99.18;2.7.11.10",
        "go_molecular_function": "GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding",
        "go_cellular_component": "",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZJ84-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZJ91-1",
        "uniprot_id": "D3ZJ91_RAT",
        "mass": 79571.0,
        "length": 699,
        "protein_name": "DDHD domain containing 2",
        "gene_name": "Ddhd2",
        "organism": "Rat",
        "refseq_name": "phospholipase DDHD2 isoform 1",
        "refseq_ac": "NP_001305345",
        "gene_names_uniprotkb": "Ddhd2",
        "gene_names_refseq": "Ddhd2",
        "protein_names_uniprotkb": "DDHD domain containing 2",
        "protein_names_refseq": "phospholipase DDHD2 isoform 1; phospholipase DDHD2",
        "tax_id": 10116,
        "disease": "hereditary spastic paraplegia 28 (Disease Ontology:DOID:0110779); hereditary spastic paraplegia 54 (Disease Ontology:DOID:0110806); hereditary spastic paraplegia (Disease Ontology:DOID:2476)",
        "pathway": " (rno:680971);  (R-RNO-1483166)",
        "pathway_count": 2,
        "publication_count": 3,
        "publication_id_list": "22673903;26790472;27198176",
        "class_list": "",
        "function": "DG lipase activity in the soluble fraction of rat brain is derived from DDHD2. DDHD2 is distributed widely in the rat brain. Immunohistochemical analysis revealed that DDHD2 is expressed in hippocampal neurons, but not in glia., [RefSeq, PubMed]; These results therefore support the idea that DDHD2 functions as a DG lipase in vivo and produces 2-AG., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0046872 metal ion binding;GO:0004806 triacylglycerol lipase activity;GO:0004620 phospholipase activity",
        "go_cellular_component": "GO:0005829 cytosol;GO:0016020 membrane;GO:0005737 cytoplasm;GO:0030134 COPII-coated ER to Golgi transport vesicle",
        "go_biological_process": "GO:0007626 locomotory behavior;GO:0008542 visual learning;GO:0019433 triglyceride catabolic process;GO:0034389 lipid droplet organization;GO:0090141 positive regulation of mitochondrial fission",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "D3ZJ91-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZJA3-1",
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        "length": 300,
        "protein_name": "Sprouty RTK signaling antagonist 4",
        "gene_name": "Spry4",
        "organism": "Rat",
        "refseq_name": "protein sprouty homolog 4",
        "refseq_ac": "NP_001099620",
        "gene_names_uniprotkb": "Spry4",
        "gene_names_refseq": "Spry4",
        "protein_names_uniprotkb": "Sprouty RTK signaling antagonist 4",
        "protein_names_refseq": "protein sprouty homolog 4; sprouty homolog 4",
        "tax_id": 10116,
        "disease": "hypogonadotropic hypogonadism 17 with or without anosmia (Disease Ontology:DOID:0090079)",
        "pathway": " (rno:291610)",
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        "publication_count": 3,
        "publication_id_list": "22384148;22673903;23982388",
        "class_list": "",
        "function": "Decreased expression of Sproutys and SPREDs during the terminal pseudoglandular stage may disrupt lung branching morphogenesis by interfering with epithelial-mesenchymal interactions contributing to PH., [RefSeq, PubMed]; Spry4 regulates neurite outgrowth reducing not only the MAPK pathway but also restricting TrkA signaling and Rac1 activation in response to NGF, [RefSeq, PubMed]",
        "predicted_glycosites": 1,
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        "go_molecular_function": "GO:0004860 protein kinase inhibitor activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0016020 membrane",
        "go_biological_process": "GO:0046580 negative regulation of Ras protein signal transduction;GO:1990830 cellular response to leukemia inhibitory factor;GO:0070373 negative regulation of ERK1 and ERK2 cascade;GO:0043407 negative regulation of MAP kinase activity;GO:1900025 negative regulation of substrate adhesion-dependent cell spreading",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "D3ZJA3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZJA4-1",
        "uniprot_id": "D3ZJA4_RAT",
        "mass": 11365.0,
        "length": 99,
        "protein_name": "Seminal vesicle secretory protein 6",
        "gene_name": "Svs6",
        "organism": "Rat",
        "refseq_name": "seminal vesicle secretory protein 6 precursor",
        "refseq_ac": "NP_001095873",
        "gene_names_uniprotkb": "Svs6",
        "gene_names_refseq": "Svp6; Svs6",
        "protein_names_uniprotkb": "Seminal vesicle secretory protein 6",
        "protein_names_refseq": "seminal vesicle secretion 6; seminal vesicle secretory protein 6 precursor; seminal vesicle secretory protein VI",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:362267)",
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        "secondary_ac_list": "",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005615 extracellular space",
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        "hit_score": 0.1,
        "record_id": "D3ZJA4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZJB7-1",
        "uniprot_id": "D3ZJB7_RAT",
        "mass": 50970.0,
        "length": 472,
        "protein_name": "Solute carrier family 30, member 10",
        "gene_name": "Slc30a10",
        "organism": "Rat",
        "refseq_name": "calcium/manganese antiporter SLC30A10",
        "refseq_ac": "NP_001099455",
        "gene_names_uniprotkb": "Slc30a10",
        "gene_names_refseq": "RGD1305098; Slc30a10",
        "protein_names_uniprotkb": "Solute carrier family 30, member 10",
        "protein_names_refseq": "calcium/manganese antiporter SLC30A10; zinc transporter 10",
        "tax_id": 10116,
        "disease": "hypermanganesemia with dystonia 1 (Disease Ontology:DOID:0080536)",
        "pathway": " (rno:289353);  (R-RNO-425410)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "38866719",
        "class_list": "",
        "function": "Elevated thyroid manganese reduces thyroid iodine to induce hypothyroidism in mice, but not rats, lacking SLC30A10 transporter., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "predicted_c_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005385 zinc ion transmembrane transporter activity;GO:0005384 manganese ion transmembrane transporter activity;GO:0140983 calcium:manganese antiporter activity",
        "go_cellular_component": "GO:0005769 early endosome;GO:0005794 Golgi apparatus;GO:0005886 plasma membrane;GO:0016020 membrane;GO:0055037 recycling endosome",
        "go_biological_process": "GO:0010312 detoxification of zinc ion;GO:1904385 cellular response to angiotensin;GO:0071577 zinc ion transmembrane transport;GO:0070374 positive regulation of ERK1 and ERK2 cascade;GO:0007173 epidermal growth factor receptor signaling pathway",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D3ZJB7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZJG3-1",
        "uniprot_id": "D3ZJG3_RAT",
        "mass": 56881.0,
        "length": 503,
        "protein_name": "Transmembrane prolyl 4-hydroxylase",
        "gene_name": "P4htm",
        "organism": "Rat",
        "refseq_name": "transmembrane prolyl 4-hydroxylase",
        "refseq_ac": "NP_001386206",
        "gene_names_uniprotkb": "P4htm",
        "gene_names_refseq": "P4htm; Ph-4; RGD1311848",
        "protein_names_uniprotkb": "Transmembrane prolyl 4-hydroxylase; 1.14.11.29; Hypoxia-inducible factor prolyl hydroxylase 4",
        "protein_names_refseq": "hypoxia-inducible factor prolyl 4-hydroxylase; transmembrane prolyl 4-hydroxylase",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:301008)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Catalyzes the post-translational formation of 4-hydroxyproline in hypoxia-inducible factor (HIF) alpha proteins. Hydroxylates HIF1A at 'Pro-402' and 'Pro-564'. May function as a cellular oxygen sensor and, under normoxic conditions, may target HIF through the hydroxylation for proteasomal degradation via the von Hippel-Lindau ubiquitination complex., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "total_reported_n_glycosites": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "1.14.11.29;1.14.11.-",
        "go_molecular_function": "GO:0005506 iron ion binding;GO:0005509 calcium ion binding;GO:0031418 L-ascorbic acid binding;GO:0016706 2-oxoglutarate-dependent dioxygenase activity;GO:0004656 procollagen-proline 4-dioxygenase activity",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0045646 regulation of erythrocyte differentiation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZJG3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZJJ3-1",
        "uniprot_id": "D3ZJJ3_RAT",
        "mass": 11930.0,
        "length": 114,
        "protein_name": "Similar to human chromosome 1 open reading frame 210",
        "gene_name": "C5h1orf210",
        "organism": "Rat",
        "refseq_name": "type III endosome membrane protein TEMP",
        "refseq_ac": "NP_001102144",
        "gene_names_uniprotkb": "C5h1orf210; RGD1305347",
        "gene_names_refseq": "C5h1orf210; RGD1305347",
        "protein_names_uniprotkb": "Similar to human chromosome 1 open reading frame 210",
        "protein_names_refseq": "type III endosome membrane protein TEMP",
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    },
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        "length": 211,
        "protein_name": "Exosomal polycystin 1 interacting protein",
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        "refseq_name": "polycystin-1-interacting protein 1 precursor",
        "refseq_ac": "NP_001102522",
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        "gene_names_refseq": "C11h21orf62; Epcip; RGD1562726",
        "protein_names_uniprotkb": "Exosomal polycystin 1 interacting protein",
        "protein_names_refseq": "polycystin-1-interacting protein 1 precursor; polycystin-1-interacting protein 1; uncharacterized protein C21orf62 homolog",
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    },
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        "length": 338,
        "protein_name": "Transcription factor AP-4",
        "gene_name": "Tfap4",
        "organism": "Rat",
        "refseq_name": "transcription factor AP-4",
        "refseq_ac": "NP_001101737",
        "gene_names_uniprotkb": "Tfap4",
        "gene_names_refseq": "Tcfap4; Tfap4",
        "protein_names_uniprotkb": "Transcription factor AP-4",
        "protein_names_refseq": "transcription factor AP-4 (activating enhancer binding protein 4); transcription factor AP-4; transcription factor AP4",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0017053 transcription repressor complex",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0008285 negative regulation of cell population proliferation;GO:0010629 negative regulation of gene expression;GO:0043065 positive regulation of apoptotic process",
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    },
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        "length": 737,
        "protein_name": "Fibronectin type III domain containing 7",
        "gene_name": "Fndc7",
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        "refseq_name": "fibronectin type III domain-containing protein 7 precursor",
        "refseq_ac": "NP_001101187",
        "gene_names_uniprotkb": "Fndc7",
        "gene_names_refseq": "Fndc7; RGD1309189",
        "protein_names_uniprotkb": "Fibronectin type III domain containing 7",
        "protein_names_refseq": "fibronectin type III domain-containing protein 7 precursor; fibronectin type III domain-containing protein 7",
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    },
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        "length": 199,
        "protein_name": "Shisa N-terminal domain-containing protein",
        "gene_name": "Shisal1",
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        "refseq_name": "protein shisa-like-1 isoform X2",
        "refseq_ac": "XP_038936243",
        "gene_names_uniprotkb": "Shisal1",
        "gene_names_refseq": "Shisal1",
        "protein_names_uniprotkb": "Shisa N-terminal domain-containing protein",
        "protein_names_refseq": "protein shisa-like-1 isoform X2",
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        "go_cellular_component": "GO:0016020 membrane",
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    },
    {
        "uniprot_canonical_ac": "D3ZK09-1",
        "uniprot_id": "D3ZK09_RAT",
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        "length": 719,
        "protein_name": "SCY1 like pseudokinase 3",
        "gene_name": "Scyl3",
        "organism": "Rat",
        "refseq_name": "protein-associating with the carboxyl-terminal domain of ezrin isoform 2",
        "refseq_ac": "NP_001416656",
        "gene_names_uniprotkb": "Scyl3",
        "gene_names_refseq": "RGD1308992; Scyl3",
        "protein_names_uniprotkb": "SCY1 like pseudokinase 3",
        "protein_names_refseq": "SCY1-like 3; SCY1-like, kinase-like 3; protein-associating with the carboxyl-terminal domain of ezrin isoform 2; protein-associating with the carboxyl-terminal domain of ezrin",
        "tax_id": 10116,
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        "pathway": " (rno:360866)",
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        "go_molecular_function": "GO:0005524 ATP binding;GO:0042802 identical protein binding",
        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005737 cytoplasm;GO:0005794 Golgi apparatus;GO:0005829 cytosol;GO:0030027 lamellipodium",
        "go_biological_process": "GO:0006954 inflammatory response;GO:0021522 spinal cord motor neuron differentiation;GO:0008104 intracellular protein localization;GO:0048666 neuron development",
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        "hit_score": 0.1,
        "record_id": "D3ZK09-1",
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    },
    {
        "uniprot_canonical_ac": "D3ZK73-1",
        "uniprot_id": "D3ZK73_RAT",
        "mass": 110812.0,
        "length": 971,
        "protein_name": "Cullin-4B",
        "gene_name": "Cul4b",
        "organism": "Rat",
        "refseq_name": "cullin-4B",
        "refseq_ac": "NP_001100421",
        "gene_names_uniprotkb": "Cul4b",
        "gene_names_refseq": "Cul4b; RGD1564494",
        "protein_names_uniprotkb": "Cullin-4B",
        "protein_names_refseq": "cullin-4B",
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        "disease": "syndromic X-linked intellectual disability Cabezas type (Disease Ontology:DOID:0060822); intellectual disability (Disease Ontology:DOID:1059)",
        "pathway": " (rno:302502);  (R-RNO-110314);  (R-RNO-5696394);  (R-RNO-5696395);  (R-RNO-5696400);  (R-RNO-6781823);  (R-RNO-6782135);  (R-RNO-6782210);  (R-RNO-8951664)",
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        "function": "CUL4B expression is up-regulated in synovium and FLS from adjuvant-induced arthritis (AIA) rats. Increased CUL4B promotes the canonical Wnt signaling and promotes the pathogenesis of AIA rats. Decreased miR-101-3p contributes to disordered CUL4B., [RefSeq, PubMed]; Circ_0011058 alleviates RA pathology through the circ_0011058/miR-335-5p/CUL4B signal axis., [RefSeq, PubMed]; MiR-674-5p Suppresses the Proliferation and Migration of Glioma Cells by Targeting Cul4b., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0031625 ubiquitin protein ligase binding;GO:0160072 ubiquitin ligase complex scaffold activity",
        "go_cellular_component": "GO:0031464 Cul4A-RING E3 ubiquitin ligase complex;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0032991 protein-containing complex",
        "go_biological_process": "GO:0048708 astrocyte differentiation;GO:0031175 neuron projection development;GO:0006974 DNA damage response;GO:0042254 ribosome biogenesis;GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process",
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    },
    {
        "uniprot_canonical_ac": "D3ZKA0-1",
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        "mass": 44249.0,
        "length": 389,
        "protein_name": "Serpin B13",
        "gene_name": "Serpinb13",
        "organism": "Rat",
        "refseq_name": "serpin B13",
        "refseq_ac": "NP_001100638",
        "gene_names_uniprotkb": "Serpinb13",
        "gene_names_refseq": "Serpinb13",
        "protein_names_uniprotkb": "Serpin B13",
        "protein_names_refseq": "serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 13; serpin B13; serpin peptidase inhibitor, clade B (ovalbumin), member 13",
        "tax_id": 10116,
        "disease": "alpha 1-antitrypsin deficiency (Disease Ontology:DOID:13372)",
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        "function": "May play a role in the proliferation or differentiation of keratinocytes., [UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005615 extracellular space;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0010951 negative regulation of endopeptidase activity;GO:1902173 negative regulation of keratinocyte apoptotic process",
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    },
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        "length": 170,
        "protein_name": "Family with sequence similarity 209",
        "gene_name": "Fam209",
        "organism": "Rat",
        "refseq_name": "family with sequence similarity 209 A precursor",
        "refseq_ac": "NP_001100018",
        "gene_names_uniprotkb": "Fam209; Fam209a",
        "gene_names_refseq": "Fam209a; Fam209; RGD1307805",
        "protein_names_uniprotkb": "Family with sequence similarity 209",
        "protein_names_refseq": "family with sequence similarity 209 A precursor; family with sequence similarity 209 member B; family with sequence similarity 209, member A",
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        "go_cellular_component": "GO:0001669 acrosomal vesicle;GO:0005637 nuclear inner membrane",
        "go_biological_process": "GO:0007286 spermatid development;GO:0001675 acrosome assembly",
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        "record_id": "D3ZKD8-1",
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        "length": 698,
        "protein_name": "UV radiation resistance associated",
        "gene_name": "Uvrag",
        "organism": "Rat",
        "refseq_name": "UV radiation resistance-associated gene protein isoform 1",
        "refseq_ac": "NP_001388471",
        "gene_names_uniprotkb": "Uvrag",
        "gene_names_refseq": "Uvrag",
        "protein_names_uniprotkb": "UV radiation resistance associated",
        "protein_names_refseq": "UV radiation resistance-associated gene protein isoform 1; UV radiation resistance-associated gene protein",
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        "disease": "colorectal cancer (Disease Ontology:DOID:9256)",
        "pathway": " (rno:308846);  (R-RNO-1632852)",
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        "publication_id_list": "15623521;22673903",
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        "function": "In cultured hippocampal neurons, MAP2 and p63 were found to concomitantly compartmentalize to the dendritic processes during neuronal differentiation., [RefSeq, PubMed]; Involved in maintaining chromosomal stability. Promotes DNA double-strand break (DSB) repair by association with DNA-dependent protein kinase complex DNA-PK and activating it in non-homologous end joining (NHEJ). Required for centrosome stability and proper chromosome segregation., [UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0000421 autophagosome membrane;GO:0005768 endosome;GO:0005769 early endosome;GO:0005783 endoplasmic reticulum;GO:0005813 centrosome",
        "go_biological_process": "GO:0097352 autophagosome maturation;GO:0097680 double-strand break repair via classical nonhomologous end joining;GO:0036092 phosphatidylinositol-3-phosphate biosynthetic process;GO:0051684 maintenance of Golgi location;GO:0006281 DNA repair",
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        "record_id": "D3ZKE1-1",
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        "length": 361,
        "protein_name": "Spermatogenesis associated 22",
        "gene_name": "Spata22",
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        "gene_names_uniprotkb": "Spata22",
        "gene_names_refseq": "RGD1565378; Sgn; Spata22",
        "protein_names_uniprotkb": "Spermatogenesis associated 22",
        "protein_names_refseq": "spermatogenesis-associated protein 22",
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        "publication_id_list": "23903057;25142975",
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        "function": "It plays an important role in meiotic prophase I and its deletion causes infertility in rats., [RefSeq, PubMed]; Spata22 may function in regulating the post-invasion DNA synthesis through interacting with Rpa on the displaced strand. Publication Status: Online-Only, [RefSeq, PubMed]",
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        "length": 198,
        "protein_name": "Nudix hydrolase 16 like 2",
        "gene_name": "Nudt16l2",
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        "refseq_name": "uncharacterized protein LOC688828 isoform X1",
        "refseq_ac": "XP_038938090",
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        "gene_names_refseq": "Nudt16l2",
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        "protein_names_refseq": "uncharacterized protein LOC688828 isoform X1",
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        "gene_name": "Slc25a45",
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        "refseq_name": "solute carrier family 25 member 45",
        "refseq_ac": "NP_001258108",
        "gene_names_uniprotkb": "Slc25a45",
        "gene_names_refseq": "Slc25a45",
        "protein_names_uniprotkb": "Solute carrier family 25 member 45",
        "protein_names_refseq": "solute carrier family 25 member 45",
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        "length": 783,
        "protein_name": "Rabenosyn, RAB effector",
        "gene_name": "Rbsn",
        "organism": "Rat",
        "refseq_name": "rabenosyn-5",
        "refseq_ac": "NP_001101345",
        "gene_names_uniprotkb": "Rbsn; Zfyve20",
        "gene_names_refseq": "Rbsn; Zfyve20",
        "protein_names_uniprotkb": "Rabenosyn, RAB effector",
        "protein_names_refseq": "rabenosyn-5; zinc finger, FYVE domain containing 20",
        "tax_id": 10116,
        "disease": "Kariminejad neurodevelopmental syndrome (Disease Ontology:DOID:0061158)",
        "pathway": " (rno:312562);  (R-RNO-168138);  (R-RNO-983231)",
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        "refseq_ac": "XP_017449880",
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        "gene_names_refseq": "Cebpzos",
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        "protein_names_refseq": "protein CEBPZOS isoform X1",
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        "gene_name": "Itprid2",
        "organism": "Rat",
        "refseq_name": "protein ITPRID2",
        "refseq_ac": "NP_001101208",
        "gene_names_uniprotkb": "Itprid2; Ssfa2",
        "gene_names_refseq": "Itprid2; Ssfa2",
        "protein_names_uniprotkb": "ITPR interacting domain containing 2",
        "protein_names_refseq": "protein ITPRID2; sperm specific antigen 2; sperm-specific antigen 3",
        "tax_id": 10116,
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        "length": 131,
        "protein_name": "Sperm microtubule inner protein 11",
        "gene_name": "Spmip11",
        "organism": "Rat",
        "refseq_name": "sperm microtubule inner protein 11",
        "refseq_ac": "NP_001128000",
        "gene_names_uniprotkb": "Spmip11; RGD1305928; Tex49",
        "gene_names_refseq": "RGD1305928; Spmip11; Tex49",
        "protein_names_uniprotkb": "Sperm microtubule inner protein 11",
        "protein_names_refseq": "sperm microtubule inner protein 11; testis expressed 49; testis-expressed protein 49",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:300207)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "mined_o_glycosites": 0,
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        "mined_s_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "total_n_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0036126 sperm flagellum;GO:0160111 axonemal A tubule inner sheath",
        "go_biological_process": "GO:0030317 flagellated sperm motility",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D3ZMG5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZMM6-1",
        "uniprot_id": "D3ZMM6_RAT",
        "mass": 35661.0,
        "length": 312,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or4f52",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr747",
        "refseq_ac": "NP_001001068",
        "gene_names_uniprotkb": "Or4f52",
        "gene_names_refseq": "Olr747; Or4f52",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 747; olfactory receptor Olr747; olfactory receptor gene Olr747",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:405956)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "reported_phosphosites": 0,
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        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZMM6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZMN0-1",
        "uniprot_id": "D3ZMN0_RAT",
        "mass": 31586.0,
        "length": 270,
        "protein_name": "Testis specific, 13",
        "gene_name": "Tsga13",
        "organism": "Rat",
        "refseq_name": "testis-specific gene 13 protein",
        "refseq_ac": "NP_001101321",
        "gene_names_uniprotkb": "Tsga13",
        "gene_names_refseq": "Tsga13",
        "protein_names_uniprotkb": "Testis specific, 13",
        "protein_names_refseq": "testis specific gene A13; testis-specific gene 13 protein",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:688848)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "29393594",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D3ZMN0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZMP9-1",
        "uniprot_id": "D3ZMP9_RAT",
        "mass": 20382.0,
        "length": 185,
        "protein_name": "Ran guanine nucleotide release factor",
        "gene_name": "Rangrf",
        "organism": "Rat",
        "refseq_name": "ran guanine nucleotide release factor",
        "refseq_ac": "NP_001099260",
        "gene_names_uniprotkb": "Rangrf",
        "gene_names_refseq": "RGD1563195; Rangrf",
        "protein_names_uniprotkb": "Ran guanine nucleotide release factor; Ran-binding protein MOG1",
        "protein_names_refseq": "ran guanine nucleotide release factor",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:287419)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "May regulate the intracellular trafficking of RAN. Promotes guanine nucleotide release from RAN and inhibits binding of new GTP by preventing the binding of the RAN guanine nucleotide exchange factor RCC1. Regulates the levels of GTP-bound RAN in the nucleus, and thereby plays a role in the regulation of RAN-dependent mitotic spindle dynamics. Enhances the expression of SCN5A at the cell membrane in cardiomyocytes., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "reported_phosphosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0017080 sodium channel regulator activity;GO:0044325 transmembrane transporter binding;GO:0005085 guanyl-nucleotide exchange factor activity;GO:0031267 small GTPase binding;GO:0099103 channel activator activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005791 rough endoplasmic reticulum;GO:0005829 cytosol",
        "go_biological_process": "GO:1900825 regulation of membrane depolarization during cardiac muscle cell action potential;GO:0090307 mitotic spindle assembly;GO:2000010 positive regulation of protein localization to cell surface;GO:0060047 heart contraction;GO:0006888 endoplasmic reticulum to Golgi vesicle-mediated transport",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZMP9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZMZ9-1",
        "uniprot_id": "D3ZMZ9_RAT",
        "mass": 71469.0,
        "length": 634,
        "protein_name": "Guanine nucleotide-binding protein-like 3-like protein",
        "gene_name": "Gnl3l",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Gnl3l",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Guanine nucleotide-binding protein-like 3-like protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "obesity (Disease Ontology:DOID:9970)",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Stabilizes TERF1 telomeric association by preventing TERF1 recruitment by PML. Stabilizes TERF1 protein by preventing its ubiquitination and hence proteasomal degradation. Does so by interfering with TERF1-binding to FBXO4 E3 ubiquitin-protein ligase. Required for cell proliferation. By stabilizing TRF1 protein during mitosis, promotes metaphase-to-anaphase transition. Stabilizes MDM2 protein by preventing its ubiquitination, and hence proteasomal degradation. By acting on MDM2, may affect TP53 activity. Required for normal processing of ribosomal pre-rRNA. Binds GTP., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "predicted_o_glycosites": 0,
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        "reported_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005525 GTP binding",
        "go_cellular_component": "GO:0005730 nucleolus;GO:0005697 telomerase holoenzyme complex",
        "go_biological_process": "GO:1904816 positive regulation of protein localization to chromosome, telomeric region;GO:0031334 positive regulation of protein-containing complex assembly;GO:0032211 negative regulation of telomere maintenance via telomerase;GO:0031647 regulation of protein stability;GO:0031397 negative regulation of protein ubiquitination",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZMZ9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZN15-1",
        "uniprot_id": "D3ZN15_RAT",
        "mass": 41682.0,
        "length": 373,
        "protein_name": "L-threonine 3-dehydrogenase, mitochondrial",
        "gene_name": "Tdh",
        "organism": "Rat",
        "refseq_name": "L-threonine 3-dehydrogenase, mitochondrial",
        "refseq_ac": "NP_001099514",
        "gene_names_uniprotkb": "Tdh",
        "gene_names_refseq": "Tdh",
        "protein_names_uniprotkb": "L-threonine 3-dehydrogenase, mitochondrial; 1.1.1.103",
        "protein_names_refseq": "L-threonine 3-dehydrogenase, mitochondrial",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:290315)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Catalyzes the NAD(+)-dependent oxidation of L-threonine to 2-amino-3-ketobutyrate, mediating L-threonine catabolism., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
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        "reported_c_glycosites_with_glycan": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "1.1.1.103",
        "go_molecular_function": "GO:0042802 identical protein binding;GO:0008743 L-threonine 3-dehydrogenase activity",
        "go_cellular_component": "GO:0005739 mitochondrion",
        "go_biological_process": "GO:0006567 L-threonine catabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZN15-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZN39-1",
        "uniprot_id": "D3ZN39_RAT",
        "mass": 122551.0,
        "length": 1081,
        "protein_name": "Ubiquitin carboxyl-terminal hydrolase 8",
        "gene_name": "Usp8",
        "organism": "Rat",
        "refseq_name": "ubiquitin carboxyl-terminal hydrolase 8",
        "refseq_ac": "NP_001099972",
        "gene_names_uniprotkb": "Usp8",
        "gene_names_refseq": "Usp8",
        "protein_names_uniprotkb": "Ubiquitin carboxyl-terminal hydrolase 8; 3.4.19.12; Deubiquitinating enzyme 8; Ubiquitin isopeptidase Y; Ubiquitin thioesterase 8; Ubiquitin-specific-processing protease 8",
        "protein_names_refseq": "ubiquitin carboxyl-terminal hydrolase 8; ubiquitin specific protease 8",
        "tax_id": 10116,
        "disease": "ACTH-secreting pituitary adenoma (Disease Ontology:DOID:7004)",
        "pathway": " (rno:296121);  (R-RNO-1358803);  (R-RNO-5689880);  (R-RNO-6807004)",
        "pathway_count": 4,
        "publication_count": 4,
        "publication_id_list": "22673903;25505317;25662281;29735556",
        "class_list": "",
        "function": "Homeostatic downscaling of synaptic strength is accompanied by an increase and decrease in Nedd4-1 and USP8 levels, respectively., [RefSeq, PubMed]; USP8 knockdown increases TrkA half-life, suggesting that the deubiquitinating activity of USP8 promotes TrkA degradation., [RefSeq, PubMed]; We identify USP8 as a key enzyme that regulates SHANK3 protein levels in neurons, [RefSeq, PubMed]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
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        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "reported_c_glycosites": 0,
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        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "3.4.19.12;2.3.2.27;2.7.11.1;2.7.10.1",
        "go_molecular_function": "GO:0017124 SH3 domain binding;GO:0004843 cysteine-type deubiquitinase activity;GO:0061578 K63-linked deubiquitinase activity;GO:1990380 K48-linked deubiquitinase activity",
        "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005769 early endosome;GO:0005829 cytosol",
        "go_biological_process": "GO:0006508 proteolysis;GO:0016579 protein deubiquitination;GO:0070536 protein K63-linked deubiquitination;GO:1905908 positive regulation of amyloid fibril formation;GO:1990090 cellular response to nerve growth factor stimulus",
        "synthesized_glycan_count": 0,
        "hit_score": 0.5,
        "record_id": "D3ZN39-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZN48-1",
        "uniprot_id": "D3ZN48_RAT",
        "mass": 28432.0,
        "length": 259,
        "protein_name": "Dickkopf WNT signaling pathway inhibitor 2",
        "gene_name": "Dkk2",
        "organism": "Rat",
        "refseq_name": "dickkopf-related protein 2 precursor",
        "refseq_ac": "NP_001099942",
        "gene_names_uniprotkb": "Dkk2",
        "gene_names_refseq": "Dkk2",
        "protein_names_uniprotkb": "Dickkopf WNT signaling pathway inhibitor 2",
        "protein_names_refseq": "dickkopf 2 homolog; dickkopf homolog 2; dickkopf homolog 4; dickkopf-related protein 2 precursor; dickkopf-related protein 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:295445);  (R-RNO-3772470)",
        "pathway_count": 2,
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        "publication_id_list": "21540552;31985779",
        "class_list": "",
        "function": "MiR-128 promotes osteogenic differentiation of bone marrow mesenchymal stem cells in rat by targeting DKK2., [RefSeq, PubMed]; There are distinct functions of DKK1 and DKK2 in controlling angiogenesis, [RefSeq, PubMed]",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0048019 receptor antagonist activity;GO:0039706 co-receptor binding",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005794 Golgi apparatus",
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    },
    {
        "uniprot_canonical_ac": "D3ZNA8-1",
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        "mass": 31637.0,
        "length": 280,
        "protein_name": "Checkpoint protein",
        "gene_name": "Hus1",
        "organism": "Rat",
        "refseq_name": "checkpoint protein HUS1 isoform 1",
        "refseq_ac": "NP_001102562",
        "gene_names_uniprotkb": "Hus1",
        "gene_names_refseq": "Hus1",
        "protein_names_uniprotkb": "Checkpoint protein",
        "protein_names_refseq": "HUS1 checkpoint homolog; Hus1 homolog; checkpoint protein HUS1 isoform 1; checkpoint protein HUS1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:498411);  (R-RNO-176187);  (R-RNO-5685938);  (R-RNO-5693607);  (R-RNO-6804756);  (R-RNO-69473)",
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        "function": "Component of the 9-1-1 cell-cycle checkpoint response complex that plays a major role in DNA repair. The 9-1-1 complex is recruited to DNA lesion upon damage by the RAD17-replication factor C (RFC) clamp loader complex. Acts then as a sliding clamp platform on DNA for several proteins involved in long-patch base excision repair (LP-BER). The 9-1-1 complex stimulates DNA polymerase beta (POLB) activity by increasing its affinity for the 3'-OH end of the primer-template and stabilizes POLB to those sites where LP-BER proceeds; endonuclease FEN1 cleavage activity on substrates with double, nick, or gap flaps of distinct sequences and lengths; and DNA ligase I (LIG1) on long-patch base excision repair substrates. The 9-1-1 complex is necessary for the recruitment of RHNO1 to sites of double-stranded breaks (DSB) occurring during the S phase., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005829 cytosol;GO:0035861 site of double-strand break",
        "go_biological_process": "GO:0009792 embryo development ending in birth or egg hatching;GO:0006468 protein phosphorylation;GO:0000723 telomere maintenance;GO:0006974 DNA damage response;GO:0009411 response to UV",
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        "hit_score": 0.1,
        "record_id": "D3ZNA8-1",
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    },
    {
        "uniprot_canonical_ac": "D3ZND8-1",
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        "length": 158,
        "protein_name": "T cell receptor beta, variable 16",
        "gene_name": "Trbv16",
        "organism": "Rat",
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        "gene_names_uniprotkb": "Trbv16; Trbvl1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "T cell receptor beta, variable 16",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (R-RNO-198933);  (R-RNO-202424);  (R-RNO-202427);  (R-RNO-202430);  (R-RNO-202433);  (R-RNO-389948)",
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        "go_cellular_component": "GO:0005886 plasma membrane;GO:0042101 T cell receptor complex",
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        "hit_score": 0.1,
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    },
    {
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        "length": 522,
        "protein_name": "Iroquois homeobox 3",
        "gene_name": "Irx3",
        "organism": "Rat",
        "refseq_name": "iroquois-class homeodomain protein IRX-3 isoform X1",
        "refseq_ac": "XP_006255254",
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        "gene_names_refseq": "Irx3",
        "protein_names_uniprotkb": "Iroquois homeobox 3",
        "protein_names_refseq": "iroquois-class homeodomain protein IRX-3 isoform X1",
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        "go_molecular_function": "GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0001228 DNA-binding transcription activator activity, RNA polymerase II-specific;GO:1990837 sequence-specific double-stranded DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0030424 axon",
        "go_biological_process": "GO:0072086 specification of loop of Henle identity;GO:0003167 atrioventricular bundle cell differentiation;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006357 regulation of transcription by RNA polymerase II;GO:0045665 negative regulation of neuron differentiation",
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    },
    {
        "uniprot_canonical_ac": "D3ZNL0-1",
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        "length": 321,
        "protein_name": "Olfactory receptor",
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        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Or10ag2; Olr561; Or10ag54b",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Olfactory receptor",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
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        "go_biological_process": "GO:0050911 detection of chemical stimulus involved in sensory perception of smell",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZNL0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZNQ5-1",
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        "length": 603,
        "protein_name": "Zinc finger protein 949",
        "gene_name": "Zfp949",
        "organism": "Rat",
        "refseq_name": "zinc finger protein 717",
        "refseq_ac": "NP_001128003",
        "gene_names_uniprotkb": "Zfp949",
        "gene_names_refseq": "Zfp949",
        "protein_names_uniprotkb": "Zinc finger protein 949",
        "protein_names_refseq": "zinc finger protein 717",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:100233177)",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0008270 zinc ion binding",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006355 regulation of DNA-templated transcription",
        "synthesized_glycan_count": 0,
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    {
        "uniprot_canonical_ac": "D3ZNW4-1",
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        "length": 275,
        "protein_name": "Alkaline ceramidase",
        "gene_name": "Acer2",
        "organism": "Rat",
        "refseq_name": "alkaline ceramidase 2",
        "refseq_ac": "NP_001101413",
        "gene_names_uniprotkb": "Acer2",
        "gene_names_refseq": "Acer2; Asah3l",
        "protein_names_uniprotkb": "Alkaline ceramidase; 3.5.1.-",
        "protein_names_refseq": "alkaline ceramidase 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:313339);  (R-RNO-9845614)",
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        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Hydrolyzes the sphingolipid ceramide into sphingosine and free fatty acid., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "3.5.1.-;3.5.1.23;3.5.1.60",
        "go_molecular_function": "GO:0046872 metal ion binding;GO:0017040 N-acylsphingosine amidohydrolase activity",
        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0016020 membrane;GO:0005794 Golgi apparatus",
        "go_biological_process": "GO:0046512 sphingosine biosynthetic process;GO:0046514 ceramide catabolic process;GO:0006672 ceramide metabolic process;GO:0008284 positive regulation of cell population proliferation;GO:0010506 regulation of autophagy",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZNW4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZP13-1",
        "uniprot_id": "D3ZP13_RAT",
        "mass": 82606.0,
        "length": 742,
        "protein_name": "Sulfhydryl oxidase",
        "gene_name": "Qsox2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Qsox2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Sulfhydryl oxidase; 1.8.3.2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:681023)",
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        "class_list": "",
        "function": "Catalyzes the oxidation of sulfhydryl groups in peptide and protein thiols to disulfides with the reduction of oxygen to hydrogen peroxide., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "ec_number_list": "1.8.3.2",
        "go_molecular_function": "GO:0016971 flavin-dependent sulfhydryl oxidase activity;GO:0003756 protein disulfide isomerase activity",
        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005615 extracellular space;GO:0005654 nucleoplasm;GO:0005794 Golgi apparatus",
        "go_biological_process": "GO:0006457 protein folding",
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    },
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        "uniprot_canonical_ac": "D3ZP88-1",
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        "length": 222,
        "protein_name": "Homeo box C5",
        "gene_name": "Hoxc5",
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        "refseq_name": "homeobox protein Hox-C5",
        "refseq_ac": "NP_001101586",
        "gene_names_uniprotkb": "Hoxc5",
        "gene_names_refseq": "Hoxc5",
        "protein_names_uniprotkb": "Homeo box C5",
        "protein_names_refseq": "homeobox protein Hox-C5",
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        "publication_id_list": "22385119",
        "class_list": "",
        "function": "Sequence-specific transcription factor which is part of a developmental regulatory system that provides cells with specific positional identities on the anterior-posterior axis., [UniProtKB, UniProtKB]; These results indicate that overexpression of HOXC5 is correlated with oral carcinogenesis and strongly contributed to the development of OSCC. HOXC5 may be a useful biomarker and has an emerging therapeutic target of OSCC., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific",
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        "protein_name": "Hexosyltransferase",
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        "refseq_ac": "NP_001102424",
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        "gene_names_refseq": "B3galt1",
        "protein_names_uniprotkb": "Hexosyltransferase; 2.4.1.-",
        "protein_names_refseq": "UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase 1; UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 1; beta-1,3-galactosyltransferase 1",
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        "go_molecular_function": "GO:0008499 N-acetyl-beta-D-glucosaminide beta-(1,3)-galactosyltransferase activity",
        "go_cellular_component": "GO:0000139 Golgi membrane",
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        "synthesized_glycan_count": 300,
        "hit_score": 0.1,
        "record_id": "D3ZPD8-1",
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    },
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        "protein_name": "ADAM metallopeptidase domain 19",
        "gene_name": "Adam19",
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        "refseq_name": "disintegrin and metalloproteinase domain-containing protein 19 precursor",
        "refseq_ac": "NP_001153700",
        "gene_names_uniprotkb": "Adam19",
        "gene_names_refseq": "Adam19; Sox30",
        "protein_names_uniprotkb": "ADAM metallopeptidase domain 19",
        "protein_names_refseq": "SRY-box containing gene 30; a disintegrin and metallopeptidase domain 19 (meltrin beta); a disintegrin and metalloproteinase domain 19 (meltrin beta); disintegrin and metalloproteinase domain-containing protein 19 precursor; disintegrin and metalloproteinase domain-containing protein 19",
        "tax_id": 10116,
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        "pathway": " (rno:303068);  (R-RNO-8941237);  (R-RNO-9762292)",
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        "publication_id_list": "24103556",
        "class_list": "",
        "function": "TGF-beta stimulation of renal cells results in a significant up-regulation of Adams 10, 17, 12, and 19, [RefSeq, PubMed]",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005794 Golgi apparatus;GO:0016020 membrane",
        "go_biological_process": "GO:0006509 membrane protein ectodomain proteolysis;GO:0007507 heart development;GO:0010628 positive regulation of gene expression;GO:0016485 protein processing;GO:0001890 placenta development",
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        "record_id": "D3ZPM7-1",
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    },
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        "protein_name": "Protocadherin 17",
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        "gene_names_uniprotkb": "Pcdh17",
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        "protein_names_uniprotkb": "Protocadherin 17",
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        "go_molecular_function": "GO:0005509 calcium ion binding;GO:0050839 cell adhesion molecule binding",
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        "go_biological_process": "GO:0007155 cell adhesion;GO:0030534 adult behavior;GO:0007156 homophilic cell adhesion via plasma membrane adhesion molecules;GO:0050805 negative regulation of synaptic transmission;GO:0099560 synaptic membrane adhesion",
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        "record_id": "D3ZPN0-1",
        "record_type": "protein"
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        "uniprot_canonical_ac": "D3ZPN5-1",
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        "length": 602,
        "protein_name": "Mitochondrial poly(A) polymerase",
        "gene_name": "Mtpap",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Mtpap",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Mitochondrial poly(A) polymerase",
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        "disease": "spastic ataxia 4 (Disease Ontology:DOID:0050943)",
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        "go_molecular_function": "GO:0000287 magnesium ion binding;GO:0005524 ATP binding;GO:0030145 manganese ion binding;GO:0042802 identical protein binding;GO:0042803 protein homodimerization activity",
        "go_cellular_component": "GO:0005739 mitochondrion",
        "go_biological_process": "GO:0000965 mitochondrial RNA 3'-end processing;GO:0097222 mitochondrial mRNA polyadenylation;GO:0071044 histone mRNA catabolic process;GO:0031123 RNA 3'-end processing;GO:0016070 RNA metabolic process",
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        "record_id": "D3ZPN5-1",
        "record_type": "protein"
    },
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        "uniprot_canonical_ac": "D3ZPP6-1",
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        "length": 1050,
        "protein_name": "HECT and RLD domain containing E3 ubiquitin protein ligase 3",
        "gene_name": "Herc3",
        "organism": "Rat",
        "refseq_name": "probable E3 ubiquitin-protein ligase HERC3 isoform 1",
        "refseq_ac": "NP_001102101",
        "gene_names_uniprotkb": "Herc3",
        "gene_names_refseq": "Herc3",
        "protein_names_uniprotkb": "HECT and RLD domain containing E3 ubiquitin protein ligase 3",
        "protein_names_refseq": "hect domain and RLD 3; probable E3 ubiquitin-protein ligase HERC3 isoform 1; probable E3 ubiquitin-protein ligase HERC3",
        "tax_id": 10116,
        "disease": "",
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        "go_molecular_function": "GO:0061630 ubiquitin protein ligase activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0016567 protein ubiquitination;GO:0006511 ubiquitin-dependent protein catabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZPP6-1",
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    },
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        "uniprot_canonical_ac": "D3ZQ49-1",
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        "length": 456,
        "protein_name": "G-protein coupled receptor 83",
        "gene_name": "Pgr15l",
        "organism": "Rat",
        "refseq_name": "G protein-coupled receptor 15-like",
        "refseq_ac": "NP_001100053",
        "gene_names_uniprotkb": "Pgr15l",
        "gene_names_refseq": "Pgr15l; RGD1562685",
        "protein_names_uniprotkb": "G-protein coupled receptor 83; Glucocorticoid-induced receptor",
        "protein_names_refseq": "G protein-coupled receptor 15-like",
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        "pathway": " (rno:296867)",
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        "function": "G-protein coupled receptor for PEN, a neuropeptide produced from the precursor protein, proSAAS (encoded by PCSK1N). Acts through a G(i)- and G(q)-alpha-mediated pathway in response to PEN. Plays a role in food intake and body weight regulation. May contribute to the regulation of anxiety-related behaviors., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004983 neuropeptide Y receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0097730 non-motile cilium",
        "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZQ49-1",
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    {
        "uniprot_canonical_ac": "D3ZQ55-1",
        "uniprot_id": "D3ZQ55_RAT",
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        "length": 660,
        "protein_name": "Junctophilin",
        "gene_name": "Jph1",
        "organism": "Rat",
        "refseq_name": "junctophilin-1",
        "refseq_ac": "NP_001100100",
        "gene_names_uniprotkb": "Jph1",
        "gene_names_refseq": "Jph1",
        "protein_names_uniprotkb": "Junctophilin",
        "protein_names_refseq": "junctophilin-1",
        "tax_id": 10116,
        "disease": "cardiomyopathy (Disease Ontology:DOID:0050700); Charcot-Marie-Tooth disease axonal type 2K (Disease Ontology:DOID:0110167)",
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        "publication_id_list": "22673903;22927069;23148318;31315980",
        "class_list": "",
        "function": "JP1 gene is expressed during the whole process of cardiogenesis, while JP1 protein only appears during the early stage., [RefSeq, PubMed]; Junctophilins contribute to the formation of junctional membrane complexes (JMCs) which link the plasma membrane with the endoplasmic or sarcoplasmic reticulum in excitable cells. Provides a structural foundation for functional cross-talk between the cell surface and intracellular calcium release channels., [UniProtKB, UniProtKB]; Molecular determinants of homo- and heteromeric interactions of Junctophilin-1 at triads in adult skeletal muscle fibers., [RefSeq, PubMed]; This study demonstrates that both JP1 and JP2 in skeletal muscle undergo Ca2+-dependent proteolysis by endogenous proteases when the intracellular Ca2+ is raised within the physiological range for a sustained period, [RefSeq, PubMed]",
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        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005783 endoplasmic reticulum;GO:0005886 plasma membrane;GO:0005789 endoplasmic reticulum membrane;GO:0030018 Z disc",
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        "protein_name": "Olfactory receptor",
        "gene_name": "Or1n2",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr417",
        "refseq_ac": "NP_001000388",
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        "gene_names_refseq": "Olr417; Or1n2",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 417; olfactory receptor Olr417; olfactory receptor gene Olr417",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
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        "length": 280,
        "protein_name": "Similar to human chromosome 5 open reading frame 15",
        "gene_name": "C10h5orf15",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "C10h5orf15; RGD1310352",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Similar to human chromosome 5 open reading frame 15",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "protein_name": "RIKEN cDNA 2200002J24 gene like",
        "gene_name": "2200002J24Rikl",
        "organism": "Rat",
        "refseq_name": "uncharacterized protein LOC688924",
        "refseq_ac": "NP_001102989",
        "gene_names_uniprotkb": "2200002J24Rikl; LOC688924",
        "gene_names_refseq": "2200002J24Rikl",
        "protein_names_uniprotkb": "RIKEN cDNA 2200002J24 gene like",
        "protein_names_refseq": "uncharacterized protein LOC688924",
        "tax_id": 10116,
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    {
        "uniprot_canonical_ac": "D3ZQB2-1",
        "uniprot_id": "D3ZQB2_RAT",
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        "length": 319,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or10q12",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr375",
        "refseq_ac": "NP_001000259",
        "gene_names_uniprotkb": "Or10q12",
        "gene_names_refseq": "Olr375; Or10q12; ratchr1-217014288-217015247_ORF",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 375; olfactory receptor Olr375; olfactory receptor gene Olr375",
        "tax_id": 10116,
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding",
        "go_cellular_component": "GO:0005886 plasma membrane",
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    {
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        "length": 308,
        "protein_name": "Adipolin",
        "gene_name": "C1qtnf12",
        "organism": "Rat",
        "refseq_name": "adipolin precursor",
        "refseq_ac": "NP_001101470",
        "gene_names_uniprotkb": "C1qtnf12; Fam132a",
        "gene_names_refseq": "C1qdc2; C1qtnf12; Fam132a; RGD1307059",
        "protein_names_uniprotkb": "Adipolin; Adipose-derived insulin-sensitizing factor; Complement C1q tumor necrosis factor-related protein 12",
        "protein_names_refseq": "C1q and tumor necrosis factor related protein 12; C1q domain containing 2; adipolin precursor; adipolin; family with sequence similarity 132, member A; protein FAM132A",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:313774)",
        "pathway_count": 1,
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        "publication_id_list": "29393594;32009080",
        "class_list": "",
        "function": "C1qtnf12 ameliorated injury in lipopolysaccharide-stimulated cardiomyocytes in an NRF2-dependent manner., [RefSeq, PubMed]; Insulin-sensitizing adipocyte-secreted protein (adipokine) that regulates glucose metabolism in liver and adipose tissue. Promotes glucose uptake in adipocytes and suppresses de novo glucose production in hepatocytes via the PI3K-Akt signaling pathway. Administration lead to reduction of blood glucose. Able to attenuate inflammation in fat tissue., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0005179 hormone activity",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0005615 extracellular space",
        "go_biological_process": "GO:0051897 positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction;GO:0010906 regulation of glucose metabolic process;GO:0035774 positive regulation of insulin secretion involved in cellular response to glucose stimulus;GO:0046324 regulation of D-glucose import;GO:0050728 negative regulation of inflammatory response",
        "synthesized_glycan_count": 0,
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        "uniprot_canonical_ac": "D3ZQM6-1",
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        "protein_name": "Methyl-CpG binding domain protein 3-like 1",
        "gene_name": "Mbd3l1",
        "organism": "Rat",
        "refseq_name": "methyl-CpG-binding domain protein 3-like 1",
        "refseq_ac": "NP_001100273",
        "gene_names_uniprotkb": "Mbd3l1",
        "gene_names_refseq": "Mbd3l1",
        "protein_names_uniprotkb": "Methyl-CpG binding domain protein 3-like 1",
        "protein_names_refseq": "methyl-CpG-binding domain protein 3-like 1",
        "tax_id": 10116,
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        "go_molecular_function": "GO:0008327 methyl-CpG binding",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006346 DNA methylation-dependent constitutive heterochromatin formation",
        "synthesized_glycan_count": 0,
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    },
    {
        "uniprot_canonical_ac": "D3ZR99-1",
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        "length": 530,
        "protein_name": "Solute carrier family 45, member 2",
        "gene_name": "Slc45a2",
        "organism": "Rat",
        "refseq_name": "membrane-associated transporter protein",
        "refseq_ac": "NP_001101123",
        "gene_names_uniprotkb": "Slc45a2",
        "gene_names_refseq": "Matp; Slc45a2",
        "protein_names_uniprotkb": "Solute carrier family 45, member 2",
        "protein_names_refseq": "membrane associated transporter protein; membrane-associated transporter protein",
        "tax_id": 10116,
        "disease": "oculocutaneous albinism (Disease Ontology:DOID:0050632); oculocutaneous albinism type IV (Disease Ontology:DOID:0070098); pigmentation disease (Disease Ontology:DOID:10123); cataract (Disease Ontology:DOID:83)",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
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    },
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        "uniprot_canonical_ac": "D3ZRW5-1",
        "uniprot_id": "D3ZRW5_RAT",
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        "length": 442,
        "protein_name": "Protein Wnt",
        "gene_name": "Wnt10a",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Wnt10a",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Protein Wnt",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "tooth agenesis (Disease Ontology:DOID:0050591); Schopf-Schulz-Passarge syndrome (Disease Ontology:DOID:0111647); ectodermal dysplasia (Disease Ontology:DOID:2121)",
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        "publication_id_list": "",
        "class_list": "",
        "function": "Ligand for members of the frizzled family of seven transmembrane receptors., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005109 frizzled binding;GO:0005125 cytokine activity;GO:0048018 receptor ligand activity",
        "go_cellular_component": "GO:0005615 extracellular space",
        "go_biological_process": "GO:0048733 sebaceous gland development;GO:0010628 positive regulation of gene expression;GO:0014033 neural crest cell differentiation;GO:0030182 neuron differentiation;GO:0001942 hair follicle development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZRW5-1",
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    },
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        "uniprot_canonical_ac": "D3ZS41-1",
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        "mass": 68982.0,
        "length": 606,
        "protein_name": "Extracellular matrix protein 2",
        "gene_name": "Ecm2",
        "organism": "Rat",
        "refseq_name": "extracellular matrix protein 2 precursor",
        "refseq_ac": "NP_001414036",
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        "gene_names_refseq": "Ecm2",
        "protein_names_uniprotkb": "Extracellular matrix protein 2",
        "protein_names_refseq": "extracellular matrix protein 2 precursor; extracellular matrix protein 2, female organ and adipocyte specific",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:100361383)",
        "pathway_count": 1,
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        "biomarker_type": "",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0008201 heparin binding;GO:0005518 collagen binding;GO:0070052 collagen V binding",
        "go_cellular_component": "GO:0031012 extracellular matrix;GO:0005614 interstitial matrix",
        "go_biological_process": "GO:0030198 extracellular matrix organization;GO:0010811 positive regulation of cell-substrate adhesion",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZS41-1",
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    },
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        "length": 98,
        "protein_name": "NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 2",
        "gene_name": "Ndufa2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ndufa2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "nuclear type mitochondrial complex I deficiency 13 (Disease Ontology:DOID:0112076); Alzheimer's disease (Disease Ontology:DOID:10652)",
        "pathway": " (rno:291660)",
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        "function": "Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005743 mitochondrial inner membrane;GO:0031966 mitochondrial membrane;GO:0045271 respiratory chain complex I",
        "go_biological_process": "GO:0022904 respiratory electron transport chain;GO:0001835 blastocyst hatching",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZS58-1",
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    },
    {
        "uniprot_canonical_ac": "D3ZS76-1",
        "uniprot_id": "D3ZS76_RAT",
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        "length": 281,
        "protein_name": "Tetratricopeptide repeat domain 9",
        "gene_name": "Ttc9",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ttc9",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Tetratricopeptide repeat domain 9",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "opiate dependence (Disease Ontology:DOID:2559)",
        "pathway": " (rno:500689)",
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        "publication_count": 1,
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        "go_molecular_function": "GO:0044183 protein folding chaperone",
        "go_cellular_component": "GO:0005740 mitochondrial envelope;GO:0005829 cytosol;GO:0016020 membrane;GO:0012505 endomembrane system",
        "go_biological_process": "GO:0043066 negative regulation of apoptotic process;GO:0006457 protein folding;GO:0060348 bone development",
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        "hit_score": 0.2,
        "record_id": "D3ZS76-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZS97-1",
        "uniprot_id": "D3ZS97_RAT",
        "mass": 39607.0,
        "length": 346,
        "protein_name": "CD226 molecule",
        "gene_name": "Cd226",
        "organism": "Rat",
        "refseq_name": "CD226 antigen isoform 1 precursor",
        "refseq_ac": "NP_001100840",
        "gene_names_uniprotkb": "Cd226",
        "gene_names_refseq": "Cd226",
        "protein_names_uniprotkb": "CD226 molecule",
        "protein_names_refseq": "CD226 antigen isoform 1 precursor; CD226 antigen",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:307199);  (R-RNO-198933)",
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        "publication_count": 2,
        "publication_id_list": "22673903;22728856",
        "class_list": "",
        "function": "His study showed that CD226 Gly307Ser may correlate with risk of neuromyelitis optica in Southern Han Chinese., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0005178 integrin binding;GO:0019901 protein kinase binding;GO:0042802 identical protein binding;GO:0050839 cell adhesion molecule binding;GO:0038023 signaling receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0009986 cell surface;GO:0009897 external side of plasma membrane",
        "go_biological_process": "GO:0050862 positive regulation of T cell receptor signaling pathway;GO:0032729 positive regulation of type II interferon production;GO:0045954 positive regulation of natural killer cell mediated cytotoxicity;GO:0042267 natural killer cell mediated cytotoxicity;GO:0002729 positive regulation of natural killer cell cytokine production",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "D3ZS97-1",
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    },
    {
        "uniprot_canonical_ac": "D3ZSC1-1",
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        "length": 621,
        "protein_name": "Sushi domain containing 5",
        "gene_name": "Susd5",
        "organism": "Rat",
        "refseq_name": "sushi domain-containing protein 5 precursor",
        "refseq_ac": "NP_001386210",
        "gene_names_uniprotkb": "Susd5",
        "gene_names_refseq": "RGD1561132; Susd5",
        "protein_names_uniprotkb": "Sushi domain containing 5",
        "protein_names_refseq": "sushi domain-containing protein 5 precursor; sushi domain-containing protein 5",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:301039)",
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        "go_molecular_function": "GO:0005540 hyaluronic acid binding",
        "go_cellular_component": "GO:0071944 cell periphery",
        "go_biological_process": "GO:0007155 cell adhesion;GO:0007219 Notch signaling pathway",
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        "hit_score": 0.1,
        "record_id": "D3ZSC1-1",
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    },
    {
        "uniprot_canonical_ac": "D3ZSC2-1",
        "uniprot_id": "D3ZSC2_RAT",
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        "length": 335,
        "protein_name": "Programmed cell death 2-like",
        "gene_name": "Pdcd2l",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Pdcd2l",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Programmed cell death 2-like",
        "protein_names_refseq": "",
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        "pathway": " (rno:689637)",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005737 cytoplasm",
        "go_biological_process": "GO:0006915 apoptotic process",
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        "length": 323,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or4k15c",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr1626",
        "refseq_ac": "NP_001000090",
        "gene_names_uniprotkb": "Or4k15c",
        "gene_names_refseq": "Olr1626; Or4k15c; ratchr15-26477126-26476155_ORF",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 1626; olfactory receptor Olr1626; olfactory receptor gene Olr1626",
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        "function": "Findings suggest that the regulation of SP6 protein stability is one of the crucial steps in amelogenesis., [RefSeq, PubMed]; Morphological differentiation and metabolism of the iron-containing pigment in ameloblasts are independently regulated during amelogenesis by means of ectopic SP6 expression., [RefSeq, PubMed]; Promotes cell proliferation. Plays a role in tooth germ growth. Plays a role in the control of enamel mineralization. Binds the AMBN promoter., [UniProtKB, UniProtKB]; Sp6 positively regulates Rock1 transcription by direct binding to the Rock1 promoter region from -206 to -150, which functionally distinct from Sp1, [RefSeq, PubMed]; Sp6 promotes amelogenesis through inhibition of follistatin gene expression. Erratum:[J Med Invest. 2008 Aug;55(3-4):303], [RefSeq, PubMed]",
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        "protein_names_refseq": "SRY (sex determining region Y)-box 7; SRY box 7; SRY-box containing gene 7; transcription factor SOX-7",
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        "function": "Demonstrated the anti-apoptosis ability of FTX during epileptogenesis and uncovered a novel FTX-mediated mechanism in status epilepticus-induced neural apoptosis by targeting miR-21-5p/SOX7 axis, which provides a new target in developing lncRNA-based strategies to reduce SE-induced hippocampal neuron apoptosis, [RefSeq, PubMed]; Findings demonstrated that SOX7 interfered with beta-catenin activity to promote neuronal apoptosis, which acted as a novel signaling mechanism in neuronal cell death., [RefSeq, PubMed]",
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        "disease": "developmental and epileptic encephalopathy 38 (Disease Ontology:DOID:0080417); lipid storage disease (Disease Ontology:DOID:9455)",
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        "mass": 77046.0,
        "length": 677,
        "protein_name": "FERM domain containing kindlin 1",
        "gene_name": "Fermt1",
        "organism": "Rat",
        "refseq_name": "fermitin family homolog 1",
        "refseq_ac": "NP_001099985",
        "gene_names_uniprotkb": "Fermt1",
        "gene_names_refseq": "Fermt1; RGD1306816",
        "protein_names_uniprotkb": "FERM domain containing kindlin 1",
        "protein_names_refseq": "UNC-112 related protein 1; fermitin family homolog 1; fermitin family member 1; kindlin 1",
        "tax_id": 10116,
        "disease": "Kindler syndrome (Disease Ontology:DOID:0060472); telangiectasis (Disease Ontology:DOID:1272); vesiculobullous skin disease (Disease Ontology:DOID:2731)",
        "pathway": " (rno:296179)",
        "pathway_count": 1,
        "publication_count": 4,
        "publication_id_list": "22623678;28845732;29677029;36740252",
        "class_list": "",
        "function": "FERM domain containing kindlin 1 knockdown attenuates inflammation induced by intracerebral hemorrhage in rats via NLR family pyrin domain containing 3/nuclear factor kappa B pathway., [RefSeq, PubMed]; Kindlin-1 silencing elevated the mechanical and thermal pain thresholds of chronic constriction injury rats., [RefSeq, PubMed]; Results therefore suggest that kindlin-1 is a potential tool for improving axon regeneration after nervous system lesions., [RefSeq, PubMed]; That kindlin-1 is a key protein in the action of hyperbaric oxygen therapy in the treatment of neuropathic pain, [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005178 integrin binding;GO:0051015 actin filament binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005925 focal adhesion;GO:0030054 cell junction;GO:0071944 cell periphery",
        "go_biological_process": "GO:0051546 keratinocyte migration;GO:0051886 negative regulation of timing of anagen;GO:2000647 negative regulation of stem cell proliferation;GO:0007155 cell adhesion;GO:0007229 integrin-mediated signaling pathway",
        "synthesized_glycan_count": 0,
        "hit_score": 0.5,
        "record_id": "D3ZTV0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZTY1-1",
        "uniprot_id": "D3ZTY1_RAT",
        "mass": 65594.0,
        "length": 601,
        "protein_name": "Zinc finger and BTB domain-containing protein 46",
        "gene_name": "Zbtb46",
        "organism": "Rat",
        "refseq_name": "zinc finger and BTB domain-containing protein 46 isoform 1",
        "refseq_ac": "NP_001101278",
        "gene_names_uniprotkb": "Zbtb46",
        "gene_names_refseq": "Btbd4; Zbtb46",
        "protein_names_uniprotkb": "Zinc finger and BTB domain-containing protein 46; BTB/POZ domain-containing protein 4",
        "protein_names_refseq": "BTB (POZ) domain containing 4; zinc finger and BTB domain-containing protein 46 isoform 1; zinc finger and BTB domain-containing protein 46",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:311718)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Transcription regulator that mediates differentiation of conventional and non-conventional dendritic cells, and which is involved in tolerance to gut microbiota. Together with RORgammaT (RORC), specifically expressed in type 3 innate lymphoid cells (ILC3s) that are required for tolerance to gut microbiota, to mediate differentiation of peripherally-induced regulatory T-cells (pTreg), which suppress inflammatory responses to commensal microorganisms. Functions as a transcription corepressor for PRDM1., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "biomarker_type": "",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific;GO:0000976 transcription cis-regulatory region binding;GO:0003712 transcription coregulator activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0000785 chromatin",
        "go_biological_process": "GO:2001200 positive regulation of dendritic cell differentiation;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0030853 negative regulation of granulocyte differentiation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D3ZTY1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZU26-1",
        "uniprot_id": "D3ZU26_RAT",
        "mass": 23681.0,
        "length": 223,
        "protein_name": "Basic helix-loop-helix family, member e23",
        "gene_name": "Bhlhe23",
        "organism": "Rat",
        "refseq_name": "class E basic helix-loop-helix protein 23",
        "refseq_ac": "NP_001102681",
        "gene_names_uniprotkb": "Bhlhe23",
        "gene_names_refseq": "Bhlhb4; Bhlhe23; RGD1559760",
        "protein_names_uniprotkb": "Basic helix-loop-helix family, member e23",
        "protein_names_refseq": "basic helix-loop-helix domain containing, class B4; class E basic helix-loop-helix protein 23",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:499952)",
        "pathway_count": 1,
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        "class_list": "",
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        "biomarker_type": "",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0046983 protein dimerization activity;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0070888 E-box binding;GO:1990837 sequence-specific double-stranded DNA binding",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0046548 retinal rod cell development;GO:0048050 post-embryonic eye morphogenesis;GO:0061564 axon development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZU26-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZU27-1",
        "uniprot_id": "D3ZU27_RAT",
        "mass": 146562.0,
        "length": 1349,
        "protein_name": "ubiquitinyl hydrolase 1",
        "gene_name": "Usp31",
        "organism": "Rat",
        "refseq_name": "ubiquitin carboxyl-terminal hydrolase 31",
        "refseq_ac": "NP_001101018",
        "gene_names_uniprotkb": "Usp31",
        "gene_names_refseq": "Usp31",
        "protein_names_uniprotkb": "ubiquitinyl hydrolase 1; 3.4.19.12",
        "protein_names_refseq": "ubiquitin carboxyl-terminal hydrolase 31; ubiquitin specific protease 31",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:308959)",
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        "publication_count": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004843 cysteine-type deubiquitinase activity",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0006508 proteolysis;GO:0016579 protein deubiquitination",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZU27-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZU37-1",
        "uniprot_id": "D3ZU37_RAT",
        "mass": 34878.0,
        "length": 310,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or8b1b",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr1240",
        "refseq_ac": "NP_001000448",
        "gene_names_uniprotkb": "Or8b1b; LOC100912054",
        "gene_names_refseq": "Olr1240; Or8b1b",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 1240; olfactory receptor 8B3-like; olfactory receptor Olr1240; olfactory receptor gene Olr1240",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:300565)",
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        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
        "predicted_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZU37-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZU52-1",
        "uniprot_id": "D3ZU52_RAT",
        "mass": 35941.0,
        "length": 322,
        "protein_name": "COP9 signalosome subunit 7B",
        "gene_name": "Cops7b",
        "organism": "Rat",
        "refseq_name": "COP9 signalosome complex subunit 7b isoform X1",
        "refseq_ac": "XP_006245476",
        "gene_names_uniprotkb": "Cops7b",
        "gene_names_refseq": "Cops7b",
        "protein_names_uniprotkb": "COP9 signalosome subunit 7B",
        "protein_names_refseq": "COP9 signalosome complex subunit 7b isoform X1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:363273);  (R-RNO-5696394);  (R-RNO-6781823);  (R-RNO-8856825);  (R-RNO-8951664)",
        "pathway_count": 5,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Component of the COP9 signalosome complex (CSN), a complex involved in various cellular and developmental processes. The CSN complex is an essential regulator of the ubiquitin (Ubl) conjugation pathway by mediating the deneddylation of the cullin subunits of SCF-type E3 ligase complexes, leading to decrease the Ubl ligase activity of SCF-type complexes such as SCF, CSA or DDB2. The complex is also involved in phosphorylation of p53/TP53, JUN, I-kappa-B-alpha/NFKBIA, ITPK1 and IRF8/ICSBP, possibly via its association with CK2 and PKD kinases. CSN-dependent phosphorylation of TP53 and JUN promotes and protects degradation by the Ubl system, respectively., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0008180 COP9 signalosome",
        "go_biological_process": "GO:0010387 COP9 signalosome assembly;GO:0000338 protein deneddylation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZU52-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZU86-1",
        "uniprot_id": "D3ZU86_RAT",
        "mass": 46005.0,
        "length": 393,
        "protein_name": "Ceramide synthase 4",
        "gene_name": "Cers4",
        "organism": "Rat",
        "refseq_name": "ceramide synthase 4",
        "refseq_ac": "NP_001100587",
        "gene_names_uniprotkb": "Cers4",
        "gene_names_refseq": "Cers4; Lass4",
        "protein_names_uniprotkb": "Ceramide synthase 4",
        "protein_names_refseq": "LAG1 homolog, ceramide synthase 4; LAG1 longevity assurance homolog 4; ceramide synthase 4; longevity assurance homolog 4",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:304208);  (R-RNO-1660661)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "29393594",
        "class_list": "",
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        "missing_score": 10000,
        "biomarker_type": "",
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0050291 sphingosine N-acyltransferase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005783 endoplasmic reticulum;GO:0005789 endoplasmic reticulum membrane;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0046513 ceramide biosynthetic process;GO:0030148 sphingolipid biosynthetic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D3ZU86-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZUA2-1",
        "uniprot_id": "D3ZUA2_RAT",
        "mass": 75709.0,
        "length": 669,
        "protein_name": "NACHT, LRR and PYD domains-containing protein 10",
        "gene_name": "Nlrp10",
        "organism": "Rat",
        "refseq_name": "NACHT, LRR and PYD domains-containing protein 10",
        "refseq_ac": "NP_001099761",
        "gene_names_uniprotkb": "Nlrp10",
        "gene_names_refseq": "Nalp10; Nlrp10",
        "protein_names_uniprotkb": "NACHT, LRR and PYD domains-containing protein 10",
        "protein_names_refseq": "NACHT, LRR and PYD domains-containing protein 10; NACHT, leucine rich repeat and PYD containing 10",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:293426)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "24197756",
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        "function": "Inhibits autoprocessing of CASP1, CASP1-dependent IL1B secretion, PYCARD aggregation and PYCARD-mediated apoptosis but not apoptosis induced by FAS or BID. Displays anti-inflammatory activity. Required for immunity against C.albicans infection. Involved in the innate immune response by contributing to pro-inflammatory cytokine release in response to invasive bacterial infection. Contributes to T-cell-mediated inflammatory responses in the skin. Plays a role in protection against periodontitis through its involvement in induction of IL1A via ERK activation in oral epithelial cells infected with periodontal pathogens. Exhibits both ATPase and GTPase activities., [UniProtKB, UniProtKB]; NLRP10 is bound to ASC protein under resting conditions. It decreases with Abeta treatment, both in vitro and in vivo. Abeta-induced cathepsin released into the cytosol degrades NLRP10, allowing dissociation of NLRP3 and formation of the inflammasome., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0003924 GTPase activity;GO:0005524 ATP binding;GO:0016887 ATP hydrolysis activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0009898 cytoplasmic side of plasma membrane;GO:0061702 canonical inflammasome complex",
        "go_biological_process": "GO:0032730 positive regulation of interleukin-1 alpha production;GO:0006954 inflammatory response;GO:0045087 innate immune response;GO:0032755 positive regulation of interleukin-6 production;GO:0002250 adaptive immune response",
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        "record_type": "protein"
    },
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        "length": 982,
        "protein_name": "NLR family, pyrin domain containing 4A",
        "gene_name": "Nlrp4a",
        "organism": "Rat",
        "refseq_name": "NACHT, LRR and PYD domains-containing protein 4A",
        "refseq_ac": "NP_001099690",
        "gene_names_uniprotkb": "Nlrp4a",
        "gene_names_refseq": "Nlrp4a; RGD1561918",
        "protein_names_uniprotkb": "NLR family, pyrin domain containing 4A",
        "protein_names_refseq": "NACHT, LRR and PYD domains-containing protein 4A",
        "tax_id": 10116,
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        "pathway": " (rno:292545)",
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        "class_list": "",
        "function": "May be involved in inflammation and recognition of cytosolic pathogen-associated molecular patterns (PAMPs) not intercepted by membrane-bound receptors., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005524 ATP binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0061702 canonical inflammasome complex",
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    },
    {
        "uniprot_canonical_ac": "D3ZUM2-1",
        "uniprot_id": "SARM1_RAT",
        "mass": 79688.0,
        "length": 724,
        "protein_name": "NAD(+) hydrolase SARM1",
        "gene_name": "Sarm1",
        "organism": "Rat",
        "refseq_name": "NAD(+) hydrolase SARM1",
        "refseq_ac": "NP_001099287",
        "gene_names_uniprotkb": "Sarm1",
        "gene_names_refseq": "Sarm1",
        "protein_names_uniprotkb": "NAD(+) hydrolase SARM1; 3.2.2.-; 3.2.2.6; NADP(+) hydrolase SARM1; NADase SARM1; Sterile alpha and TIR motif-containing protein 1",
        "protein_names_refseq": "NAD(+) hydrolase SARM1; NADP(+) hydrolase SARM1; NADase SARM1; sterile alpha and TIR motif-containing protein 1",
        "tax_id": 10116,
        "disease": "neurodegenerative disease (Disease Ontology:DOID:1289); amyotrophic lateral sclerosis (Disease Ontology:DOID:332)",
        "pathway": " (rno:287545);  (R-RNO-166166);  (R-RNO-936964);  (R-RNO-937041);  (R-RNO-937072)",
        "pathway_count": 5,
        "publication_count": 4,
        "publication_id_list": "32968873;33318563;36287202;38334594",
        "class_list": "",
        "function": "A SARM1-mitochondrial feedback loop drives neuropathogenesis in a Charcot-Marie-Tooth disease type 2A rat model. Publication Status: Online-Only, [RefSeq, PubMed]; Cisplatin induced neurotoxicity is mediated by Sarm1 and calpain activation. Publication Status: Online-Only, [RefSeq, PubMed]; NAD(+) hydrolase, which plays a key role in axonal degeneration following injury by regulating NAD(+) metabolism. Acts as a negative regulator of MYD88- and TRIF-dependent toll-like receptor signaling pathway by promoting Wallerian degeneration, an injury-induced form of programmed subcellular death which involves degeneration of an axon distal to the injury site. Wallerian degeneration is triggered by NAD(+) depletion: in response to injury, SARM1 is activated and catalyzes cleavage of NAD(+) into ADP-D-ribose (ADPR), cyclic ADPR (cADPR) and nicotinamide; NAD(+) cleavage promoting cytoskeletal degradation and axon destruction. Also able to hydrolyze NADP(+), but not other NAD(+)-related molecules. Can activate neuronal cell death in response to stress. Regulates dendritic arborization through the MAPK4-JNK pathway. Involved in innate immune response: inhibits both TICAM1/TRIF- and MYD88-dependent activation of JUN/AP-1, TRIF-dependent activation of NF-kappa-B and IRF3, and the phosphorylation of MAPK14/p38. Acts as a non-self dsDNA sensor in a sequence-independent manner to elicit NAD(+) degradation and thus to promote programmed cell death (By similarity)., [UniProtKB, UniProtKB, UniProtKB]; Phosphorylation at S548 as a Functional Switch of Sterile Alpha and TIR Motif-Containing 1 in Cerebral Ischemia/Reperfusion Injury in Rats., [RefSeq, PubMed]; Synergistic Protection of Retinal Ganglion Cells (RGCs) by SARM1 Inactivation with CNTF in a Rodent Model of Nonarteritic Anterior Ischemic Optic Neuropathy. Publication Status: Online-Only, [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0042802 identical protein binding;GO:0003690 double-stranded DNA binding;GO:0035591 signaling adaptor activity;GO:0003953 NAD+ nucleosidase activity;GO:0061809 NAD+ nucleosidase activity, cyclic ADP-ribose generating",
        "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005737 cytoplasm;GO:0005739 mitochondrion;GO:0005741 mitochondrial outer membrane;GO:0005874 microtubule",
        "go_biological_process": "GO:0019677 NAD+ catabolic process;GO:0070585 protein localization to mitochondrion;GO:0007165 signal transduction;GO:0007399 nervous system development;GO:0030154 cell differentiation",
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        "protein_name": "GDP-fucose protein O-fucosyltransferase 2",
        "gene_name": "Pofut2",
        "organism": "Rat",
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        "gene_names_uniprotkb": "Pofut2",
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        "protein_names_uniprotkb": "GDP-fucose protein O-fucosyltransferase 2; 2.4.1.221; Peptide-O-fucosyltransferase 2",
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        "tax_id": 10116,
        "disease": "Down syndrome (Disease Ontology:DOID:14250)",
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        "gene_names_uniprotkb": "Dnajb1",
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        "protein_names_uniprotkb": "DnaJ heat shock protein family (Hsp40) member B1",
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        "go_molecular_function": "GO:0051082 unfolded protein binding;GO:0051087 protein-folding chaperone binding;GO:0051117 ATPase binding;GO:0003714 transcription corepressor activity;GO:0001671 ATPase activator activity",
        "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0061827 sperm head;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0090084 negative regulation of inclusion body assembly;GO:1903334 positive regulation of protein folding;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0030900 forebrain development;GO:0034605 cellular response to heat",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZUU5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZUV1-1",
        "uniprot_id": "D3ZUV1_RAT",
        "mass": 39114.0,
        "length": 359,
        "protein_name": "NIPA magnesium transporter 2",
        "gene_name": "Nipa2",
        "organism": "Rat",
        "refseq_name": "magnesium transporter NIPA2",
        "refseq_ac": "NP_001100988",
        "gene_names_uniprotkb": "Nipa2",
        "gene_names_refseq": "Nipa2; RGD1306051; SLC56A2",
        "protein_names_uniprotkb": "NIPA magnesium transporter 2",
        "protein_names_refseq": "magnesium transporter NIPA2; non imprinted in Prader-Willi/Angelman syndrome 2 homolog; solute carrier family 56 member 2",
        "tax_id": 10116,
        "disease": "hereditary spastic paraplegia (Disease Ontology:DOID:2476)",
        "pathway": " (rno:308667);  (R-RNO-5223345)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "29393594",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 1,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0015095 magnesium ion transmembrane transporter activity",
        "go_cellular_component": "GO:0005769 early endosome;GO:0005886 plasma membrane;GO:0016020 membrane",
        "go_biological_process": "GO:0015693 magnesium ion transport",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D3ZUV1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZUV2-1",
        "uniprot_id": "D3ZUV2_RAT",
        "mass": 110118.0,
        "length": 1006,
        "protein_name": "E3 ubiquitin-protein ligase MIB1",
        "gene_name": "Mib1",
        "organism": "Rat",
        "refseq_name": "E3 ubiquitin-protein ligase MIB1",
        "refseq_ac": "NP_001100875",
        "gene_names_uniprotkb": "Mib1",
        "gene_names_refseq": "Mib1",
        "protein_names_uniprotkb": "E3 ubiquitin-protein ligase MIB1; 2.3.2.27; DAPK-interacting protein 1; E3 ubiquitin-protein ligase mib1; Mind bomb homolog 1; RING-type E3 ubiquitin transferase MIB1",
        "protein_names_refseq": "E3 ubiquitin-protein ligase MIB1; mindbomb E3 ubiquitin protein ligase 1; mindbomb homolog 1",
        "tax_id": 10116,
        "disease": "left ventricular noncompaction (Disease Ontology:DOID:0060480); epilepsy (Disease Ontology:DOID:1826)",
        "pathway": " (rno:307594)",
        "pathway_count": 1,
        "publication_count": 2,
        "publication_id_list": "25931508;34954392",
        "class_list": "",
        "function": "E3 ubiquitin ligase mind bomb 1 overexpression reduces apoptosis and inflammation of cardiac microvascular endothelial cells in coronary microvascular dysfunction., [RefSeq, PubMed]; Mib1 analysis provides a comprehensive interactome for investigating its role in signaling networks and neuronal development., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0061630 ubiquitin protein ligase activity",
        "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005737 cytoplasm;GO:0005813 centrosome;GO:0014069 postsynaptic density;GO:0015630 microtubule cytoskeleton",
        "go_biological_process": "GO:0001701 in utero embryonic development;GO:0006897 endocytosis;GO:0007219 Notch signaling pathway;GO:0007507 heart development;GO:0045665 negative regulation of neuron differentiation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "D3ZUV2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZUY0-1",
        "uniprot_id": "D3ZUY0_RAT",
        "mass": 36196.0,
        "length": 334,
        "protein_name": "Retinol dehydrogenase 14",
        "gene_name": "Rdh14",
        "organism": "Rat",
        "refseq_name": "retinol dehydrogenase 14",
        "refseq_ac": "NP_001102746",
        "gene_names_uniprotkb": "Rdh14",
        "gene_names_refseq": "RGD1565196; Rdh14",
        "protein_names_uniprotkb": "Retinol dehydrogenase 14; 1.1.1.300; Alcohol dehydrogenase PAN2",
        "protein_names_refseq": "retinol dehydrogenase 14 (all-trans and 9-cis)9; retinol dehydrogenase 14 (all-trans and 9-cis); retinol dehydrogenase 14 (all-trans/9-cis/11-cis); retinol dehydrogenase 14",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:500629);  (R-RNO-5365859)",
        "pathway_count": 2,
        "publication_count": 0,
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        "class_list": "",
        "function": "",
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "1.1.1.300;1.1.1.184;1.1.1.122;1.1.1.30;1.1.1.104;1.1.1.-;1.1.1.21;1.1.1.372;1.1.1.54",
        "go_molecular_function": "GO:0008106 alcohol dehydrogenase (NADP+) activity;GO:0052650 all-trans-retinol dehydrogenase (NADP+) activity",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005783 endoplasmic reticulum;GO:0005829 cytosol",
        "go_biological_process": "GO:0042572 retinol metabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZUY0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZV26-1",
        "uniprot_id": "D3ZV26_RAT",
        "mass": 22351.0,
        "length": 217,
        "protein_name": "Vesicle transport protein",
        "gene_name": "Sft2d3",
        "organism": "Rat",
        "refseq_name": "vesicle transport protein SFT2C",
        "refseq_ac": "NP_001102357",
        "gene_names_uniprotkb": "Sft2d3",
        "gene_names_refseq": "RGD1561764; Sft2d3",
        "protein_names_uniprotkb": "Vesicle transport protein",
        "protein_names_refseq": "vesicle transport protein SFT2C",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:364835)",
        "pathway_count": 1,
        "publication_count": 0,
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        "class_list": "",
        "function": "May be involved in fusion of retrograde transport vesicles derived from an endocytic compartment with the Golgi complex., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0016020 membrane;GO:0012505 endomembrane system",
        "go_biological_process": "GO:0015031 protein transport;GO:0016192 vesicle-mediated transport",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZV26-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZV70-1",
        "uniprot_id": "D3ZV70_RAT",
        "mass": 25354.0,
        "length": 226,
        "protein_name": "A-kinase interacting protein 1",
        "gene_name": "Akip1",
        "organism": "Rat",
        "refseq_name": "A-kinase-interacting protein 1 isoform 1",
        "refseq_ac": "NP_001101967",
        "gene_names_uniprotkb": "Akip1",
        "gene_names_refseq": "Akip1; RGD1306959",
        "protein_names_uniprotkb": "A-kinase interacting protein 1",
        "protein_names_refseq": "A kinase (PRKA) interacting protein 1; A-kinase-interacting protein 1 isoform 1; proline-rich protein BCA3",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:361624)",
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        "publication_id_list": "23319652;24169435;24236204;30181740",
        "class_list": "",
        "function": "AKIP1 expression modulates mitochondrial function in rat neonatal cardiomyocytes. Publication Status: Online-Only, [RefSeq, PubMed]; Data indicate A-kinase interacting protein 1 (AKIP1) as a critical molecular regulator and a therapeutic control point for stress adaptation in the heart., [RefSeq, PubMed]; MiR-320 plays an important role in regulating cardiomyocyte apoptosis induced by ischemia-reperfusion injury by targeting AKIP1 and inducing the mitochondrial apoptotic pathway. Publication Status: Online-Only, [RefSeq, PubMed]; Our results show that AKIP1 is induced in hypertrophic hearts and can stimulate adaptive cardiomyocyte growth, which involves Akt signaling Publication Status: Online-Only, [RefSeq, PubMed]",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005654 nucleoplasm",
        "go_biological_process": "GO:1901222 regulation of non-canonical NF-kappaB signal transduction;GO:0034446 substrate adhesion-dependent cell spreading",
        "synthesized_glycan_count": 0,
        "hit_score": 0.5,
        "record_id": "D3ZV70-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZV90-1",
        "uniprot_id": "D3ZV90_RAT",
        "mass": 31649.0,
        "length": 290,
        "protein_name": "Empty spiracles homeobox 1",
        "gene_name": "Emx1",
        "organism": "Rat",
        "refseq_name": "homeobox protein EMX1",
        "refseq_ac": "NP_001414509",
        "gene_names_uniprotkb": "Emx1",
        "gene_names_refseq": "Emx1; RGD1564002",
        "protein_names_uniprotkb": "Empty spiracles homeobox 1",
        "protein_names_refseq": "empty spiracles homolog 1; homeobox protein EMX1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:500235)",
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        "go_molecular_function": "GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:1990837 sequence-specific double-stranded DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005730 nucleolus",
        "go_biological_process": "GO:0001701 in utero embryonic development;GO:0006357 regulation of transcription by RNA polymerase II;GO:0021987 cerebral cortex development;GO:0007417 central nervous system development;GO:0007420 brain development",
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        "record_id": "D3ZV90-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZVA5-1",
        "uniprot_id": "D3ZVA5_RAT",
        "mass": 33853.0,
        "length": 324,
        "protein_name": "Fibrillarin-like 1",
        "gene_name": "Fbll1",
        "organism": "Rat",
        "refseq_name": "rRNA/tRNA 2'-O-methyltransferase fibrillarin-like protein 1",
        "refseq_ac": "NP_001102294",
        "gene_names_uniprotkb": "Fbll1",
        "gene_names_refseq": "Fbll1; RGD1562841",
        "protein_names_uniprotkb": "Fibrillarin-like 1",
        "protein_names_refseq": "fibrillarin rRNA 2'-O-methyltransferase like 1; fibrillarin-like 1; rRNA/tRNA 2'-O-methyltransferase fibrillarin-like protein 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:363563)",
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003723 RNA binding;GO:0008649 rRNA methyltransferase activity;GO:1990259 histone H2AQ104 methyltransferase activity;GO:0062105 RNA 2'-O-methyltransferase activity;GO:0008168 methyltransferase activity",
        "go_cellular_component": "GO:0005730 nucleolus;GO:0001650 fibrillar center;GO:0015030 Cajal body;GO:0031428 box C/D methylation guide snoRNP complex;GO:0032040 small-subunit processome",
        "go_biological_process": "GO:0031167 rRNA methylation;GO:0048255 mRNA stabilization;GO:0001835 blastocyst hatching;GO:0000494 box C/D sno(s)RNA 3'-end processing;GO:0006364 rRNA processing",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZVA5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZVH0-1",
        "uniprot_id": "D3ZVH0_RAT",
        "mass": 46899.0,
        "length": 418,
        "protein_name": "STE20-related kinase adapter protein beta",
        "gene_name": "Stradb",
        "organism": "Rat",
        "refseq_name": "STE20-related kinase adapter protein beta",
        "refseq_ac": "NP_001102777",
        "gene_names_uniprotkb": "Stradb",
        "gene_names_refseq": "Als2cr2; RGD1559449; Stradb",
        "protein_names_uniprotkb": "STE20-related kinase adapter protein beta; Pseudokinase ALS2CR2",
        "protein_names_refseq": "STE20-related kinase adapter protein beta; STE20-related kinase adaptor beta; amyotrophic lateral sclerosis 2 (juvenile) chromosome region, candidate 2; polyploidy associated protein kinase PAPK-A",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:501146);  (R-RNO-380972)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Pseudokinase which, in complex with CAB39/MO25 (CAB39/MO25alpha or CAB39L/MO25beta), binds to and activates STK11/LKB1. Adopts a closed conformation typical of active protein kinases and binds STK11/LKB1 as a pseudosubstrate, promoting conformational change of STK11/LKB1 in an active conformation., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004672 protein kinase activity;GO:0005524 ATP binding;GO:0043539 protein serine/threonine kinase activator activity",
        "go_cellular_component": "GO:1902554 serine/threonine protein kinase complex;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0007254 JNK cascade;GO:0000902 cell morphogenesis;GO:0032147 activation of protein kinase activity;GO:2001240 negative regulation of extrinsic apoptotic signaling pathway in absence of ligand;GO:0006611 protein export from nucleus",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZVH0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZVM7-1",
        "uniprot_id": "D3ZVM7_RAT",
        "mass": 26528.0,
        "length": 247,
        "protein_name": "MyoD family inhibitor domain containing",
        "gene_name": "Mdfic",
        "organism": "Rat",
        "refseq_name": "myoD family inhibitor domain-containing protein",
        "refseq_ac": "NP_001099138",
        "gene_names_uniprotkb": "Mdfic",
        "gene_names_refseq": "Kdt1; Mdfic",
        "protein_names_uniprotkb": "MyoD family inhibitor domain containing",
        "protein_names_refseq": "MyoD family inhibitor domain containing protein; kidney cell line derived transcript 1; myoD family inhibitor domain-containing protein",
        "tax_id": 10116,
        "disease": "hereditary lymphedema (Disease Ontology:DOID:0050580); central conducting lymphatic anomaly (Disease Ontology:DOID:0081030)",
        "pathway": " (rno:362325)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 2,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0030957 Tat protein binding;GO:0030332 cyclin binding;GO:0140297 DNA-binding transcription factor binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0045892 negative regulation of DNA-templated transcription;GO:0045893 positive regulation of DNA-templated transcription;GO:0030111 regulation of Wnt signaling pathway;GO:0042308 negative regulation of protein import into nucleus;GO:0046328 regulation of JNK cascade",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZVM7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZVU3-1",
        "uniprot_id": "D3ZVU3_RAT",
        "mass": 28233.0,
        "length": 255,
        "protein_name": "Myogenic factor",
        "gene_name": "Myf5",
        "organism": "Rat",
        "refseq_name": "myogenic factor 5",
        "refseq_ac": "NP_001100253",
        "gene_names_uniprotkb": "Myf5",
        "gene_names_refseq": "Myf5",
        "protein_names_uniprotkb": "Myogenic factor",
        "protein_names_refseq": "myogenic factor 5",
        "tax_id": 10116,
        "disease": "Duchenne muscular dystrophy (Disease Ontology:DOID:11723); musculoskeletal system disease (Disease Ontology:DOID:17)",
        "pathway": " (rno:299766);  (R-RNO-525793)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "21258934",
        "class_list": "",
        "function": "Induces fibroblasts to differentiate into myoblasts. Acts as a transcriptional activator that promotes transcription of muscle-specific target genes and plays a role in muscle differentiation., [UniProtKB, UniProtKB]; Myf 5 mRNA and protein expression were not altered in the CDH group., [RefSeq, PubMed]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 2,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0046983 protein dimerization activity;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0043565 sequence-specific DNA binding;GO:0001228 DNA-binding transcription activator activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0043403 skeletal muscle tissue regeneration;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0030198 extracellular matrix organization;GO:0045944 positive regulation of transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D3ZVU3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZW78-1",
        "uniprot_id": "D3ZW78_RAT",
        "mass": 92012.0,
        "length": 835,
        "protein_name": "Probable carboxypeptidase X1",
        "gene_name": "Cpxm1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Cpxm1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Probable carboxypeptidase X1; Metallocarboxypeptidase CPX-1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:296156)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "May be involved in cell-cell interactions. No carboxypeptidase activity was found yet., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
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        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0004181 metallocarboxypeptidase activity",
        "go_cellular_component": "GO:0005615 extracellular space",
        "go_biological_process": "GO:0006508 proteolysis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZW78-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZW90-1",
        "uniprot_id": "D3ZW90_RAT",
        "mass": 69286.0,
        "length": 611,
        "protein_name": "Rho-related BTB domain-containing protein 3",
        "gene_name": "Rhobtb3",
        "organism": "Rat",
        "refseq_name": "rho-related BTB domain-containing protein 3",
        "refseq_ac": "NP_001101115",
        "gene_names_uniprotkb": "Rhobtb3",
        "gene_names_refseq": "Rhobtb3",
        "protein_names_uniprotkb": "Rho-related BTB domain-containing protein 3",
        "protein_names_refseq": "rho-related BTB domain-containing protein 3",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:309922);  (R-RNO-6811440);  (R-RNO-9706019)",
        "pathway_count": 3,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Rab9-regulated ATPase required for endosome to Golgi transport. Involved in transport vesicle docking at the Golgi complex, possibly by participating in release M6PRBP1/TIP47 from vesicles to permit their efficient docking and fusion at the Golgi. Specifically binds Rab9, but not other Rab proteins. Has low intrinsic ATPase activity due to autoinhibition, which is relieved by Rab9., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003924 GTPase activity;GO:0005524 ATP binding;GO:0005525 GTP binding;GO:0016887 ATP hydrolysis activity;GO:0031625 ubiquitin protein ligase binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005794 Golgi apparatus;GO:0005829 cytosol",
        "go_biological_process": "GO:0008584 male gonad development;GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process;GO:0030162 regulation of proteolysis;GO:0042147 retrograde transport, endosome to Golgi",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZW90-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZWD7-1",
        "uniprot_id": "D3ZWD7_RAT",
        "mass": 35222.0,
        "length": 312,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or4f14f",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr780",
        "refseq_ac": "NP_001000606",
        "gene_names_uniprotkb": "Or4f14f",
        "gene_names_refseq": "Olr780; Or4f14f",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 780; olfactory receptor Olr780; olfactory receptor gene Olr780",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:404795)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZWD7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZWF5-1",
        "uniprot_id": "D3ZWF5_RAT",
        "mass": 11429.0,
        "length": 100,
        "protein_name": "Transcription and mRNA export factor ENY2",
        "gene_name": "Eny2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Eny2; ENY2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Transcription and mRNA export factor ENY2; Enhancer of yellow 2 transcription factor homolog",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:685258)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Involved in mRNA export coupled transcription activation by association with both the TREX-2 and the SAGA complexes. The transcription regulatory histone acetylation (HAT) complex SAGA is a multiprotein complex that activates transcription by remodeling chromatin and mediating histone acetylation and deubiquitination. Within the SAGA complex, participates to a subcomplex that specifically deubiquitinates both histones H2A and H2B. The SAGA complex is recruited to specific gene promoters by activators such as MYC, where it is required for transcription. Required for nuclear receptor-mediated transactivation. The TREX-2 complex functions in docking export-competent ribonucleoprotein particles (mRNPs) to the nuclear entrance of the nuclear pore complex (nuclear basket). TREX-2 participates in mRNA export and accurate chromatin positioning in the nucleus by tethering genes to the nuclear periphery., [UniProtKB, HAMAP, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003713 transcription coactivator activity;GO:0003682 chromatin binding",
        "go_cellular_component": "GO:0044615 nuclear pore nuclear basket;GO:0005654 nucleoplasm;GO:0071819 DUBm complex;GO:0070390 transcription export complex 2;GO:0000124 SAGA complex",
        "go_biological_process": "GO:0016973 poly(A)+ mRNA export from nucleus;GO:0006357 regulation of transcription by RNA polymerase II;GO:0015031 protein transport;GO:0045893 positive regulation of DNA-templated transcription;GO:0061179 negative regulation of insulin secretion involved in cellular response to glucose stimulus",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZWF5-1",
        "record_type": "protein"
    },
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        "length": 286,
        "protein_name": "Homeo box B13",
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        "refseq_name": "homeobox protein Hox-B13",
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        "function": "A microRNA175p/homeobox B13 axis participates in the phenotypic modulation of vascular smooth muscle cells., [RefSeq, PubMed]",
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        "length": 330,
        "protein_name": "Olfactory receptor family 14 subfamily N member 1",
        "gene_name": "Or14n1",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr20",
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        "gene_names_uniprotkb": "Or14n1",
        "gene_names_refseq": "Olr20; Or14n1",
        "protein_names_uniprotkb": "Olfactory receptor family 14 subfamily N member 1",
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        "protein_names_uniprotkb": "Matrix metalloproteinase-17; Membrane-type matrix metalloproteinase 4; Membrane-type-4 matrix metalloproteinase",
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        "protein_names_uniprotkb": "Elongation factor-like GTPase 1; Elongation factor Tu GTP-binding domain-containing protein 1; Elongation factor-like 1; Protein FAM42A",
        "protein_names_refseq": "elongation factor Tu GTP binding domain containing 1; elongation factor Tu GTP-binding domain-containing protein 1; elongation factor-like GTPase 1",
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        "function": "GTPase involved in the biogenesis of the 60S ribosomal subunit and translational activation of ribosomes. Together with SBDS, triggers the GTP-dependent release of EIF6 from 60S pre-ribosomes in the cytoplasm, thereby activating ribosomes for translation competence by allowing 80S ribosome assembly and facilitating EIF6 recycling to the nucleus, where it is required for 60S rRNA processing and nuclear export., [UniProtKB, UniProtKB, UniProtKB]",
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        "protein_names_refseq": "BTB/POZ domain-containing protein KCTD4; potassium channel tetramerisation domain containing 4",
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        "protein_name": "ADAM metallopeptidase with thrombospondin type 1 motif, 15",
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        "refseq_name": "A disintegrin and metalloproteinase with thrombospondin motifs 15 precursor",
        "refseq_ac": "NP_001100280",
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        "protein_names_refseq": "A disintegrin and metalloproteinase with thrombospondin motifs 15 precursor; A disintegrin and metalloproteinase with thrombospondin motifs 15; a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 15",
        "tax_id": 10116,
        "disease": "distal arthrogryposis (Disease Ontology:DOID:0050646)",
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        "protein_names_refseq": "leucine-rich repeat-containing protein 4C precursor; leucine-rich repeat-containing protein 4C",
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        "protein_name": "Similar to human chromosome 1 open reading frame 198",
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        "organism": "Rat",
        "refseq_name": "uncharacterized protein C1orf198 homolog",
        "refseq_ac": "NP_001102604",
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        "gene_names_refseq": "C19h1orf198; RGD1559896",
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        "protein_names_refseq": "uncharacterized protein C1orf198 homolog",
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        "organism": "Rat",
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        "gene_names_uniprotkb": "Or9a4",
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        "protein_name": "Leucine rich repeat containing 38",
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        "organism": "Rat",
        "refseq_name": "leucine-rich repeat-containing protein 38 precursor",
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        "gene_names_uniprotkb": "Lrrc38",
        "gene_names_refseq": "Lrrc38; RGD1311416",
        "protein_names_uniprotkb": "Leucine rich repeat containing 38",
        "protein_names_refseq": "leucine-rich repeat-containing protein 38 precursor; leucine-rich repeat-containing protein 38",
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        "gene_name": "Nudt11",
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        "refseq_name": "diphosphoinositol polyphosphate phosphohydrolase 3-beta",
        "refseq_ac": "NP_001388133",
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        "protein_names_uniprotkb": "Diphosphoinositol polyphosphate phosphohydrolase 3-alpha; Nudix hydrolase 11",
        "protein_names_refseq": "diphosphoinositol polyphosphate phosphohydrolase 3-beta; nudix (nucleoside diphosphate linked moiety X)-type motif 11",
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        "gene_names_refseq": "Olr879; Or6c38",
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        "protein_names_refseq": "olfactory receptor 879; olfactory receptor Olr879; olfactory receptor gene Olr879",
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        "refseq_name": "zinc finger protein 663",
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        "protein_names_uniprotkb": "Zinc finger protein 663",
        "protein_names_refseq": "rCG32328-like; zinc finger protein 663; zinc finger protein 84-like; zinc finger protein 883-like",
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        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II",
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        "length": 400,
        "protein_name": "Zinc finger CCHC-type containing 3",
        "gene_name": "Zcchc3",
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        "refseq_name": "zinc finger CCHC domain-containing protein 3",
        "refseq_ac": "NP_001386550",
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        "protein_names_refseq": "zinc finger CCHC domain-containing protein 3; zinc finger, CCHC domain containing 3",
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        "go_molecular_function": "GO:0003723 RNA binding;GO:0008270 zinc ion binding;GO:0003690 double-stranded DNA binding",
        "go_cellular_component": "GO:0005737 cytoplasm",
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    },
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        "protein_name": "Proline rich and Gla domain 4",
        "gene_name": "Prrg4",
        "organism": "Rat",
        "refseq_name": "transmembrane gamma-carboxyglutamic acid protein 4 precursor",
        "refseq_ac": "NP_001102673",
        "gene_names_uniprotkb": "Prrg4",
        "gene_names_refseq": "Prrg4; RGD1560542",
        "protein_names_uniprotkb": "Proline rich and Gla domain 4",
        "protein_names_refseq": "proline rich Gla (G-carboxyglutamic acid) 4 (transmembrane); transmembrane gamma-carboxyglutamic acid protein 4 precursor; transmembrane gamma-carboxyglutamic acid protein 4",
        "tax_id": 10116,
        "disease": "cholangiocarcinoma (Disease Ontology:DOID:4947)",
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        "go_molecular_function": "GO:0005509 calcium ion binding;GO:0050699 WW domain binding",
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        "uniprot_canonical_ac": "D3ZZC5-1",
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        "mass": 34530.0,
        "length": 310,
        "protein_name": "Tumor necrosis factor receptor type 1-associated DEATH domain protein",
        "gene_name": "Tradd",
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        "refseq_name": "tumor necrosis factor receptor type 1-associated DEATH domain protein",
        "refseq_ac": "NP_001093950",
        "gene_names_uniprotkb": "Tradd",
        "gene_names_refseq": "Tradd",
        "protein_names_uniprotkb": "Tumor necrosis factor receptor type 1-associated DEATH domain protein; TNFRSF1A-associated via death domain",
        "protein_names_refseq": "tumor necrosis factor receptor type 1-associated DEATH domain protein",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:246756);  (R-RNO-3371378);  (R-RNO-5218900);  (R-RNO-5357786);  (R-RNO-5357905);  (R-RNO-5357956);  (R-RNO-5675482);  (R-RNO-69416);  (R-RNO-75893)",
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        "function": "Adapter molecule for TNFRSF1A/TNFR1 that specifically associates with the cytoplasmic domain of activated TNFRSF1A/TNFR1 mediating its interaction with FADD. Overexpression of TRADD leads to two major TNF-induced responses, apoptosis and activation of NF-kappa-B. The nuclear form acts as a tumor suppressor by preventing ubiquitination and degradation of isoform p19ARF/ARF of CDKN2A by TRIP12: acts by interacting with TRIP12, leading to disrupt interaction between TRIP12 and isoform p19ARF/ARF of CDKN2A., [UniProtKB, UniProtKB, UniProtKB]; Results show that both infliximab and methylprednisolone (MP) could lower the expressions of NF-kappaB, TRADD, and FADD 24 hours after the acute spinal cord injury (ASCI)., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0005068 transmembrane receptor protein tyrosine kinase adaptor activity;GO:0070513 death domain binding;GO:0030674 protein-macromolecule adaptor activity;GO:0042802 identical protein binding;GO:0019900 kinase binding",
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        "gene_name": "Dcp1b",
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        "refseq_name": "mRNA-decapping enzyme 1B isoform 1",
        "refseq_ac": "NP_001418769",
        "gene_names_uniprotkb": "Dcp1b",
        "gene_names_refseq": "Dcp1b; RGD1562214",
        "protein_names_uniprotkb": "5'-(N(7)-methylguanosine 5'-triphospho)-[mRNA] hydrolase; 3.6.1.62",
        "protein_names_refseq": "DCP1 decapping enzyme homolog b; mRNA-decapping enzyme 1B isoform 1; mRNA-decapping enzyme 1B",
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        "refseq_name": "potassium voltage-gated channel subfamily V member 2",
        "refseq_ac": "NP_001099840",
        "gene_names_uniprotkb": "Kcnv2",
        "gene_names_refseq": "Kcnv2",
        "protein_names_uniprotkb": "Potassium voltage-gated channel subfamily V member 2; Voltage-gated potassium channel subunit Kv8.2",
        "protein_names_refseq": "potassium channel, subfamily V, member 2; potassium channel, voltage-gated modifier subfamily V, member 2; potassium voltage-gated channel subfamily V member 2",
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        "disease": "cone dystrophy with supernormal rod responses (Disease Ontology:DOID:0081022)",
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        "function": "Potassium channel subunit. Modulates channel activity by shifting the threshold and the half-maximal activation to more negative values., [UniProtKB, UniProtKB]; The present data provide evidence that the transcriptional regulation of Kcnv2 and Kv2.1 is a way through which the retinal clock system drives the functional adaptation of visual function to the marked daily changes in environmental lighting conditions. Publication Status: Online-Only, [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0015459 potassium channel regulator activity;GO:0005249 voltage-gated potassium channel activity",
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        "protein_name": "peptidylprolyl isomerase",
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        "gene_names_uniprotkb": "Fkbp2",
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        "protein_names_uniprotkb": "peptidylprolyl isomerase; 5.2.1.8",
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        "tax_id": 10116,
        "disease": "Huntington's disease (Disease Ontology:DOID:12858)",
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        "function": "PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides., [UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "5.2.1.8",
        "go_molecular_function": "GO:0003755 peptidyl-prolyl cis-trans isomerase activity",
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        "record_id": "D3ZZR9-1",
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    {
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        "uniprot_id": "D3ZZU8_RAT",
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        "length": 309,
        "protein_name": "protein-ribulosamine 3-kinase",
        "gene_name": "Fn3k",
        "organism": "Rat",
        "refseq_name": "fructosamine-3-kinase",
        "refseq_ac": "NP_001102521",
        "gene_names_uniprotkb": "Fn3k",
        "gene_names_refseq": "Fn3k; Fnsk",
        "protein_names_uniprotkb": "protein-ribulosamine 3-kinase; 2.7.1.172",
        "protein_names_refseq": "fructosamine-3-kinase",
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        "pathway": " (rno:498034);  (R-RNO-163841)",
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        "publication_id_list": "15331600",
        "class_list": "",
        "function": "Fructosamine 3-kinase and fructosamine 3-kinase-related protein have roles in repairing damage caused by ribose 5-phosphate [FN3K, FN3K-RP], [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005829 cytosol",
        "go_biological_process": "GO:0030389 fructosamine metabolic process;GO:0030855 epithelial cell differentiation;GO:0036528 peptidyl-lysine deglycation;GO:0036525 protein deglycation",
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        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "D4A029-1",
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        "protein_name": "2-oxoglutarate and iron-dependent oxygenase JMJD4",
        "gene_name": "Jmjd4",
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        "gene_names_uniprotkb": "Jmjd4",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "2-oxoglutarate and iron-dependent oxygenase JMJD4; JmjC domain-containing protein 4; Jumonji domain-containing protein 4; Lysyl-hydroxylase JMJD4",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "go_molecular_function": "GO:0043565 sequence-specific DNA binding;GO:0016706 2-oxoglutarate-dependent dioxygenase activity;GO:0106156 peptidyl-lysine 4-dioxygenase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm",
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        "length": 222,
        "protein_name": "STING ER exit protein",
        "gene_name": "Steep1",
        "organism": "Rat",
        "refseq_name": "STING ER exit protein",
        "refseq_ac": "NP_001101420",
        "gene_names_uniprotkb": "Steep1; RGD1564541",
        "gene_names_refseq": "RGD1564541; Steep1",
        "protein_names_uniprotkb": "STING ER exit protein",
        "protein_names_refseq": "STING ER exit protein; UPF0428 protein CXorf56 homolog",
        "tax_id": 10116,
        "disease": "non-syndromic X-linked intellectual disability 107 (Disease Ontology:DOID:0112054)",
        "pathway": " (rno:313433);  (R-RNO-72163)",
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        "class_list": "",
        "function": "Molecular adapter that stimulates membrane curvature formation and subsequent endoplasmic reticulum exit site (ERES) establishment by recruiting PI3K complex I, leading to COPII vesicle-mediated transport. Promotes endoplasmic reticulum (ER) exit of cGAMP-activated STING1 oligomers., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0030674 protein-macromolecule adaptor activity",
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        "go_biological_process": "GO:0090158 endoplasmic reticulum membrane organization;GO:0006888 endoplasmic reticulum to Golgi vesicle-mediated transport;GO:0032527 protein exit from endoplasmic reticulum",
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        "protein_name": "Serine hydrolase-like 2",
        "gene_name": "Serhl2",
        "organism": "Rat",
        "refseq_name": "serine hydrolase-like protein 2 isoform X1",
        "refseq_ac": "XP_008763997",
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        "gene_names_refseq": "RGD1563386; Serhl2",
        "protein_names_uniprotkb": "Serine hydrolase-like 2",
        "protein_names_refseq": "serine hydrolase-like protein 2 isoform X1",
        "tax_id": 10116,
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        "pathway": " (rno:500911)",
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        "go_molecular_function": "GO:0016787 hydrolase activity",
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        "length": 312,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or51k2",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr135",
        "refseq_ac": "NP_001001288",
        "gene_names_uniprotkb": "Or51k2",
        "gene_names_refseq": "Olr135; Or51k2",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 135; olfactory receptor Olr135; olfactory receptor gene Olr135",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "protein_name": "Olfactory receptor",
        "gene_name": "Or4m1",
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        "refseq_name": "olfactory receptor Olr1612",
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        "gene_names_refseq": "Olr1612; Or4m1",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 1612; olfactory receptor Olr1612; olfactory receptor gene Olr1612",
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        "uniprot_id": "D4A099_RAT",
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        "length": 460,
        "protein_name": "5-cytosine rRNA methyltransferase NSUN4",
        "gene_name": "Nsun4",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Nsun4",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "5-cytosine rRNA methyltransferase NSUN4; 5-cytosine tRNA methyltransferase NSUN4; NOL1/NOP2/Sun domain family member 4",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "go_molecular_function": "GO:0009383 rRNA (cytosine-C5-)-methyltransferase activity;GO:0008168 methyltransferase activity;GO:0008649 rRNA methyltransferase activity;GO:0008173 RNA methyltransferase activity;GO:0070181 small ribosomal subunit rRNA binding",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005759 mitochondrial matrix",
        "go_biological_process": "GO:0031167 rRNA methylation;GO:0006364 rRNA processing;GO:0000957 mitochondrial RNA catabolic process;GO:1902775 mitochondrial large ribosomal subunit assembly;GO:1900864 mitochondrial RNA modification",
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    },
    {
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        "length": 636,
        "protein_name": "Protein arginine N-methyltransferase 5",
        "gene_name": "Prmt5",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Prmt5",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Protein arginine N-methyltransferase 5; 2.1.1.320",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "idiopathic scoliosis (Disease Ontology:DOID:0060250); Leydig cell tumor (Disease Ontology:DOID:2696); asthma (Disease Ontology:DOID:2841); seminoma (Disease Ontology:DOID:4440)",
        "pathway": " (rno:364382);  (R-RNO-191859);  (R-RNO-3214858);  (R-RNO-6804760)",
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        "class_list": "",
        "function": "Arginine methyltransferase that can both catalyze the formation of omega-N monomethylarginine (MMA) and symmetrical dimethylarginine (sDMA)., [UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "2.1.1.320;2.3.1.48;3.6.1.15;3.6.4.13;2.7.11.22;2.1.1.321;3.6.4.-",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005794 Golgi apparatus;GO:0005829 cytosol",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006338 chromatin remodeling;GO:0048714 positive regulation of oligodendrocyte differentiation;GO:0006355 regulation of DNA-templated transcription;GO:0006479 protein methylation",
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        "organism": "Rat",
        "refseq_name": "polyhomeotic-like protein 2",
        "refseq_ac": "NP_001013187",
        "gene_names_uniprotkb": "Phc2",
        "gene_names_refseq": "Phc2",
        "protein_names_uniprotkb": "Polyhomeotic homolog 2",
        "protein_names_refseq": "polyhomeotic-like 2; polyhomeotic-like protein 2",
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        "disease": "cancer (Disease Ontology:DOID:162)",
        "pathway": " (rno:313038);  (R-RNO-2559580);  (R-RNO-3108214);  (R-RNO-3899300);  (R-RNO-4551638);  (R-RNO-4570464);  (R-RNO-8939243);  (R-RNO-8943724)",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0003682 chromatin binding;GO:0008270 zinc ion binding;GO:0042802 identical protein binding;GO:0042393 histone binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0000792 heterochromatin;GO:0031519 PcG protein complex;GO:0035102 PRC1 complex",
        "go_biological_process": "GO:0007283 spermatogenesis;GO:0045892 negative regulation of DNA-templated transcription",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D4A0M3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A0U6-1",
        "uniprot_id": "D4A0U6_RAT",
        "mass": 104496.0,
        "length": 911,
        "protein_name": "DNA ligase",
        "gene_name": "Lig4",
        "organism": "Rat",
        "refseq_name": "DNA ligase 4",
        "refseq_ac": "NP_001099565",
        "gene_names_uniprotkb": "Lig4",
        "gene_names_refseq": "Lig4",
        "protein_names_uniprotkb": "DNA ligase; 6.5.1.1",
        "protein_names_refseq": "DNA ligase (ATP) 4; DNA ligase 4; ligase IV, DNA, ATP-dependent",
        "tax_id": 10116,
        "disease": "DNA ligase IV deficiency (Disease Ontology:DOID:0060021); prostate cancer (Disease Ontology:DOID:10283); pancreatic cancer (Disease Ontology:DOID:1793); high grade glioma (Disease Ontology:DOID:3070); colorectal cancer (Disease Ontology:DOID:9256); multiple myeloma (Disease Ontology:DOID:9538)",
        "pathway": " (rno:290907);  (R-RNO-5693571)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "29393594",
        "class_list": "",
        "function": "DNA ligase involved in DNA non-homologous end joining (NHEJ); required for double-strand break (DSB) repair and V(D)J recombination. Catalyzes the NHEJ ligation step of the broken DNA during DSB repair by resealing the DNA breaks after the gap filling is completed. Joins single-strand breaks in a double-stranded polydeoxynucleotide in an ATP-dependent reaction. LIG4 is mechanistically flexible: it can ligate nicks as well as compatible DNA overhangs alone, while in the presence of XRCC4, it can ligate ends with 2-nucleotides (nt) microhomology and 1-nt gaps. Forms a subcomplex with XRCC4; the LIG4-XRCC4 subcomplex is responsible for the NHEJ ligation step and XRCC4 enhances the joining activity of LIG4. Binding of the LIG4-XRCC4 complex to DNA ends is dependent on the assembly of the DNA-dependent protein kinase complex DNA-PK to these DNA ends. LIG4 regulates nuclear localization of XRCC4., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "reported_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "total_n_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 6,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "2.7.11.1;6.5.1.1;4.2.99.18;5.6.2.4;2.7.7.7;4.2.99.-;3.1.-.-",
        "go_molecular_function": "GO:0003909 DNA ligase activity;GO:0000287 magnesium ion binding;GO:0003677 DNA binding;GO:0005524 ATP binding;GO:0016208 AMP binding",
        "go_cellular_component": "GO:0070419 nonhomologous end joining complex;GO:0032807 DNA ligase IV complex;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0000793 condensed chromosome",
        "go_biological_process": "GO:0071897 DNA biosynthetic process;GO:0002328 pro-B cell differentiation;GO:0006297 nucleotide-excision repair, DNA gap filling;GO:0097680 double-strand break repair via classical nonhomologous end joining;GO:2001252 positive regulation of chromosome organization",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D4A0U6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A0W0-1",
        "uniprot_id": "D4A0W0_RAT",
        "mass": 23299.0,
        "length": 207,
        "protein_name": "Lysozyme-like 1",
        "gene_name": "Lyzl1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Lyzl1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Lysozyme-like 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "viral infectious disease (Disease Ontology:DOID:934)",
        "pathway": " (rno:364745)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_o_glycosites": 0,
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        "mined_s_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
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        "total_reported_o_glycosites": 0,
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        "total_n_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003796 lysozyme activity",
        "go_cellular_component": "",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4A0W0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A0W2-1",
        "uniprot_id": "D4A0W2_RAT",
        "mass": 16980.0,
        "length": 151,
        "protein_name": "Similar to RIKEN cDNA 9530003J23",
        "gene_name": "RGD1306474",
        "organism": "Rat",
        "refseq_name": "uncharacterized protein LOC362881 precursor",
        "refseq_ac": "NP_001102216",
        "gene_names_uniprotkb": "RGD1306474",
        "gene_names_refseq": "Lyzf1; RGD1306474",
        "protein_names_uniprotkb": "Similar to RIKEN cDNA 9530003J23",
        "protein_names_refseq": "lysozyme f1; uncharacterized protein LOC362881 precursor",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:362881)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003796 lysozyme activity",
        "go_cellular_component": "GO:0005615 extracellular space",
        "go_biological_process": "GO:0050829 defense response to Gram-negative bacterium;GO:0050830 defense response to Gram-positive bacterium",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4A0W2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A109-1",
        "uniprot_id": "D4A109_RAT",
        "mass": 37480.0,
        "length": 330,
        "protein_name": "Interferon gamma receptor 2",
        "gene_name": "Ifngr2",
        "organism": "Rat",
        "refseq_name": "interferon gamma receptor 2 precursor",
        "refseq_ac": "NP_001101783",
        "gene_names_uniprotkb": "Ifngr2",
        "gene_names_refseq": "Ifngr2",
        "protein_names_uniprotkb": "Interferon gamma receptor 2",
        "protein_names_refseq": "interferon gamma receptor 2 precursor",
        "tax_id": 10116,
        "disease": "immunodeficiency 28 (Disease Ontology:DOID:0111995); congenital heart disease (Disease Ontology:DOID:1682); pulmonary tuberculosis (Disease Ontology:DOID:2957); acute myocardial infarction (Disease Ontology:DOID:9408); allergic asthma (Disease Ontology:DOID:9415); type 1 diabetes mellitus (Disease Ontology:DOID:9744)",
        "pathway": " (rno:360697);  (R-RNO-877300);  (R-RNO-877312);  (R-RNO-9732724)",
        "pathway_count": 4,
        "publication_count": 1,
        "publication_id_list": "29393594",
        "class_list": "",
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        "predicted_glycosites": 1,
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        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004906 type II interferon receptor activity;GO:0004896 cytokine receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0001774 microglial cell activation;GO:0051607 defense response to virus;GO:0019221 cytokine-mediated signaling pathway;GO:1900451 positive regulation of glutamate receptor signaling pathway;GO:0038196 type III interferon-mediated signaling pathway",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D4A109-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A175-1",
        "uniprot_id": "D4A175_RAT",
        "mass": 53667.0,
        "length": 479,
        "protein_name": "tRNA dimethylallyltransferase",
        "gene_name": "Trit1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Trit1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "tRNA dimethylallyltransferase; 2.5.1.75",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "combined oxidative phosphorylation deficiency 35 (Disease Ontology:DOID:0111464); lung cancer (Disease Ontology:DOID:1324)",
        "pathway": " (rno:362586)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "29393594",
        "class_list": "",
        "function": "Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 of both cytosolic and mitochondrial tRNAs, leading to the formation of N6-(dimethylallyl)adenosine (i6A37). Mediates modification of a limited subset of tRNAs: tRNA(Ser)(AGA), tRNA(Ser)(CGA), tRNA(Ser)(UGA), as well as partial modification of the selenocysteine tRNA(Ser)(UCA). TRIT1 is therefore required for selenoprotein expression., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
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        "reported_c_glycosites_with_glycan": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "2.5.1.75",
        "go_molecular_function": "GO:0005524 ATP binding;GO:0008270 zinc ion binding;GO:0052381 tRNA dimethylallyltransferase activity",
        "go_cellular_component": "GO:0005739 mitochondrion",
        "go_biological_process": "GO:0006400 tRNA modification;GO:0070900 mitochondrial tRNA modification",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D4A175-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A188-1",
        "uniprot_id": "D4A188_RAT",
        "mass": 49301.0,
        "length": 449,
        "protein_name": "Repulsive guidance molecule BMP co-receptor a",
        "gene_name": "Rgma",
        "organism": "Rat",
        "refseq_name": "repulsive guidance molecule A precursor",
        "refseq_ac": "NP_001100994",
        "gene_names_uniprotkb": "Rgma",
        "gene_names_refseq": "Rgma",
        "protein_names_uniprotkb": "Repulsive guidance molecule BMP co-receptor a",
        "protein_names_refseq": "RGM domain family, member A; repulsive guidance molecule A precursor; repulsive guidance molecule A; repulsive guidance molecule family member A",
        "tax_id": 10116,
        "disease": "sciatic neuropathy (Disease Ontology:DOID:11446); multiple sclerosis (Disease Ontology:DOID:2377); temporal lobe epilepsy (Disease Ontology:DOID:3328); middle cerebral artery infarction (Disease Ontology:DOID:3525)",
        "pathway": " (rno:308739)",
        "pathway_count": 1,
        "publication_count": 6,
        "publication_id_list": "15845084;26843113;29061393;29396549;32779334;38306928",
        "class_list": "",
        "function": "Inhibition of repulsive guidance molecule-a ameliorates compromised blood-spinal cord barrier integrity associated with neuromyelitis optica in rats., [RefSeq, PubMed]; Overexpression of RGMa inhibited hyper-excitability of hippocampal neurons., [RefSeq, PubMed]; RGMa might suppress angiogenesis via VEGF, Ang2, Ang1 and BDNF after cerebral ischemia/reperfusion injury, [RefSeq, PubMed]; RGMa promotes reactive astrogliosis and glial scar formation by forming a complex with ALK5 and Smad2/3 to promote ALK5-Smad2/3 interaction to facilitate TGFbeta1/Smad2/3 signaling, thereby inhibiting neurological functional recovery., [RefSeq, PubMed]; Silencing miR-20a-5p inhibits axonal growth and neuronal branching and prevents epileptogenesis through RGMa-RhoA-mediated synaptic plasticity., [RefSeq, PubMed]; The expression of repulsive guidance molecule (RGM) is studied in the spinal cord of rats with spinal cord injury (SCI). After SCI, RGM+ cells accumulate in lesions and peri-lesional areas., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 4,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005102 signaling receptor binding;GO:0015026 coreceptor activity;GO:1990459 transferrin receptor binding",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005886 plasma membrane;GO:0009986 cell surface;GO:0098552 side of membrane",
        "go_biological_process": "GO:0010976 positive regulation of neuron projection development;GO:0031175 neuron projection development;GO:0043547 positive regulation of GTPase activity;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0051044 positive regulation of membrane protein ectodomain proteolysis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.7,
        "record_id": "D4A188-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A1E8-1",
        "uniprot_id": "D4A1E8_RAT",
        "mass": 29632.0,
        "length": 269,
        "protein_name": "Lck interacting transmembrane adaptor 1",
        "gene_name": "Lime1",
        "organism": "Rat",
        "refseq_name": "lck-interacting transmembrane adapter 1",
        "refseq_ac": "NP_001102084",
        "gene_names_uniprotkb": "Lime1",
        "gene_names_refseq": "Lime1; RGD1562795",
        "protein_names_uniprotkb": "Lck interacting transmembrane adaptor 1",
        "protein_names_refseq": "lck-interacting transmembrane adapter 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:362289)",
        "pathway_count": 1,
        "publication_count": 0,
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        "predicted_glycosites": 1,
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        "reported_n_glycosites_with_glycan": 0,
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        "protein_name": "Transcription termination factor 1",
        "gene_name": "Ttf1",
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        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ttf1",
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        "protein_names_uniprotkb": "Transcription termination factor 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:499766);  (R-RNO-5683826);  (R-RNO-73762);  (R-RNO-73863)",
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        "refseq_ac": "NP_001292376",
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        "gene_names_refseq": "Bivm",
        "protein_names_uniprotkb": "Basic immunoglobulin-like variable motif-containing protein",
        "protein_names_refseq": "basic immunoglobulin-like variable motif-containing protein; rCG22223-like",
        "tax_id": 10116,
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        "pathway": " (rno:102548228)",
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        "length": 548,
        "protein_name": "Solute carrier family 22, member 15",
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        "refseq_name": "solute carrier family 22 member 15",
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        "gene_names_refseq": "Slc22a15",
        "protein_names_uniprotkb": "Solute carrier family 22, member 15",
        "protein_names_refseq": "solute carrier family 22 (organic cation transporter), member 15; solute carrier family 22 member 15",
        "tax_id": 10116,
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        "pathway": " (rno:310732);  (R-RNO-549127)",
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        "go_molecular_function": "GO:0015199 amino-acid betaine transmembrane transporter activity;GO:0022857 transmembrane transporter activity",
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        "length": 355,
        "protein_name": "Similar to human chromosome 19 open reading frame 67",
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        "refseq_name": "UPF0575 protein C19orf67 homolog isoform X1",
        "refseq_ac": "XP_001066168",
        "gene_names_uniprotkb": "C19h19orf67; LOC100365832; LOC686013",
        "gene_names_refseq": "C19h19orf67",
        "protein_names_uniprotkb": "Similar to human chromosome 19 open reading frame 67",
        "protein_names_refseq": "UPF0575 protein C19orf67 homolog isoform X1",
        "tax_id": 10116,
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        "go_molecular_function": "",
        "go_cellular_component": "",
        "go_biological_process": "GO:0001701 in utero embryonic development",
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        "length": 369,
        "protein_name": "Beta-1,4-galactosyltransferase",
        "gene_name": "B4galt2",
        "organism": "Rat",
        "refseq_name": "beta-1,4-galactosyltransferase 2",
        "refseq_ac": "NP_001101435",
        "gene_names_uniprotkb": "B4galt2",
        "gene_names_refseq": "B4galt2",
        "protein_names_uniprotkb": "Beta-1,4-galactosyltransferase; 2.4.1.-; Beta-1,4-GalTase",
        "protein_names_refseq": "UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 2; beta-1,4-galactosyltransferase 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:313536);  (R-RNO-2022854);  (R-RNO-975577)",
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        "class_list": "",
        "function": "Responsible for the synthesis of complex-type N-linked oligosaccharides in many glycoproteins as well as the carbohydrate moieties of glycolipids., [UniProtKB, UniProtKB, UniProtKB]",
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        "predicted_n_glycosites": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "2.4.1.-;2.4.1.274;2.4.1.275;2.4.1.22;2.4.1.38;2.4.1.90",
        "go_molecular_function": "GO:0008378 galactosyltransferase activity;GO:0046872 metal ion binding;GO:0003945 N-acetyllactosamine synthase activity;GO:0003831 beta-N-acetylglucosaminylglycopeptide beta-1,4-galactosyltransferase activity",
        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005794 Golgi apparatus;GO:0032580 Golgi cisterna membrane",
        "go_biological_process": "GO:0005975 carbohydrate metabolic process;GO:0009101 glycoprotein biosynthetic process;GO:0007613 memory;GO:0007626 locomotory behavior;GO:0008542 visual learning",
        "synthesized_glycan_count": 10444,
        "hit_score": 0.1,
        "record_id": "D4A2A5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A2B4-1",
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        "length": 229,
        "protein_name": "Claudin",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Cldn24",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Claudin",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "function": "Claudins function as major constituents of the tight junction complexes that regulate the permeability of epithelia., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005198 structural molecule activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0005923 bicellular tight junction;GO:0016324 apical plasma membrane",
        "go_biological_process": "",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A2G1-1",
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        "mass": 66762.0,
        "length": 618,
        "protein_name": "Leucine rich repeat and Ig domain containing 4",
        "gene_name": "Lingo4",
        "organism": "Rat",
        "refseq_name": "leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 4 precursor",
        "refseq_ac": "NP_001102659",
        "gene_names_uniprotkb": "Lingo4",
        "gene_names_refseq": "Lingo4; RGD1562025",
        "protein_names_uniprotkb": "Leucine rich repeat and Ig domain containing 4",
        "protein_names_refseq": "leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 4 precursor",
        "tax_id": 10116,
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        "pathway": " (rno:499668)",
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        "function": "",
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        "go_molecular_function": "GO:0038023 signaling receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0051965 positive regulation of synapse assembly",
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        "record_id": "D4A2G1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A2G4-1",
        "uniprot_id": "D4A2G4_RAT",
        "mass": 86359.0,
        "length": 773,
        "protein_name": "Microprocessor complex subunit DGCR8",
        "gene_name": "Dgcr8",
        "organism": "Rat",
        "refseq_name": "microprocessor complex subunit DGCR8 isoform 1",
        "refseq_ac": "NP_001099335",
        "gene_names_uniprotkb": "Dgcr8",
        "gene_names_refseq": "Dgcr8",
        "protein_names_uniprotkb": "Microprocessor complex subunit DGCR8",
        "protein_names_refseq": "DiGeorge syndrome critical region gene 8; microprocessor complex subunit DGCR8 isoform 1; microprocessor complex subunit DGCR8",
        "tax_id": 10116,
        "disease": "alcohol dependence (Disease Ontology:DOID:0050741); chromosome 22q11.2 deletion syndrome, distal (Disease Ontology:DOID:0060413)",
        "pathway": " (rno:287954)",
        "pathway_count": 1,
        "publication_count": 3,
        "publication_id_list": "22673903;34413501;36222340",
        "class_list": "",
        "function": "CCR1 enhances SUMOylation of DGCR8 by up-regulating ERK phosphorylation to promote spinal nerve ligation-induced neuropathic pain., [RefSeq, PubMed]; The 24-h pattern of dgcr8, drosha, and dicer expression in the rat suprachiasmatic nuclei and peripheral tissues and its modulation by angiotensin II., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "go_molecular_function": "GO:0030674 protein-macromolecule adaptor activity;GO:0042802 identical protein binding;GO:0042803 protein homodimerization activity;GO:0046872 metal ion binding;GO:0003725 double-stranded RNA binding",
        "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0006974 DNA damage response;GO:0072091 regulation of stem cell proliferation;GO:0031053 primary miRNA processing;GO:2000633 positive regulation of pre-miRNA processing",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "D4A2G4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A2G9-1",
        "uniprot_id": "D4A2G9_RAT",
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        "length": 219,
        "protein_name": "Ran-specific GTPase-activating protein",
        "gene_name": "Ranbp1l1; Ranbp1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ranbp1l1; Ranbp1; RGD1565297; Ranbp1l1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ran-specific GTPase-activating protein; Ran-binding protein 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "sciatic neuropathy (Disease Ontology:DOID:11446); dilated cardiomyopathy (Disease Ontology:DOID:12930); myocardial infarction (Disease Ontology:DOID:5844)",
        "pathway": " (rno:360739);  (rno:498088)",
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        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Plays a role in RAN-dependent nucleocytoplasmic transport. Alleviates the TNPO1-dependent inhibition of RAN GTPase activity and mediates the dissociation of RAN from proteins involved in transport into the nucleus. Induces a conformation change in the complex formed by XPO1 and RAN that triggers the release of the nuclear export signal of cargo proteins. Promotes the disassembly of the complex formed by RAN and importin beta. Promotes dissociation of RAN from a complex with KPNA2 and CSE1L. Required for normal mitotic spindle assembly and normal progress through mitosis via its effect on RAN. Does not increase the RAN GTPase activity by itself, but increases GTP hydrolysis mediated by RANGAP1. Inhibits RCC1-dependent exchange of RAN-bound GDP by GTP., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0005092 GDP-dissociation inhibitor activity;GO:0005096 GTPase activator activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005813 centrosome;GO:0005829 cytosol;GO:1904115 axon cytoplasm;GO:0032838 plasma membrane bounded cell projection cytoplasm",
        "go_biological_process": "GO:0072750 cellular response to leptomycin B;GO:0006913 nucleocytoplasmic transport;GO:0010976 positive regulation of neuron projection development;GO:0051592 response to calcium ion;GO:0071466 cellular response to xenobiotic stimulus",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D4A2G9-1",
        "record_type": "protein"
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        "uniprot_canonical_ac": "D4A2R5-1",
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        "mass": 67965.0,
        "length": 646,
        "protein_name": "Mex-3 RNA binding family member C",
        "gene_name": "Mex3c",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Mex3c",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Mex-3 RNA binding family member C",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-983168)",
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        "publication_count": 1,
        "publication_id_list": "22673903",
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        "biomarker_type": "",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0003723 RNA binding;GO:0008270 zinc ion binding;GO:0061630 ubiquitin protein ligase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0003415 chondrocyte hypertrophy;GO:0097009 energy homeostasis;GO:0045598 regulation of fat cell differentiation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D4A2R5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A2T8-1",
        "uniprot_id": "D4A2T8_RAT",
        "mass": 20265.0,
        "length": 176,
        "protein_name": "Interleukin family protein",
        "gene_name": "Il20",
        "organism": "Rat",
        "refseq_name": "interleukin-20",
        "refseq_ac": "NP_001137353",
        "gene_names_uniprotkb": "Il20",
        "gene_names_refseq": "If2d; Il20",
        "protein_names_uniprotkb": "Interleukin family protein",
        "protein_names_refseq": "interferon 2d; interleukin-20",
        "tax_id": 10116,
        "disease": "rheumatoid arthritis (Disease Ontology:DOID:7148); end stage renal disease (Disease Ontology:DOID:783); psoriasis (Disease Ontology:DOID:8893)",
        "pathway": " (rno:681112);  (R-RNO-8854691)",
        "pathway_count": 2,
        "publication_count": 4,
        "publication_id_list": "19342680;28253513;31953216;36835229",
        "class_list": "",
        "function": "Dual Role of Interleukin-20 in Different Stages of Osteoclast Differentiation and Its Osteoimmune Regulation during Alveolar Bone Remodeling. Publication Status: Online-Only, [RefSeq, PubMed]; IL-20 promotes hypoxia/reoxygenation-induced mitochondrial dysfunction and apoptosis in cardiomyocytes by upregulating oxidative stress by activating the PKC/NADPH oxidase pathway., [RefSeq, PubMed]; IL-20 was responsive to hypoxia in vitro and in the ischemic stroke model and that up-regulation of IL-20 in the ischemic brain may contribute to brain injury, [RefSeq, PubMed]; Immune regulatory cytokine., [UniProtKB, UniProtKB]; Microarray analysis revealed 880 transcripts showing 2.0-fold change following Unilateral Ureteral Obstruction, enriched mainly in immune response related processes. The most up-regulated genes were MMPs and members of IL-20 cytokine subfamily., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "predicted_c_glycosites": 0,
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        "total_reported_n_glycosites": 0,
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        "glyco_site_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0045517 interleukin-20 receptor binding;GO:0045518 interleukin-22 receptor binding;GO:0005125 cytokine activity",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0030876 interleukin-20 receptor complex",
        "go_biological_process": "GO:0006955 immune response;GO:0045672 positive regulation of osteoclast differentiation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.5,
        "record_id": "D4A2T8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A2V6-1",
        "uniprot_id": "D4A2V6_RAT",
        "mass": 36751.0,
        "length": 338,
        "protein_name": "Junctional sarcoplasmic reticulum protein 1",
        "gene_name": "Jsrp1",
        "organism": "Rat",
        "refseq_name": "junctional sarcoplasmic reticulum protein 1",
        "refseq_ac": "NP_001103061",
        "gene_names_uniprotkb": "Jsrp1",
        "gene_names_refseq": "Jsrp1",
        "protein_names_uniprotkb": "Junctional sarcoplasmic reticulum protein 1",
        "protein_names_refseq": "junctional sarcoplasmic reticulum protein 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:690423)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
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        "predicted_glycosites": 1,
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        "total_reported_n_glycosites": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0016529 sarcoplasmic reticulum",
        "go_biological_process": "GO:0003009 skeletal muscle contraction;GO:0072657 protein localization to membrane;GO:0060314 regulation of ryanodine-sensitive calcium-release channel activity",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D4A2V6-1",
        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "D4A2Y7-1",
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        "length": 778,
        "protein_name": "N-acetylated-alpha-linked acidic dipeptidase 2",
        "gene_name": "Naalad2",
        "organism": "Rat",
        "refseq_name": "N-acetylated-alpha-linked acidic dipeptidase 2 isoform 1",
        "refseq_ac": "NP_001100272",
        "gene_names_uniprotkb": "Naalad2",
        "gene_names_refseq": "Naalad2",
        "protein_names_uniprotkb": "N-acetylated-alpha-linked acidic dipeptidase 2; 3.4.17.21; Glutamate carboxypeptidase III; N-acetylated-alpha-linked acidic dipeptidase II",
        "protein_names_refseq": "N-acetylated-alpha-linked acidic dipeptidase 2 isoform 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:300384);  (R-RNO-8963693)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Has N-acetylated-alpha-linked-acidic dipeptidase (NAALADase) activity. Also exhibits a dipeptidyl-peptidase IV type activity. Inactivates the peptide neurotransmitter N-acetylaspartylglutamate., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "protein_names_refseq": "EGF-like-domain, multiple 5; multiple epidermal growth factor-like domains protein 9 precursor; multiple epidermal growth factor-like domains protein 9",
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        "protein_names_uniprotkb": "polynucleotide adenylyltransferase; 2.7.7.19",
        "protein_names_refseq": "family with sequence similarity 46, member D; terminal nucleotidyltransferase 5D",
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        "protein_name": "Cytoplasmic protein",
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        "refseq_name": "cytoplasmic protein NCK2",
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        "protein_names_refseq": "NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 6 (B14); NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 6",
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        "protein_names_uniprotkb": "Cytochrome c oxidase assembly homolog COX15",
        "protein_names_refseq": "COX15 cytochrome c oxidase assembly homolog; COX15 homolog, cytochrome c oxidase assembly protein; COX15 homolog; cytochrome c oxidase assembly homolog 15; cytochrome c oxidase assembly homolog COX15; cytochrome c oxidase assembly protein COX15 homolog",
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        "disease": "mitochondrial complex IV deficiency nuclear type 6 (Disease Ontology:DOID:0080358); hypertrophic cardiomyopathy (Disease Ontology:DOID:11984); ovarian dysfunction (Disease Ontology:DOID:1414); Leigh disease (Disease Ontology:DOID:3652)",
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        "protein_names_uniprotkb": "ATP-dependent RNA helicase homolog DQX1; DEAQ box polypeptide 1",
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        "protein_names_refseq": "39S ribosomal protein L19, mitochondrial; large ribosomal subunit protein bL19m; ribosomal protein, mitochondrial, L15",
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        "gene_names_refseq": "Supt16h",
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        "function": "Component of the FACT complex, a general chromatin factor that acts to reorganize nucleosomes. The FACT complex is involved in multiple processes that require DNA as a template such as mRNA elongation, DNA replication and DNA repair. During transcription elongation the FACT complex acts as a histone chaperone that both destabilizes and restores nucleosomal structure. It facilitates the passage of RNA polymerase II and transcription by promoting the dissociation of one histone H2A-H2B dimer from the nucleosome, then subsequently promotes the reestablishment of the nucleosome following the passage of RNA polymerase II. The FACT complex is probably also involved in phosphorylation of 'Ser-392' of p53/TP53 via its association with CK2 (casein kinase II)., [UniProtKB, UniProtKB, UniProtKB]",
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        "gene_names_refseq": "Hdlbpl2; RGD1563104",
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        "go_biological_process": "GO:0008090 retrograde axonal transport;GO:0021987 cerebral cortex development;GO:0071456 cellular response to hypoxia;GO:0006626 protein targeting to mitochondrion;GO:0008089 anterograde axonal transport",
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        "protein_name": "Lin-37 DREAM MuvB core complex component",
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        "refseq_name": "protein lin-37 homolog",
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        "gene_names_refseq": "Lin37; RGD1308901",
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        "protein_names_refseq": "lin-37 homolog; protein lin-37 homolog",
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        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008289 lipid binding",
        "go_cellular_component": "GO:0005576 extracellular region",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4A5H4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A5K6-1",
        "uniprot_id": "D4A5K6_RAT",
        "mass": 54848.0,
        "length": 475,
        "protein_name": "CAAX prenyl protease",
        "gene_name": "Zmpste24",
        "organism": "Rat",
        "refseq_name": "CAAX prenyl protease 1 homolog",
        "refseq_ac": "NP_001101444",
        "gene_names_uniprotkb": "Zmpste24",
        "gene_names_refseq": "Zmpste24",
        "protein_names_uniprotkb": "CAAX prenyl protease; 3.4.24.84",
        "protein_names_refseq": "CAAX prenyl protease 1 homolog; zinc metallopeptidase, STE24 homolog; zinc metalloproteinase, STE24 homolog",
        "tax_id": 10116,
        "disease": "familial partial lipodystrophy (Disease Ontology:DOID:0050440); restrictive dermopathy (Disease Ontology:DOID:0060762); restrictive dermopathy 1 (Disease Ontology:DOID:0070369); metabolic dysfunction-associated steatotic liver disease (Disease Ontology:DOID:0080208); mandibuloacral dysplasia type B lipodystrophy (Disease Ontology:DOID:0081129); Emery-Dreifuss muscular dystrophy (Disease Ontology:DOID:11726); progeria (Disease Ontology:DOID:3911); type 2 diabetes mellitus (Disease Ontology:DOID:9352)",
        "pathway": " (rno:313564)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Proteolytically removes the C-terminal three residues of farnesylated proteins., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 8,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004175 endopeptidase activity;GO:0004222 metalloendopeptidase activity;GO:0046872 metal ion binding;GO:0003690 double-stranded DNA binding",
        "go_cellular_component": "GO:0005635 nuclear envelope;GO:0016020 membrane;GO:0005789 endoplasmic reticulum membrane;GO:0032991 protein-containing complex",
        "go_biological_process": "GO:0071586 CAAX-box protein processing;GO:1903799 negative regulation of miRNA processing;GO:0060993 kidney morphogenesis;GO:0043516 regulation of DNA damage response, signal transduction by p53 class mediator;GO:0003231 cardiac ventricle development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4A5K6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A5L7-1",
        "uniprot_id": "D4A5L7_RAT",
        "mass": 44628.0,
        "length": 420,
        "protein_name": "Solute carrier family 35, member D3",
        "gene_name": "Slc35d3",
        "organism": "Rat",
        "refseq_name": "solute carrier family 35 member D3",
        "refseq_ac": "NP_001100992",
        "gene_names_uniprotkb": "Slc35d3",
        "gene_names_refseq": "Slc35d3",
        "protein_names_uniprotkb": "Solute carrier family 35, member D3",
        "protein_names_refseq": "solute carrier family 35 member D3",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:308717)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0030674 protein-macromolecule adaptor activity;GO:0015297 antiporter activity;GO:0005460 UDP-glucose transmembrane transporter activity",
        "go_cellular_component": "GO:0005769 early endosome;GO:0005783 endoplasmic reticulum;GO:0005794 Golgi apparatus;GO:0031901 early endosome membrane;GO:0030672 synaptic vesicle membrane",
        "go_biological_process": "GO:0055085 transmembrane transport;GO:0097009 energy homeostasis;GO:0010508 positive regulation of autophagy;GO:0060155 platelet dense granule organization;GO:0070863 positive regulation of protein exit from endoplasmic reticulum",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D4A5L7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A5S1-1",
        "uniprot_id": "D4A5S1_RAT",
        "mass": 94128.0,
        "length": 827,
        "protein_name": "Ubiquitin carboxyl-terminal hydrolase",
        "gene_name": "Usp26",
        "organism": "Rat",
        "refseq_name": "ubiquitin carboxyl-terminal hydrolase 26",
        "refseq_ac": "NP_001100418",
        "gene_names_uniprotkb": "Usp26",
        "gene_names_refseq": "RGD1563443; Usp26",
        "protein_names_uniprotkb": "Ubiquitin carboxyl-terminal hydrolase; 3.4.19.12",
        "protein_names_refseq": "ubiquitin carboxyl-terminal hydrolase 26",
        "tax_id": 10116,
        "disease": "X-linked spermatogenic failure 6 (Disease Ontology:DOID:0070597)",
        "pathway": " (rno:302488);  (R-RNO-5689880)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Deubiquitinating enzyme that removes conjugated ubiquitin from specific proteins to regulate different cellular processes., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "3.4.19.12",
        "go_molecular_function": "GO:0004843 cysteine-type deubiquitinase activity;GO:1990380 K48-linked deubiquitinase activity;GO:0101005 deubiquitinase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005829 cytosol;GO:0036126 sperm flagellum",
        "go_biological_process": "GO:0006508 proteolysis;GO:0007283 spermatogenesis;GO:0016579 protein deubiquitination;GO:0031647 regulation of protein stability;GO:0000082 G1/S transition of mitotic cell cycle",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4A5S1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A5S6-1",
        "uniprot_id": "D4A5S6_RAT",
        "mass": 52680.0,
        "length": 465,
        "protein_name": "Chitobiosyldiphosphodolichol beta-mannosyltransferase",
        "gene_name": "Alg1",
        "organism": "Rat",
        "refseq_name": "chitobiosyldiphosphodolichol beta-mannosyltransferase",
        "refseq_ac": "NP_001101734",
        "gene_names_uniprotkb": "Alg1",
        "gene_names_refseq": "Alg1",
        "protein_names_uniprotkb": "Chitobiosyldiphosphodolichol beta-mannosyltransferase; 2.4.1.142; Asparagine-linked glycosylation protein 1 homolog; Beta-1,4-mannosyltransferase; GDP-Man:GlcNAc2-PP-dolichol mannosyltransferase; GDP-mannose-dolichol diphosphochitobiose mannosyltransferase",
        "protein_names_refseq": "asparagine-linked glycosylation 1 homolog (S. cerevisiae, beta-1,4-mannosyltransferase); asparagine-linked glycosylation 1 homolog (yeast, beta-1,4-mannosyltransferase); asparagine-linked glycosylation 1, beta-1,4-mannosyltransferase homolog; chitobiosyldiphosphodolichol beta-mannosyltransferase",
        "tax_id": 10116,
        "disease": "congenital disorder of glycosylation type I (Disease Ontology:DOID:0050570); congenital disorder of glycosylation Ik (Disease Ontology:DOID:0080563); congenital disorder of glycosylation (Disease Ontology:DOID:5212)",
        "pathway": " (rno:360475);  (R-RNO-446193)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Mannosyltransferase that operates in the biosynthetic pathway of dolichol-linked oligosaccharides, the glycan precursors employed in protein asparagine (N)-glycosylation. The assembly of dolichol-linked oligosaccharides begins on the cytosolic side of the endoplasmic reticulum membrane and finishes in its lumen. The sequential addition of sugars to dolichol pyrophosphate produces dolichol-linked oligosaccharides containing fourteen sugars, including two GlcNAcs, nine mannoses and three glucoses. Once assembled, the oligosaccharide is transferred from the lipid to nascent proteins by oligosaccharyltransferases. Catalyzes, on the cytoplasmic face of the endoplasmic reticulum, the addition of the first mannose residues to the dolichol-linked oligosaccharide chain, to produce Man1GlcNAc(2)-PP-dolichol core oligosaccharide. Man1GlcNAc(2)-PP-dolichol is a substrate for ALG2, the following enzyme in the biosynthetic pathway., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 3,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "2.4.1.142",
        "go_molecular_function": "GO:0000030 mannosyltransferase activity;GO:0004578 chitobiosyldiphosphodolichol beta-mannosyltransferase activity",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0006488 dolichol-linked oligosaccharide biosynthetic process;GO:0006487 protein N-linked glycosylation",
        "synthesized_glycan_count": 15150,
        "hit_score": 0.1,
        "record_id": "D4A5S6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A5T3-1",
        "uniprot_id": "D4A5T3_RAT",
        "mass": 7965.0,
        "length": 68,
        "protein_name": "Small integral membrane protein 45",
        "gene_name": "Smim45",
        "organism": "Rat",
        "refseq_name": "small integral membrane protein 45",
        "refseq_ac": "NP_001382896",
        "gene_names_uniprotkb": "Smim45; LOC688613",
        "gene_names_refseq": "Smim45",
        "protein_names_uniprotkb": "Small integral membrane protein 45",
        "protein_names_refseq": "small integral membrane protein 45",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0042551 neuron maturation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4A5T3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A5T8-1",
        "uniprot_id": "D4A5T8_RAT",
        "mass": 204147.0,
        "length": 1754,
        "protein_name": "Periplakin",
        "gene_name": "Ppl",
        "organism": "Rat",
        "refseq_name": "periplakin",
        "refseq_ac": "NP_001100446",
        "gene_names_uniprotkb": "Ppl",
        "gene_names_refseq": "Ppl",
        "protein_names_uniprotkb": "Periplakin",
        "protein_names_refseq": "periplakin",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:302934);  (R-RNO-6809371);  (R-RNO-8851680)",
        "pathway_count": 3,
        "publication_count": 3,
        "publication_id_list": "15590649;16641100;22673903",
        "class_list": "",
        "function": "Component of the cornified envelope of keratinocytes. May link the cornified envelope to desmosomes and intermediate filaments. May act as a localization signal in PKB/AKT-mediated signaling., [UniProtKB, UniProtKB]; Periplakin interferes with G protein activation by the melanin-concentrating hormone receptor-1 by binding to the proximal segment of the receptor C-terminal tail, [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005198 structural molecule activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005856 cytoskeleton;GO:0005886 plasma membrane;GO:0016020 membrane;GO:0001533 cornified envelope",
        "go_biological_process": "GO:0031424 keratinization;GO:0009612 response to mechanical stimulus;GO:0042060 wound healing;GO:0045104 intermediate filament cytoskeleton organization;GO:0002786 regulation of antibacterial peptide production",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "D4A5T8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A5X2-1",
        "uniprot_id": "D4A5X2_RAT",
        "mass": 13143.0,
        "length": 128,
        "protein_name": "Family with sequence similarity 229, member A",
        "gene_name": "Fam229a",
        "organism": "Rat",
        "refseq_name": "protein FAM229A",
        "refseq_ac": "NP_001102736",
        "gene_names_uniprotkb": "Fam229a; RGD1564163",
        "gene_names_refseq": "Fam229a; RGD1564163",
        "protein_names_uniprotkb": "Family with sequence similarity 229, member A",
        "protein_names_refseq": "protein FAM229A",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:500554)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4A5X2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A5Z8-1",
        "uniprot_id": "D4A5Z8_RAT",
        "mass": 36574.0,
        "length": 326,
        "protein_name": "Olfactory receptor family 5 subfamily D member 37",
        "gene_name": "Or5d37",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr608",
        "refseq_ac": "NP_001000655",
        "gene_names_uniprotkb": "Or5d37",
        "gene_names_refseq": "Olr608; Or5d37",
        "protein_names_uniprotkb": "Olfactory receptor family 5 subfamily D member 37",
        "protein_names_refseq": "olfactory receptor 608; olfactory receptor Olr608; olfactory receptor gene Olr608",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:404853)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Odorant receptor., [UniProtKB, UniProtKB]; Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4A5Z8-1",
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    },
    {
        "uniprot_canonical_ac": "D4A670-1",
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        "length": 368,
        "protein_name": "Left-right determination factor",
        "gene_name": "Lefty1",
        "organism": "Rat",
        "refseq_name": "left-right determination factor 1 precursor",
        "refseq_ac": "NP_001102550",
        "gene_names_uniprotkb": "Lefty1",
        "gene_names_refseq": "Lefty1; RGD1561867",
        "protein_names_uniprotkb": "Left-right determination factor",
        "protein_names_refseq": "left-right determination factor 1 precursor",
        "tax_id": 10116,
        "disease": "congenital heart disease (Disease Ontology:DOID:1682)",
        "pathway": " (rno:498299);  (R-RNO-114608)",
        "pathway_count": 2,
        "publication_count": 2,
        "publication_id_list": "29286065;33409963",
        "class_list": "",
        "function": "Lefty1 Ameliorates Post-infarction Fibrosis by Suppressing p-Smad2 and p-ERK1/2 Signaling Pathways., [RefSeq, PubMed]; Lefty1 may ameliorate renal tubulointerstitial inflammation by suppressing NFkappaB signaling., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
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        "total_reported_n_glycosites": 0,
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        "biomarker_type": "",
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        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005125 cytokine activity;GO:0005160 transforming growth factor beta receptor binding;GO:0008083 growth factor activity;GO:0038100 nodal binding",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0005615 extracellular space",
        "go_biological_process": "GO:1900108 negative regulation of nodal signaling pathway;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0008285 negative regulation of cell population proliferation;GO:0032526 response to retinoic acid;GO:0003007 heart morphogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "D4A670-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A6G2-1",
        "uniprot_id": "D4A6G2_RAT",
        "mass": 92214.0,
        "length": 837,
        "protein_name": "Semaphorin-4G",
        "gene_name": "Sema4g",
        "organism": "Rat",
        "refseq_name": "semaphorin-4G precursor",
        "refseq_ac": "NP_001101996",
        "gene_names_uniprotkb": "Sema4g",
        "gene_names_refseq": "Sema4g",
        "protein_names_uniprotkb": "Semaphorin-4G",
        "protein_names_refseq": "sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4G; semaphorin-4G precursor",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:361764)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "38843836",
        "class_list": "",
        "function": "Cell surface receptor for PLXNB2. May play a role in axon guidance., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 2,
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0030215 semaphorin receptor binding;GO:0038191 neuropilin binding;GO:0045499 chemorepellent activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0030335 positive regulation of cell migration;GO:0071526 semaphorin-plexin signaling pathway;GO:0001755 neural crest cell migration;GO:0050919 negative chemotaxis;GO:0007411 axon guidance",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "D4A6G2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A6S9-1",
        "uniprot_id": "D4A6S9_RAT",
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        "length": 480,
        "protein_name": "Solute carrier family 46, member 2",
        "gene_name": "Slc46a2",
        "organism": "Rat",
        "refseq_name": "solute carrier family 46 member 2",
        "refseq_ac": "NP_001100122",
        "gene_names_uniprotkb": "Slc46a2",
        "gene_names_refseq": "Slc46a2; Tscot",
        "protein_names_uniprotkb": "Solute carrier family 46, member 2",
        "protein_names_refseq": "solute carrier family 46 member 2; thymic stromal cotransporter homolog",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:298034)",
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        "publication_id_list": "29393594",
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        "go_molecular_function": "GO:0022857 transmembrane transporter activity;GO:0140360 cyclic-GMP-AMP transmembrane transporter activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0009986 cell surface;GO:0016020 membrane",
        "go_biological_process": "GO:0070430 positive regulation of nucleotide-binding oligomerization domain containing 1 signaling pathway;GO:0055085 transmembrane transport;GO:0045580 regulation of T cell differentiation;GO:0048538 thymus development;GO:0043029 T cell homeostasis",
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        "hit_score": 0.2,
        "record_id": "D4A6S9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A6T2-1",
        "uniprot_id": "D4A6T2_RAT",
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        "length": 320,
        "protein_name": "RNA pseudouridine synthase D3",
        "gene_name": "Rpusd3",
        "organism": "Rat",
        "refseq_name": "mitochondrial mRNA pseudouridine synthase RPUSD3 isoform 2",
        "refseq_ac": "NP_001102111",
        "gene_names_uniprotkb": "Rpusd3",
        "gene_names_refseq": "RGD1307582; Rpusd3",
        "protein_names_uniprotkb": "RNA pseudouridine synthase D3",
        "protein_names_refseq": "RNA pseudouridylate synthase domain containing 3; RNA pseudouridylate synthase domain-containing protein 3; mitochondrial mRNA pseudouridine synthase RPUSD3 isoform 2; mitochondrial mRNA pseudouridine synthase RPUSD3",
        "tax_id": 10116,
        "disease": "",
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        "go_molecular_function": "GO:0003723 RNA binding;GO:0009982 pseudouridine synthase activity",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005759 mitochondrial matrix;GO:0035770 ribonucleoprotein granule",
        "go_biological_process": "GO:0000455 enzyme-directed rRNA pseudouridine synthesis;GO:1990481 mRNA pseudouridine synthesis;GO:0070131 positive regulation of mitochondrial translation;GO:0001522 pseudouridine synthesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4A6T2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A750-1",
        "uniprot_id": "D4A750_RAT",
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        "length": 1033,
        "protein_name": "Beta-1,4-N-acetylgalactosaminyltransferase",
        "gene_name": "B4galnt4",
        "organism": "Rat",
        "refseq_name": "N-acetyl-beta-glucosaminyl-glycoprotein 4-beta-N-acetylgalactosaminyltransferase 1",
        "refseq_ac": "NP_001101032",
        "gene_names_uniprotkb": "B4galnt4",
        "gene_names_refseq": "B4galnt4; RGD1310052",
        "protein_names_uniprotkb": "Beta-1,4-N-acetylgalactosaminyltransferase; 2.4.1.244",
        "protein_names_refseq": "N-acetyl-beta-glucosaminyl-glycoprotein 4-beta-N-acetylgalactosaminyltransferase 1; beta 1,4-N-acetylgalactosaminyltransferase-transferase 4",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:309105)",
        "pathway_count": 1,
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        "publication_id_list": "29393594",
        "class_list": "",
        "function": "Transfers N-acetylgalactosamine (GalNAc) from UDP-GalNAc to N-acetylglucosamine-beta-benzyl with a beta-1,4-linkage to form N,N'-diacetyllactosediamine, GalNAc-beta-1,4-GlcNAc structures in N-linked glycans and probably O-linked glycans., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "2.4.1.244",
        "go_molecular_function": "GO:0008376 acetylgalactosaminyltransferase activity;GO:0033842 N-acetyl-beta-glucosaminyl-derivative 4-beta-N-acetylgalactosaminyltransferase activity;GO:0047238 glucuronosyl-N-acetylgalactosaminyl-proteoglycan 4-beta-N-acetylgalactosaminyltransferase activity",
        "go_cellular_component": "GO:0032580 Golgi cisterna membrane",
        "go_biological_process": "GO:0050650 chondroitin sulfate proteoglycan biosynthetic process",
        "synthesized_glycan_count": 865,
        "hit_score": 0.2,
        "record_id": "D4A750-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A789-1",
        "uniprot_id": "D4A789_RAT",
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        "length": 463,
        "protein_name": "Signal-regulatory protein beta 3",
        "gene_name": "Sirpb3",
        "organism": "Rat",
        "refseq_name": "uncharacterized protein LOC296149 isoform b",
        "refseq_ac": "NP_001127987",
        "gene_names_uniprotkb": "Sirpb3",
        "gene_names_refseq": "RGD1566226; Sirpb3",
        "protein_names_uniprotkb": "Signal-regulatory protein beta 3",
        "protein_names_refseq": "uncharacterized protein LOC296149 isoform b",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:296149)",
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        "biomarker_type": "",
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    {
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        "protein_name": "Charged multivesicular body protein 7",
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        "protein_names_uniprotkb": "Charged multivesicular body protein 7; Chromatin-modifying protein 7",
        "protein_names_refseq": "CHMP family, member 7; charged multivesicular body protein 7",
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        "pathway": " (rno:364419);  (R-RNO-1632852);  (R-RNO-5620971);  (R-RNO-917729);  (R-RNO-9668328)",
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        "go_biological_process": "GO:0001778 plasma membrane repair;GO:0031468 nuclear membrane reassembly;GO:0039702 viral budding via host ESCRT complex;GO:0071985 multivesicular body sorting pathway;GO:0097352 autophagosome maturation",
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        "protein_names_refseq": "mediator of RNA polymerase II transcription subunit 31; mediator of RNA polymerase II transcription, subunit 31 homolog",
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        "protein_names_refseq": "mediator of RNA polymerase II transcription subunit 10; mediator of RNA polymerase II transcription, subunit 10 homolog (NUT2, S. cerevisiae)",
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        "protein_names_refseq": "olfactory receptor 1314; olfactory receptor 148-like; olfactory receptor Olr1314; olfactory receptor gene Olr1314",
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        "protein_name": "Protocadherin beta 20",
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        "gene_names_uniprotkb": "Pcdhb20",
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        "protein_names_uniprotkb": "Protocadherin beta 20",
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        "go_molecular_function": "GO:0005509 calcium ion binding;GO:0050839 cell adhesion molecule binding",
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        "length": 355,
        "protein_name": "N-formylpeptide chemoattractant receptor",
        "gene_name": "Fpr1",
        "organism": "Rat",
        "refseq_name": "fMet-Leu-Phe receptor",
        "refseq_ac": "NP_001099686",
        "gene_names_uniprotkb": "Fpr1",
        "gene_names_refseq": "Fpr1",
        "protein_names_uniprotkb": "N-formylpeptide chemoattractant receptor",
        "protein_names_refseq": "fMet-Leu-Phe receptor",
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        "pathway": " (rno:292409);  (R-RNO-418594);  (R-RNO-444473);  (R-RNO-6798695)",
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        "publication_id_list": "16516855;27173446;27782092;29393594;34565207",
        "class_list": "",
        "function": "ANXA1 promotes microglial activation and migration during oxygen-glucose deprivation/reperfusion via FPR, and CK2 target alpha-E-catenin phosphorylation is involved in this process. Publication Status: Online-Only, [RefSeq, PubMed]; Formyl peptide receptor 1 promotes podocyte injury through regulation of mitogen-activated protein kinase pathways., [RefSeq, PubMed]; Our results suggest that Nordy was capable of reducing the level of malignancy of glioma cells., [RefSeq, PubMed]; Reports showed that both Fpr1 and Fpr2 are expressed on NSCs and both receptors mediate the migration of neural stem cells (NSCs) in vitro and in vivo, and promote the differentiation of NSCs to neuron through F-actin polymerization. Publication Status: Online-Only, [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0004875 complement receptor activity;GO:0005124 scavenger receptor binding;GO:0050786 RAGE receptor binding;GO:0004930 G protein-coupled receptor activity;GO:0001664 G protein-coupled receptor binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005886 plasma membrane",
        "go_biological_process": "GO:0002430 complement receptor mediated signaling pathway;GO:0006935 chemotaxis;GO:0006954 inflammatory response;GO:0007186 G protein-coupled receptor signaling pathway;GO:0007204 positive regulation of cytosolic calcium ion concentration",
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        "length": 102,
        "protein_name": "U6 snRNA-associated Sm-like protein LSm3",
        "gene_name": "Lsm3",
        "organism": "Rat",
        "refseq_name": "U6 snRNA-associated Sm-like protein LSm3",
        "refseq_ac": "NP_001100081",
        "gene_names_uniprotkb": "Lsm3; LSM3",
        "gene_names_refseq": "Lsm3",
        "protein_names_uniprotkb": "U6 snRNA-associated Sm-like protein LSm3",
        "protein_names_refseq": "LSM3 U6 small nuclear RNA and mRNA degradation associated; LSM3 homolog, U6 small nuclear RNA associated; U6 snRNA-associated Sm-like protein LSm3",
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        "function": "Binds specifically to the 3'-terminal U-tract of U6 snRNA., [UniProtKB, UniProtKB]; Plays a role in pre-mRNA splicing as component of the U4/U6-U5 tri-snRNP complex that is involved in spliceosome assembly, and as component of the precatalytic spliceosome (spliceosome B complex). The heptameric LSM2-8 complex binds specifically to the 3'-terminal U-tract of U6 snRNA., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003723 RNA binding;GO:0030629 U6 snRNA 3'-end binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005681 spliceosomal complex;GO:0000932 P-body;GO:0071013 catalytic step 2 spliceosome",
        "go_biological_process": "GO:0000398 mRNA splicing, via spliceosome;GO:0033962 P-body assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4A7U6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A7V6-1",
        "uniprot_id": "D4A7V6_RAT",
        "mass": 219690.0,
        "length": 1962,
        "protein_name": "CASP8-associated protein 2",
        "gene_name": "Casp8ap2",
        "organism": "Rat",
        "refseq_name": "CASP8-associated protein 2",
        "refseq_ac": "NP_001101391",
        "gene_names_uniprotkb": "Casp8ap2",
        "gene_names_refseq": "Casp8ap2",
        "protein_names_uniprotkb": "CASP8-associated protein 2; FLICE-associated huge protein",
        "protein_names_refseq": "CASP8-associated protein 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:313128);  (R-RNO-3899300)",
        "pathway_count": 2,
        "publication_count": 7,
        "publication_id_list": "16641100;19721136;22482882;22673903;29393594;33234216;33882492",
        "class_list": "",
        "function": "Data identified FLICE-associated huge protein (FLASH)/caspase-8-associated protein-2 (Casp8ap2) in (PC)MSCs as the target gene of miR-210., [RefSeq, PubMed]; Participates in TNF-induced blockade of glucocorticoid receptor (GR) transactivation at the nuclear receptor coactivator level, upstream and independently of NF-kappa-B. Suppresses both NCOA2- and NCOA3-induced enhancement of GR transactivation. Involved in TNF-induced activation of NF-kappa-B via a TRAF2-dependent pathway. Acts as a downstream mediator for CASP8-induced activation of NF-kappa-B. Required for the activation of CASP8 in FAS-mediated apoptosis. Involved for histone gene transcription and progression through S phase: required for the generation of mature histone mRNAs following the 3' end cleavage of histone pre-mRNAs., [UniProtKB, UniProtKB, UniProtKB]; The MicroRNA-210/Casp8ap2 Pathway Alleviates Hypoxia-Induced Injury in Myocardial Cells by Regulating Apoptosis and Autophagy. Publication Status: Online-Only, [RefSeq, PubMed]; The ischemic preconditioning (IPC) enhances stem cell survival via the combined participation of hypoxia responsive miRs miR-107 and miR-210 via their respective putative target genes Pdcd10 and Casp8ap2., [RefSeq, PubMed]; The microRNA-210/Casp8ap2 Axis Alleviates Hypoxia-Induced Myocardial Injury by Regulating Apoptosis and Autophagy., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 0,
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        "reported_s_glycosites_with_glycan": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0002020 protease binding;GO:0042802 identical protein binding;GO:0003714 transcription corepressor activity;GO:0008656 cysteine-type endopeptidase activator activity involved in apoptotic process;GO:0032184 SUMO polymer binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005739 mitochondrion;GO:0016605 PML body",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0071260 cellular response to mechanical stimulus;GO:0008625 extrinsic apoptotic signaling pathway via death domain receptors;GO:0036337 Fas signaling pathway;GO:0097190 apoptotic signaling pathway",
        "synthesized_glycan_count": 0,
        "hit_score": 0.8,
        "record_id": "D4A7V6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A7X9-1",
        "uniprot_id": "D4A7X9_RAT",
        "mass": 125319.0,
        "length": 1098,
        "protein_name": "Myosin IF",
        "gene_name": "Myo1f",
        "organism": "Rat",
        "refseq_name": "unconventional myosin-If",
        "refseq_ac": "NP_001101546",
        "gene_names_uniprotkb": "Myo1f",
        "gene_names_refseq": "Myo1f",
        "protein_names_uniprotkb": "Myosin IF",
        "protein_names_refseq": "myosin-If; unconventional myosin-If",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:314654)",
        "pathway_count": 1,
        "publication_count": 2,
        "publication_id_list": "22673903;29393594",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005516 calmodulin binding;GO:0005524 ATP binding;GO:0051015 actin filament binding;GO:0000146 microfilament motor activity;GO:0003779 actin binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005886 plasma membrane;GO:0015629 actin cytoskeleton;GO:0005902 microvillus;GO:0016459 myosin complex",
        "go_biological_process": "GO:0006897 endocytosis;GO:0007015 actin filament organization;GO:0007162 negative regulation of cell adhesion;GO:0030335 positive regulation of cell migration;GO:0032956 regulation of actin cytoskeleton organization",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "D4A7X9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A810-1",
        "uniprot_id": "D4A810_RAT",
        "mass": 53891.0,
        "length": 489,
        "protein_name": "Potassium voltage-gated channel subfamily A member 7",
        "gene_name": "Kcna7",
        "organism": "Rat",
        "refseq_name": "potassium voltage-gated channel subfamily A member 7",
        "refseq_ac": "NP_001102384",
        "gene_names_uniprotkb": "Kcna7",
        "gene_names_refseq": "Kcna7",
        "protein_names_uniprotkb": "Potassium voltage-gated channel subfamily A member 7; Voltage-gated potassium channel subunit Kv1.7",
        "protein_names_refseq": "potassium channel, voltage gated shaker related subfamily A, member 7; potassium voltage-gated channel subfamily A member 7; potassium voltage-gated channel, shaker-related subfamily, member 7",
        "tax_id": 10116,
        "disease": "episodic ataxia type 1 (Disease Ontology:DOID:0050989); epilepsy (Disease Ontology:DOID:1826)",
        "pathway": " (rno:365241);  (R-RNO-1296072)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
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        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 2,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "1.8.-.-",
        "go_molecular_function": "GO:0005251 delayed rectifier potassium channel activity;GO:0005249 voltage-gated potassium channel activity",
        "go_cellular_component": "GO:0016020 membrane;GO:0008076 voltage-gated potassium channel complex",
        "go_biological_process": "GO:0051260 protein homooligomerization;GO:0001508 action potential;GO:0071805 potassium ion transmembrane transport",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4A810-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A834-1",
        "uniprot_id": "D4A834_RAT",
        "mass": 25534.0,
        "length": 225,
        "protein_name": "Proteoglycan 3, pro eosinophil major basic protein 2",
        "gene_name": "Prg3",
        "organism": "Rat",
        "refseq_name": "proteoglycan 3 precursor",
        "refseq_ac": "NP_001099957",
        "gene_names_uniprotkb": "Prg3",
        "gene_names_refseq": "Prg3",
        "protein_names_uniprotkb": "Proteoglycan 3, pro eosinophil major basic protein 2",
        "protein_names_refseq": "proteoglycan 3 precursor",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:295706);  (R-RNO-6798695)",
        "pathway_count": 2,
        "publication_count": 0,
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        "class_list": "",
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        "predicted_glycosites": 0,
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        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_s_glycosites": 0,
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        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0030246 carbohydrate binding",
        "go_cellular_component": "",
        "go_biological_process": "GO:0006955 immune response;GO:0017148 negative regulation of translation;GO:0032757 positive regulation of interleukin-8 production;GO:0019370 leukotriene biosynthetic process;GO:0042119 neutrophil activation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4A834-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A838-1",
        "uniprot_id": "D4A838_RAT",
        "mass": 35917.0,
        "length": 318,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or10v9b",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Or10v9b; Olr318; Or10v5",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:309221)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "predicted_c_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
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        "reported_phosphosites": 0,
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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4A838-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A857-1",
        "uniprot_id": "D4A857_RAT",
        "mass": 116012.0,
        "length": 1041,
        "protein_name": "Importin 9",
        "gene_name": "Ipo9",
        "organism": "Rat",
        "refseq_name": "importin-9",
        "refseq_ac": "NP_001100650",
        "gene_names_uniprotkb": "Ipo9",
        "gene_names_refseq": "Ipo9",
        "protein_names_uniprotkb": "Importin 9",
        "protein_names_refseq": "importin-9",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:304817)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "15992958",
        "class_list": "",
        "function": "Results describe the structure of the rat importin 9 gene, together with its transcripts and the encoded protein with its putative functional domains., [RefSeq, PubMed]",
        "predicted_glycosites": 2,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 2,
        "predicted_c_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 2,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0031267 small GTPase binding;GO:0042393 histone binding;GO:0061608 nuclear import signal receptor activity;GO:0140713 histone chaperone activity",
        "go_cellular_component": "GO:0005635 nuclear envelope;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005634 nucleus",
        "go_biological_process": "GO:0006606 protein import into nucleus;GO:0031144 proteasome localization;GO:0006886 intracellular protein transport",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D4A857-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A8H3-1",
        "uniprot_id": "D4A8H3_RAT",
        "mass": 117931.0,
        "length": 1053,
        "protein_name": "Ubiquitin-like modifier-activating enzyme 6",
        "gene_name": "Uba6",
        "organism": "Rat",
        "refseq_name": "ubiquitin-like modifier-activating enzyme 6",
        "refseq_ac": "NP_001100683",
        "gene_names_uniprotkb": "Uba6",
        "gene_names_refseq": "RGD1308324; Uba6; Ube1l2",
        "protein_names_uniprotkb": "Ubiquitin-like modifier-activating enzyme 6; 6.2.1.45; Ubiquitin-activating enzyme E1-like protein 2",
        "protein_names_refseq": "ubiquitin-activating enzyme E1-like 2; ubiquitin-like modifier-activating enzyme 6",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:305268);  (R-RNO-8866652);  (R-RNO-983168)",
        "pathway_count": 3,
        "publication_count": 2,
        "publication_id_list": "22673903;32497710",
        "class_list": "",
        "function": "Down-regulation of UBA6 exacerbates brain injury by inhibiting the activation of Notch signaling pathway to promote cerebral cell apoptosis in rat acute cerebral infarction model. Erratum:[Mol Cell Probes. 2021 Dec;60:101773. PMID: 34649757], [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "predicted_o_glycosites": 0,
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity",
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        "protein_name": "Similar to human chromosome 9 open reading frame 153",
        "gene_name": "C17h9orf153",
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        "refseq_name": "uncharacterized protein C9orf153 homolog isoform 1",
        "refseq_ac": "NP_001389383",
        "gene_names_uniprotkb": "C17h9orf153; LOC100912252; LOC683621",
        "gene_names_refseq": "C17h9orf153",
        "protein_names_uniprotkb": "Similar to human chromosome 9 open reading frame 153",
        "protein_names_refseq": "uncharacterized protein C9orf153 homolog isoform 1; uncharacterized protein C9orf153 homolog",
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        "length": 776,
        "protein_name": "17S U2 SnRNP complex component HTATSF1",
        "gene_name": "Htatsf1",
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        "refseq_name": "17S U2 SnRNP complex component HTATSF1",
        "refseq_ac": "NP_001101729",
        "gene_names_uniprotkb": "Htatsf1",
        "gene_names_refseq": "Htatsf1; RGD1563377",
        "protein_names_uniprotkb": "17S U2 SnRNP complex component HTATSF1",
        "protein_names_refseq": "17S U2 SnRNP complex component HTATSF1; HIV TAT specific factor 1; HIV Tat-specific factor 1",
        "tax_id": 10116,
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        "pathway": " (rno:317612);  (R-RNO-9770562)",
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        "go_molecular_function": "GO:0003723 RNA binding;GO:0140463 chromatin-protein adaptor activity;GO:0160004 poly-ADP-D-ribose modification-dependent protein binding",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0035861 site of double-strand break;GO:0005686 U2 snRNP;GO:0005684 U2-type spliceosomal complex",
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        "uniprot_canonical_ac": "D4A9G4-1",
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        "length": 530,
        "protein_name": "Tyrosinase",
        "gene_name": "Tyr",
        "organism": "Rat",
        "refseq_name": "tyrosinase precursor",
        "refseq_ac": "NP_001101005",
        "gene_names_uniprotkb": "Tyr",
        "gene_names_refseq": "Tyr",
        "protein_names_uniprotkb": "Tyrosinase; 1.14.18.1; Monophenol monooxygenase",
        "protein_names_refseq": "tyrosinase precursor",
        "tax_id": 10116,
        "disease": "oculocutaneous albinism (Disease Ontology:DOID:0050632); ocular albinism 1 (Disease Ontology:DOID:0050633); oculocutaneous albinism type IA (Disease Ontology:DOID:0070094); oculocutaneous albinism type IB (Disease Ontology:DOID:0070095); pigmentation disease (Disease Ontology:DOID:10123); buphthalmos (Disease Ontology:DOID:11211); vitiligo (Disease Ontology:DOID:12306); color blindness (Disease Ontology:DOID:13399); melanoma (Disease Ontology:DOID:1909); retinoschisis (Disease Ontology:DOID:8465); skin melanoma (Disease Ontology:DOID:8923)",
        "pathway": " (rno:308800);  (R-RNO-5662702)",
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        "function": "This is a copper-containing oxidase that functions in the formation of pigments such as melanins and other polyphenolic compounds. Catalyzes the initial and rate limiting step in the cascade of reactions leading to melanin production from tyrosine. In addition to hydroxylating tyrosine to DOPA (3,4-dihydroxyphenylalanine), also catalyzes the oxidation of DOPA to DOPA-quinone, and possibly the oxidation of DHI (5,6-dihydroxyindole) to indole-5,6 quinone., [UniProtKB, UniProtKB]",
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        "ec_number_list": "1.14.18.1",
        "go_molecular_function": "GO:0042802 identical protein binding;GO:0042803 protein homodimerization activity;GO:0005507 copper ion binding;GO:0004503 tyrosinase activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0048471 perinuclear region of cytoplasm;GO:0042470 melanosome;GO:0033162 melanosome membrane",
        "go_biological_process": "GO:0008283 cell population proliferation;GO:0048538 thymus development;GO:0009411 response to UV;GO:0051591 response to cAMP;GO:0033280 response to vitamin D",
        "synthesized_glycan_count": 0,
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    },
    {
        "uniprot_canonical_ac": "D4A9L2-1",
        "uniprot_id": "D4A9L2_RAT",
        "mass": 27745.0,
        "length": 248,
        "protein_name": "Serine/arginine-rich splicing factor 1",
        "gene_name": "Srsf1",
        "organism": "Rat",
        "refseq_name": "serine/arginine-rich splicing factor 1",
        "refseq_ac": "NP_001103022",
        "gene_names_uniprotkb": "Srsf1",
        "gene_names_refseq": "Sfrs1; Srsf1",
        "protein_names_uniprotkb": "Serine/arginine-rich splicing factor 1; Splicing factor, arginine/serine-rich 1",
        "protein_names_refseq": "serine/arginine-rich splicing factor 1; splicing factor, arginine/serine-rich 1B",
        "tax_id": 10116,
        "disease": "neurodevelopmental disorder with dysmorphic facies and behavioral abnormalities (Disease Ontology:DOID:0070513); stomach cancer (Disease Ontology:DOID:10534); renovascular hypertension (Disease Ontology:DOID:1591); colon cancer (Disease Ontology:DOID:219); lung squamous cell carcinoma (Disease Ontology:DOID:3907); lung non-small cell carcinoma (Disease Ontology:DOID:3908); lung adenocarcinoma (Disease Ontology:DOID:3910); clear cell renal cell carcinoma (Disease Ontology:DOID:4467); myocardial infarction (Disease Ontology:DOID:5844); myositis (Disease Ontology:DOID:633); hepatocellular carcinoma (Disease Ontology:DOID:684); chronic myeloid leukemia (Disease Ontology:DOID:8552); myeloid leukemia (Disease Ontology:DOID:8692); cervix uteri carcinoma in situ (Disease Ontology:DOID:8991)",
        "pathway": " (rno:689890);  (R-RNO-159236);  (R-RNO-72163);  (R-RNO-72165);  (R-RNO-72203);  (R-RNO-9770562)",
        "pathway_count": 6,
        "publication_count": 3,
        "publication_id_list": "22673903;28799539;29974845",
        "class_list": "",
        "function": "Present results suggested that pathologically high cyclic stretch induces the shuttling of SRSF1 which results in the secretive pattern splicing of VEGFA and finally contributes to the proliferation of vascular smooth muscle cells. Publication Status: Online-Only, [RefSeq, PubMed]; SRSF1 promotes vascular smooth muscle cell (VSMC) proliferation and injury-induced neointima formation. SRSF1 favors the induction of a truncated p53 isoform, Delta133p53, which has an equal proliferative effect and in turn transcriptionally activates Kruppel-like factor 5 (KLF5) via the Delta133p53-EGR1 complex, resulting in an accelerated cell-cycle progression and increased VSMC proliferation. Publication Status: Online-Only, [RefSeq, PubMed]",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003723 RNA binding;GO:0003729 mRNA binding;GO:0043422 protein kinase B binding;GO:0044547 DNA topoisomerase binding;GO:0050733 RS domain binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005635 nuclear envelope;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0033120 positive regulation of RNA splicing;GO:0001701 in utero embryonic development;GO:0048255 mRNA stabilization;GO:0008380 RNA splicing;GO:0060048 cardiac muscle contraction",
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        "record_id": "D4A9L2-1",
        "record_type": "protein"
    },
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        "uniprot_canonical_ac": "D4A9P9-1",
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        "mass": 56378.0,
        "length": 503,
        "protein_name": "Hedgehog acyltransferase-like",
        "gene_name": "Hhatl",
        "organism": "Rat",
        "refseq_name": "protein-cysteine N-palmitoyltransferase HHAT-like protein",
        "refseq_ac": "NP_001100338",
        "gene_names_uniprotkb": "Hhatl",
        "gene_names_refseq": "Gup1; Hhatl; RGD1311911",
        "protein_names_uniprotkb": "Hedgehog acyltransferase-like",
        "protein_names_refseq": "Gup1, glycerol uptake/transporter homolog; protein-cysteine N-palmitoyltransferase HHAT-like protein",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:301073)",
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        "publication_count": 1,
        "publication_id_list": "38719175",
        "class_list": "",
        "function": "Downregulation of HHATL promotes cardiac hypertrophy via activation of SHH/DRP1., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0048471 perinuclear region of cytoplasm;GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0060262 negative regulation of N-terminal protein palmitoylation;GO:0031399 regulation of protein modification process",
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        "record_id": "D4A9P9-1",
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    {
        "uniprot_canonical_ac": "D4A9T2-1",
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        "length": 222,
        "protein_name": "Twisted gastrulation BMP signaling modulator 1",
        "gene_name": "Twsg1",
        "organism": "Rat",
        "refseq_name": "twisted gastrulation protein homolog 1 precursor",
        "refseq_ac": "NP_001102281",
        "gene_names_uniprotkb": "Twsg1",
        "gene_names_refseq": "Twsg1",
        "protein_names_uniprotkb": "Twisted gastrulation BMP signaling modulator 1",
        "protein_names_refseq": "twisted gastrulation homolog 1; twisted gastrulation protein homolog 1 precursor; twisted gastrulation protein homolog 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:363294)",
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        "publication_count": 0,
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        "ec_number_list": "",
        "go_molecular_function": "GO:0008201 heparin binding;GO:0050431 transforming growth factor beta binding",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005813 centrosome;GO:0005829 cytosol",
        "go_biological_process": "GO:0030154 cell differentiation;GO:0030900 forebrain development;GO:0030509 BMP signaling pathway;GO:0030514 negative regulation of BMP signaling pathway;GO:0030097 hemopoiesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4A9T2-1",
        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "D4A9T6-1",
        "uniprot_id": "D4A9T6_RAT",
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        "length": 290,
        "protein_name": "Aquaporin",
        "gene_name": "Aqp12a",
        "organism": "Rat",
        "refseq_name": "aquaporin-12",
        "refseq_ac": "NP_001102479",
        "gene_names_uniprotkb": "Aqp12a",
        "gene_names_refseq": "Aqp12a; Aqp12b; Aqp12; RGD1562727",
        "protein_names_uniprotkb": "Aquaporin",
        "protein_names_refseq": "aquaporin 12B; aquaporin-12",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:367316);  (R-RNO-432047)",
        "pathway_count": 2,
        "publication_count": 2,
        "publication_id_list": "32735865;38511591",
        "class_list": "",
        "function": "Aquaporin-7 and aquaporin-12 modulate the inflammatory phenotype of endocrine pancreatic beta-cells., [RefSeq, PubMed]; Expression of AQP-10, -11 and -12 in the rat stria vascularis., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0015267 channel activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0016020 membrane",
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        "hit_score": 0.3,
        "record_id": "D4A9T6-1",
        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "D4A9V0-1",
        "uniprot_id": "D4A9V0_RAT",
        "mass": 63691.0,
        "length": 563,
        "protein_name": "serine C-palmitoyltransferase",
        "gene_name": "Sptlc3",
        "organism": "Rat",
        "refseq_name": "serine palmitoyltransferase 3",
        "refseq_ac": "NP_001099987",
        "gene_names_uniprotkb": "Sptlc3",
        "gene_names_refseq": "RGD1310030; Sptlc3",
        "protein_names_uniprotkb": "serine C-palmitoyltransferase; 2.3.1.50",
        "protein_names_refseq": "serine palmitoyltransferase 3",
        "tax_id": 10116,
        "disease": "hereditary sensory and autonomic neuropathy type 1 (Disease Ontology:DOID:0070162)",
        "pathway": " (rno:296188);  (R-RNO-1660661)",
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        "go_molecular_function": "GO:0004758 serine C-palmitoyltransferase activity;GO:0030170 pyridoxal phosphate binding",
        "go_cellular_component": "GO:0017059 serine palmitoyltransferase complex;GO:0005783 endoplasmic reticulum;GO:0016020 membrane",
        "go_biological_process": "GO:0046513 ceramide biosynthetic process;GO:0046512 sphingosine biosynthetic process;GO:0046520 sphingoid biosynthetic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4A9V0-1",
        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "D4A9V4-1",
        "uniprot_id": "D4A9V4_RAT",
        "mass": 43941.0,
        "length": 412,
        "protein_name": "E2F transcription factor 4",
        "gene_name": "E2f4",
        "organism": "Rat",
        "refseq_name": "transcription factor E2F4",
        "refseq_ac": "NP_001258274",
        "gene_names_uniprotkb": "E2f4",
        "gene_names_refseq": "E2f4",
        "protein_names_uniprotkb": "E2F transcription factor 4",
        "protein_names_refseq": "E2F transcription factor 4, p107/p130-binding; transcription factor E2F4",
        "tax_id": 10116,
        "disease": "otitis media (Disease Ontology:DOID:10754); Lynch syndrome (Disease Ontology:DOID:3883)",
        "pathway": " (rno:100360427);  (R-RNO-1538133);  (R-RNO-2173796);  (R-RNO-69231)",
        "pathway_count": 4,
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        "publication_id_list": "22985930",
        "class_list": "",
        "function": "E2F4 is part of a transcriptional repressor complex comprising p130 and HDAC1 in cardiac myocytes. Relief from E2F4-dependent gene silencing induces the expression of pro-apoptotic genes., [RefSeq, PubMed]",
        "predicted_glycosites": 1,
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        "secondary_ac_list": "",
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0003682 chromatin binding;GO:0003700 DNA-binding transcription factor activity;GO:0019904 protein domain specific binding;GO:0046983 protein dimerization activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0000785 chromatin;GO:0090575 RNA polymerase II transcription regulator complex",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0042127 regulation of cell population proliferation;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0006355 regulation of DNA-templated transcription",
        "synthesized_glycan_count": 0,
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        "record_id": "D4A9V4-1",
        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "D4A9Z2-1",
        "uniprot_id": "D4A9Z2_RAT",
        "mass": 96850.0,
        "length": 862,
        "protein_name": "DNA topoisomerase",
        "gene_name": "Top3b",
        "organism": "Rat",
        "refseq_name": "DNA topoisomerase 3-beta-1",
        "refseq_ac": "NP_001099331",
        "gene_names_uniprotkb": "Top3b",
        "gene_names_refseq": "Top3b",
        "protein_names_uniprotkb": "DNA topoisomerase; 5.6.2.1",
        "protein_names_refseq": "DNA topoisomerase 3-beta-1; topoisomerase (DNA) III beta",
        "tax_id": 10116,
        "disease": "type 2 diabetes mellitus (Disease Ontology:DOID:9352)",
        "pathway": " (rno:287930)",
        "pathway_count": 1,
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        "publication_id_list": "",
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        "function": "Introduces a single-strand break via transesterification at a target site in duplex DNA. Releases the supercoiling and torsional tension of DNA introduced during the DNA replication and transcription by transiently cleaving and rejoining one strand of the DNA duplex. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand., [UniProtKB, UniProtKB]",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0003917 DNA topoisomerase type I (single strand cut, ATP-independent) activity;GO:0140226 RNA topoisomerase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0000793 condensed chromosome;GO:0140225 DNA topoisomerase III-beta-TDRD3 complex",
        "go_biological_process": "GO:0006281 DNA repair;GO:0006310 DNA recombination;GO:0007059 chromosome segregation;GO:0006265 DNA topological change",
        "synthesized_glycan_count": 0,
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        "record_id": "D4A9Z2-1",
        "record_type": "protein"
    },
    {
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        "length": 627,
        "protein_name": "Zinc finger protein 697",
        "gene_name": "Zfp697",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Zfp697",
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        "protein_names_uniprotkb": "Zinc finger protein 697",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (rno:295310)",
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        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "RNA-interacting protein with a high number of miRNA targets. Acts as a damage-induced regulator of muscle remodeling by mediating the interferon gamma response in muscle cells., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003700 DNA-binding transcription factor activity;GO:0008270 zinc ion binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0035198 miRNA binding",
        "go_cellular_component": "GO:0005634 nucleus",
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    },
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        "length": 322,
        "protein_name": "Protein atonal homolog 8",
        "gene_name": "Atoh8",
        "organism": "Rat",
        "refseq_name": "transcription factor ATOH8",
        "refseq_ac": "NP_001102711",
        "gene_names_uniprotkb": "Atoh8",
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        "protein_names_uniprotkb": "Protein atonal homolog 8",
        "protein_names_refseq": "protein atonal homolog 8; transcription factor ATOH8",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:500200)",
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        "go_molecular_function": "GO:0003700 DNA-binding transcription factor activity;GO:0046983 protein dimerization activity;GO:0070888 E-box binding;GO:0140297 DNA-binding transcription factor binding",
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        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0010629 negative regulation of gene expression;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0010595 positive regulation of endothelial cell migration;GO:0045892 negative regulation of DNA-templated transcription",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4AA32-1",
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        "length": 529,
        "protein_name": "DEP domain-containing protein 1B",
        "gene_name": "Depdc1b",
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        "refseq_name": "DEP domain-containing protein 1B",
        "refseq_ac": "NP_001101121",
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        "gene_names_refseq": "Depdc1b",
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        "protein_names_refseq": "DEP domain-containing protein 1B",
        "tax_id": 10116,
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        "pathway": " (rno:310074);  (R-RNO-8980692);  (R-RNO-9013026);  (R-RNO-9013106);  (R-RNO-9013148);  (R-RNO-9013149);  (R-RNO-9013404);  (R-RNO-9013406);  (R-RNO-9013408);  (R-RNO-9013409);  (R-RNO-9013420);  (R-RNO-9013423);  (R-RNO-9013424);  (R-RNO-9035034);  (R-RNO-9696264);  (R-RNO-9696270);  (R-RNO-9696273)",
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        "go_molecular_function": "GO:0005096 GTPase activator activity",
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        "go_biological_process": "GO:0016477 cell migration;GO:0035556 intracellular signal transduction;GO:0030177 positive regulation of Wnt signaling pathway",
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        "record_id": "D4AA32-1",
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    },
    {
        "uniprot_canonical_ac": "D4AA36-1",
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        "length": 656,
        "protein_name": "SIM bHLH transcription factor 2",
        "gene_name": "Sim2",
        "organism": "Rat",
        "refseq_name": "single-minded homolog 2",
        "refseq_ac": "NP_001100578",
        "gene_names_uniprotkb": "Sim2",
        "gene_names_refseq": "Sim2",
        "protein_names_uniprotkb": "SIM bHLH transcription factor 2",
        "protein_names_refseq": "single-minded 2; single-minded family bHLH transcription factor 2; single-minded homolog 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:304071)",
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        "publication_id_list": "16641100;23333261;25319570",
        "class_list": "",
        "function": "Ethanol at different concentrations induced Sim2 accumulation in primary cultures of rat neurons., [RefSeq, PubMed]; Sim2 may mediate neurotoxicity during hyperglycaemia and thereby play a critical role in the development of hyperglycaemia-induced cognitive deficits., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0046982 protein heterodimerization activity;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0016604 nuclear body",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0007399 nervous system development;GO:0030154 cell differentiation",
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        "record_id": "D4AA36-1",
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    },
    {
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        "uniprot_id": "D4AA62_RAT",
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        "length": 282,
        "protein_name": "PAK4-inhibitor INKA1",
        "gene_name": "Inka1",
        "organism": "Rat",
        "refseq_name": "PAK4-inhibitor INKA1",
        "refseq_ac": "NP_001101657",
        "gene_names_uniprotkb": "Inka1; Fam212a",
        "gene_names_refseq": "Fam212a; Inka1; RGD1560778",
        "protein_names_uniprotkb": "PAK4-inhibitor INKA1; Induced in neural crest by AP2-alpha protein homolog; Inka-box actin regulator 1; PAK4-inhibitor inka1",
        "protein_names_refseq": "PAK4-inhibitor INKA1; family with sequence similarity 212, member A",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:316001)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Inhibitor of the serine/threonine-protein kinase PAK4. Acts by binding PAK4 in a substrate-like manner, inhibiting the protein kinase activity., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0019901 protein kinase binding;GO:0030291 protein serine/threonine kinase inhibitor activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0021915 neural tube development",
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        "hit_score": 0.1,
        "record_id": "D4AA62-1",
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    },
    {
        "uniprot_canonical_ac": "D4AAE7-1",
        "uniprot_id": "D4AAE7_RAT",
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        "length": 143,
        "protein_name": "Copper transport protein",
        "gene_name": "Slc31a2",
        "organism": "Rat",
        "refseq_name": "protein SLC31A2",
        "refseq_ac": "NP_001028865",
        "gene_names_uniprotkb": "Slc31a2",
        "gene_names_refseq": "Slc31a2",
        "protein_names_uniprotkb": "Copper transport protein",
        "protein_names_refseq": "probable low affinity copper uptake protein 2; protein SLC31A2; solute carrier family 31 (copper transporter), member 2; solute carrier family 31 (copper transporters), member 2",
        "tax_id": 10116,
        "disease": "Wilson disease (Disease Ontology:DOID:893)",
        "pathway": " (rno:298091)",
        "pathway_count": 1,
        "publication_count": 2,
        "publication_id_list": "17944601;22673903",
        "class_list": "",
        "function": "Ctr2 promotes copper uptake at the plasma membrane and plays a role in regulating copper levels in COS-7 cells, [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0005375 copper ion transmembrane transporter activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane;GO:0055037 recycling endosome;GO:0005765 lysosomal membrane;GO:0031902 late endosome membrane",
        "go_biological_process": "GO:0006878 intracellular copper ion homeostasis;GO:0006825 copper ion transport;GO:0015677 copper ion import;GO:1902311 regulation of copper ion transmembrane transport",
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    {
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        "length": 342,
        "protein_name": "Cell cycle control protein",
        "gene_name": "Tmem30c",
        "organism": "Rat",
        "refseq_name": "cell cycle control protein 50C",
        "refseq_ac": "NP_001099359",
        "gene_names_uniprotkb": "Tmem30c",
        "gene_names_refseq": "RGD1306090; Tmem30c",
        "protein_names_uniprotkb": "Cell cycle control protein",
        "protein_names_refseq": "cell cycle control protein 50C",
        "tax_id": 10116,
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        "pathway": " (rno:288175)",
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        "length": 273,
        "protein_name": "Transmembrane protein 45A",
        "gene_name": "Tmem45a",
        "organism": "Rat",
        "refseq_name": "transmembrane protein 45A",
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        "gene_names_uniprotkb": "Tmem45a",
        "gene_names_refseq": "Tmem45al; Tmem45a",
        "protein_names_uniprotkb": "Transmembrane protein 45A",
        "protein_names_refseq": "transmembrane protein 45A-like; transmembrane protein 45A",
        "tax_id": 10116,
        "disease": "",
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        "publication_id_list": "22673903;31585906",
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        "function": "TMEM45A is involved in renal fibrosis in rats by regulating Jagged1/Notch pathway. Publication Status: Online-Only, [RefSeq, PubMed]",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0016020 membrane",
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        "hit_score": 0.3,
        "record_id": "D4AAI6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4AAM1-1",
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        "length": 123,
        "protein_name": "Similar to human chromosome 11 open reading frame 98",
        "gene_name": "C1h11orf98",
        "organism": "Rat",
        "refseq_name": "uncharacterized protein C11orf98 homolog",
        "refseq_ac": "NP_001103051",
        "gene_names_uniprotkb": "C1h11orf98; LOC690349; Lbhd1l1; Lbhd1; RGD1597339",
        "gene_names_refseq": "C1h11orf98; Lbhd1; RGD1304652; RGD1597339",
        "protein_names_uniprotkb": "Similar to human chromosome 11 open reading frame 98",
        "protein_names_refseq": "LBH domain containing 1; uncharacterized protein C11orf98 homolog",
        "tax_id": 10116,
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        "pathway": " (rno:690349)",
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        "function": "",
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        "record_id": "D4AAM1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4AAN8-1",
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        "mass": 122407.0,
        "length": 1087,
        "protein_name": "DNA helicase B",
        "gene_name": "Helb",
        "organism": "Rat",
        "refseq_name": "DNA helicase B",
        "refseq_ac": "NP_001386765",
        "gene_names_uniprotkb": "Helb",
        "gene_names_refseq": "Helb; RGD1560103",
        "protein_names_uniprotkb": "DNA helicase B; 3.6.4.12",
        "protein_names_refseq": "DNA helicase B; helicase (DNA) B",
        "tax_id": 10116,
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        "pathway": " (rno:500837)",
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        "publication_id_list": "22673903;29393594",
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        "function": "5'-3' DNA helicase involved in DNA damage response by acting as an inhibitor of DNA end resection. Recruitment to single-stranded DNA (ssDNA) following DNA damage leads to inhibit the nucleases catalyzing resection, such as EXO1, BLM and DNA2, possibly via the 5'-3' ssDNA translocase activity of HELB. As cells approach S phase, DNA end resection is promoted by the nuclear export of HELB following phosphorylation. Acts independently of TP53BP1. Unwinds duplex DNA with 5'-3' polarity. Has single-strand DNA-dependent ATPase and DNA helicase activities. Prefers ATP and dATP as substrates. During S phase, may facilitate cellular recovery from replication stress., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "ec_number_list": "5.6.2.3;3.6.4.13;3.6.4.12;2.7.11.1;3.6.1.5;3.6.4.10;3.6.4.-;2.3.2.27;5.6.2.4;3.6.5.-;5.6.2.-;3.1.-.-;2.7.7.7;2.7.7.49;3.1.13.1;4.2.99.18;7.6.2.2;7.6.2.3;7.6.2.-;5.6.1.6;7.2.2.-;3.6.1.15;3.6.4.6;3.1.3.1;3.9.1.1;6.1.1.12;3.6.1.-;2.7.4.3;3.1.4.-;3.4.24.-;3.6.-.-;3.4.21.53;5.6.2.5",
        "go_molecular_function": "GO:0003723 RNA binding;GO:0005524 ATP binding;GO:0016787 hydrolase activity;GO:0044877 protein-containing complex binding;GO:0004386 helicase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005681 spliceosomal complex",
        "go_biological_process": "GO:2000042 negative regulation of double-strand break repair via homologous recombination;GO:0006260 DNA replication;GO:0006974 DNA damage response;GO:0006269 DNA replication, synthesis of primer;GO:0006261 DNA-templated DNA replication",
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        "record_type": "protein"
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        "length": 318,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or2f2",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr808",
        "refseq_ac": "NP_001000850",
        "gene_names_uniprotkb": "Or2f2",
        "gene_names_refseq": "Olr808; Or2f2",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 808; olfactory receptor Olr808; olfactory receptor gene Olr808",
        "tax_id": 10116,
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        "pathway": " (rno:405140)",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0050911 detection of chemical stimulus involved in sensory perception of smell",
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        "hit_score": 0.1,
        "record_id": "D4AAR1-1",
        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "D4AAU8-1",
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        "mass": 31092.0,
        "length": 273,
        "protein_name": "Leucine-rich repeat-containing protein 10",
        "gene_name": "Lrrc10",
        "organism": "Rat",
        "refseq_name": "leucine-rich repeat-containing protein 10",
        "refseq_ac": "NP_001101566",
        "gene_names_uniprotkb": "Lrrc10",
        "gene_names_refseq": "Lrrc10",
        "protein_names_uniprotkb": "Leucine-rich repeat-containing protein 10",
        "protein_names_refseq": "leucine-rich repeat-containing protein 10-like; leucine-rich repeat-containing protein 10",
        "tax_id": 10116,
        "disease": "dilated cardiomyopathy (Disease Ontology:DOID:12930)",
        "pathway": " (rno:314848)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "May play important roles in cardiac development and/or cardiac function., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003779 actin binding;GO:0051393 alpha-actinin binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005739 mitochondrion;GO:0005856 cytoskeleton;GO:0030017 sarcomere;GO:0030016 myofibril",
        "go_biological_process": "GO:0055013 cardiac muscle cell development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D4AAU8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4AB91-1",
        "uniprot_id": "D4AB91_RAT",
        "mass": 27349.0,
        "length": 248,
        "protein_name": "Zinc finger protein 575",
        "gene_name": "Zfp575",
        "organism": "Rat",
        "refseq_name": "zinc finger protein 575 isoform X1",
        "refseq_ac": "XP_038967287",
        "gene_names_uniprotkb": "Zfp575",
        "gene_names_refseq": "Zfp575; Znf575",
        "protein_names_uniprotkb": "Zinc finger protein 575",
        "protein_names_refseq": "zinc finger protein 575 isoform X1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:308430)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB]",
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific",
        "go_cellular_component": "",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4AB91-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4AB92-1",
        "uniprot_id": "D4AB92_RAT",
        "mass": 24810.0,
        "length": 217,
        "protein_name": "AFG2 interacting ribosome maturation factor",
        "gene_name": "Airim",
        "organism": "Rat",
        "refseq_name": "AFG2-interacting ribosome maturation factor",
        "refseq_ac": "NP_001102734",
        "gene_names_uniprotkb": "Airim; C5h1orf109; RGD1560436",
        "gene_names_refseq": "Airim; C5h1orf109; RGD1560436",
        "protein_names_uniprotkb": "AFG2 interacting ribosome maturation factor",
        "protein_names_refseq": "AFG2-interacting ribosome maturation factor; ribosome biogenesis protein C1orf109 homolog; uncharacterized protein C1orf109 homolog",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:500546)",
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        "secondary_ac_list": "",
        "ec_number_list": "",
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        "protein_names_refseq": "rCG30099-like; testis expressed 52 isoform 1; testis-expressed protein 52",
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        "protein_name": "Serine protease 41",
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        "refseq_name": "serine protease 41 precursor",
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        "gene_names_refseq": "Prss41; RGD1304769; Tessp1",
        "protein_names_uniprotkb": "Serine protease 41",
        "protein_names_refseq": "protease, serine, 21 (testisin); protease, serine, 41; serine protease 41 precursor; testis serine protease 1; testis-specific serine protease 1",
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        "length": 362,
        "protein_name": "Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase",
        "gene_name": "Hacd3",
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        "refseq_name": "very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 3",
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        "protein_names_uniprotkb": "Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase; 4.2.1.134",
        "protein_names_refseq": "protein tyrosine phosphatase-like A domain containing 1; very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 3",
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        "function": "Catalyzes the third of the four reactions of the long-chain fatty acids elongation cycle. This endoplasmic reticulum-bound enzymatic process, allows the addition of two carbons to the chain of long- and very long-chain fatty acids/VLCFAs per cycle. This enzyme catalyzes the dehydration of the 3-hydroxyacyl-CoA intermediate into trans-2,3-enoyl-CoA, within each cycle of fatty acid elongation. Thereby, it participates to the production of VLCFAs of different chain lengths that are involved in multiple biological processes as precursors of membrane lipids and lipid mediators., [UniProtKB, UniProtKB]; PTPLAD1 (HACD3)is in complex with insulin receptor in rat's liver plasma membrane and golgi-endosome(G/E). PTPLAD1 compartmentalization between PM and G/E is insulin-dependent. SiRNA-mediated knockdown of PTPLAD1 increased IR tyrosine phosphorylation and affect IR endocytosis in HEK293. PTPLAD1 depletion enhanced insulin effect on Glut2 translocation in HEK293 cells and it increased AKT-ser473 phosphorylation. [PTPLAD1], [RefSeq, PubMed]",
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        "protein_names_refseq": "probable G-protein coupled receptor 101",
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        "disease": "growth hormone secreting pituitary adenoma 2 (Disease Ontology:DOID:0112007)",
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        "function": "Increased GPCR101 mRNA expression in supraoptic and paraventricular nuclei from late pregnancy to late lactation may reflect the functional importance of this receptor in the regulation of neurons of these nuclei during this period., [RefSeq, PubMed]",
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        "length": 301,
        "protein_name": "Transmembrane 4 L six family member 5",
        "gene_name": "Tm4sf5",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Tm4sf5",
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        "protein_names_uniprotkb": "Transmembrane 4 L six family member 5",
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        "protein_name": "Zinc finger and BTB domain containing 2",
        "gene_name": "Zbtb2",
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        "gene_names_uniprotkb": "Zbtb2",
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        "protein_names_uniprotkb": "Zinc finger and BTB domain containing 2",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0042802 identical protein binding;GO:1990837 sequence-specific double-stranded DNA binding",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005634 nucleus",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0002682 regulation of immune system process;GO:0001817 regulation of cytokine production",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
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    {
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        "length": 629,
        "protein_name": "G protein-coupled receptor 153",
        "gene_name": "Gpr153",
        "organism": "Rat",
        "refseq_name": "probable G-protein coupled receptor 153 isoform 1",
        "refseq_ac": "NP_001426138",
        "gene_names_uniprotkb": "Gpr153",
        "gene_names_refseq": "Gpr153",
        "protein_names_uniprotkb": "G protein-coupled receptor 153",
        "protein_names_refseq": "probable G-protein coupled receptor 153 isoform 1; probable G-protein coupled receptor 153",
        "tax_id": 10116,
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        "class_list": "",
        "function": "Antisense oligodeoxynucleotide knockdown of Gpr153 caused a slight reduction in food intake and elevated plus maze test showed significant reduction in the percentage of time spent in centre square, which points towards probable role in decision making., [RefSeq, PubMed]",
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        "gene_name": "Emc6",
        "organism": "Rat",
        "refseq_name": "ER membrane protein complex subunit 6",
        "refseq_ac": "NP_001099276",
        "gene_names_uniprotkb": "Emc6",
        "gene_names_refseq": "Emc6; RGD1309231; Tmem93",
        "protein_names_uniprotkb": "ER membrane protein complex subunit 6; Transmembrane protein 93",
        "protein_names_refseq": "ER membrane protein complex subunit 6; transmembrane protein 93",
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        "go_cellular_component": "GO:0072546 EMC complex;GO:0016020 membrane;GO:0005789 endoplasmic reticulum membrane;GO:1903349 omegasome membrane",
        "go_biological_process": "GO:0000045 autophagosome assembly;GO:0071816 tail-anchored membrane protein insertion into ER membrane;GO:0045050 protein insertion into ER membrane by stop-transfer membrane-anchor sequence",
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        "protein_names_uniprotkb": "Kelch-like family member 28",
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    {
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        "protein_names_uniprotkb": "Leucine-rich repeat transmembrane protein FLRT1",
        "protein_names_refseq": "fibronectin leucine rich transmembrane protein 3; leucine-rich repeat transmembrane protein FLRT1",
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        "function": "Plays a role in fibroblast growth factor-mediated signaling cascades that lead to the activation of MAP kinases. Promotes neurite outgrowth via FGFR1-mediated activation of downstream MAP kinases. Promotes an increase both in neurite number and in neurite length. May play a role in cell-cell adhesion and cell guidance via its interaction with ADGRL1/LPHN1 and ADGRL3., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005104 fibroblast growth factor receptor binding",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005886 plasma membrane;GO:0005911 cell-cell junction;GO:0005925 focal adhesion;GO:0048471 perinuclear region of cytoplasm",
        "go_biological_process": "GO:0007155 cell adhesion;GO:0016358 dendrite development;GO:0051965 positive regulation of synapse assembly;GO:1990138 neuron projection extension;GO:0008543 fibroblast growth factor receptor signaling pathway",
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    {
        "uniprot_canonical_ac": "D4AC56-1",
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        "length": 510,
        "protein_name": "ETS variant transcription factor 5",
        "gene_name": "Etv5",
        "organism": "Rat",
        "refseq_name": "ETS translocation variant 5",
        "refseq_ac": "NP_001100552",
        "gene_names_uniprotkb": "Etv5",
        "gene_names_refseq": "Etv5",
        "protein_names_uniprotkb": "ETS variant transcription factor 5",
        "protein_names_refseq": "ETS translocation variant 5; ets variant gene 5 (ets-related molecule)",
        "tax_id": 10116,
        "disease": "bipolar disorder (Disease Ontology:DOID:3312); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (rno:303828)",
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        "publication_id_list": "16394217;24089499;24710089;27909004;29393594;33883060;37876309",
        "class_list": "",
        "function": "ETV5 regulates proliferation and cell cycle genes in the INS-1 (832/13) cell line independently of the concentration of secreted insulin., [RefSeq, PubMed]; Gene transfer of Etv5 in the VTA/SNpc did not affect measures of energy balance or performances in a progressive ratio schedule Publication Status: Online-Only, [RefSeq, PubMed]; Maternal undernutrition during pregnancy and lactation increases transcription factors, ETV5 and GDNF, and alters regulation of apoptosis and heat shock proteins in the testis of adult offspring in the rat., [RefSeq, PubMed]; The data suggest that ETV4 family members regulate their own expression, and that they regulate transcription of a subset of genes that are dependent upon testicular luminal fluid factors., [RefSeq, PubMed]; These data establish Etv4 and Etv5 as essential molecules of the transcriptional program linking neurotrophin signaling to sensory neuronal differentiation, [RefSeq, PubMed]; This study demonstrates that Etv4 and Etv5 transcription factors are expressed in hippocampal pyramidal neurons during the main period of dendritogenesis; reveals a novel role for Etv4 and Etv5 transcription factors for hippocampal circuit development and the coordination of synaptic maturation; and indicates that both factors are essential in the transcriptional program linking BDNF signaling to dendrite development., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0003700 DNA-binding transcription factor activity;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0000976 transcription cis-regulatory region binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0001228 DNA-binding transcription activator activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005886 plasma membrane;GO:0045202 synapse",
        "go_biological_process": "GO:0060762 regulation of branching involved in mammary gland duct morphogenesis;GO:0048133 male germ-line stem cell asymmetric division;GO:0060252 positive regulation of glial cell proliferation;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006357 regulation of transcription by RNA polymerase II",
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        "uniprot_id": "D4ACB8_RAT",
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        "protein_name": "T-complex protein 1 subunit theta",
        "gene_name": "Cct8",
        "organism": "Rat",
        "refseq_name": "T-complex protein 1 subunit theta",
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        "protein_names_uniprotkb": "T-complex protein 1 subunit theta; CCT-theta",
        "protein_names_refseq": "T-complex protein 1 subunit theta; chaperonin containing Tcp1, subunit 8 (theta); chaperonin subunit 8 (theta)",
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        "disease": "",
        "pathway": " (rno:288305);  (R-RNO-390471);  (R-RNO-5620922);  (R-RNO-6798695);  (R-RNO-6814122)",
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        "publication_id_list": "18683930;29393594",
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        "ec_number_list": "5.6.2.3;3.6.4.13;3.6.4.12;2.7.11.1;3.6.1.5;3.6.4.10;3.6.4.-;2.3.2.27;5.6.2.4;3.6.5.-;5.6.2.-;3.1.-.-;2.7.7.7;2.7.7.49;3.1.13.1;4.2.99.18;7.6.2.2;7.6.2.3;7.6.2.-;5.6.1.6;7.2.2.-;3.6.1.15;3.6.4.6;3.1.3.1;3.9.1.1;6.1.1.12;3.6.1.-;2.7.4.3;3.1.4.-;3.4.24.-;3.6.-.-;3.4.21.53;5.6.2.5",
        "go_molecular_function": "GO:0005524 ATP binding;GO:0051082 unfolded protein binding;GO:0016887 ATP hydrolysis activity;GO:0044183 protein folding chaperone;GO:0140662 ATP-dependent protein folding chaperone",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005813 centrosome;GO:0005829 cytosol;GO:0005874 microtubule;GO:0044297 cell body",
        "go_biological_process": "GO:0007339 binding of sperm to zona pellucida;GO:0032212 positive regulation of telomere maintenance via telomerase;GO:0050821 protein stabilization;GO:0006457 protein folding",
        "synthesized_glycan_count": 0,
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        "protein_name": "Pseudouridylate synthase RPUSD2",
        "gene_name": "Rpusd2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Rpusd2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Pseudouridylate synthase RPUSD2; RNA pseudouridylate synthase domain-containing protein 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
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        "pathway_count": 0,
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        "class_list": "",
        "function": "Pseudouridine synthase that catalyzes pseudouridylation of mRNAs., [UniProtKB, UniProtKB]",
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        "ec_number_list": "5.4.99.-;5.4.99.12;5.4.99.25",
        "go_molecular_function": "GO:0003723 RNA binding;GO:0009982 pseudouridine synthase activity",
        "go_cellular_component": "",
        "go_biological_process": "GO:0000455 enzyme-directed rRNA pseudouridine synthesis;GO:1990481 mRNA pseudouridine synthesis",
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        "record_id": "D4ACD4-1",
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    {
        "uniprot_canonical_ac": "D4ACF4-1",
        "uniprot_id": "D4ACF4_RAT",
        "mass": 26102.0,
        "length": 238,
        "protein_name": "Neural retina-specific leucine zipper protein",
        "gene_name": "Nrl",
        "organism": "Rat",
        "refseq_name": "neural retina-specific leucine zipper protein",
        "refseq_ac": "NP_001099506",
        "gene_names_uniprotkb": "Nrl",
        "gene_names_refseq": "Nrl",
        "protein_names_uniprotkb": "Neural retina-specific leucine zipper protein",
        "protein_names_refseq": "neural retina-specific leucine zipper protein",
        "tax_id": 10116,
        "disease": "enhanced S-cone syndrome 2 (Disease Ontology:DOID:0061232); enhanced S-cone syndrome (Disease Ontology:DOID:0090059); retinitis pigmentosa 27 (Disease Ontology:DOID:0110397); retinitis pigmentosa (Disease Ontology:DOID:10584)",
        "pathway": " (rno:290221)",
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        "publication_count": 1,
        "publication_id_list": "16854989",
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        "function": "Acts as a transcriptional activator which regulates the expression of several rod-specific genes, including RHO and PDE6B. Also functions as a transcriptional coactivator, stimulating transcription mediated by the transcription factor CRX and NR2E3. Binds to the rhodopsin promoter in a sequence-specific manner., [UniProtKB, UniProtKB]; Signaling by RA via RA receptors regulates the expression of NRL, providing a framework for delineating early steps in photoreceptor cell fate determination, [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0003700 DNA-binding transcription factor activity;GO:0043522 leucine zipper domain binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0001228 DNA-binding transcription activator activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0010628 positive regulation of gene expression;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0006355 regulation of DNA-templated transcription",
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        "refseq_name": "protein GAPT",
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        "gene_names_uniprotkb": "Gapt",
        "gene_names_refseq": "Gapt",
        "protein_names_uniprotkb": "Grb2-binding adaptor protein, transmembrane",
        "protein_names_refseq": "protein GAPT",
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        "go_cellular_component": "GO:0005886 plasma membrane",
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    },
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        "protein_name": "Fucose mutarotase",
        "gene_name": "Fuom",
        "organism": "Rat",
        "refseq_name": "fucose mutarotase",
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        "gene_names_uniprotkb": "Fuom",
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        "protein_names_uniprotkb": "Fucose mutarotase; 5.1.3.29",
        "protein_names_refseq": "fucose mutarotase",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:293587);  (R-RNO-6787639)",
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        "class_list": "",
        "function": "Involved in the interconversion between alpha- and beta-L-fucoses. L-Fucose (6-deoxy-L-galactose) exists as alpha-L-fucose (29.5%) and beta-L-fucose (70.5%), the beta-form is metabolized through the salvage pathway. GDP-L-fucose formed either by the de novo or salvage pathways is transported into the endoplasmic reticulum, where it serves as a substrate for N- and O-glycosylations by fucosyltransferases. Fucosylated structures expressed on cell surfaces or secreted in biological fluids are believed to play a critical role in cell-cell adhesion and recognition processes., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005829 cytosol",
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        "protein_names_refseq": "Ras association (RalGDS/AF-6) domain family 3; Ras association (RalGDS/AF-6) domain family member 3; ras association domain-containing protein 3",
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        "go_molecular_function": "GO:0042802 identical protein binding",
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        "protein_name": "Zinc finger CCCH-type containing 12B",
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        "refseq_name": "probable ribonuclease ZC3H12B isoform 1",
        "refseq_ac": "NP_001419803",
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        "gene_names_refseq": "RGD1560891; Zc3h12b",
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        "protein_names_refseq": "probable ribonuclease ZC3H12B isoform 1; probable ribonuclease ZC3H12B",
        "tax_id": 10116,
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        "go_molecular_function": "GO:0003729 mRNA binding;GO:0008270 zinc ion binding;GO:0016787 hydrolase activity;GO:0004521 RNA endonuclease activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0036464 cytoplasmic ribonucleoprotein granule",
        "go_biological_process": "GO:0061158 3'-UTR-mediated mRNA destabilization",
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        "record_id": "D4ACQ4-1",
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    },
    {
        "uniprot_canonical_ac": "D4ACV0-1",
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        "length": 631,
        "protein_name": "Negative elongation factor complex member B",
        "gene_name": "Nelfb",
        "organism": "Rat",
        "refseq_name": "negative elongation factor B",
        "refseq_ac": "NP_001101287",
        "gene_names_uniprotkb": "Nelfb",
        "gene_names_refseq": "Cobra1; Nelfb; RGD1307832",
        "protein_names_uniprotkb": "Negative elongation factor complex member B",
        "protein_names_refseq": "cofactor of BRCA1; negative elongation factor B; negative elongation factor protein B",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:311796);  (R-RNO-112382);  (R-RNO-113418);  (R-RNO-674695);  (R-RNO-6796648);  (R-RNO-75955)",
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        "class_list": "",
        "function": "These studies allow us to position the actions of two new modulators of GR-regulated transactivation, NELF-A and NELF-B, relative to other factors in the overall gene induction sequence., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0140870 RNA polymerase inhibitor activity",
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    {
        "uniprot_canonical_ac": "D4ACZ1-1",
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        "mass": 40907.0,
        "length": 359,
        "protein_name": "Mab-21 like 2",
        "gene_name": "Mab21l2",
        "organism": "Rat",
        "refseq_name": "protein mab-21-like 2",
        "refseq_ac": "NP_001102861",
        "gene_names_uniprotkb": "Mab21l2",
        "gene_names_refseq": "Mab21l2",
        "protein_names_uniprotkb": "Mab-21 like 2",
        "protein_names_refseq": "protein mab-21-like 2",
        "tax_id": 10116,
        "disease": "syndromic microphthalmia 14 (Disease Ontology:DOID:0111802); microphthalmia (Disease Ontology:DOID:10629); coloboma (Disease Ontology:DOID:12270)",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0010172 embryonic body morphogenesis;GO:0008283 cell population proliferation;GO:0008284 positive regulation of cell population proliferation;GO:0001654 eye development;GO:0043010 camera-type eye development",
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    {
        "uniprot_canonical_ac": "D4AD29-1",
        "uniprot_id": "D4AD29_RAT",
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        "length": 99,
        "protein_name": "Ragulator complex protein LAMTOR4",
        "gene_name": "Lamtor4",
        "organism": "Rat",
        "refseq_name": "ragulator complex protein LAMTOR4",
        "refseq_ac": "NP_001101800",
        "gene_names_uniprotkb": "Lamtor4",
        "gene_names_refseq": "Lamtor4; RGD1309735",
        "protein_names_uniprotkb": "Ragulator complex protein LAMTOR4; Late endosomal/lysosomal adaptor and MAPK and MTOR activator 4",
        "protein_names_refseq": "ragulator complex protein LAMTOR4",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:360776);  (R-RNO-1632852);  (R-RNO-165159);  (R-RNO-166208);  (R-RNO-380972);  (R-RNO-5628897);  (R-RNO-8943724);  (R-RNO-9639288)",
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        "function": "As part of the Ragulator complex it is involved in amino acid sensing and activation of mTORC1, a signaling complex promoting cell growth in response to growth factors, energy levels, and amino acids. Activated by amino acids through a mechanism involving the lysosomal V-ATPase, the Ragulator plays a dual role for the small GTPases Rag (RagA/RRAGA, RagB/RRAGB, RagC/RRAGC and/or RagD/RRAGD): it (1) acts as a guanine nucleotide exchange factor (GEF), activating the small GTPases Rag and (2) mediates recruitment of Rag GTPases to the lysosome membrane. Activated Ragulator and Rag GTPases function as a scaffold recruiting mTORC1 to lysosomes where it is in turn activated., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0060090 molecular adaptor activity;GO:0005085 guanyl-nucleotide exchange factor activity",
        "go_cellular_component": "GO:0005764 lysosome;GO:0005765 lysosomal membrane;GO:0071986 Ragulator complex;GO:1990877 FNIP-folliculin RagC/D GAP",
        "go_biological_process": "GO:1904263 positive regulation of TORC1 signaling;GO:0032008 positive regulation of TOR signaling;GO:0071230 cellular response to amino acid stimulus;GO:0061462 protein localization to lysosome;GO:0008361 regulation of cell size",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4AD29-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4AD66-1",
        "uniprot_id": "D4AD66_RAT",
        "mass": 57266.0,
        "length": 506,
        "protein_name": "Potassium voltage-gated channel modifier subfamily G member 4",
        "gene_name": "Kcng4",
        "organism": "Rat",
        "refseq_name": "potassium voltage-gated channel subfamily G member 4",
        "refseq_ac": "NP_001100905",
        "gene_names_uniprotkb": "Kcng4",
        "gene_names_refseq": "Kcng4",
        "protein_names_uniprotkb": "Potassium voltage-gated channel modifier subfamily G member 4",
        "protein_names_refseq": "potassium channel, voltage gated modifier subfamily G, member 4; potassium voltage-gated channel subfamily G member 4; potassium voltage-gated channel, subfamily G, member 4",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:307900);  (R-RNO-1296072)",
        "pathway_count": 2,
        "publication_count": 0,
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        "class_list": "",
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        "biomarker_type": "",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0015459 potassium channel regulator activity;GO:0044325 transmembrane transporter binding;GO:0005249 voltage-gated potassium channel activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane;GO:0008076 voltage-gated potassium channel complex",
        "go_biological_process": "GO:1901379 regulation of potassium ion transmembrane transport;GO:0051260 protein homooligomerization;GO:0001508 action potential;GO:0043266 regulation of potassium ion transport;GO:0071805 potassium ion transmembrane transport",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4AD66-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4ADE5-1",
        "uniprot_id": "D4ADE5_RAT",
        "mass": 40508.0,
        "length": 366,
        "protein_name": "Histone-lysine N-methyltransferase SETD7",
        "gene_name": "Setd7",
        "organism": "Rat",
        "refseq_name": "histone-lysine N-methyltransferase SETD7",
        "refseq_ac": "NP_001103028",
        "gene_names_uniprotkb": "Setd7",
        "gene_names_refseq": "Setd7",
        "protein_names_uniprotkb": "Histone-lysine N-methyltransferase SETD7; 2.1.1.-; SET domain-containing protein 7",
        "protein_names_refseq": "SET domain containing (lysine methyltransferase) 7; histone-lysine N-methyltransferase SETD7",
        "tax_id": 10116,
        "disease": "fetal alcohol spectrum disorder (Disease Ontology:DOID:0050696); extrahepatic cholestasis (Disease Ontology:DOID:13619)",
        "pathway": " (rno:689954);  (R-RNO-3214841)",
        "pathway_count": 2,
        "publication_count": 5,
        "publication_id_list": "30119254;31505256;32448511;34592314;35259059",
        "class_list": "",
        "function": "Histone methyltransferase that specifically monomethylates 'Lys-4' of histone H3. H3 'Lys-4' methylation represents a specific tag for epigenetic transcriptional activation. Plays a central role in the transcriptional activation of genes such as collagenase or insulin. Recruited by IPF1/PDX-1 to the insulin promoter, leading to activate transcription. Also has methyltransferase activity toward non-histone proteins such as CGAS, p53/TP53, TAF10, and possibly TAF7 by recognizing and binding the [KR]-[STA]-K in substrate proteins. Monomethylates 'Lys-189' of TAF10, leading to increase the affinity of TAF10 for RNA polymerase II. Monomethylates 'Lys-372' of p53/TP53, stabilizing p53/TP53 and increasing p53/TP53-mediated transcriptional activation. Monomethylates 'Lys-491' of CGAS, promoting interaction between SGF29 and CGAS., [UniProtKB, UniProtKB, UniProtKB]; Role of SET7/9 in the progression of ischemic renal injury in diabetic and non-diabetic rats., [RefSeq, PubMed]; SET domain containing 7 promotes oxygen-glucose deprivation/reoxygenation-induced PC12 cell inflammation and oxidative stress by regulating Keap1/Nrf2/ARE and NF-kappaB pathways., [RefSeq, PubMed]; SETD7 gene silencing attenuates hypoxia/reoxygenation-induced injury of cardiomyocytes via the down-regulation of Keap1 and promotion of the Nrf2-mediated anti-oxidation signaling pathway., [RefSeq, PubMed]; SETD7 mediates spinal microgliosis and neuropathic pain in a rat model of peripheral nerve injury., [RefSeq, PubMed]; SetD7 (Set7/9) is a novel target of PPARgamma that promotes the adaptive pancreatic beta-cell glycemic response., [RefSeq, PubMed]",
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        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 2,
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        "secondary_ac_list": "",
        "ec_number_list": "2.1.1.361;2.1.1.364;2.1.1.370;2.1.1.371;2.1.1.359;2.1.1.-;2.1.1.85;2.1.1.355;2.1.1.354;2.1.1.362",
        "go_molecular_function": "GO:0003682 chromatin binding;GO:0042054 histone methyltransferase activity;GO:0002039 p53 binding;GO:0016279 protein-lysine N-methyltransferase activity;GO:0140945 histone H3K4 monomethyltransferase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005730 nucleolus;GO:0005694 chromosome",
        "go_biological_process": "GO:0097305 response to alcohol;GO:0006351 DNA-templated transcription;GO:0045471 response to ethanol;GO:0006974 DNA damage response;GO:0045893 positive regulation of DNA-templated transcription",
        "synthesized_glycan_count": 0,
        "hit_score": 0.6,
        "record_id": "D4ADE5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4ADF5-1",
        "uniprot_id": "D4ADF5_RAT",
        "mass": 14204.0,
        "length": 125,
        "protein_name": "Programmed cell death protein 5",
        "gene_name": "Pdcd5",
        "organism": "Rat",
        "refseq_name": "programmed cell death protein 5",
        "refseq_ac": "NP_001099717",
        "gene_names_uniprotkb": "Pdcd5",
        "gene_names_refseq": "Pdcd5",
        "protein_names_uniprotkb": "Programmed cell death protein 5",
        "protein_names_refseq": "programmed cell death protein 5",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:292814)",
        "pathway_count": 1,
        "publication_count": 4,
        "publication_id_list": "22673903;23638963;24614334;34936294",
        "class_list": "",
        "function": "May function in the process of apoptosis., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; MiR-10b-3p Protects Cerebral I/R Injury through Targeting Programmed Cell Death 5 (PDCD5)., [RefSeq, PubMed]; PDCD5 was a key regulator of autophagy that might play an important role following middle cerebral artery occlusion/reperfusion injury., [RefSeq, PubMed]; PDCD5-induced apoptosis and over-expression of PDCD5 are harmful to ischemic neurons in cerebral ischemia/reperfusion injury., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0008201 heparin binding;GO:0048487 beta-tubulin binding;GO:0010698 acetyltransferase activator activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005829 cytosol",
        "go_biological_process": "GO:0006915 apoptotic process;GO:0010628 positive regulation of gene expression;GO:0043065 positive regulation of apoptotic process;GO:0042981 regulation of apoptotic process;GO:0071560 cellular response to transforming growth factor beta stimulus",
        "synthesized_glycan_count": 0,
        "hit_score": 0.5,
        "record_id": "D4ADF5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4ADI8-1",
        "uniprot_id": "D4ADI8_RAT",
        "mass": 106823.0,
        "length": 981,
        "protein_name": "Cell division cycle associated 2",
        "gene_name": "Cdca2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Cdca2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Cell division cycle associated 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:305984)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0019888 protein phosphatase regulator activity;GO:0140693 molecular condensate scaffold activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0000793 condensed chromosome;GO:0005694 chromosome",
        "go_biological_process": "GO:0007059 chromosome segregation;GO:0007088 regulation of mitotic nuclear division;GO:0051321 meiotic cell cycle",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D4ADI8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4ADR1-1",
        "uniprot_id": "D4ADR1_RAT",
        "mass": 42922.0,
        "length": 384,
        "protein_name": "Lysophosphatidic acid receptor 5",
        "gene_name": "Lpar5",
        "organism": "Rat",
        "refseq_name": "lysophosphatidic acid receptor 5 isoform X1",
        "refseq_ac": "XP_006237451",
        "gene_names_uniprotkb": "Lpar5",
        "gene_names_refseq": "Gpr92; Lpar5; RGD1562580",
        "protein_names_uniprotkb": "Lysophosphatidic acid receptor 5",
        "protein_names_refseq": "lysophosphatidic acid receptor 5 isoform X1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-416476);  (R-RNO-418594);  (R-RNO-419408)",
        "pathway_count": 3,
        "publication_count": 1,
        "publication_id_list": "29393594",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "total_n_glycosites": 0,
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        "reported_mutagensis": 0,
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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0048266 behavioral response to pain",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D4ADR1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4ADS5-1",
        "uniprot_id": "D4ADS5_RAT",
        "mass": 49185.0,
        "length": 462,
        "protein_name": "Kremen protein",
        "gene_name": "Kremen2",
        "organism": "Rat",
        "refseq_name": "kremen protein 2 precursor",
        "refseq_ac": "NP_001382036",
        "gene_names_uniprotkb": "Kremen2",
        "gene_names_refseq": "Kremen2",
        "protein_names_uniprotkb": "Kremen protein; Kringle-containing protein marking the eye and the nose",
        "protein_names_refseq": "kremen protein 2 precursor; kremen protein 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-3772470)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Receptor for Dickkopf proteins. Cooperates with DKK1/2 to inhibit Wnt/beta-catenin signaling by promoting the endocytosis of Wnt receptors LRP5 and LRP6. Plays a role in limb development; attenuates Wnt signaling in the developing limb to allow normal limb patterning and can also negatively regulate bone formation., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004888 transmembrane signaling receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0007165 signal transduction;GO:0016055 Wnt signaling pathway;GO:0060173 limb development;GO:0030279 negative regulation of ossification",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4ADS5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4ADX7-1",
        "uniprot_id": "KCNF1_RAT",
        "mass": 55663.0,
        "length": 493,
        "protein_name": "Voltage-gated potassium channel regulatory subunit KCNF1",
        "gene_name": "Kcnf1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Kcnf1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Voltage-gated potassium channel regulatory subunit KCNF1; Potassium voltage-gated channel subfamily F member 1; Voltage-gated potassium channel subunit Kv5.1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:298908);  (R-RNO-1296072)",
        "pathway_count": 2,
        "publication_count": 3,
        "publication_id_list": "1740690;9305895;9696692",
        "class_list": "",
        "function": "Regulatory alpha-subunit of the voltage-gated potassium (Kv) channel which, when coassembled with KCNB1 or KCNB2, can modulate their expression and their gating kinetics by acting on deactivation upon repolarization and inactivation during maintained depolarization (PubMed:9305895, PubMed:9696692). Accelerates inactivation but has relatively little effect on deactivation (PubMed:9696692). Coexpression with KCNB1 or KCNB2 markedly slows inactivation (PubMed:9305895). Each modulatory subunit has its own specific properties of regulation, and can lead to extensive inhibitions, to large changes in kinetics, and/or to large shifts in the voltage dependencies of the inactivation process (PubMed:9305895). The gating kinetics depends on the nature and stoichiometry of the associated regulatory sunbunit (PubMed:9305895, PubMed:9696692). Fails to produce a potassium current when expressed alone (PubMed:9305895)., [UniProtKB, PubMed, PubMed, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0015459 potassium channel regulator activity;GO:0005249 voltage-gated potassium channel activity",
        "go_cellular_component": "GO:0016020 membrane;GO:0008076 voltage-gated potassium channel complex;GO:0097546 ciliary base",
        "go_biological_process": "GO:0051260 protein homooligomerization;GO:0001508 action potential;GO:0006813 potassium ion transport;GO:0043266 regulation of potassium ion transport;GO:1905515 non-motile cilium assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "D4ADX7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4AE11-1",
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        "length": 232,
        "protein_name": "Polycomb group RING finger protein 6 like 1",
        "gene_name": "Pcgf6l1",
        "organism": "Rat",
        "refseq_name": "uncharacterized protein LOC302366",
        "refseq_ac": "NP_001100405",
        "gene_names_uniprotkb": "Pcgf6l1; RGD1562871",
        "gene_names_refseq": "Pcgf6l1; RGD1562871",
        "protein_names_uniprotkb": "Polycomb group RING finger protein 6 like 1",
        "protein_names_refseq": "uncharacterized protein LOC302366",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:302366)",
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        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding",
        "go_cellular_component": "GO:0031519 PcG protein complex",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4AE11-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4AE21-1",
        "uniprot_id": "D4AE21_RAT",
        "mass": 45420.0,
        "length": 419,
        "protein_name": "MANSC domain containing 1",
        "gene_name": "Mansc1",
        "organism": "Rat",
        "refseq_name": "MANSC domain-containing protein 1 precursor",
        "refseq_ac": "NP_001103073",
        "gene_names_uniprotkb": "Mansc1",
        "gene_names_refseq": "Mansc1",
        "protein_names_uniprotkb": "MANSC domain containing 1",
        "protein_names_refseq": "MANSC domain-containing protein 1 precursor; MANSC domain-containing protein 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:690606)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 1,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005794 Golgi apparatus;GO:0016020 membrane",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4AE21-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4AE24-1",
        "uniprot_id": "D4AE24_RAT",
        "mass": 49348.0,
        "length": 444,
        "protein_name": "Ribosomal protein S6 kinase beta-2",
        "gene_name": "Rps6kb2",
        "organism": "Rat",
        "refseq_name": "ribosomal protein S6 kinase beta-2 isoform X1",
        "refseq_ac": "XP_063124245",
        "gene_names_uniprotkb": "Rps6kb2",
        "gene_names_refseq": "Rps6kb2",
        "protein_names_uniprotkb": "Ribosomal protein S6 kinase beta-2; 2.7.11.1; 70 kDa ribosomal protein S6 kinase 2; p70 ribosomal S6 kinase beta",
        "protein_names_refseq": "ribosomal protein S6 kinase beta-2 isoform X1",
        "tax_id": 10116,
        "disease": "alcohol dependence (Disease Ontology:DOID:0050741); glucose metabolism disease (Disease Ontology:DOID:4194); type 2 diabetes mellitus (Disease Ontology:DOID:9352)",
        "pathway": " (R-RNO-198693)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Phosphorylates specifically ribosomal protein S6. Seems to act downstream of mTOR signaling in response to growth factors and nutrients to promote cell proliferation, cell growth and cell cycle progression in an alternative pathway regulated by MEAK7., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "2.7.11.1;2.7.12.1;2.7.1.153;2.7.1.137;2.7.11.24;2.7.11.25;2.7.11.22;2.7.11.23;2.7.4.6;2.7.1.154;2.7.11.38;2.7.11.17;2.7.11.21;2.7.12.2;2.7.1.40;2.7.11.12;2.7.11.26;2.7.11.34;2.7.10.2;2.7.1.150;2.7.11.13;4.1.1.32;2.7.11.19;2.7.2.3;2.7.11.11;2.7.11.31;3.1.3.16;2.7.11.4;2.3.1.48;3.1.11.-;2.7.13.3;2.7.4.18;3.1.24.-;3.4.19.12;2.7.11.39;2.4.99.18;2.7.11.10",
        "go_molecular_function": "GO:0004711 ribosomal protein S6 kinase activity;GO:0004672 protein kinase activity;GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding;GO:0042277 peptide binding",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0046627 negative regulation of insulin receptor signaling pathway;GO:0006468 protein phosphorylation;GO:0031929 TOR signaling;GO:0038202 TORC1 signaling;GO:0045948 positive regulation of translational initiation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4AE24-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4AE25-1",
        "uniprot_id": "D4AE25_RAT",
        "mass": 33047.0,
        "length": 290,
        "protein_name": "Programmed cell death 1 ligand 1",
        "gene_name": "Cd274",
        "organism": "Rat",
        "refseq_name": "programmed cell death 1 ligand 1 precursor",
        "refseq_ac": "NP_001178883",
        "gene_names_uniprotkb": "Cd274",
        "gene_names_refseq": "Cd274; Pdcd1lg1; RGD1566211",
        "protein_names_uniprotkb": "Programmed cell death 1 ligand 1; B7 homolog 1",
        "protein_names_refseq": "programmed cell death 1 ligand 1 precursor; programmed cell death 1 ligand 1",
        "tax_id": 10116,
        "disease": "adult T-cell leukemia/lymphoma (Disease Ontology:DOID:0050523); infantile onset multisystem autoimmune disease 5 (Disease Ontology:DOID:0061164); Cryptococcal meningitis (Disease Ontology:DOID:0080159); nasal type extranodal NK/T-cell lymphoma (Disease Ontology:DOID:0080797); stomach cancer (Disease Ontology:DOID:10534); pre-eclampsia (Disease Ontology:DOID:10591); Human papillomavirus infectious disease (Disease Ontology:DOID:11166); toxic shock syndrome (Disease Ontology:DOID:14115); hepatitis C (Disease Ontology:DOID:1883); pulmonary tuberculosis (Disease Ontology:DOID:2957); tuberculosis (Disease Ontology:DOID:399); human immunodeficiency virus infectious disease (Disease Ontology:DOID:526); hepatocellular carcinoma (Disease Ontology:DOID:684); periodontitis (Disease Ontology:DOID:824); influenza (Disease Ontology:DOID:8469); cervix uteri carcinoma in situ (Disease Ontology:DOID:8991)",
        "pathway": " (rno:499342);  (R-RNO-389948);  (R-RNO-9929356);  (R-RNO-9929491);  (R-RNO-9931269);  (R-RNO-9931295)",
        "pathway_count": 6,
        "publication_count": 2,
        "publication_id_list": "32631356;38203304",
        "class_list": "",
        "function": "PD-L1 and AKT Overexpressing Adipose-Derived Mesenchymal Stem Cells Enhance Myocardial Protection by Upregulating CD25[+] T Cells in Acute Myocardial Infarction Rat Model. Publication Status: Online-Only, [RefSeq, PubMed]; Pulmonary endothelium-derived PD-L1 induced by the H9N2 avian influenza virus inhibits the immune response of T cells. Publication Status: Online-Only, [RefSeq, PubMed]; The PDCD1-mediated inhibitory pathway is exploited by tumors to attenuate anti-tumor immunity and escape destruction by the immune system, thereby facilitating tumor survival. The interaction with PDCD1/PD-1 inhibits cytotoxic T lymphocytes (CTLs) effector function. The blockage of the PDCD1-mediated pathway results in the reversal of the exhausted T-cell phenotype and the normalization of the anti-tumor response, providing a rationale for cancer immunotherapy., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003713 transcription coactivator activity;GO:0048018 receptor ligand activity",
        "go_cellular_component": "GO:0009897 external side of plasma membrane;GO:0031901 early endosome membrane;GO:0055038 recycling endosome membrane;GO:0005886 plasma membrane;GO:0009986 cell surface",
        "go_biological_process": "GO:0006955 immune response;GO:0007166 cell surface receptor signaling pathway;GO:0031295 T cell costimulation;GO:0042130 negative regulation of T cell proliferation;GO:0071222 cellular response to lipopolysaccharide",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "D4AE25-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4AE44-1",
        "uniprot_id": "D4AE44_RAT",
        "mass": 38989.0,
        "length": 348,
        "protein_name": "Calcium homeostasis modulator 1",
        "gene_name": "Calhm1",
        "organism": "Rat",
        "refseq_name": "calcium homeostasis modulator protein 1",
        "refseq_ac": "NP_001102638",
        "gene_names_uniprotkb": "Calhm1",
        "gene_names_refseq": "Calhm1; Fam26c; RGD1564891",
        "protein_names_uniprotkb": "Calcium homeostasis modulator 1",
        "protein_names_refseq": "calcium homeostasis modulator protein 1; family with sequence similarity 26, member C",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:499367)",
        "pathway_count": 1,
        "publication_count": 3,
        "publication_id_list": "26781424;28334404;38689353",
        "class_list": "",
        "function": "CALHM1 was increased in painful diabetic neuropathy compared with controls., [RefSeq, PubMed]; Control of astrocytic Ca[2+] signaling by nitric oxide-dependent S-nitrosylation of Ca[2+] homeostasis modulator 1 channels. Publication Status: Online-Only, [RefSeq, PubMed]; Findings indicate that communication between salt-detecting cells and nerve endings might involve ATP release by CALMH1 channels., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0042802 identical protein binding;GO:0005227 calcium-activated cation channel activity;GO:0005244 voltage-gated monoatomic ion channel activity;GO:0005261 monoatomic cation channel activity;GO:0005245 voltage-gated calcium channel activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0016323 basolateral plasma membrane;GO:0044853 plasma membrane raft",
        "go_biological_process": "GO:0051260 protein homooligomerization;GO:0051291 protein heterooligomerization;GO:0006812 monoatomic cation transport;GO:0034765 regulation of monoatomic ion transmembrane transport;GO:0050909 sensory perception of taste",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "D4AE44-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4AE63-1",
        "uniprot_id": "D4AE63_RAT",
        "mass": 81343.0,
        "length": 716,
        "protein_name": "Alpha-galactosidase MYORG",
        "gene_name": "Myorg",
        "organism": "Rat",
        "refseq_name": "myogenesis-regulating glycosidase",
        "refseq_ac": "NP_001102441",
        "gene_names_uniprotkb": "Myorg; RGD1309821",
        "gene_names_refseq": "Myorg; RGD1309821",
        "protein_names_uniprotkb": "Alpha-galactosidase MYORG; 3.2.1.22; Myogenesis regulating glycosidase; Nuclear envelope transmembrane protein 37",
        "protein_names_refseq": "myogenesis-regulating glycosidase",
        "tax_id": 10116,
        "disease": "basal ganglia calcification (Disease Ontology:DOID:0060230)",
        "pathway": " (rno:366360)",
        "pathway_count": 1,
        "publication_count": 2,
        "publication_id_list": "16641100;38843836",
        "class_list": "",
        "function": "Alpha-galactosidase with unusual specificity for the Gal-alpha1,4-Glc structure, whose in vivo substrate is still unknown. Promotes myogenesis by activating AKT signaling through the maturation and secretion of IGF2., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 1,
        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "reported_phosphosites": 0,
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        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 0,
        "biomarker_type": "",
        "glycan_count": 1,
        "disease_count": 1,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004557 alpha-galactosidase activity",
        "go_cellular_component": "GO:0031965 nuclear membrane;GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0051897 positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction;GO:0005975 carbohydrate metabolic process;GO:0048741 skeletal muscle fiber development;GO:0043568 positive regulation of insulin-like growth factor receptor signaling pathway",
        "synthesized_glycan_count": 0,
        "hit_score": 0.5,
        "record_id": "D4AE63-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4AE65-1",
        "uniprot_id": "D4AE65_RAT",
        "mass": 32341.0,
        "length": 280,
        "protein_name": "Ribosomal RNA-processing protein 7 homolog A",
        "gene_name": "Rrp7a",
        "organism": "Rat",
        "refseq_name": "ribosomal RNA-processing protein 7 homolog A",
        "refseq_ac": "NP_001124040",
        "gene_names_uniprotkb": "Rrp7a",
        "gene_names_refseq": "Cgi-96; RGD1311547; Rrp7a",
        "protein_names_uniprotkb": "Ribosomal RNA-processing protein 7 homolog A",
        "protein_names_refseq": "gastric cancer antigen Zg14; ribosomal RNA-processing protein 7 homolog A",
        "tax_id": 10116,
        "disease": "primary autosomal recessive microcephaly 28 (Disease Ontology:DOID:0051039); primary microcephaly (Disease Ontology:DOID:0070297)",
        "pathway": " (rno:362967);  (R-RNO-6791226)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Nucleolar protein that is involved in ribosomal RNA (rRNA) processing. Also plays a role in primary cilia resorption, and cell cycle progression in neurogenesis and neocortex development. Part of the small subunit (SSU) processome, first precursor of the small eukaryotic ribosomal subunit. During the assembly of the SSU processome in the nucleolus, many ribosome biogenesis factors, an RNA chaperone and ribosomal proteins associate with the nascent pre-rRNA and work in concert to generate RNA folding, modifications, rearrangements and cleavage as well as targeted degradation of pre-ribosomal RNA by the RNA exosome., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 2,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003723 RNA binding",
        "go_cellular_component": "GO:0005730 nucleolus;GO:0005737 cytoplasm;GO:0005813 centrosome;GO:0005929 cilium;GO:0032040 small-subunit processome",
        "go_biological_process": "GO:1902570 protein localization to nucleolus;GO:0042254 ribosome biogenesis;GO:0006364 rRNA processing;GO:0001825 blastocyst formation;GO:0042274 ribosomal small subunit biogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4AE65-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4AE69-1",
        "uniprot_id": "D4AE69_RAT",
        "mass": 27309.0,
        "length": 249,
        "protein_name": "Transmembrane protein 51",
        "gene_name": "Tmem51",
        "organism": "Rat",
        "refseq_name": "transmembrane protein 51",
        "refseq_ac": "NP_001102743",
        "gene_names_uniprotkb": "Tmem51",
        "gene_names_refseq": "RGD1565452; Tmem51",
        "protein_names_uniprotkb": "Transmembrane protein 51",
        "protein_names_refseq": "transmembrane protein 51",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:500578)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "",
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D4AE69-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4AEG0-1",
        "uniprot_id": "D4AEG0_RAT",
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        "length": 515,
        "protein_name": "Recombining binding protein suppressor of hairless-like protein",
        "gene_name": "Rbpjl",
        "organism": "Rat",
        "refseq_name": "recombining binding protein suppressor of hairless-like protein",
        "refseq_ac": "NP_001102074",
        "gene_names_uniprotkb": "Rbpjl",
        "gene_names_refseq": "Rbpjl; Rbpsuhl",
        "protein_names_uniprotkb": "Recombining binding protein suppressor of hairless-like protein; Transcription factor RBP-L",
        "protein_names_refseq": "recombining binding protein suppressor of hairless-like protein",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:362268)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Putative transcription factor, which cooperates with EBNA2 to activate transcription., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
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        "predicted_c_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0003682 chromatin binding;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005667 transcription regulator complex",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0045893 positive regulation of DNA-templated transcription",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4AEG0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4AEG6-1",
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        "length": 260,
        "protein_name": "Large ribosomal subunit protein bL32m",
        "gene_name": "Mrpl32",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Mrpl32",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Large ribosomal subunit protein bL32m; 39S ribosomal protein L32, mitochondrial",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-5389840);  (R-RNO-5419276);  (R-RNO-9837999);  (R-RNO-9937383)",
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        "publication_count": 0,
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        "class_list": "",
        "function": "Component of the mitochondrial large ribosomal subunit (mt-LSU). The mitochondrial ribosome (mitoribosome) is a large ribonucleoprotein complex responsible for the synthesis of proteins inside mitochondria., [UniProtKB, UniProtKB]",
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        "reported_phosphosites": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
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        "ec_number_list": "",
        "go_molecular_function": "GO:0003735 structural constituent of ribosome",
        "go_cellular_component": "GO:0005762 mitochondrial large ribosomal subunit;GO:0005739 mitochondrion;GO:0005829 cytosol",
        "go_biological_process": "GO:0006412 translation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4AEG6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4AEG8-1",
        "uniprot_id": "D4AEG8_RAT",
        "mass": 14655.0,
        "length": 133,
        "protein_name": "Ankyrin repeat and KH domain containing 1",
        "gene_name": "Eif4ebp3",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Eif4ebp3; Ankhd1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ankyrin repeat and KH domain containing 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:100365872)",
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        "publication_count": 0,
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        "class_list": "",
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008190 eukaryotic initiation factor 4E binding",
        "go_cellular_component": "",
        "go_biological_process": "GO:0045947 negative regulation of translational initiation",
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        "record_id": "D4AEG8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4AEG9-1",
        "uniprot_id": "D4AEG9_RAT",
        "mass": 21573.0,
        "length": 185,
        "protein_name": "Homeobox expressed in ES cells 1",
        "gene_name": "Hesx1",
        "organism": "Rat",
        "refseq_name": "homeobox expressed in ES cells 1",
        "refseq_ac": "NP_001102576",
        "gene_names_uniprotkb": "Hesx1",
        "gene_names_refseq": "Hesx1; RGD1563858",
        "protein_names_uniprotkb": "Homeobox expressed in ES cells 1; Homeobox protein ANF",
        "protein_names_refseq": "homeo box gene expressed in ES cells; homeobox expressed in ES cells 1",
        "tax_id": 10116,
        "disease": "septooptic dysplasia (Disease Ontology:DOID:0060857); hypopituitarism (Disease Ontology:DOID:9406)",
        "pathway": " (rno:498575)",
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0003682 chromatin binding;GO:0042803 protein homodimerization activity;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0030878 thyroid gland development;GO:0043584 nose development;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006357 regulation of transcription by RNA polymerase II;GO:0030900 forebrain development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4AEG9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "E9PT19-1",
        "uniprot_id": "E9PT19_RAT",
        "mass": 118713.0,
        "length": 1065,
        "protein_name": "Helicase POLQ-like",
        "gene_name": "Helq",
        "organism": "Rat",
        "refseq_name": "helicase POLQ-like",
        "refseq_ac": "NP_001014156",
        "gene_names_uniprotkb": "Helq",
        "gene_names_refseq": "Hel308; Helq",
        "protein_names_uniprotkb": "Helicase POLQ-like; 5.6.2.4; Mus308-like helicase; POLQ-like helicase",
        "protein_names_refseq": "DNA helicase HEL308; helicase POLQ-like",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:360912)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Single-stranded 3'-5' DNA helicase that plays a key role in homology-driven double-strand break (DSB) repair. Involved in different DSB repair mechanisms that are guided by annealing of extensive stretches of complementary bases at break ends, such as microhomology-mediated end-joining (MMEJ), single-strand annealing (SSA) or synthesis-dependent strand annealing (SDSA). Possesses both DNA unwinding and annealing activities. Forms a complex with RAD51, stimulating HELQ DNA helicase activity and ability to unwing DNA. Efficiently unwinds substrates containing 3' overhangs or a D-loop. In contrast, interaction with the replication protein A (RPA/RP-A) complex inhibits DNA unwinding by HELQ but strongly stimulates DNA strand annealing. Triggers displacement of RPA from single-stranded DNA to facilitate annealing of complementary sequences., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "5.6.2.3;3.6.4.13;3.6.4.12;2.7.11.1;3.6.1.5;3.6.4.10;3.6.4.-;2.3.2.27;5.6.2.4;3.6.5.-;5.6.2.-;3.1.-.-;2.7.7.7;2.7.7.49;3.1.13.1;4.2.99.18;7.6.2.2;7.6.2.3;7.6.2.-;5.6.1.6;7.2.2.-;3.6.1.15;3.6.4.6;3.1.3.1;3.9.1.1;6.1.1.12;3.6.1.-;2.7.4.3;3.1.4.-;3.4.24.-;3.6.-.-;3.4.21.53;5.6.2.5",
        "go_molecular_function": "GO:1990518 single-stranded 3'-5' DNA helicase activity;GO:0003677 DNA binding;GO:0005524 ATP binding;GO:0016787 hydrolase activity;GO:0017116 single-stranded DNA helicase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0090734 site of DNA damage",
        "go_biological_process": "GO:0097681 double-strand break repair via alternative nonhomologous end joining;GO:0000724 double-strand break repair via homologous recombination;GO:0010792 DNA double-strand break processing involved in repair via single-strand annealing;GO:1905168 positive regulation of double-strand break repair via homologous recombination;GO:0045003 double-strand break repair via synthesis-dependent strand annealing",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "E9PT19-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "E9PT51-1",
        "uniprot_id": "E9PT51_RAT",
        "mass": 41797.0,
        "length": 368,
        "protein_name": "Polymerase delta-interacting protein 2",
        "gene_name": "Poldip2",
        "organism": "Rat",
        "refseq_name": "polymerase delta-interacting protein 2",
        "refseq_ac": "NP_001388912",
        "gene_names_uniprotkb": "Poldip2",
        "gene_names_refseq": "PDIP38; Poldip2",
        "protein_names_uniprotkb": "Polymerase delta-interacting protein 2",
        "protein_names_refseq": "DNA-directed polymerase delta interacting protein 2; polymerase (DNA) delta interacting protein 2; polymerase (DNA-directed), delta interacting protein 2; polymerase delta-interacting protein 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:287544)",
        "pathway_count": 1,
        "publication_count": 4,
        "publication_id_list": "17623671;30354218;36123704;38843836",
        "class_list": "",
        "function": "Integrin engagement during cell attachment activates Poldip2/Nox4 to oxidize actin, which modulates filamentous actin assembly and its interaction with vinculin., [RefSeq, PubMed]; Involved in DNA damage tolerance by regulating translesion synthesis (TLS) of templates carrying DNA damage lesions such as 8oxoG and abasic sites. May act by stimulating activity of DNA polymerases involved in TLS, such as PRIMPOL and polymerase delta (POLD1)., [UniProtKB, UniProtKB, UniProtKB]; PDIP38 can shuttle between the cytoplasmic and the nuclear compartments and that its subcellular localization is regulated by CEACAM1, [RefSeq, PubMed]; ZEB1 regulates bone metabolism in osteoporotic rats through inducing POLDIP2 transcription. Publication Status: Online-Only, [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 1,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 1,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 1,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 1,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 0,
        "biomarker_type": "",
        "glycan_count": 1,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "C8YL70",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0030674 protein-macromolecule adaptor activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0042645 mitochondrial nucleoid;GO:0005739 mitochondrion;GO:0005759 mitochondrial matrix;GO:0005911 cell-cell junction",
        "go_biological_process": "GO:0006281 DNA repair;GO:0070987 error-free translesion synthesis;GO:0045931 positive regulation of mitotic cell cycle;GO:0090307 mitotic spindle assembly;GO:0051894 positive regulation of focal adhesion assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.7,
        "record_id": "E9PT51-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "E9PTP3-1",
        "uniprot_id": "E9PTP3_RAT",
        "mass": 30188.0,
        "length": 278,
        "protein_name": "Gap junction protein",
        "gene_name": "Gjd3",
        "organism": "Rat",
        "refseq_name": "gap junction delta-3 protein",
        "refseq_ac": "XP_343966",
        "gene_names_uniprotkb": "Gjd3",
        "gene_names_refseq": "Gjd3",
        "protein_names_uniprotkb": "Gap junction protein",
        "protein_names_refseq": "gap junction delta-3 protein",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:363677);  (R-RNO-190861)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "One gap junction consists of a cluster of closely packed pairs of transmembrane channels, the connexons, through which materials of low MW diffuse from one cell to a neighboring cell., [UniProtKB, UniProtKB]; Structural component of the gap junction, a specialized intercellular structure consisting of a cluster of closely packed pairs of transmembrane channels, the connexons, that allow passage of small molecules and electrical signals between neighboring cells. Forms homotypic and heterotypic channels gated by transjunctional voltage. Involved in intercellular innate immune signaling. Mediates translocation of 2',3'-cGAMP and 2',5'-oligoadenylates (2-5A) second messengers from virus-infected cells to macrophages and uninfected neighboring cells to propagate and amplify the antiviral immune response., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005216 monoatomic ion channel activity;GO:0086077 gap junction channel activity involved in AV node cell-bundle of His cell electrical coupling;GO:0005243 gap junction channel activity",
        "go_cellular_component": "GO:0009986 cell surface;GO:0005921 gap junction;GO:0005922 connexin complex",
        "go_biological_process": "GO:0007267 cell-cell signaling;GO:0010459 negative regulation of heart rate;GO:0009749 response to glucose;GO:0086053 AV node cell to bundle of His cell communication by electrical coupling;GO:0016264 gap junction assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "E9PTP3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "E9PU07-1",
        "uniprot_id": "E9PU07_RAT",
        "mass": 16925.0,
        "length": 151,
        "protein_name": "Eosinophil-associated, ribonuclease A family, member 1",
        "gene_name": "Ear1",
        "organism": "Rat",
        "refseq_name": "eosinophil-associated, ribonuclease A family, member 1 precursor",
        "refseq_ac": "NP_001395600",
        "gene_names_uniprotkb": "Ear1; LOC100361909",
        "gene_names_refseq": "Ear1; Ear3; Raf4",
        "protein_names_uniprotkb": "Eosinophil-associated, ribonuclease A family, member 1",
        "protein_names_refseq": "eosinophil-associated ribonuclease 3-like; eosinophil-associated ribonuclease 3; eosinophil-associated, ribonuclease A family, member 1 precursor; ribonuclease A f4",
        "tax_id": 10116,
        "disease": "idiopathic pulmonary fibrosis (Disease Ontology:DOID:0050156)",
        "pathway": " (rno:100361909);  (R-RNO-6798695);  (R-RNO-6803157)",
        "pathway_count": 3,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0016787 hydrolase activity;GO:0003676 nucleic acid binding;GO:0004519 endonuclease activity;GO:0004540 RNA nuclease activity",
        "go_cellular_component": "GO:0005615 extracellular space",
        "go_biological_process": "GO:0006935 chemotaxis;GO:0050830 defense response to Gram-positive bacterium;GO:0002227 innate immune response in mucosa",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "E9PU07-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "E9PU29-1",
        "uniprot_id": "E9PU29_RAT",
        "mass": 119245.0,
        "length": 1062,
        "protein_name": "RBR-type E3 ubiquitin transferase",
        "gene_name": "Rnf31",
        "organism": "Rat",
        "refseq_name": "E3 ubiquitin-protein ligase RNF31",
        "refseq_ac": "NP_001102338",
        "gene_names_uniprotkb": "Rnf31",
        "gene_names_refseq": "Rnf31",
        "protein_names_uniprotkb": "RBR-type E3 ubiquitin transferase; 2.3.2.31",
        "protein_names_refseq": "E3 ubiquitin-protein ligase RNF31",
        "tax_id": 10116,
        "disease": "immunodeficiency 115 (Disease Ontology:DOID:0061081)",
        "pathway": " (rno:364386);  (R-RNO-5357786);  (R-RNO-5357905);  (R-RNO-5357956)",
        "pathway_count": 4,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
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        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "3.4.19.12;2.7.11.10;2.3.2.27;2.3.2.23;2.7.11.1;2.3.2.31;2.7.11.25",
        "go_molecular_function": "GO:0036435 K48-linked polyubiquitin modification-dependent protein binding;GO:0008270 zinc ion binding;GO:0042802 identical protein binding;GO:0031625 ubiquitin protein ligase binding;GO:0061630 ubiquitin protein ligase activity",
        "go_cellular_component": "GO:0005829 cytosol;GO:0009898 cytoplasmic side of plasma membrane;GO:0035631 CD40 receptor complex;GO:0071797 LUBAC complex",
        "go_biological_process": "GO:0097039 protein linear polyubiquitination;GO:0023035 CD40 signaling pathway;GO:0050852 T cell receptor signaling pathway;GO:0043123 positive regulation of canonical NF-kappaB signal transduction;GO:0016567 protein ubiquitination",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "E9PU29-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F1LMV9-1",
        "uniprot_id": "F1LMV9_RAT",
        "mass": 54964.0,
        "length": 480,
        "protein_name": "Coronin",
        "gene_name": "Coro2b",
        "organism": "Rat",
        "refseq_name": "coronin-2B",
        "refseq_ac": "NP_001413961",
        "gene_names_uniprotkb": "Coro2b",
        "gene_names_refseq": "Coro2b",
        "protein_names_uniprotkb": "Coronin",
        "protein_names_refseq": "coronin, actin binding protein, 2B; coronin-2B",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:300768)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
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        "total_c_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0051015 actin filament binding;GO:0017166 vinculin binding;GO:1990147 talin binding",
        "go_cellular_component": "GO:0005884 actin filament;GO:0005886 plasma membrane;GO:0005925 focal adhesion",
        "go_biological_process": "GO:1904951 positive regulation of establishment of protein localization;GO:0007015 actin filament organization;GO:0032956 regulation of actin cytoskeleton organization;GO:0003093 regulation of glomerular filtration;GO:0048041 focal adhesion assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F1LMV9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F1LNP8-1",
        "uniprot_id": "F1LNP8_RAT",
        "mass": 57156.0,
        "length": 515,
        "protein_name": "Nectin-1",
        "gene_name": "Nectin1",
        "organism": "Rat",
        "refseq_name": "nectin-1 precursor",
        "refseq_ac": "NP_001093946",
        "gene_names_uniprotkb": "Nectin1; Pvrl1",
        "gene_names_refseq": "HveC; Nectin1; Pvrl1; nectin-1",
        "protein_names_uniprotkb": "Nectin-1; Herpes virus entry mediator C; Nectin cell adhesion molecule 1; Poliovirus receptor-related protein 1",
        "protein_names_refseq": "nectin); nectin-1 precursor; poliovirus receptor-related 1 (herpesvirus entry mediator C; poliovirus receptor-related protein 1",
        "tax_id": 10116,
        "disease": "cleft lip-palate-ectodermal dysplasia syndrome (Disease Ontology:DOID:0060773); ectodermal dysplasia (Disease Ontology:DOID:2121); cleft palate (Disease Ontology:DOID:674); cleft lip (Disease Ontology:DOID:9296)",
        "pathway": " (rno:192183);  (R-RNO-418990);  (R-RNO-420597)",
        "pathway_count": 3,
        "publication_count": 3,
        "publication_id_list": "22673903;23418609;24090084",
        "class_list": "",
        "function": "Cell adhesion molecule that promotes cell-cell contacts and plays important roles in the development of the nervous system. Acts by forming homophilic or heterophilic trans-dimers. Heterophilic interactions have been detected between NECTIN1 and NECTIN3 and between NECTIN1 and NECTIN4. Involved in axon guidance by promoting contacts between the commissural axons and the floor plate cells. Involved in synaptogegesis. Has some neurite outgrowth-promoting activity. Promotes formation of checkerboard-like cellular pattern of hair cells and supporting cells in the auditory epithelium via heterophilic interaction with NECTIN3: NECTIN1 is present in the membrane of hair cells and associates with NECTIN3 on supporting cells, thereby mediating heterotypic adhesion between these two cell types. Required for enamel mineralization., [UniProtKB, UniProtKB, UniProtKB]; Data indicate that contextual fear conditioning showed transient nectin-1 upregulation in synapse-enriched hippocampal fractions at about 2 h posttraining., [RefSeq, PubMed]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 1,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 1,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 1,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 2,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 0,
        "biomarker_type": "",
        "glycan_count": 4,
        "disease_count": 4,
        "glyco_site_count": 2,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0042802 identical protein binding;GO:0042803 protein homodimerization activity;GO:0050839 cell adhesion molecule binding;GO:0044877 protein-containing complex binding;GO:0030246 carbohydrate binding",
        "go_cellular_component": "GO:0032584 growth cone membrane;GO:0048787 presynaptic active zone membrane;GO:0005886 plasma membrane;GO:0005912 adherens junction;GO:0030424 axon",
        "go_biological_process": "GO:0098609 cell-cell adhesion;GO:0046598 positive regulation of viral entry into host cell;GO:0060041 retina development in camera-type eye;GO:0046718 symbiont entry into host cell;GO:0051963 regulation of synapse assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.9,
        "record_id": "F1LNP8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F1LPB5-1",
        "uniprot_id": "F1LPB5_RAT",
        "mass": 25122.0,
        "length": 215,
        "protein_name": "ER lumen protein-retaining receptor",
        "gene_name": "Kdelr3",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Kdelr3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "ER lumen protein-retaining receptor",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:315131);  (R-RNO-6807878);  (R-RNO-6811434)",
        "pathway_count": 3,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "B1WC77",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005046 KDEL sequence binding;GO:0046923 ER retention sequence binding",
        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005783 endoplasmic reticulum;GO:0005789 endoplasmic reticulum membrane;GO:0005801 cis-Golgi network;GO:0030663 COPI-coated vesicle membrane",
        "go_biological_process": "GO:0015031 protein transport;GO:0006890 retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum;GO:0006621 protein retention in ER lumen",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F1LPB5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F1LPI3-1",
        "uniprot_id": "F1LPI3_RAT",
        "mass": 57350.0,
        "length": 510,
        "protein_name": "Gap junction protein",
        "gene_name": "Gja10",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Gja10",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Gap junction protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:313126);  (R-RNO-112303);  (R-RNO-190861)",
        "pathway_count": 3,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Structural component of the gap junction, a specialized intercellular structure consisting of a cluster of closely packed pairs of transmembrane channels, the connexons, that allow passage of small molecules and electrical signals between neighboring cells. Forms homotypic and heterotypic channels gated by transjunctional voltage. Involved in intercellular innate immune signaling. Mediates translocation of 2',3'-cGAMP and 2',5'-oligoadenylates (2-5A) second messengers from virus-infected cells to macrophages and uninfected neighboring cells to propagate and amplify the antiviral immune response., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005243 gap junction channel activity",
        "go_cellular_component": "GO:0005921 gap junction;GO:0005922 connexin complex",
        "go_biological_process": "GO:0007267 cell-cell signaling;GO:0007416 synapse assembly;GO:0009416 response to light stimulus;GO:0050908 detection of light stimulus involved in visual perception;GO:0007276 gamete generation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F1LPI3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F1LPI5-1",
        "uniprot_id": "F1LPI5_RAT",
        "mass": 129114.0,
        "length": 1172,
        "protein_name": "Laminin subunit beta-3",
        "gene_name": "Lamb3",
        "organism": "Rat",
        "refseq_name": "laminin subunit beta-3 precursor",
        "refseq_ac": "NP_001094311",
        "gene_names_uniprotkb": "Lamb3",
        "gene_names_refseq": "Lamb3",
        "protein_names_uniprotkb": "Laminin subunit beta-3; Epiligrin subunit beta; Kalinin B1 chain; Kalinin subunit beta; Laminin-5 subunit beta; Nicein subunit beta",
        "protein_names_refseq": "laminin chain; laminin subunit beta-3 precursor; laminin, beta 3",
        "tax_id": 10116,
        "disease": "junctional epidermolysis bullosa Herlitz type (Disease Ontology:DOID:0060737); junctional epidermolysis bullosa non-Herlitz type (Disease Ontology:DOID:0060738); amelogenesis imperfecta type 1A (Disease Ontology:DOID:0110054); junctional epidermolysis bullosa (Disease Ontology:DOID:3209); lung non-small cell carcinoma (Disease Ontology:DOID:3908); lung small cell carcinoma (Disease Ontology:DOID:5409)",
        "pathway": " (rno:305078)",
        "pathway_count": 1,
        "publication_count": 2,
        "publication_id_list": "20039268;20301201",
        "class_list": "",
        "function": "Binding sites for alpha3beta1 and alpha6beta4 are closely spaced in the Ln-332 LG domains where they regulate alternative cell functions, namely adhesion/migration or hemidesmosome anchoring., [RefSeq, PubMed]; Binding to cells via a high affinity receptor, laminin is thought to mediate the attachment, migration and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; In bladder carcinoma laminin-332 can suppress the number of invadopodia that form by interacting with a3b1 integrin and altering the cellular balance of FAK and Src kinase activity., [RefSeq, PubMed]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
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        "total_o_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 6,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0044877 protein-containing complex binding",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0043256 laminin complex;GO:0005604 basement membrane;GO:0005610 laminin-5 complex",
        "go_biological_process": "GO:0016477 cell migration;GO:0009887 animal organ morphogenesis;GO:0034446 substrate adhesion-dependent cell spreading;GO:0007411 axon guidance;GO:0009888 tissue development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "F1LPI5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F1LRL4-1",
        "uniprot_id": "F1LRL4_RAT",
        "mass": 141939.0,
        "length": 1263,
        "protein_name": "TBC1 domain family member 9B",
        "gene_name": "Tbc1d9b",
        "organism": "Rat",
        "refseq_name": "TBC1 domain family member 9B isoform 1",
        "refseq_ac": "NP_001381172",
        "gene_names_uniprotkb": "Tbc1d9b",
        "gene_names_refseq": "RGD1310147; Tbc1d9b",
        "protein_names_uniprotkb": "TBC1 domain family member 9B",
        "protein_names_refseq": "BUB2-like protein 1; TBC1 domain family member 9B isoform 1; TBC1 domain family, member 9B (with GRAM domain); vascular Rab-GAP/TBC-containing",
        "tax_id": 10116,
        "disease": "nephrotic syndrome type 20 (Disease Ontology:DOID:0070357)",
        "pathway": " (rno:360520)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "May act as a GTPase-activating protein for Rab family protein(s)., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
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        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "total_n_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005096 GTPase activator activity;GO:0005509 calcium ion binding",
        "go_cellular_component": "GO:0016020 membrane",
        "go_biological_process": "GO:0003008 system process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "F1LRL4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F1LS86-1",
        "uniprot_id": "F1LS86_RAT",
        "mass": 144286.0,
        "length": 1262,
        "protein_name": "Isoleucine--tRNA ligase, cytoplasmic",
        "gene_name": "Iars1",
        "organism": "Rat",
        "refseq_name": "isoleucine--tRNA ligase, cytoplasmic",
        "refseq_ac": "NP_001094042",
        "gene_names_uniprotkb": "Iars1; Iars",
        "gene_names_refseq": "Iars1; Iarsl; Iars",
        "protein_names_uniprotkb": "Isoleucine--tRNA ligase, cytoplasmic; 6.1.1.5; Isoleucyl-tRNA synthetase",
        "protein_names_refseq": "isoleucine--tRNA ligase, cytoplasmic-like; isoleucine--tRNA ligase, cytoplasmic; isoleucine-tRNA synthetase; isoleucyl tRNA synthetase; isoleucyl-tRNA synthetase, cytoplasmic",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:306804);  (R-RNO-9856649)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "29393594",
        "class_list": "",
        "function": "Catalyzes the specific attachment of an amino acid to its cognate tRNA in a 2 step reaction: the amino acid (AA) is first activated by ATP to form AA-AMP and then transferred to the acceptor end of the tRNA., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "6.1.1.5;6.1.1.15;6.1.1.17;6.1.1.10;6.1.1.12;3.6.4.12;2.7.11.24;6.1.1.19;2.7.7.-;6.1.1.6;6.1.1.18",
        "go_molecular_function": "GO:0002161 aminoacyl-tRNA deacylase activity;GO:0004822 isoleucine-tRNA ligase activity;GO:0005524 ATP binding;GO:0000049 tRNA binding;GO:0051020 GTPase binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0017101 aminoacyl-tRNA synthetase multienzyme complex",
        "go_biological_process": "GO:0006428 isoleucyl-tRNA aminoacylation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "F1LS86-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F1LT82-1",
        "uniprot_id": "F1LT82_RAT",
        "mass": 46484.0,
        "length": 449,
        "protein_name": "Paired box 1",
        "gene_name": "Pax1",
        "organism": "Rat",
        "refseq_name": "paired box protein Pax-1",
        "refseq_ac": "NP_001388828",
        "gene_names_uniprotkb": "Pax1",
        "gene_names_refseq": "Pax-1; Pax1",
        "protein_names_uniprotkb": "Paired box 1",
        "protein_names_refseq": "Paired box homeotic gene 1; paired box gene 1; paired box protein Pax-1",
        "tax_id": 10116,
        "disease": "branchiootorenal syndrome (Disease Ontology:DOID:14702)",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 1,
        "publication_id_list": "34453169",
        "class_list": "",
        "function": "Aberrant Epigenetic Alteration of PAX1 Expression Contributes to Parathyroid Tumorigenesis., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0001228 DNA-binding transcription activator activity, RNA polymerase II-specific;GO:1990837 sequence-specific double-stranded DNA binding",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0043367 CD4-positive, alpha-beta T cell differentiation;GO:0043374 CD8-positive, alpha-beta T cell differentiation;GO:0060017 parathyroid gland development;GO:0006351 DNA-templated transcription;GO:0008283 cell population proliferation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "F1LT82-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F1LU70-1",
        "uniprot_id": "F1LU70_RAT",
        "mass": 103203.0,
        "length": 930,
        "protein_name": "G patch domain containing 1",
        "gene_name": "Gpatch1",
        "organism": "Rat",
        "refseq_name": "G patch domain-containing protein 1",
        "refseq_ac": "NP_001099716",
        "gene_names_uniprotkb": "Gpatch1",
        "gene_names_refseq": "Gpatc1; Gpatch1",
        "protein_names_uniprotkb": "G patch domain containing 1",
        "protein_names_refseq": "G patch domain-containing protein 1",
        "tax_id": 10116,
        "disease": "progressive myoclonus epilepsy 3 (Disease Ontology:DOID:0111446)",
        "pathway": " (rno:292810);  (R-RNO-72163)",
        "pathway_count": 2,
        "publication_count": 2,
        "publication_id_list": "16641100;22673903",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003723 RNA binding;GO:0003676 nucleic acid binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0071013 catalytic step 2 spliceosome",
        "go_biological_process": "GO:0006397 mRNA processing",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "F1LU70-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F1LUI6-1",
        "uniprot_id": "F1LUI6_RAT",
        "mass": 20154.0,
        "length": 188,
        "protein_name": "Achaete-scute family bHLH transcription factor 5",
        "gene_name": "Ascl5",
        "organism": "Rat",
        "refseq_name": "achaete-scute homolog 5",
        "refseq_ac": "NP_001385517",
        "gene_names_uniprotkb": "Ascl5",
        "gene_names_refseq": "Ascl5; RGD1561854",
        "protein_names_uniprotkb": "Achaete-scute family bHLH transcription factor 5",
        "protein_names_refseq": "achaete-scute complex homolog 5; achaete-scute homolog 5",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:363991)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
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        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0046983 protein dimerization activity;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0000785 chromatin;GO:0090575 RNA polymerase II transcription regulator complex",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0097186 amelogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F1LUI6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F1LW77-1",
        "uniprot_id": "F1LW77_RAT",
        "mass": 25753.0,
        "length": 229,
        "protein_name": "small monomeric GTPase",
        "gene_name": "Rab33b",
        "organism": "Rat",
        "refseq_name": "ras-related protein Rab-33B",
        "refseq_ac": "NP_001102414",
        "gene_names_uniprotkb": "Rab33b",
        "gene_names_refseq": "Rab33b",
        "protein_names_uniprotkb": "small monomeric GTPase; 3.6.5.2",
        "protein_names_refseq": "RAB33B, member of RAS oncogene family; ras-related protein Rab-33B",
        "tax_id": 10116,
        "disease": "Smith-McCort dysplasia 2 (Disease Ontology:DOID:0081271)",
        "pathway": " (rno:365793);  (R-RNO-6811438);  (R-RNO-8854214);  (R-RNO-8873719)",
        "pathway_count": 4,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "total_n_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "3.6.5.2;3.6.1.1;3.6.5.-;3.6.5.3;2.3.2.27;2.7.11.1;3.6.5.5;3.6.1.5;2.5.1.60;3.6.1.-;3.6.5.4",
        "go_molecular_function": "GO:0003924 GTPase activity;GO:0005525 GTP binding;GO:0003925 G protein activity",
        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005768 endosome;GO:0005794 Golgi apparatus;GO:0005796 Golgi lumen;GO:0034045 phagophore assembly site membrane",
        "go_biological_process": "GO:0000045 autophagosome assembly;GO:0034497 protein localization to phagophore assembly site;GO:0048705 skeletal system morphogenesis;GO:0034067 protein localization to Golgi apparatus;GO:2000156 regulation of retrograde vesicle-mediated transport, Golgi to ER",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F1LW77-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F1LWG4-1",
        "uniprot_id": "F1LWG4_RAT",
        "mass": 37782.0,
        "length": 328,
        "protein_name": "Complex I intermediate-associated protein 30, mitochondrial",
        "gene_name": "Ndufaf1",
        "organism": "Rat",
        "refseq_name": "complex I intermediate-associated protein 30, mitochondrial",
        "refseq_ac": "NP_001099970",
        "gene_names_uniprotkb": "Ndufaf1",
        "gene_names_refseq": "Cia30; Ndufaf1",
        "protein_names_uniprotkb": "Complex I intermediate-associated protein 30, mitochondrial; NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 1",
        "protein_names_refseq": "NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, assembly factor 1; NADH dehydrogenase (ubiquinone) complex I, assembly factor 1; complex I intermediate-associated protein 30, mitochondrial",
        "tax_id": 10116,
        "disease": "nuclear type mitochondrial complex I deficiency 11 (Disease Ontology:DOID:0112089); mitochondrial metabolism disease (Disease Ontology:DOID:700)",
        "pathway": " (rno:296086);  (R-RNO-6799198)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "As part of the MCIA complex, involved in the assembly of the mitochondrial complex I., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 2,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0051082 unfolded protein binding",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0160295 mitochondrial complex I intermediate assembly complex",
        "go_biological_process": "GO:0032981 mitochondrial respiratory chain complex I assembly;GO:0006120 mitochondrial electron transport, NADH to ubiquinone;GO:0051131 chaperone-mediated protein complex assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F1LWG4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F1LX20-1",
        "uniprot_id": "F1LX20_RAT",
        "mass": 27051.0,
        "length": 231,
        "protein_name": "TNF alpha induced protein 8 like 3",
        "gene_name": "Tnfaip8l3",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Tnfaip8l3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "TNF alpha induced protein 8 like 3",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:315673);  (R-RNO-1483255)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
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        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
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        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0035091 phosphatidylinositol binding;GO:0008526 phosphatidylinositol transfer activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005886 plasma membrane",
        "go_biological_process": "GO:0070374 positive regulation of ERK1 and ERK2 cascade;GO:0015914 phospholipid transport;GO:0042981 regulation of apoptotic process;GO:1902531 regulation of intracellular signal transduction;GO:1902633 1-phosphatidyl-1D-myo-inositol 4,5-bisphosphate metabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "F1LX20-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F1LYF5-1",
        "uniprot_id": "F1LYF5_RAT",
        "mass": 34611.0,
        "length": 311,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or5b24",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr344",
        "refseq_ac": "NP_001001043",
        "gene_names_uniprotkb": "Or5b24",
        "gene_names_refseq": "Olr344; Or5b24",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 344; olfactory receptor Olr344; olfactory receptor gene Olr344",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:405929)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Odorant receptor., [UniProtKB, UniProtKB]; Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_s_glycosites": 0,
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        "reported_phosphosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F1LYF5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F1LYG2-1",
        "uniprot_id": "F1LYG2_RAT",
        "mass": 194929.0,
        "length": 1776,
        "protein_name": "Signal-induced proliferation-associated 1 like 3",
        "gene_name": "Sipa1l3",
        "organism": "Rat",
        "refseq_name": "signal-induced proliferation-associated 1-like protein 3",
        "refseq_ac": "NP_001358027",
        "gene_names_uniprotkb": "Sipa1l3",
        "gene_names_refseq": "Sipa1l3",
        "protein_names_uniprotkb": "Signal-induced proliferation-associated 1 like 3",
        "protein_names_refseq": "signal-induced proliferation-associated 1-like protein 3",
        "tax_id": 10116,
        "disease": "cataract 45 (Disease Ontology:DOID:0110262); cataract (Disease Ontology:DOID:83)",
        "pathway": " (rno:292771)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 4,
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        "predicted_o_glycosites": 4,
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        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
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        "mined_s_glycosites": 0,
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        "reported_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
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        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 1,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 2,
        "glyco_site_count": 4,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005096 GTPase activator activity",
        "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005794 Golgi apparatus;GO:0005886 plasma membrane;GO:0045177 apical part of cell;GO:0001725 stress fiber",
        "go_biological_process": "GO:0051056 regulation of small GTPase mediated signal transduction;GO:0007010 cytoskeleton organization;GO:0003382 epithelial cell morphogenesis;GO:0002244 hematopoietic progenitor cell differentiation;GO:0090162 establishment of epithelial cell polarity",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "F1LYG2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F1LYL9-1",
        "uniprot_id": "SOX9_RAT",
        "mass": 56124.0,
        "length": 507,
        "protein_name": "Transcription factor SOX-9",
        "gene_name": "Sox9",
        "organism": "Rat",
        "refseq_name": "transcription factor SOX-9",
        "refseq_ac": "NP_536328",
        "gene_names_uniprotkb": "Sox9",
        "gene_names_refseq": "SRY; Sox9",
        "protein_names_uniprotkb": "Transcription factor SOX-9",
        "protein_names_refseq": "SRY (sex determining region Y)-box 9 (campomelic dysplasia, autosomal sex-reversal); SRY box 9; SRY-box containing gene 9; transcription factor SOX-9",
        "tax_id": 10116,
        "disease": "campomelic dysplasia (Disease Ontology:DOID:0050463); 46,XX sex reversal 2 (Disease Ontology:DOID:0111763); 46,XY sex reversal 10 (Disease Ontology:DOID:0111775); lung cancer (Disease Ontology:DOID:1324); lung carcinoma (Disease Ontology:DOID:3905)",
        "pathway": " (rno:140586);  (R-RNO-3769402)",
        "pathway_count": 2,
        "publication_count": 6,
        "publication_id_list": "26150426;33811247;35634668;36192639;36642539;38901791",
        "class_list": "",
        "function": "H3K18 lactylation accelerates liver fibrosis progression through facilitating SOX9 transcription., [RefSeq, PubMed]; Knockdown of SOX9 alleviates tracheal fibrosis through the Wnt/beta-catenin signaling pathway., [RefSeq, PubMed]; SRY-box transcription factor 9 modulates Muller cell gliosis in diabetic retinopathy by upregulating TXNIP transcription., [RefSeq, PubMed]; Sublytic C5b-9 induces glomerular mesangial cell proliferation via ERK1/2-dependent SOX9 phosphorylation and acetylation by enhancing Cyclin D1 in rat Thy-1 nephritis., [RefSeq, PubMed]; Transcription factor that plays a key role in chondrocytes differentiation and skeletal development (By similarity). Specifically binds the 5'-ACAAAG-3' DNA motif present in enhancers and super-enhancers and promotes expression of genes important for chondrogenesis, including cartilage matrix protein-coding genes COL2A1, COL4A2, COL9A1, COL11A2 and ACAN, SOX5 and SOX6 (PubMed:26150426). Also binds to some promoter regions (By similarity). Plays a central role in successive steps of chondrocyte differentiation (By similarity). Absolutely required for precartilaginous condensation, the first step in chondrogenesis during which skeletal progenitors differentiate into prechondrocytes (By similarity). Together with SOX5 and SOX6, required for overt chondrogenesis when condensed prechondrocytes differentiate into early stage chondrocytes, the second step in chondrogenesis (By similarity). Later, required to direct hypertrophic maturation and block osteoblast differentiation of growth plate chondrocytes: maintains chondrocyte columnar proliferation, delays prehypertrophy and then prevents osteoblastic differentiation of chondrocytes by lowering beta-catenin (CTNNB1) signaling and RUNX2 expression (By similarity). Also required for chondrocyte hypertrophy, both indirectly, by keeping the lineage fate of chondrocytes, and directly, by remaining present in upper hypertrophic cells and transactivating COL10A1 along with MEF2C (By similarity). Low lipid levels are the main nutritional determinant for chondrogenic commitment of skeletal progenitor cells: when lipids levels are low, FOXO (FOXO1 and FOXO3) transcription factors promote expression of SOX9, which induces chondrogenic commitment and suppresses fatty acid oxidation (By similarity). Mechanistically, helps, but is not required, to remove epigenetic signatures of transcriptional repression and deposit active promoter and enhancer marks at chondrocyte-specific genes (By similarity). Acts in cooperation with the Hedgehog pathway-dependent GLI (GLI1 and GLI3) transcription factors (By similarity). In addition to cartilage development, also acts as a regulator of proliferation and differentiation in epithelial stem/progenitor cells: involved in the lung epithelium during branching morphogenesis, by balancing proliferation and differentiation and regulating the extracellular matrix (By similarity). Controls epithelial branching during kidney development (By similarity)., [UniProtKB, UniProtKB, PubMed]; [Repair impact of vibration exercise with different frequencies on articular cartilage of rats with early knee osteoarthritis and its JNK/NF-kappaB, SOX9 mechanisms]., [RefSeq, PubMed]",
        "predicted_glycosites": 2,
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        "mined_s_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "gene_names_refseq": "Jcad; RGD1562037",
        "protein_names_uniprotkb": "Junctional cadherin 5 associated",
        "protein_names_refseq": "junctional cadherin 5-associated protein; junctional protein associated with coronary artery disease",
        "tax_id": 10116,
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        "pathway_count": 0,
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005911 cell-cell junction;GO:0005912 adherens junction;GO:0030054 cell junction;GO:0048471 perinuclear region of cytoplasm;GO:0032587 ruffle membrane",
        "go_biological_process": "GO:1903672 positive regulation of sprouting angiogenesis;GO:0043410 positive regulation of MAPK cascade;GO:0090050 positive regulation of cell migration involved in sprouting angiogenesis;GO:1900748 positive regulation of vascular endothelial growth factor signaling pathway;GO:1903589 positive regulation of blood vessel endothelial cell proliferation involved in sprouting angiogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "F1M6T3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F1M6U9-1",
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        "mass": 35171.0,
        "length": 312,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or52h2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Or52h2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Olfactory receptor",
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        "function": "Odorant receptor., [UniProtKB, UniProtKB]",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
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        "record_id": "F1M6U9-1",
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    },
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        "length": 481,
        "protein_name": "Low-density lipoprotein receptor-related protein 11",
        "gene_name": "Lrp11",
        "organism": "Rat",
        "refseq_name": "low-density lipoprotein receptor-related protein 11 isoform X1",
        "refseq_ac": "XP_038959502",
        "gene_names_uniprotkb": "Lrp11",
        "gene_names_refseq": "Lrp11",
        "protein_names_uniprotkb": "Low-density lipoprotein receptor-related protein 11",
        "protein_names_refseq": "low-density lipoprotein receptor-related protein 11 isoform X1",
        "tax_id": 10116,
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        "ec_number_list": "",
        "go_molecular_function": "GO:0051219 phosphoprotein binding",
        "go_cellular_component": "GO:0016020 membrane",
        "go_biological_process": "GO:0009409 response to cold;GO:0042594 response to starvation;GO:0009612 response to mechanical stimulus;GO:0009414 response to water deprivation;GO:0009408 response to heat",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F1M753-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F1M798-1",
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        "mass": 111648.0,
        "length": 990,
        "protein_name": "Metalloendopeptidase",
        "gene_name": "Bmp1",
        "organism": "Rat",
        "refseq_name": "bone morphogenetic protein 1 precursor",
        "refseq_ac": "NP_112613",
        "gene_names_uniprotkb": "Bmp1",
        "gene_names_refseq": "Bmp1",
        "protein_names_uniprotkb": "Metalloendopeptidase; 3.4.24.-",
        "protein_names_refseq": "bone morphogenetic protein 1 precursor; procollagen C-proteinase",
        "tax_id": 10116,
        "disease": "osteogenesis imperfecta type 13 (Disease Ontology:DOID:0110342); osteogenesis imperfecta (Disease Ontology:DOID:12347)",
        "pathway": " (rno:83470);  (R-RNO-1650814);  (R-RNO-2214320);  (R-RNO-2243919);  (R-RNO-8963896)",
        "pathway_count": 5,
        "publication_count": 3,
        "publication_id_list": "17071617;21415150;28684382",
        "class_list": "",
        "function": "Bone morphogenetic protein 1 is inhibited by native and altered forms of alpha2-macroglobulin, [RefSeq, PubMed]; Circulating bone morphogenetic protein 1-3 isoform increases renal fibrosis., [RefSeq, PubMed]; Collectively, the results indicate that androgen and IGF-I mutually interact and accelerate progesterone production, at least in part, by regulating endogenous BMP signaling in rat granulosa cells., [RefSeq, PubMed]",
        "predicted_glycosites": 2,
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        "missing_score": 10000,
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        "ec_number_list": "1.4.3.13;3.4.24.-",
        "go_molecular_function": "GO:0004222 metalloendopeptidase activity;GO:0008270 zinc ion binding;GO:0042802 identical protein binding;GO:0005509 calcium ion binding;GO:0008233 peptidase activity",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0031982 vesicle",
        "go_biological_process": "GO:0006508 proteolysis;GO:0016485 protein processing;GO:0009953 dorsal/ventral pattern formation;GO:0061036 positive regulation of cartilage development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "F1M798-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F1M801-1",
        "uniprot_id": "F1M801_RAT",
        "mass": 216079.0,
        "length": 1944,
        "protein_name": "Anaphase-promoting complex subunit 1",
        "gene_name": "Anapc1",
        "organism": "Rat",
        "refseq_name": "anaphase-promoting complex subunit 1",
        "refseq_ac": "NP_001101241",
        "gene_names_uniprotkb": "Anapc1",
        "gene_names_refseq": "Anapc1",
        "protein_names_uniprotkb": "Anaphase-promoting complex subunit 1; Cyclosome subunit 1; Mitotic checkpoint regulator; Testis-specific gene 24 protein",
        "protein_names_refseq": "anaphase-promoting complex subunit 1",
        "tax_id": 10116,
        "disease": "Rothmund-Thomson syndrome (Disease Ontology:DOID:2732)",
        "pathway": " (rno:311412);  (R-RNO-141430);  (R-RNO-174048);  (R-RNO-174084);  (R-RNO-174154);  (R-RNO-174178);  (R-RNO-174184);  (R-RNO-176407);  (R-RNO-176408);  (R-RNO-176412);  (R-RNO-179409);  (R-RNO-2467813);  (R-RNO-2559582);  (R-RNO-68867);  (R-RNO-69017);  (R-RNO-983168)",
        "pathway_count": 16,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Component of the anaphase promoting complex/cyclosome (APC/C), a cell cycle-regulated E3 ubiquitin ligase that controls progression through mitosis and the G1 phase of the cell cycle. The APC/C complex acts by mediating ubiquitination and subsequent degradation of target proteins: it mainly mediates the formation of 'Lys-11'-linked polyubiquitin chains and, to a lower extent, the formation of 'Lys-48'- and 'Lys-63'-linked polyubiquitin chains. The APC/C complex catalyzes assembly of branched 'Lys-11'-/'Lys-48'-linked branched ubiquitin chains on target proteins., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0060090 molecular adaptor activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005680 anaphase-promoting complex",
        "go_biological_process": "GO:0051301 cell division;GO:0031145 anaphase-promoting complex-dependent catabolic process;GO:0070979 protein K11-linked ubiquitination;GO:0070936 protein K48-linked ubiquitination;GO:0141198 protein branched polyubiquitination",
        "synthesized_glycan_count": 0,
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        "record_id": "F1M801-1",
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    },
    {
        "uniprot_canonical_ac": "F1M9B2-1",
        "uniprot_id": "F1M9B2_RAT",
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        "length": 373,
        "protein_name": "Insulin-like growth factor-binding protein 7",
        "gene_name": "Igfbp7",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Igfbp7",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Insulin-like growth factor-binding protein 7; MAC25 protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "metabolic dysfunction-associated steatotic liver disease (Disease Ontology:DOID:0080208); renal cell carcinoma (Disease Ontology:DOID:4450)",
        "pathway": " (R-RNO-381426);  (R-RNO-8957275)",
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        "function": "Binds IGF1 and IGF2 with a relatively low affinity. Stimulates prostacyclin (PGI2) production. Stimulates cell adhesion. Acts as a ligand for CD93 to play a role in angiogenesis., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0005520 insulin-like growth factor binding;GO:0048018 receptor ligand activity",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005576 extracellular region",
        "go_biological_process": "GO:0001525 angiogenesis;GO:0007155 cell adhesion;GO:0071380 cellular response to prostaglandin E stimulus;GO:0032526 response to retinoic acid;GO:0032870 cellular response to hormone stimulus",
        "synthesized_glycan_count": 0,
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    {
        "uniprot_canonical_ac": "F1MAQ8-1",
        "uniprot_id": "F1MAQ8_RAT",
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        "length": 814,
        "protein_name": "PNN interacting serine and arginine rich protein",
        "gene_name": "Pnisr",
        "organism": "Rat",
        "refseq_name": "arginine/serine-rich protein PNISR",
        "refseq_ac": "NP_001020445",
        "gene_names_uniprotkb": "Pnisr",
        "gene_names_refseq": "Pnisr; RGD1307395; Sfrs18; Srsf18",
        "protein_names_uniprotkb": "PNN interacting serine and arginine rich protein",
        "protein_names_refseq": "PNN-interacting serine/arginine-rich protein; arginine/serine-rich protein PNISR; serine/arginine-rich splicing factor 18; splicing factor, arginine/serine-rich 18",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:297942)",
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        "missing_score": 10000,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0016607 nuclear speck;GO:0048786 presynaptic active zone",
        "go_biological_process": "",
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        "record_id": "F1MAQ8-1",
        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "F1MAS1-1",
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        "length": 700,
        "protein_name": "CACN subunit beta associated regulatory protein",
        "gene_name": "Cbarp",
        "organism": "Rat",
        "refseq_name": "voltage-dependent calcium channel beta subunit-associated regulatory protein isoform X2",
        "refseq_ac": "XP_038934912",
        "gene_names_uniprotkb": "Cbarp; Dos",
        "gene_names_refseq": "Cbarp; Dos",
        "protein_names_uniprotkb": "CACN subunit beta associated regulatory protein",
        "protein_names_refseq": "voltage-dependent calcium channel beta subunit-associated regulatory protein isoform X2",
        "tax_id": 10116,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0044325 transmembrane transporter binding",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0030141 secretory granule;GO:0030426 growth cone",
        "go_biological_process": "GO:0045955 negative regulation of calcium ion-dependent exocytosis;GO:1903170 negative regulation of calcium ion transmembrane transport;GO:1901386 negative regulation of voltage-gated calcium channel activity",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "F1MAS1-1",
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    },
    {
        "uniprot_canonical_ac": "F6WEQ6-1",
        "uniprot_id": "ZN692_RAT",
        "mass": 59219.0,
        "length": 533,
        "protein_name": "Zinc finger protein 692",
        "gene_name": "Zfp692; Znf692",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Zfp692; Znf692; Arebp; Zfp692",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger protein 692; AICAR responsive element binding protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 1,
        "publication_id_list": "17097062",
        "class_list": "",
        "function": "May act as an transcriptional repressor for PCK1 gene expression, in turns may participate in the hepatic gluconeogenesis regulation through the activated AMPK signaling pathway., [UniProtKB, PubMed]",
        "predicted_glycosites": 0,
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        "secondary_ac_list": "B2GUW5",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006357 regulation of transcription by RNA polymerase II;GO:0006111 regulation of gluconeogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "F6WEQ6-1",
        "record_type": "protein"
    },
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        "length": 443,
        "protein_name": "Oligodendrocyte-myelin glycoprotein",
        "gene_name": "Omg",
        "organism": "Rat",
        "refseq_name": "oligodendrocyte-myelin glycoprotein precursor",
        "refseq_ac": "NP_001005898",
        "gene_names_uniprotkb": "Omg",
        "gene_names_refseq": "Omg",
        "protein_names_uniprotkb": "Oligodendrocyte-myelin glycoprotein",
        "protein_names_refseq": "oligodendrocyte-myelin glycoprotein precursor",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:450224);  (R-RNO-193634)",
        "pathway_count": 2,
        "publication_count": 3,
        "publication_id_list": "18809489;24090084;38843836",
        "class_list": "",
        "function": "Cell adhesion molecule contributing to the interactive process required for myelination in the central nervous system., [UniProtKB, UniProtKB]; The change of neuronal OMgp expression might be involved in reconnection of neural circuit between axotomized facial neuron and upper motor neuron after transection, [RefSeq, PubMed]",
        "predicted_glycosites": 1,
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        "go_molecular_function": "GO:0042802 identical protein binding",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0098552 side of membrane",
        "go_biological_process": "GO:0007155 cell adhesion;GO:0031102 neuron projection regeneration;GO:0048683 regulation of collateral sprouting of intact axon in response to injury",
        "synthesized_glycan_count": 0,
        "hit_score": 0.6,
        "record_id": "F7EYB9-1",
        "record_type": "protein"
    },
    {
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        "length": 223,
        "protein_name": "Interleukin-18-binding protein",
        "gene_name": "Il18bp",
        "organism": "Rat",
        "refseq_name": "interleukin-18-binding protein isoform X1",
        "refseq_ac": "XP_008758027",
        "gene_names_uniprotkb": "Il18bp",
        "gene_names_refseq": "Igifbp; Il18bp",
        "protein_names_uniprotkb": "Interleukin-18-binding protein",
        "protein_names_refseq": "interleukin-18-binding protein isoform X1",
        "tax_id": 10116,
        "disease": "alcoholic liver cirrhosis (Disease Ontology:DOID:14018); cystic fibrosis (Disease Ontology:DOID:1485); allergic contact dermatitis (Disease Ontology:DOID:3042); chronic obstructive pulmonary disease (Disease Ontology:DOID:3083); liver cirrhosis (Disease Ontology:DOID:5082); myocardial infarction (Disease Ontology:DOID:5844)",
        "pathway": " (R-RNO-9012546)",
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        "go_molecular_function": "GO:0042007 interleukin-18 binding",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0140368 decoy receptor complex",
        "go_biological_process": "GO:0032496 response to lipopolysaccharide;GO:0042088 T-helper 1 type immune response;GO:0070301 cellular response to hydrogen peroxide;GO:0071356 cellular response to tumor necrosis factor",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F7F5P4-1",
        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "F7F6L0-1",
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        "length": 468,
        "protein_name": "Mgat4 family, member E-like",
        "gene_name": "Mgat4f",
        "organism": "Rat",
        "refseq_name": "Mgat4 family, member E-like precursor",
        "refseq_ac": "NP_001013894",
        "gene_names_uniprotkb": "Mgat4f; LOC289035",
        "gene_names_refseq": "Mgat4e-like; Mgat4el; Mgat4f",
        "protein_names_uniprotkb": "Mgat4 family, member E-like",
        "protein_names_refseq": "Mgat4 family, member E-like precursor; Mgat4 family, member E-like; alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase MGAT4E-like",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:289035)",
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        "go_molecular_function": "GO:0008375 acetylglucosaminyltransferase activity",
        "go_cellular_component": "",
        "go_biological_process": "GO:0006487 protein N-linked glycosylation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F7F6L0-1",
        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "F7F7W7-1",
        "uniprot_id": "F7F7W7_RAT",
        "mass": 12128.0,
        "length": 109,
        "protein_name": "C-X-C motif chemokine ligand 13",
        "gene_name": "Cxcl13",
        "organism": "Rat",
        "refseq_name": "C-X-C motif chemokine 13 isoform 1 precursor",
        "refseq_ac": "NP_001406128",
        "gene_names_uniprotkb": "Cxcl13",
        "gene_names_refseq": "Cxcl13",
        "protein_names_uniprotkb": "C-X-C motif chemokine ligand 13",
        "protein_names_refseq": "C-X-C motif chemokine 13 isoform 1 precursor; C-X-C motif chemokine 13; chemokine (C-X-C motif) ligand 13",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-380108);  (R-RNO-418594)",
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        "publication_count": 5,
        "publication_id_list": "28359934;31589828;35075718;37622691;38526919",
        "class_list": "",
        "function": "CXCL13/CXCR5 promote chronic postsurgical pain and astrocyte activation in rats by targeting NLRP3., [RefSeq, PubMed]; LncRNA NONRATT009773.2 promotes bone cancer pain progression through the miR-708-5p/CXCL13 axis., [RefSeq, PubMed]; Mechanism of IRF5-regulated CXCL13/CXCR5 Signaling Axis in CCI-induced Neuropathic Pain in Rats., [RefSeq, PubMed]; Study highlighted the contribution of IL-17 pathway in the trafficking of CXCL13-induced GluN2B-containing N-methyl-d-aspartate receptor in the pathogenesis of remifentanil-induced hyperalgesia., [RefSeq, PubMed]; The roles of chemokine (C-X-C motif) ligand 13 in spinal cord ischemia-reperfusion injury in rats., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0008201 heparin binding;GO:0048018 receptor ligand activity;GO:0017134 fibroblast growth factor binding;GO:0031724 CXCR5 chemokine receptor binding;GO:0008009 chemokine activity",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0005615 extracellular space",
        "go_biological_process": "GO:0032487 regulation of Rap protein signal transduction;GO:0006954 inflammatory response;GO:0007166 cell surface receptor signaling pathway;GO:0007204 positive regulation of cytosolic calcium ion concentration;GO:0007267 cell-cell signaling",
        "synthesized_glycan_count": 0,
        "hit_score": 0.6,
        "record_id": "F7F7W7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7FD99-1",
        "uniprot_id": "F7FD99_RAT",
        "mass": 39478.0,
        "length": 342,
        "protein_name": "Similar to human chromosome 10 open reading frame 120",
        "gene_name": "C1h10orf120",
        "organism": "Rat",
        "refseq_name": "similar to RIKEN cDNA 1700022C21",
        "refseq_ac": "NP_001388001",
        "gene_names_uniprotkb": "C1h10orf120; LOC499276",
        "gene_names_refseq": "C1h10orf120",
        "protein_names_uniprotkb": "Similar to human chromosome 10 open reading frame 120",
        "protein_names_refseq": "similar to RIKEN cDNA 1700022C21; uncharacterized protein C10orf120 homolog",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:499276)",
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
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        "record_id": "F7FD99-1",
        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "F7FL00-1",
        "uniprot_id": "F7FL00_RAT",
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        "length": 454,
        "protein_name": "Carbonic anhydrase",
        "gene_name": "Ca9",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ca9; Car9",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Carbonic anhydrase; 4.2.1.1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "endometrial hyperplasia (Disease Ontology:DOID:0080365); urinary bladder cancer (Disease Ontology:DOID:11054); hepatitis B (Disease Ontology:DOID:2043); transitional cell carcinoma (Disease Ontology:DOID:2671); breast carcinoma (Disease Ontology:DOID:3459); Lynch syndrome (Disease Ontology:DOID:3883); lung non-small cell carcinoma (Disease Ontology:DOID:3908); renal cell carcinoma (Disease Ontology:DOID:4450); hepatocellular carcinoma (Disease Ontology:DOID:684)",
        "pathway": " (R-RNO-1475029)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Reversible hydration of carbon dioxide., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 9,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "A2IBE1",
        "ec_number_list": "4.2.1.1;4.2.1.69",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0004089 carbonate dehydratase activity;GO:0140677 molecular function activator activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0016323 basolateral plasma membrane",
        "go_biological_process": "GO:0001666 response to hypoxia;GO:0009410 response to xenobiotic stimulus;GO:0033574 response to testosterone",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F7FL00-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7FL39-1",
        "uniprot_id": "F7FL39_RAT",
        "mass": 44131.0,
        "length": 428,
        "protein_name": "Homeo box B3",
        "gene_name": "Hoxb3",
        "organism": "Rat",
        "refseq_name": "homeobox protein Hox-B3 isoform X2",
        "refseq_ac": "XP_006247256",
        "gene_names_uniprotkb": "Hoxb3",
        "gene_names_refseq": "Hoxb3",
        "protein_names_uniprotkb": "Homeo box B3",
        "protein_names_refseq": "homeobox protein Hox-B3 isoform X2",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Sequence-specific transcription factor which is part of a developmental regulatory system that provides cells with specific positional identities on the anterior-posterior axis., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
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        "reported_c_glycosites_with_glycan": 0,
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        "biomarker_type": "",
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        "binding_glycan_count": 0,
        "secondary_ac_list": "B2RYQ0",
        "ec_number_list": "",
        "go_molecular_function": "GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0001228 DNA-binding transcription activator activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0030878 thyroid gland development;GO:0021546 rhombomere development;GO:0021615 glossopharyngeal nerve morphogenesis;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0001525 angiogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F7FL39-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F8WFN8-1",
        "uniprot_id": "F8WFN8_RAT",
        "mass": 15698.0,
        "length": 139,
        "protein_name": "DPY30 domain containing 2",
        "gene_name": "Dydc2",
        "organism": "Rat",
        "refseq_name": "DPY30 domain-containing protein 2",
        "refseq_ac": "NP_001128269",
        "gene_names_uniprotkb": "Dydc2",
        "gene_names_refseq": "Dydc2",
        "protein_names_uniprotkb": "DPY30 domain containing 2",
        "protein_names_refseq": "DPY30 domain-containing protein 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:688422)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005930 axoneme;GO:0048188 Set1C/COMPASS complex",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F8WFN8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V671-1",
        "uniprot_id": "G3V671_RAT",
        "mass": 36310.0,
        "length": 321,
        "protein_name": "T-lymphocyte activation antigen CD80",
        "gene_name": "Cd80",
        "organism": "Rat",
        "refseq_name": "T-lymphocyte activation antigen CD80 precursor",
        "refseq_ac": "NP_001405592",
        "gene_names_uniprotkb": "Cd80",
        "gene_names_refseq": "B7-1; Cd80",
        "protein_names_uniprotkb": "T-lymphocyte activation antigen CD80; Activation B7-1 antigen",
        "protein_names_refseq": "CD80 antigen; CD80-like; Cd80 a rat homolog of the human CD28/CTLA - 4 ligand (B7-1); T-lymphocyte activation antigen CD80 precursor",
        "tax_id": 10116,
        "disease": "adult T-cell leukemia/lymphoma (Disease Ontology:DOID:0050523); kidney failure (Disease Ontology:DOID:1074); relapsing-remitting multiple sclerosis (Disease Ontology:DOID:2378); high grade glioma (Disease Ontology:DOID:3070); chronic obstructive pulmonary disease (Disease Ontology:DOID:3083); demyelinating disease (Disease Ontology:DOID:3213); periodontal disease (Disease Ontology:DOID:3388); anti-basement membrane glomerulonephritis (Disease Ontology:DOID:4780); rheumatoid arthritis (Disease Ontology:DOID:7148); systemic lupus erythematosus (Disease Ontology:DOID:9074); type 1 diabetes mellitus (Disease Ontology:DOID:9744)",
        "pathway": " (R-RNO-1257604);  (R-RNO-389356);  (R-RNO-389357);  (R-RNO-389359);  (R-RNO-389513);  (R-RNO-6811558)",
        "pathway_count": 6,
        "publication_count": 3,
        "publication_id_list": "29360807;32733939;34129205",
        "class_list": "",
        "function": "Diabetes-Mediated Toxicity Resulted in the Expression of CD80 and CD86 on Neutrophils after Delayed Wound Healing in Male Rats. Publication Status: Online-Only, [RefSeq, PubMed]; ETRA antagonist restores podocyte foot process effacement as well as the aberrant expression of TLR-3, nuclear factor-kappaB (NF-kappaB), and CD80 in puromycin aminonucleoside-injured kidneys, [RefSeq, PubMed]; Losartan Protects Podocytes against High Glucose-induced Injury by Inhibiting B7-1 Expression., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0015026 coreceptor activity;GO:0048018 receptor ligand activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0009986 cell surface;GO:0009897 external side of plasma membrane;GO:0098636 protein complex involved in cell adhesion",
        "go_biological_process": "GO:0002710 negative regulation of T cell mediated immunity;GO:0006955 immune response;GO:0007166 cell surface receptor signaling pathway;GO:0031295 T cell costimulation;GO:0042110 T cell activation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "G3V671-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V672-1",
        "uniprot_id": "G3V672_RAT",
        "mass": 126687.0,
        "length": 1162,
        "protein_name": "Nuclear receptor interacting protein 1",
        "gene_name": "Nrip1",
        "organism": "Rat",
        "refseq_name": "nuclear receptor-interacting protein 1",
        "refseq_ac": "NP_001094030",
        "gene_names_uniprotkb": "Nrip1",
        "gene_names_refseq": "Nrip1; RIP140",
        "protein_names_uniprotkb": "Nuclear receptor interacting protein 1",
        "protein_names_refseq": "nuclear receptor-interacting protein 1; receptor-interacting protein 140",
        "tax_id": 10116,
        "disease": "congenital anomalies of the kidney and urinary tract (Disease Ontology:DOID:0080205); osteoporosis (Disease Ontology:DOID:11476)",
        "pathway": " (rno:304157);  (R-RNO-3899300);  (R-RNO-9018519)",
        "pathway_count": 3,
        "publication_count": 5,
        "publication_id_list": "22923231;24823858;27614093;27639592;29393594",
        "class_list": "",
        "function": "In skeletal muscle cells, RIP140 expression significantly impacts palmitate uptake and oxidation and that alterations in gene expression and Akt-atypical protein kinaseC-theta signalling can partly explain these changes., [RefSeq, PubMed]; Overexpression of RIP140 induced proinflammatory gene expression and cytokine release in neonatal cardiomyocytes, which could be reversed by p65-NF-kappaB inhibition, [RefSeq, PubMed]; RIP140 aggravates metabolic repression, mitochondrial malfunction, and further accelerates the transition to heart failure in response to myocardial infarction stress., [RefSeq, PubMed]; This study indicates that suppression of SIRT3 by RIP140 facilitates the development of cardiomyocyte hypertrophy, mitochondrial dysfunction and energy metabolic dysfunction., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "predicted_c_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003713 transcription coactivator activity;GO:0005102 signaling receptor binding;GO:0003714 transcription corepressor activity;GO:0035259 nuclear glucocorticoid receptor binding;GO:0042826 histone deacetylase binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0016607 nuclear speck;GO:0000785 chromatin",
        "go_biological_process": "GO:0001543 ovarian follicle rupture;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006357 regulation of transcription by RNA polymerase II;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0007623 circadian rhythm",
        "synthesized_glycan_count": 0,
        "hit_score": 0.6,
        "record_id": "G3V672-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V674-1",
        "uniprot_id": "G3V674_RAT",
        "mass": 39296.0,
        "length": 352,
        "protein_name": "Claudin domain-containing protein 1",
        "gene_name": "Cldnd1",
        "organism": "Rat",
        "refseq_name": "claudin domain-containing protein 1 isoform X1",
        "refseq_ac": "XP_006248266",
        "gene_names_uniprotkb": "Cldnd1",
        "gene_names_refseq": "Cldnd1",
        "protein_names_uniprotkb": "Claudin domain-containing protein 1; Claudin-25",
        "protein_names_refseq": "claudin domain-containing protein 1 isoform X1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:288182)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Plays a role in negatively regulating the permeability of cells to small molecules., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
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        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
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        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
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        "reported_phosphosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0016324 apical plasma membrane;GO:0016020 membrane",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "G3V674-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V681-1",
        "uniprot_id": "G3V681_RAT",
        "mass": 96571.0,
        "length": 862,
        "protein_name": "DNA replication licensing factor MCM4",
        "gene_name": "Mcm4",
        "organism": "Rat",
        "refseq_name": "DNA replication licensing factor MCM4",
        "refseq_ac": "NP_387500",
        "gene_names_uniprotkb": "Mcm4",
        "gene_names_refseq": "Mcm4; Mcmd4",
        "protein_names_uniprotkb": "DNA replication licensing factor MCM4; 3.6.4.12",
        "protein_names_refseq": "DNA replication licensing factor MCM4; mini chromosome maintenance deficient 4 homolog; minichromosome maintenance deficient 4 homolog",
        "tax_id": 10116,
        "disease": "immunodeficiency 54 (Disease Ontology:DOID:0111967)",
        "pathway": " (rno:29728);  (R-RNO-176187);  (R-RNO-68867);  (R-RNO-68949);  (R-RNO-68962)",
        "pathway_count": 5,
        "publication_count": 2,
        "publication_id_list": "22673903;23264620",
        "class_list": "",
        "function": "Acts as a component of the MCM2-7 complex (MCM complex) which is the replicative helicase essential for 'once per cell cycle' DNA replication initiation and elongation in eukaryotic cells. Core component of CDC45-MCM-GINS (CMG) helicase, the molecular machine that unwinds template DNA during replication, and around which the replisome is built. The active ATPase sites in the MCM2-7 ring are formed through the interaction surfaces of two neighboring subunits such that a critical structure of a conserved arginine finger motif is provided in trans relative to the ATP-binding site of the Walker A box of the adjacent subunit. The six ATPase active sites, however, are likely to contribute differentially to the complex helicase activity., [UniProtKB, UniProtKB]; Acts as component of the MCM2-7 complex (MCM complex) which is the replicative helicase essential for 'once per cell cycle' DNA replication initiation and elongation in eukaryotic cells. The active ATPase sites in the MCM2-7 ring are formed through the interaction surfaces of two neighboring subunits such that a critical structure of a conserved arginine finger motif is provided in trans relative to the ATP-binding site of the Walker A box of the adjacent subunit. The six ATPase active sites, however, are likely to contribute differentially to the complex helicase activity., [UniProtKB, UniProtKB]; Peroxisome proliferator-activated receptor gamma coactivator 1beta (PGC-1beta) protein attenuates vascular lesion formation by inhibition of chromatin loading of minichromosome maintenance complex in smooth muscle cells, [RefSeq, PubMed]",
        "predicted_glycosites": 2,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 2,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
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        "reported_n_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "total_n_glycosites": 0,
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        "reported_mutagensis": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 2,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "5.6.2.3;3.6.4.13;3.6.4.12;2.7.11.1;3.6.1.5;3.6.4.10;3.6.4.-;2.3.2.27;5.6.2.4;3.6.5.-;5.6.2.-;2.7.7.7;3.1.-.-;2.7.7.49;3.1.13.1;4.2.99.18;2.7.7.-;7.6.2.2;7.6.2.3;7.6.2.-;5.6.1.6;7.2.2.-;3.6.1.15;3.6.4.6;3.1.3.1;3.9.1.1;6.1.1.12;3.6.1.-;2.7.4.3;2.7.11.22;3.1.4.-;3.4.24.-;3.6.-.-;3.4.21.53;5.6.2.5",
        "go_molecular_function": "GO:0005524 ATP binding;GO:0016787 hydrolase activity;GO:0003697 single-stranded DNA binding;GO:0003678 DNA helicase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0042555 MCM complex;GO:0071162 CMG complex",
        "go_biological_process": "GO:0006271 DNA strand elongation involved in DNA replication;GO:0006260 DNA replication;GO:1902975 mitotic DNA replication initiation;GO:0000727 double-strand break repair via break-induced replication",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "G3V681-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V6C3-1",
        "uniprot_id": "G3V6C3_RAT",
        "mass": 26293.0,
        "length": 228,
        "protein_name": "Polysaccharide biosynthesis domain containing 1",
        "gene_name": "Pbdc1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Pbdc1; RGD1562502",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Polysaccharide biosynthesis domain containing 1",
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    },
    {
        "uniprot_canonical_ac": "G3V6G8-1",
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        "length": 490,
        "protein_name": "Membrane-associated tyrosine- and threonine-specific cdc2-inhibitory kinase",
        "gene_name": "Pkmyt1",
        "organism": "Rat",
        "refseq_name": "membrane-associated tyrosine- and threonine-specific cdc2-inhibitory kinase",
        "refseq_ac": "NP_001099236",
        "gene_names_uniprotkb": "Pkmyt1",
        "gene_names_refseq": "Pkmyt1; RGD1305434",
        "protein_names_uniprotkb": "Membrane-associated tyrosine- and threonine-specific cdc2-inhibitory kinase; 2.7.11.1; Myt1 kinase",
        "protein_names_refseq": "membrane-associated tyrosine- and threonine-specific cdc2-inhibitory kinase",
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        "disease": "",
        "pathway": " (rno:287101);  (R-RNO-156711);  (R-RNO-69273);  (R-RNO-69478)",
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        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Acts as a negative regulator of entry into mitosis (G2 to M transition) by phosphorylation of the CDK1 kinase specifically when CDK1 is complexed to cyclins. Mediates phosphorylation of CDK1 predominantly on 'Thr-14'. Also involved in Golgi fragmentation. May be involved in phosphorylation of CDK1 on 'Tyr-15' to a lesser degree, however tyrosine kinase activity is unclear and may be indirect., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "2.7.11.1;2.7.12.1;2.7.1.153;2.7.1.137;2.7.11.24;2.7.11.25;2.7.11.22;2.7.11.23;2.7.4.6;2.7.1.154;2.7.11.38;2.7.11.17;2.7.11.21;2.7.12.2;2.7.1.40;2.7.11.12;2.7.11.26;2.7.11.34;2.7.10.2;2.7.1.150;2.7.11.13;4.1.1.32;2.7.11.19;2.7.2.3;2.7.11.11;2.7.11.31;3.1.3.16;2.7.11.4;2.3.1.48;3.1.11.-;2.7.13.3;2.7.4.18;3.1.24.-;3.4.19.12;2.7.11.39;2.4.99.18;2.7.11.10",
        "go_molecular_function": "GO:0004672 protein kinase activity;GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding;GO:0046872 metal ion binding;GO:0016301 kinase activity",
        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005794 Golgi apparatus",
        "go_biological_process": "GO:0010972 negative regulation of G2/M transition of mitotic cell cycle;GO:0051321 meiotic cell cycle;GO:0110031 negative regulation of G2/MI transition of meiotic cell cycle",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "G3V6G8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V6K7-1",
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        "length": 527,
        "protein_name": "V(D)J recombination-activating protein 2",
        "gene_name": "Rag2",
        "organism": "Rat",
        "refseq_name": "V(D)J recombination-activating protein 2",
        "refseq_ac": "NP_001093998",
        "gene_names_uniprotkb": "Rag2",
        "gene_names_refseq": "Rag2",
        "protein_names_uniprotkb": "V(D)J recombination-activating protein 2",
        "protein_names_refseq": "V(D)J recombination-activating protein 2; recombination activating gene 2; recombination activating protein 2",
        "tax_id": 10116,
        "disease": "Omenn syndrome (Disease Ontology:DOID:0060010); severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive (Disease Ontology:DOID:0090013); combined cellular and humoral immune defects with granulomas (Disease Ontology:DOID:0112253); severe combined immunodeficiency (Disease Ontology:DOID:627)",
        "pathway": " (rno:295953)",
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        "go_molecular_function": "GO:0003682 chromatin binding;GO:0005546 phosphatidylinositol-4,5-bisphosphate binding;GO:0005547 phosphatidylinositol-3,4,5-trisphosphate binding;GO:0008270 zinc ion binding;GO:0043325 phosphatidylinositol-3,4-bisphosphate binding",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0097519 DNA recombinase complex",
        "go_biological_process": "GO:0002360 T cell lineage commitment;GO:0030183 B cell differentiation;GO:0042742 defense response to bacterium;GO:0033077 T cell differentiation in thymus;GO:0046622 positive regulation of organ growth",
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    {
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        "length": 311,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or8g23",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr1278",
        "refseq_ac": "NP_775152",
        "gene_names_uniprotkb": "Or8g23",
        "gene_names_refseq": "Olr1278; Or8g23",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor (U131); olfactory receptor 1278; olfactory receptor 144-like; olfactory receptor 8G1-like; olfactory receptor Olr1278; olfactory receptor gene Olr1278",
        "tax_id": 10116,
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        "pathway": " (rno:286913)",
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        "class_list": "",
        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell",
        "synthesized_glycan_count": 0,
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        "record_id": "G3V6Q8-1",
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    },
    {
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        "uniprot_id": "G3V6V6_RAT",
        "mass": 40696.0,
        "length": 367,
        "protein_name": "LIM homeobox 8",
        "gene_name": "Lhx8",
        "organism": "Rat",
        "refseq_name": "LIM/homeobox protein Lhx8 isoform 1",
        "refseq_ac": "NP_001402020",
        "gene_names_uniprotkb": "Lhx8",
        "gene_names_refseq": "Lhx7; Lhx8",
        "protein_names_uniprotkb": "LIM homeobox 8",
        "protein_names_refseq": "LIM homeobox protein 8; LIM/homeobox protein Lhx8 isoform 1; LIM/homeobox protein Lhx8",
        "tax_id": 10116,
        "disease": "depressive disorder (Disease Ontology:DOID:1596)",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 5,
        "publication_id_list": "11801365;23150137;23385486;24265310;25475040",
        "class_list": "",
        "function": "Although the potential interaction of Lhx8 with other factors remains unknown, our results suggested that neuronal subtype specification can be directly manipulated in the stage of immature newborn neurons by a specific transcription factor in vitro., [RefSeq, PubMed]; Combined expression of Lhx7 and Gbx1 plays a role in the development of the cholinergic system of the basal forebrain., [RefSeq, PubMed]; Data indicate that LIM homeobox 8 (Lhx8) regulates functions of cholinergic neurons by modulating tropomyosin receptor kinase A (TrkA) expression., [RefSeq, PubMed]; Lhx8 plays role as a suppressor gene of cell proliferation., [RefSeq, PubMed]; Lhx8 was not associated with the MAP2-positive neurons differentiation on adherent conditions, but played a role in the specification of cholinergic neurons derived from hippocampal neural stem/progenitor cells in vitro, [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "secondary_ac_list": "Q5FVG3",
        "ec_number_list": "",
        "go_molecular_function": "GO:0046872 metal ion binding;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:1990837 sequence-specific double-stranded DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0001674 female germ cell nucleus",
        "go_biological_process": "GO:0021879 forebrain neuron differentiation;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0007611 learning or memory;GO:0045471 response to ethanol",
        "synthesized_glycan_count": 0,
        "hit_score": 0.6,
        "record_id": "G3V6V6-1",
        "record_type": "protein"
    },
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        "uniprot_id": "G3V6V8_RAT",
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        "length": 481,
        "protein_name": "Hyaluronidase",
        "gene_name": "Hyal4",
        "organism": "Rat",
        "refseq_name": "hyaluronidase-4",
        "refseq_ac": "NP_001094250",
        "gene_names_uniprotkb": "Hyal4",
        "gene_names_refseq": "Hyal4",
        "protein_names_uniprotkb": "Hyaluronidase; 3.2.1.35",
        "protein_names_refseq": "hyaluronidase-4; hyaluronoglucosaminidase 4",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:404783);  (R-RNO-2024101);  (R-RNO-2160916)",
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        "secondary_ac_list": "",
        "ec_number_list": "3.2.1.35",
        "go_molecular_function": "GO:0004415 hyalurononglucosaminidase activity;GO:0052757 chondroitin hydrolase activity",
        "go_cellular_component": "GO:0009986 cell surface;GO:0005764 lysosome;GO:0031410 cytoplasmic vesicle",
        "go_biological_process": "GO:0005975 carbohydrate metabolic process;GO:0006027 glycosaminoglycan catabolic process;GO:0030207 chondroitin sulfate proteoglycan catabolic process;GO:0030214 hyaluronan catabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "G3V6V8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V6W8-1",
        "uniprot_id": "G3V6W8_RAT",
        "mass": 49199.0,
        "length": 430,
        "protein_name": "Bone morphogenetic protein 7",
        "gene_name": "Bmp7",
        "organism": "Rat",
        "refseq_name": "bone morphogenetic protein 7 isoform 1 precursor",
        "refseq_ac": "NP_001178785",
        "gene_names_uniprotkb": "Bmp7",
        "gene_names_refseq": "BMP-7; Bmp7",
        "protein_names_uniprotkb": "Bone morphogenetic protein 7; Osteogenic protein 1",
        "protein_names_refseq": "bone moorphogenic protein-7; bone morphogenetic protein 7 isoform 1 precursor",
        "tax_id": 10116,
        "disease": "obstructive sleep apnea (Disease Ontology:DOID:0050848); prostate cancer (Disease Ontology:DOID:10283); pyelonephritis (Disease Ontology:DOID:11400); acute kidney tubular necrosis (Disease Ontology:DOID:12556); Marfan syndrome (Disease Ontology:DOID:14323); breast cancer (Disease Ontology:DOID:1612); nephroblastoma (Disease Ontology:DOID:2154); ovarian carcinoma (Disease Ontology:DOID:4001); renal cell carcinoma (Disease Ontology:DOID:4450); kidney disease (Disease Ontology:DOID:557); osteoarthritis (Disease Ontology:DOID:8398); diabetes mellitus (Disease Ontology:DOID:9351); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (rno:85272);  (R-RNO-2129379)",
        "pathway_count": 2,
        "publication_count": 5,
        "publication_id_list": "36542543;36613483;36765143;36858954;37293506",
        "class_list": "",
        "function": "BMP7 ameliorates intervertebral disc degeneration in type 1 diabetic rats by inhibiting pyroptosis of nucleus pulposus cells and NLRP3 inflammasome activity. Publication Status: Online-Only, [RefSeq, PubMed]; Bone morphogenetic protein-7 attenuates pancreatic damage under diabetic conditions and prevents progression to diabetic nephropathy via inhibition of ferroptosis. Publication Status: Online-Only, [RefSeq, PubMed]; Conserved miR-370-3p/BMP-7 axis regulates the phenotypic change of human vascular smooth muscle cells. Publication Status: Online-Only, [RefSeq, PubMed]; Differentiation of rat bone marrow mesenchymal stem cells into neurons induced by bone morphogenetic protein 7 in vitro., [RefSeq, PubMed]; Imbalance in Bone Morphogenic Proteins 2 and 7 Is Associated with Renal and Cardiovascular Damage in Chronic Kidney Disease. Publication Status: Online-Only, [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0008201 heparin binding;GO:0005125 cytokine activity;GO:0008083 growth factor activity;GO:0070700 BMP receptor binding",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0031012 extracellular matrix;GO:0031982 vesicle;GO:0005576 extracellular region",
        "go_biological_process": "GO:0007507 heart development;GO:0008285 negative regulation of cell population proliferation;GO:0010628 positive regulation of gene expression;GO:0030855 epithelial cell differentiation;GO:0043065 positive regulation of apoptotic process",
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    },
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        "length": 358,
        "protein_name": "Caspase activity and apoptosis inhibitor 1",
        "gene_name": "Caap1",
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        "refseq_name": "caspase activity and apoptosis inhibitor 1 isoform 1",
        "refseq_ac": "NP_001402884",
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        "gene_names_refseq": "Caap1",
        "protein_names_uniprotkb": "Caspase activity and apoptosis inhibitor 1",
        "protein_names_refseq": "caspase activity and apoptosis inhibitor 1 isoform 1",
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        "secondary_ac_list": "Q3KR90",
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        "go_biological_process": "GO:0043066 negative regulation of apoptotic process;GO:0042981 regulation of apoptotic process",
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    },
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        "protein_name": "Homeobox protein Hox-B1",
        "gene_name": "Hoxb1",
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        "refseq_name": "homeobox protein Hox-B1",
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        "gene_names_refseq": "Hoxb1",
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        "protein_names_refseq": "homeobox protein Hox-B1",
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        "function": "Sequence-specific transcription factor which is part of a developmental regulatory system that provides cells with specific positional identities on the anterior-posterior axis. Acts on the anterior body structures., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0019904 protein domain specific binding;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0021570 rhombomere 4 development;GO:0021571 rhombomere 5 development;GO:0021754 facial nucleus development;GO:0021546 rhombomere development;GO:0006351 DNA-templated transcription",
        "synthesized_glycan_count": 0,
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    },
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        "length": 204,
        "protein_name": "MRG domain binding protein",
        "gene_name": "Mrgbp",
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        "refseq_name": "MRG/MORF4L-binding protein",
        "refseq_ac": "NP_001167210",
        "gene_names_uniprotkb": "Mrgbp",
        "gene_names_refseq": "Mrgbp; RGD1308612",
        "protein_names_uniprotkb": "MRG domain binding protein",
        "protein_names_refseq": "MRG-binding protein; MRG/MORF4L binding protein; MRG/MORF4L-binding protein",
        "tax_id": 10116,
        "disease": "prostate cancer (Disease Ontology:DOID:10283)",
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        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0035267 NuA4 histone acetyltransferase complex;GO:0000786 nucleosome;GO:0043189 H4/H2A histone acetyltransferase complex",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0006325 chromatin organization;GO:0051726 regulation of cell cycle;GO:1905168 positive regulation of double-strand break repair via homologous recombination",
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    },
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Gfus; Tsta3",
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        "protein_names_uniprotkb": "GDP-L-fucose synthase; 1.1.1.271; GDP-4-keto-6-deoxy-D-mannose-3,5-epimerase-4-reductase",
        "protein_names_refseq": "",
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        "function": "Catalyzes the two-step NADP-dependent conversion of GDP-4-dehydro-6-deoxy-D-mannose to GDP-fucose, involving an epimerase and a reductase reaction., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005829 cytosol",
        "go_biological_process": "GO:0019673 GDP-mannose metabolic process;GO:0042351 'de novo' GDP-L-fucose biosynthetic process;GO:0010595 positive regulation of endothelial cell migration;GO:0001913 T cell mediated cytotoxicity;GO:1904906 positive regulation of endothelial cell-matrix adhesion via fibronectin",
        "synthesized_glycan_count": 0,
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    {
        "uniprot_canonical_ac": "G3V7A3-1",
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        "length": 405,
        "protein_name": "Serpin family I member 2",
        "gene_name": "Serpini2",
        "organism": "Rat",
        "refseq_name": "serpin I2 precursor",
        "refseq_ac": "NP_001127881",
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        "gene_names_refseq": "Serpini2",
        "protein_names_uniprotkb": "Serpin family I member 2",
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        "tax_id": 10116,
        "disease": "familial encephalopathy with neuroserpin inclusion bodies (Disease Ontology:DOID:0050831); Shwachman-Diamond syndrome (Disease Ontology:DOID:0060479)",
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        "publication_id_list": "12438159",
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        "function": "Neuroserpin may play a role in cell communication, cell adhesion, and/or cell migration, [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0004867 serine-type endopeptidase inhibitor activity",
        "go_cellular_component": "GO:0005615 extracellular space",
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    {
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        "length": 397,
        "protein_name": "DNA excision repair protein ERCC-8",
        "gene_name": "Ercc8",
        "organism": "Rat",
        "refseq_name": "DNA excision repair protein ERCC-8",
        "refseq_ac": "NP_001101120",
        "gene_names_uniprotkb": "Ercc8",
        "gene_names_refseq": "Ckn1; Ercc8",
        "protein_names_uniprotkb": "DNA excision repair protein ERCC-8",
        "protein_names_refseq": "Cockayne syndrome 1 (classical); DNA excision repair protein ERCC-8; excision repair cross-complementation group 8; excision repair cross-complementing rodent repair deficiency, complementation group 8; excision repaiross-complementing rodent repair deficiency, complementation group 8",
        "tax_id": 10116,
        "disease": "UV-sensitive syndrome (Disease Ontology:DOID:0060240); Cockayne syndrome A (Disease Ontology:DOID:0080907); Cockayne syndrome (Disease Ontology:DOID:2962)",
        "pathway": " (rno:310071)",
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        "publication_count": 0,
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        "function": "Substrate-recognition component of the CSA complex, a DCX (DDB1-CUL4-X-box) E3 ubiquitin-protein ligase complex, involved in transcription-coupled nucleotide excision repair (TC-NER), a process during which RNA polymerase II-blocking lesions are rapidly removed from the transcribed strand of active genes. Following recruitment to lesion-stalled RNA polymerase II (Pol II), the CSA complex mediates ubiquitination of Pol II subunit POLR2A/RPB1 at 'Lys-1268', a critical TC-NER checkpoint, governing RNA Pol II stability and initiating DNA damage excision by TFIIH recruitment. The CSA complex also promotes the ubiquitination and subsequent proteasomal degradation of ERCC6/CSB in a UV-dependent manner; ERCC6 degradation is essential for the recovery of RNA synthesis after transcription-coupled repair. Also plays a role in DNA double-strand breaks (DSSBs) repair by non-homologous end joining (NHEJ)., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:1990756 ubiquitin-like ligase-substrate adaptor activity",
        "go_cellular_component": "GO:0031464 Cul4A-RING E3 ubiquitin ligase complex;GO:0000109 nucleotide-excision repair complex;GO:0005634 nucleus;GO:0043204 perikaryon;GO:0016363 nuclear matrix",
        "go_biological_process": "GO:0097680 double-strand break repair via classical nonhomologous end joining;GO:0006979 response to oxidative stress;GO:0006974 DNA damage response;GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process;GO:0010996 response to auditory stimulus",
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        "record_id": "G3V7B8-1",
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    {
        "uniprot_canonical_ac": "G3V7E0-1",
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        "length": 325,
        "protein_name": "Homeobox protein orthopedia",
        "gene_name": "Otp",
        "organism": "Rat",
        "refseq_name": "homeobox protein orthopedia",
        "refseq_ac": "NP_001093993",
        "gene_names_uniprotkb": "Otp",
        "gene_names_refseq": "Otp",
        "protein_names_uniprotkb": "Homeobox protein orthopedia",
        "protein_names_refseq": "homeobox protein orthopedia; orthopedia homolog",
        "tax_id": 10116,
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        "pathway": " (rno:294640)",
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        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 2,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0021879 forebrain neuron differentiation;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0030182 neuron differentiation;GO:0002052 positive regulation of neuroblast proliferation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "G3V7E0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V7E7-1",
        "uniprot_id": "G3V7E7_RAT",
        "mass": 27950.0,
        "length": 256,
        "protein_name": "Homeobox protein goosecoid",
        "gene_name": "Gsc",
        "organism": "Rat",
        "refseq_name": "homeobox protein goosecoid",
        "refseq_ac": "NP_001178802",
        "gene_names_uniprotkb": "Gsc",
        "gene_names_refseq": "Gsc",
        "protein_names_uniprotkb": "Homeobox protein goosecoid",
        "protein_names_refseq": "homeobox protein goosecoid-like; homeobox protein goosecoid",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:317715)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "The protein encoded by this gene is likely a homeobox transcription factor. [provided by RefSeq, Jul 2008]., [RefSeq]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
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        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "total_n_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0061629 RNA polymerase II-specific DNA-binding transcription factor binding;GO:1990837 sequence-specific double-stranded DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0016607 nuclear speck;GO:0005667 transcription regulator complex",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006357 regulation of transcription by RNA polymerase II;GO:0030900 forebrain development;GO:0030178 negative regulation of Wnt signaling pathway;GO:0042474 middle ear morphogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "G3V7E7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V7K0-1",
        "uniprot_id": "G3V7K0_RAT",
        "mass": 39420.0,
        "length": 361,
        "protein_name": "Visual system homeobox 2",
        "gene_name": "Vsx2",
        "organism": "Rat",
        "refseq_name": "visual system homeobox 2",
        "refseq_ac": "NP_001162599",
        "gene_names_uniprotkb": "Vsx2",
        "gene_names_refseq": "Chx10; Vsx2",
        "protein_names_uniprotkb": "Visual system homeobox 2; Ceh-10 homeodomain-containing homolog; Homeobox protein CHX10",
        "protein_names_refseq": "ceh-10 homeo domain containing homolog; visual system homeobox 2",
        "tax_id": 10116,
        "disease": "isolated microphthalmia 2 (Disease Ontology:DOID:0060839); blindness (Disease Ontology:DOID:1432)",
        "pathway": " (rno:171360)",
        "pathway_count": 1,
        "publication_count": 2,
        "publication_id_list": "16236706;16547132",
        "class_list": "",
        "function": "CHX10 may target specific motifs to inhibit rod photoreceptor gene expression in bipolar cells, [RefSeq, PubMed]; Chx10 directly controls bipolar cell genesis by inhibiting rod differentiation independent of its temporally limited early effect on retinal progenitor cell proliferation, [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "reported_phosphosites": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific;GO:1990837 sequence-specific double-stranded DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0060042 retina morphogenesis in camera-type eye;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0008284 positive regulation of cell population proliferation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "G3V7K0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V7T6-1",
        "uniprot_id": "G3V7T6_RAT",
        "mass": 145830.0,
        "length": 1304,
        "protein_name": "Splicing factor 3B subunit 1",
        "gene_name": "Sf3b1",
        "organism": "Rat",
        "refseq_name": "splicing factor 3B subunit 1",
        "refseq_ac": "NP_445878",
        "gene_names_uniprotkb": "Sf3b1",
        "gene_names_refseq": "Sap155; Sf3b1",
        "protein_names_uniprotkb": "Splicing factor 3B subunit 1; Pre-mRNA-splicing factor SF3b 155 kDa subunit; Spliceosome-associated protein 155",
        "protein_names_refseq": "splicing factor 3B subunit 1; splicing factor 3b, subunit 1, 155kD",
        "tax_id": 10116,
        "disease": "myelodysplastic syndrome (Disease Ontology:DOID:0050908); uterine corpus endometrial carcinoma (Disease Ontology:DOID:0050939); bladder urothelial carcinoma (Disease Ontology:DOID:4006); hepatocellular carcinoma (Disease Ontology:DOID:684); acute myeloid leukemia (Disease Ontology:DOID:9119)",
        "pathway": " (rno:84486);  (R-RNO-5250924);  (R-RNO-72163);  (R-RNO-72165);  (R-RNO-9770562);  (R-RNO-9943411)",
        "pathway_count": 6,
        "publication_count": 2,
        "publication_id_list": "22673903;35039052",
        "class_list": "",
        "function": "The SF3B1(R625H) mutation promotes prolactinoma tumor progression through aberrant splicing of DLG1. Publication Status: Online-Only, [RefSeq, PubMed]",
        "predicted_glycosites": 4,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 4,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 4,
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        "go_molecular_function": "GO:0036002 pre-mRNA binding;GO:0003682 chromatin binding;GO:0003729 mRNA binding;GO:1990935 splicing factor binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0016607 nuclear speck;GO:0005681 spliceosomal complex;GO:0016363 nuclear matrix;GO:0000785 chromatin",
        "go_biological_process": "GO:0009952 anterior/posterior pattern specification;GO:0045945 positive regulation of transcription by RNA polymerase III;GO:0000398 mRNA splicing, via spliceosome;GO:0000245 spliceosomal complex assembly;GO:0001825 blastocyst formation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "G3V7T6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V7X1-1",
        "uniprot_id": "G3V7X1_RAT",
        "mass": 33077.0,
        "length": 303,
        "protein_name": "Fibroblast growth factor",
        "gene_name": "Fgf11",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Fgf11",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Fibroblast growth factor; FGF",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
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        "pathway_count": 0,
        "publication_count": 0,
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        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0017080 sodium channel regulator activity;GO:0008083 growth factor activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0022008 neurogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "G3V7X1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "M0R8V6-1",
        "uniprot_id": "M0R8V6_RAT",
        "mass": 21352.0,
        "length": 191,
        "protein_name": "Similar to human chromosome 17 open reading frame 50",
        "gene_name": "C10h17orf50",
        "organism": "Rat",
        "refseq_name": "similar to human chromosome 17 open reading frame 50",
        "refseq_ac": "NP_001417207",
        "gene_names_uniprotkb": "C10h17orf50; LOC689039",
        "gene_names_refseq": "C10h17orf50",
        "protein_names_uniprotkb": "Similar to human chromosome 17 open reading frame 50",
        "protein_names_refseq": "similar to human chromosome 17 open reading frame 50; uncharacterized protein C17orf50 homolog",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:689039)",
        "pathway_count": 1,
        "publication_count": 0,
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        "function": "",
        "predicted_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005654 nucleoplasm",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "M0R8V6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZLC1-1",
        "uniprot_id": "D3ZLC1_RAT",
        "mass": 71183.0,
        "length": 640,
        "protein_name": "Lamin B2",
        "gene_name": "Lmnb2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Lmnb2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Lamin B2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "congenital muscular dystrophy (Disease Ontology:DOID:0050557); autosomal dominant primary microcephaly 27 (Disease Ontology:DOID:0051038); familial partial lipodystrophy type 2 (Disease Ontology:DOID:0070202); autosomal dominant Emery-Dreifuss muscular dystrophy 2 (Disease Ontology:DOID:0070247); autosomal recessive Emery-Dreifuss muscular dystrophy 3 (Disease Ontology:DOID:0070248); partial lipodystrophy (Disease Ontology:DOID:0080299); dilated cardiomyopathy 1A (Disease Ontology:DOID:0110425); congenital muscular dystrophy due to LMNA mutation (Disease Ontology:DOID:0110640); progressive myoclonus epilepsy 9 (Disease Ontology:DOID:0111450); Emery-Dreifuss muscular dystrophy (Disease Ontology:DOID:11726); progeria (Disease Ontology:DOID:3911); myopathy (Disease Ontology:DOID:423); muscular dystrophy (Disease Ontology:DOID:9884)",
        "pathway": " (rno:299625)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "",
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005200 structural constituent of cytoskeleton;GO:0042802 identical protein binding",
        "go_cellular_component": "GO:0031981 nuclear lumen;GO:0005882 intermediate filament;GO:0005634 nucleus;GO:0005635 nuclear envelope;GO:0031965 nuclear membrane",
        "go_biological_process": "GO:0090435 protein localization to nuclear envelope;GO:0006998 nuclear envelope organization;GO:0031507 heterochromatin formation;GO:0007097 nuclear migration;GO:0051664 nuclear pore localization",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D3ZLC1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZXU0-1",
        "uniprot_id": "D3ZXU0_RAT",
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        "length": 960,
        "protein_name": "Zinc finger with KRAB and SCAN domains 2",
        "gene_name": "Zkscan2",
        "organism": "Rat",
        "refseq_name": "zinc finger protein with KRAB and SCAN domains 2",
        "refseq_ac": "NP_001419304",
        "gene_names_uniprotkb": "Zkscan2",
        "gene_names_refseq": "Zkscan2",
        "protein_names_uniprotkb": "Zinc finger with KRAB and SCAN domains 2",
        "protein_names_refseq": "zinc finger protein with KRAB and SCAN domains 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:368120)",
        "pathway_count": 1,
        "publication_count": 0,
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        "class_list": "",
        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB]",
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus",
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        "refseq_name": "E1A-binding protein p400 isoform X3",
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        "protein_names_uniprotkb": "E1A-binding protein p400; Domino homolog; p400 kDa SWI2/SNF2-related protein",
        "protein_names_refseq": "E1A-binding protein p400 isoform X3",
        "tax_id": 10116,
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    },
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        "protein_name": "Rho GTPase activating protein 22",
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        "refseq_name": "rho GTPase-activating protein 22 isoform X2",
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        "pathway": " (rno:306279);  (R-RNO-8980692);  (R-RNO-9013148);  (R-RNO-9013149)",
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    },
    {
        "uniprot_canonical_ac": "A0A0G2JUY1-1",
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        "length": 1221,
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        "refseq_name": "E3 ubiquitin-protein ligase NEDD4-like isoform X4",
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        "protein_names_uniprotkb": "E3 ubiquitin-protein ligase NEDD4-like; 2.3.2.26; HECT-type E3 ubiquitin transferase NED4L",
        "protein_names_refseq": "E3 ubiquitin-protein ligase NEDD4-like isoform X4",
        "tax_id": 10116,
        "disease": "periventricular nodular heterotopia (Disease Ontology:DOID:0050454); Liddle syndrome (Disease Ontology:DOID:0050477); stroke (Disease Ontology:DOID:0051061)",
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        "go_molecular_function": "GO:0061630 ubiquitin protein ligase activity;GO:0019870 potassium channel inhibitor activity;GO:0019871 sodium channel inhibitor activity;GO:0044325 transmembrane transporter binding;GO:0017080 sodium channel regulator activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0016324 apical plasma membrane;GO:0098978 glutamatergic synapse;GO:0005886 plasma membrane;GO:0098794 postsynapse",
        "go_biological_process": "GO:0016567 protein ubiquitination;GO:0006511 ubiquitin-dependent protein catabolic process;GO:1903861 positive regulation of dendrite extension;GO:1903765 negative regulation of potassium ion export across plasma membrane;GO:0060306 regulation of membrane repolarization",
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    {
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        "protein_name": "Proliferation-associated SNF2-like protein",
        "gene_name": "Hells",
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        "refseq_name": "lymphoid-specific helicase",
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        "protein_names_uniprotkb": "Proliferation-associated SNF2-like protein",
        "protein_names_refseq": "TBC1D12: TBC1 domain family, member 12; lymphocyte-specific helicase-like; lymphoid-specific helicase",
        "tax_id": 10116,
        "disease": "immunodeficiency-centromeric instability-facial anomalies syndrome 4 (Disease Ontology:DOID:0090011); high grade glioma (Disease Ontology:DOID:3070)",
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        "function": "ATP-dependent chromatin remodeler that regulates chromatin accessibility, DNA methylation, and histone modifications. It facilitates de novo DNA methylation at repetitive sequences and promotes transcriptional silencing via recruitment of DNA methyltransferases (DNMTs) and histone deacetylases (HDACs), contributing to heterochromatin formation and repression of transposable elements. Also involved in DNA repair by recruiting DNA damage response mediators to double-strand breaks in heterochromatin, promoting homologous recombination via RBBP8/CtIP-dependent end resection. During meiosis, it is recruited by PRDM9 to recombination hotspots, aiding chromatin opening. Through these diverse roles, is crucial for processes such as development, differentiation, and genomic stability. Involved in regulation of the expansion or survival of lymphoid cells., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005524 ATP binding;GO:0016787 hydrolase activity;GO:0004386 helicase activity;GO:0003682 chromatin binding;GO:0140463 chromatin-protein adaptor activity",
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        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0051301 cell division;GO:0031508 pericentric heterochromatin formation;GO:0001822 kidney development;GO:0000724 double-strand break repair via homologous recombination",
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    },
    {
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        "protein_name": "Phosphomevalonate kinase",
        "gene_name": "Pmvk",
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        "refseq_name": "phosphomevalonate kinase",
        "refseq_ac": "NP_001008353",
        "gene_names_uniprotkb": "Pmvk",
        "gene_names_refseq": "Pmvk",
        "protein_names_uniprotkb": "Phosphomevalonate kinase; 2.7.4.2; PMKase",
        "protein_names_refseq": "phosphomevalonate kinase",
        "tax_id": 10116,
        "disease": "porokeratosis (Disease Ontology:DOID:3805)",
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        "class_list": "",
        "function": "Catalyzes the reversible ATP-dependent phosphorylation of mevalonate 5-phosphate to produce mevalonate diphosphate and ADP, a key step in the mevalonic acid mediated biosynthesis of isopentenyl diphosphate and other polyisoprenoid metabolites., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "ec_number_list": "2.7.4.2",
        "go_molecular_function": "GO:0005524 ATP binding;GO:0004631 phosphomevalonate kinase activity",
        "go_cellular_component": "GO:0005829 cytosol;GO:0005777 peroxisome",
        "go_biological_process": "GO:0006695 cholesterol biosynthetic process;GO:0019287 isopentenyl diphosphate biosynthetic process, mevalonate pathway;GO:0016126 sterol biosynthetic process;GO:0033386 geranylgeranyl diphosphate biosynthetic process;GO:0033489 cholesterol biosynthetic process via desmosterol",
        "synthesized_glycan_count": 0,
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        "record_id": "Q5RK24-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V8Z9-1",
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        "length": 294,
        "protein_name": "COP9 signalosome subunit 7A",
        "gene_name": "Cops7a",
        "organism": "Rat",
        "refseq_name": "COP9 signalosome complex subunit 7a isoform X2",
        "refseq_ac": "XP_038963603",
        "gene_names_uniprotkb": "Cops7a",
        "gene_names_refseq": "Cops7a",
        "protein_names_uniprotkb": "COP9 signalosome subunit 7A",
        "protein_names_refseq": "COP9 signalosome complex subunit 7a isoform X2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:312710);  (R-RNO-5696394);  (R-RNO-6781823);  (R-RNO-8856825);  (R-RNO-8951664)",
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        "class_list": "",
        "function": "Component of the COP9 signalosome complex (CSN), a complex involved in various cellular and developmental processes. The CSN complex is an essential regulator of the ubiquitin (Ubl) conjugation pathway by mediating the deneddylation of the cullin subunits of SCF-type E3 ligase complexes, leading to decrease the Ubl ligase activity of SCF-type complexes such as SCF, CSA or DDB2. The complex is also involved in phosphorylation of p53/TP53, JUN, I-kappa-B-alpha/NFKBIA, ITPK1 and IRF8/ICSBP, possibly via its association with CK2 and PKD kinases. CSN-dependent phosphorylation of TP53 and JUN promotes and protects degradation by the Ubl system, respectively., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "reported_fully_resolved_glycans": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0008180 COP9 signalosome;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0010387 COP9 signalosome assembly;GO:0000338 protein deneddylation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "G3V8Z9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZKG1-1",
        "uniprot_id": "D3ZKG1_RAT",
        "mass": 92036.0,
        "length": 833,
        "protein_name": "Methylmalonyl-CoA mutase, mitochondrial",
        "gene_name": "Mmut",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Mmut; LOC100361295; Mut",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Methylmalonyl-CoA mutase, mitochondrial; 5.4.99.2; Methylmalonyl-CoA isomerase",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency (Disease Ontology:DOID:0060740); methylmalonic acidemia (Disease Ontology:DOID:14749)",
        "pathway": " (R-RNO-71032);  (R-RNO-9759218)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Catalyzes the reversible isomerization of methylmalonyl-CoA (MMCoA) (generated from branched-chain amino acid metabolism and degradation of dietary odd chain fatty acids and cholesterol) to succinyl-CoA (3-carboxypropionyl-CoA), a key intermediate of the tricarboxylic acid cycle., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "5.4.99.2",
        "go_molecular_function": "GO:0046872 metal ion binding;GO:0031419 cobalamin binding;GO:0004494 methylmalonyl-CoA mutase activity;GO:0003924 GTPase activity;GO:0042802 identical protein binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005739 mitochondrion;GO:0005759 mitochondrial matrix",
        "go_biological_process": "GO:0006790 sulfur compound metabolic process;GO:0043547 positive regulation of GTPase activity;GO:0009791 post-embryonic development;GO:0050667 homocysteine metabolic process;GO:1901290 succinyl-CoA biosynthetic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZKG1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F1M5R1-1",
        "uniprot_id": "F1M5R1_RAT",
        "mass": 66235.0,
        "length": 595,
        "protein_name": "REL proto-oncogene, NF-kB subunit",
        "gene_name": "Rel",
        "organism": "Rat",
        "refseq_name": "proto-oncogene c-Rel",
        "refseq_ac": "NP_001408243",
        "gene_names_uniprotkb": "Rel",
        "gene_names_refseq": "Rel",
        "protein_names_uniprotkb": "REL proto-oncogene, NF-kB subunit",
        "protein_names_refseq": "proto-oncogene c-Rel; reticuloendotheliosis oncogene; v-rel avian reticuloendotheliosis viral oncogene homolog; v-rel reticuloendotheliosis viral oncogene homolog",
        "tax_id": 10116,
        "disease": "immunodeficiency 92 (Disease Ontology:DOID:0061062); bacterial infectious disease (Disease Ontology:DOID:104); breast cancer (Disease Ontology:DOID:1612); transitional cell carcinoma (Disease Ontology:DOID:2671)",
        "pathway": " (rno:305584);  (R-RNO-1169091)",
        "pathway_count": 2,
        "publication_count": 3,
        "publication_id_list": "23564451;24605601;24853588",
        "class_list": "",
        "function": "Data indicate that C-rel binding on the interleukin-2 (IL-2) promoter region declined in the aged CD4+T cells., [RefSeq, PubMed]; Expression of p65 and c-Rel implies that these subunits of NF-kappaB appear to contribute to the mechanisms of brain adaptation to severe hypoxia., [RefSeq, PubMed]; PACAP promotes both survival and neuritogenesis in PC12 cells by activating NF-kappaB pathway, most likely via classical and alternative signaling cascades involving ERK1/2 kinases, Ca(2+), and c-Rel/p52 dimers., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "predicted_o_glycosites": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0003700 DNA-binding transcription factor activity;GO:0043565 sequence-specific DNA binding;GO:0001228 DNA-binding transcription activator activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006954 inflammatory response;GO:0045087 innate immune response;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0034097 response to cytokine",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "F1M5R1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F1LW91-1",
        "uniprot_id": "F1LW91_RAT",
        "mass": 236744.0,
        "length": 2106,
        "protein_name": "Nuclear mitotic apparatus protein 1",
        "gene_name": "Numa1",
        "organism": "Rat",
        "refseq_name": "nuclear mitotic apparatus protein 1 isoform X2",
        "refseq_ac": "XP_038969278",
        "gene_names_uniprotkb": "Numa1",
        "gene_names_refseq": "Numa1",
        "protein_names_uniprotkb": "Nuclear mitotic apparatus protein 1",
        "protein_names_refseq": "nuclear mitotic apparatus protein 1 isoform X2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:308870);  (R-RNO-380320);  (R-RNO-68875)",
        "pathway_count": 3,
        "publication_count": 2,
        "publication_id_list": "22673903;29393594",
        "class_list": "",
        "function": "",
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        "total_reported_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0008017 microtubule binding;GO:0019904 protein domain specific binding;GO:0044877 protein-containing complex binding;GO:0051010 microtubule plus-end binding;GO:0070840 dynein complex binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0055028 cortical microtubule;GO:1905720 cytoplasmic microtubule bundle;GO:0000922 spindle pole;GO:0005634 nucleus",
        "go_biological_process": "GO:0055048 anastral spindle assembly;GO:1902365 positive regulation of protein localization to spindle pole body;GO:1902846 positive regulation of mitotic spindle elongation;GO:1905820 positive regulation of chromosome separation;GO:0051984 positive regulation of chromosome segregation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "F1LW91-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q5PQK2-1",
        "uniprot_id": "Q5PQK2_RAT",
        "mass": 52371.0,
        "length": 515,
        "protein_name": "RNA-binding protein FUS",
        "gene_name": "Fus",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Fus",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "RNA-binding protein FUS",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "amyotrophic lateral sclerosis type 6 (Disease Ontology:DOID:0060198); essential tremor 4 (Disease Ontology:DOID:0111431); sarcoma (Disease Ontology:DOID:1115); neurodegenerative disease (Disease Ontology:DOID:1289); amyotrophic lateral sclerosis (Disease Ontology:DOID:332); liposarcoma (Disease Ontology:DOID:3382); frontotemporal dementia (Disease Ontology:DOID:9255)",
        "pathway": " (rno:317385);  (R-RNO-72163);  (R-RNO-72203);  (R-RNO-9770562)",
        "pathway_count": 4,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "DNA/RNA-binding protein that plays a role in various cellular processes such as transcription regulation, RNA splicing, RNA transport, DNA repair and damage response. Binds to ssRNA containing the consensus sequence 5'-AGGUAA-3'. Binds to nascent pre-mRNAs and acts as a molecular mediator between RNA polymerase II and U1 small nuclear ribonucleoprotein thereby coupling transcription and splicing. Also binds its own pre-mRNA and autoregulates its expression; this autoregulation mechanism is mediated by non-sense-mediated decay. Plays a role in DNA repair mechanisms by promoting D-loop formation and homologous recombination during DNA double-strand break repair. In neuronal cells, plays crucial roles in dendritic spine formation and stability, RNA transport, mRNA stability and synaptic homeostasis., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003723 RNA binding;GO:0008270 zinc ion binding;GO:0003682 chromatin binding;GO:0003713 transcription coactivator activity;GO:0042802 identical protein binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0098978 glutamatergic synapse;GO:0098982 GABA-ergic synapse;GO:0005654 nucleoplasm;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0006355 regulation of DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0048255 mRNA stabilization;GO:0051260 protein homooligomerization;GO:1990000 amyloid fibril formation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "Q5PQK2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A0G2JYJ7-1",
        "uniprot_id": "A0A0G2JYJ7_RAT",
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        "length": 405,
        "protein_name": "RNA binding motif, single stranded interacting protein 2",
        "gene_name": "Rbms2",
        "organism": "Rat",
        "refseq_name": "RNA-binding motif, single-stranded-interacting protein 2 isoform X1",
        "refseq_ac": "XP_063119154",
        "gene_names_uniprotkb": "Rbms2",
        "gene_names_refseq": "Rbms2",
        "protein_names_uniprotkb": "RNA binding motif, single stranded interacting protein 2",
        "protein_names_refseq": "RNA-binding motif, single-stranded-interacting protein 2 isoform X1",
        "tax_id": 10116,
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        "pathway_count": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003723 RNA binding;GO:0003730 mRNA 3'-UTR binding;GO:0008143 poly(A) binding;GO:0008266 poly(U) RNA binding",
        "go_cellular_component": "GO:1990904 ribonucleoprotein complex;GO:0005634 nucleus;GO:0005829 cytosol",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A0G2JYJ7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A0G2K0G9-1",
        "uniprot_id": "A0A0G2K0G9_RAT",
        "mass": 107717.0,
        "length": 984,
        "protein_name": "Ras and Rab interactor 3",
        "gene_name": "Rin3",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Rin3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ras and Rab interactor 3",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:314397);  (R-RNO-8876198)",
        "pathway_count": 2,
        "publication_count": 0,
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        "class_list": "",
        "function": "",
        "predicted_glycosites": 3,
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        "go_molecular_function": "GO:0005096 GTPase activator activity;GO:0005085 guanyl-nucleotide exchange factor activity;GO:0031267 small GTPase binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005769 early endosome;GO:0005829 cytosol;GO:0030424 axon;GO:0030425 dendrite",
        "go_biological_process": "GO:0007165 signal transduction;GO:0016192 vesicle-mediated transport;GO:0097494 regulation of vesicle size;GO:0002091 negative regulation of receptor internalization;GO:0060755 negative regulation of mast cell chemotaxis",
        "synthesized_glycan_count": 0,
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        "record_id": "A0A0G2K0G9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V8L0-1",
        "uniprot_id": "G3V8L0_RAT",
        "mass": 88267.0,
        "length": 790,
        "protein_name": "GATOR2 complex protein WDR24",
        "gene_name": "Wdr24",
        "organism": "Rat",
        "refseq_name": "GATOR2 complex protein WDR24",
        "refseq_ac": "NP_001178013",
        "gene_names_uniprotkb": "Wdr24",
        "gene_names_refseq": "RGD1304803; Wdr24",
        "protein_names_uniprotkb": "GATOR2 complex protein WDR24; 2.3.2.27; WD repeat-containing protein 24",
        "protein_names_refseq": "GATOR complex protein WDR24; GATOR2 complex protein WDR24; WD repeat-containing protein 24",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:360497);  (R-RNO-9639288)",
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        "publication_id_list": "",
        "class_list": "",
        "function": "Catalytic component of the GATOR2 complex, a multiprotein complex that acts as an activator of the amino acid-sensing branch of the mTORC1 signaling pathway. The GATOR2 complex indirectly activates mTORC1 through the inhibition of the GATOR1 subcomplex. GATOR2 probably acts as an E3 ubiquitin-protein ligase toward GATOR1. In the presence of abundant amino acids, the GATOR2 complex mediates ubiquitination of the NPRL2 core component of the GATOR1 complex, leading to GATOR1 inactivation. In the absence of amino acids, GATOR2 is inhibited, activating the GATOR1 complex. In addition to its role in regulation of the mTORC1 complex, promotes the acidification of lysosomes and facilitates autophagic flux. Within the GATOR2 complex, WDR24 constitutes the catalytic subunit that mediates 'Lys-6'-linked ubiquitination of NPRL2., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
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        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "7.1.2.2;2.1.1.-;2.3.2.27;2.7.10.2;2.7.11.1;3.6.5.-",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0061630 ubiquitin protein ligase activity",
        "go_cellular_component": "GO:0005765 lysosomal membrane;GO:0061700 GATOR2 complex;GO:0005829 cytosol;GO:0005774 vacuolar membrane",
        "go_biological_process": "GO:1904263 positive regulation of TORC1 signaling;GO:0010506 regulation of autophagy;GO:0006914 autophagy;GO:0034198 cellular response to amino acid starvation;GO:0085020 protein K6-linked ubiquitination",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "G3V8L0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A0G2K1B6-1",
        "uniprot_id": "A0A0G2K1B6_RAT",
        "mass": 54206.0,
        "length": 494,
        "protein_name": "Nuclear factor 1",
        "gene_name": "Nfix",
        "organism": "Rat",
        "refseq_name": "nuclear factor 1 X-type isoform X5",
        "refseq_ac": "XP_063134373",
        "gene_names_uniprotkb": "Nfix; Nf1x",
        "gene_names_refseq": "Nf1x; Nfix",
        "protein_names_uniprotkb": "Nuclear factor 1",
        "protein_names_refseq": "nuclear factor 1 X-type isoform X5",
        "tax_id": 10116,
        "disease": "Marshall-Smith syndrome (Disease Ontology:DOID:0050858); Sotos syndrome 2 (Disease Ontology:DOID:0112102); Scheuermann's disease (Disease Ontology:DOID:13300)",
        "pathway": " (rno:81524)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Recognizes and binds the palindromic sequence 5'-TTGGCNNNNNGCCAA-3' present in viral and cellular promoters and in the origin of replication of adenovirus type 2. These proteins are individually capable of activating transcription and replication., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_c_glycosites": 0,
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        "reported_c_glycosites": 0,
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        "reported_phosphosites": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 3,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0003700 DNA-binding transcription factor activity;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0003682 chromatin binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006260 DNA replication;GO:0045893 positive regulation of DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0014016 neuroblast differentiation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A0G2K1B6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A0G2K0P1-1",
        "uniprot_id": "A0A0G2K0P1_RAT",
        "mass": 96060.0,
        "length": 838,
        "protein_name": "Kinesin-associated protein 3",
        "gene_name": "Kifap3",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Kifap3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Kinesin-associated protein 3",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-2132295);  (R-RNO-5620924);  (R-RNO-6811434);  (R-RNO-983189)",
        "pathway_count": 4,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
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        "reported_o_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
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        "reported_c_glycosites_with_glycan": 0,
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        "reported_mutagensis": 0,
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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0019894 kinesin binding;GO:0019903 protein phosphatase binding;GO:0120170 intraciliary transport particle B binding",
        "go_cellular_component": "GO:0005871 kinesin complex;GO:0098978 glutamatergic synapse;GO:0000794 condensed nuclear chromosome;GO:0005783 endoplasmic reticulum;GO:0005794 Golgi apparatus",
        "go_biological_process": "GO:0098971 anterograde dendritic transport of neurotransmitter receptor complex;GO:0046587 positive regulation of calcium-dependent cell-cell adhesion;GO:0008285 negative regulation of cell population proliferation;GO:0043066 negative regulation of apoptotic process;GO:0007018 microtubule-based movement",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A0G2K0P1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "M0R629-1",
        "uniprot_id": "M0R629_RAT",
        "mass": 50250.0,
        "length": 457,
        "protein_name": "Adenylosuccinate synthetase isozyme 1",
        "gene_name": "Adss1",
        "organism": "Rat",
        "refseq_name": "adenylosuccinate synthase 1 isoform 1",
        "refseq_ac": "NP_001419071",
        "gene_names_uniprotkb": "Adss1; ADSS1; ADSSL1; Adssl1",
        "gene_names_refseq": "AdSS 1; Adss1; Adssl1",
        "protein_names_uniprotkb": "Adenylosuccinate synthetase isozyme 1; 6.3.4.4; AMPSase 1; AdSS 1; Adenylosuccinate synthetase, basic isozyme; Adenylosuccinate synthetase, muscle isozyme; IMP--aspartate ligase 1; M-type adenylosuccinate synthetase",
        "protein_names_refseq": "AMPSase 1; IMP--aspartate ligase 1; adenylosuccinate synthase 1 isoform 1; adenylosuccinate synthase like 1; adenylosuccinate synthetase isozyme 1; adenylosuccinate synthetase, muscle isozyme",
        "tax_id": 10116,
        "disease": "sarcoma (Disease Ontology:DOID:1115)",
        "pathway": " (rno:684425);  (R-RNO-73817)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Component of the purine nucleotide cycle (PNC), which interconverts IMP and AMP to regulate the nucleotide levels in various tissues, and which contributes to glycolysis and ammoniagenesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP., [UniProtKB, UniProtKB, HAMAP]; Plays an important role in the de novo pathway and in the salvage pathway of purine nucleotide biosynthesis. Catalyzes the first commited step in the biosynthesis of AMP from IMP., [UniProtKB, HAMAP]; Plays an important role in the de novo pathway of purine nucleotide biosynthesis., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
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        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "reported_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
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        "reported_c_glycosites_with_glycan": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "6.3.4.4",
        "go_molecular_function": "GO:0000287 magnesium ion binding;GO:0005525 GTP binding;GO:0004019 adenylosuccinate synthase activity;GO:0003924 GTPase activity;GO:0042802 identical protein binding",
        "go_cellular_component": "GO:0005737 cytoplasm",
        "go_biological_process": "GO:0044209 AMP salvage;GO:0044208 'de novo' AMP biosynthetic process;GO:0042594 response to starvation;GO:0046040 IMP metabolic process;GO:0071466 cellular response to xenobiotic stimulus",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "M0R629-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A0G2K069-1",
        "uniprot_id": "A0A0G2K069_RAT",
        "mass": 171721.0,
        "length": 1736,
        "protein_name": "Collagen alpha-2(XI) chain",
        "gene_name": "Col11a2",
        "organism": "Rat",
        "refseq_name": "collagen alpha-2(XI) chain isoform 1 precursor",
        "refseq_ac": "NP_001388231",
        "gene_names_uniprotkb": "Col11a2",
        "gene_names_refseq": "Col11a2",
        "protein_names_uniprotkb": "Collagen alpha-2(XI) chain",
        "protein_names_refseq": "collagen alpha-2(XI) chain isoform 1 precursor; collagen alpha-2(XI) chain-like; collagen, type XI, alpha 2; procollagen, type XI, alpha 2; type XI collagen alpha2 chain",
        "tax_id": 10116,
        "disease": "otospondylomegaepiphyseal dysplasia, autosomal recessive (Disease Ontology:DOID:0080026); Stickler syndrome (Disease Ontology:DOID:0080046); fibrochondrogenesis 2 (Disease Ontology:DOID:0080673); otospondylomegaepiphyseal dysplasia, autosomal dominant (Disease Ontology:DOID:0080677); autosomal recessive nonsyndromic deafness 53 (Disease Ontology:DOID:0110509); autosomal dominant nonsyndromic deafness 13 (Disease Ontology:DOID:0110545); osteochondrodysplasia (Disease Ontology:DOID:2256); cleft palate (Disease Ontology:DOID:674)",
        "pathway": " (rno:294279);  (R-RNO-1442490);  (R-RNO-1650814);  (R-RNO-2022090);  (R-RNO-3000171);  (R-RNO-8874081);  (R-RNO-8948216)",
        "pathway_count": 7,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "May play an important role in fibrillogenesis by controlling lateral growth of collagen II fibrils., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 8,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 8,
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        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
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        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
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        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 8,
        "glyco_site_count": 8,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005201 extracellular matrix structural constituent;GO:0046872 metal ion binding;GO:0030020 extracellular matrix structural constituent conferring tensile strength",
        "go_cellular_component": "GO:0031012 extracellular matrix;GO:0005576 extracellular region;GO:0005581 collagen trimer;GO:0005585 collagen type II trimer",
        "go_biological_process": "GO:0030199 collagen fibril organization;GO:0007605 sensory perception of sound;GO:0048705 skeletal system morphogenesis;GO:0051216 cartilage development;GO:0001894 tissue homeostasis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A0G2K069-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A0G2JVY9-1",
        "uniprot_id": "A0A0G2JVY9_RAT",
        "mass": 47054.0,
        "length": 418,
        "protein_name": "Cyclin-A2",
        "gene_name": "Ccna2",
        "organism": "Rat",
        "refseq_name": "cyclin-A2",
        "refseq_ac": "NP_446154",
        "gene_names_uniprotkb": "Ccna2",
        "gene_names_refseq": "Ccna2",
        "protein_names_uniprotkb": "Cyclin-A2",
        "protein_names_refseq": "cyclin-A2",
        "tax_id": 10116,
        "disease": "embryonal carcinoma (Disease Ontology:DOID:3308); myocardial infarction (Disease Ontology:DOID:5844)",
        "pathway": " (rno:114494);  (R-RNO-1538133);  (R-RNO-171319);  (R-RNO-174184);  (R-RNO-176408);  (R-RNO-187577);  (R-RNO-2559582);  (R-RNO-2559586);  (R-RNO-5689880);  (R-RNO-5693607);  (R-RNO-6804116);  (R-RNO-6804756);  (R-RNO-6804757);  (R-RNO-68911);  (R-RNO-68949);  (R-RNO-69017);  (R-RNO-69273);  (R-RNO-69478);  (R-RNO-69563);  (R-RNO-69656);  (R-RNO-75035)",
        "pathway_count": 21,
        "publication_count": 1,
        "publication_id_list": "27414783",
        "class_list": "",
        "function": "Cyclin which controls both the G1/S and the G2/M transition phases of the cell cycle. Functions through the formation of specific serine/threonine kinase holoenzyme complexes with the cyclin-dependent protein kinases CDK1 and CDK2. The cyclin subunit confers the substrate specificity of these complexes and differentially interacts with and activates CDK1 and CDK2 throughout the cell cycle., [UniProtKB, UniProtKB, UniProtKB]; SPINK3 along with Ccna2 and EGFR accelerated cell proliferation during rat liver regeneration via P38 MAPK, PKC, JAK-STAT and AKT pathways., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 2,
        "glyco_site_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0019901 protein kinase binding;GO:0019904 protein domain specific binding;GO:0016538 cyclin-dependent protein serine/threonine kinase regulator activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005815 microtubule organizing center",
        "go_biological_process": "GO:0043687 post-translational protein modification;GO:0051301 cell division;GO:0000086 G2/M transition of mitotic cell cycle;GO:0071456 cellular response to hypoxia;GO:0007265 Ras protein signal transduction",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A0G2JVY9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A096MJA9-1",
        "uniprot_id": "A0A096MJA9_RAT",
        "mass": 81087.0,
        "length": 722,
        "protein_name": "Aspartyl/asparaginyl beta-hydroxylase",
        "gene_name": "Asph",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Asph",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Aspartyl/asparaginyl beta-hydroxylase; 1.14.11.16; Aspartate beta-hydroxylase; Peptide-aspartate beta-dioxygenase",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "chromosome 16p11.2 deletion syndrome, 593-kb (Disease Ontology:DOID:0070515); cholangiocarcinoma (Disease Ontology:DOID:4947)",
        "pathway": " (R-RNO-2672351);  (R-RNO-5578775)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "38843836",
        "class_list": "",
        "function": "Specifically hydroxylates an Asp or Asn residue in certain epidermal growth factor-like (EGF) domains of a number of proteins., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "protein_name": "Transcriptional regulating factor 1",
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        "refseq_name": "transcriptional-regulating factor 1 isoform 1",
        "refseq_ac": "NP_001419757",
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        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0071393 cellular response to progesterone stimulus;GO:0006357 regulation of transcription by RNA polymerase II;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0045892 negative regulation of DNA-templated transcription",
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        "protein_name": "hyaluronoglucosaminidase",
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        "refseq_name": "inactive cell surface hyaluronidase CEMIP2",
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        "protein_names_refseq": "cell surface hyaluronidase; inactive cell surface hyaluronidase CEMIP2; transmembrane protein 2",
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        "protein_names_refseq": "intraflagellar transport 88 homolog; intraflagellar transport protein 88 homolog; tetratricopeptide repeat domain 10",
        "tax_id": 10116,
        "disease": "autosomal recessive polycystic kidney disease (Disease Ontology:DOID:0110861); silicosis (Disease Ontology:DOID:10325); scimitar syndrome (Disease Ontology:DOID:4297); mitral valve disease (Disease Ontology:DOID:61); autosomal dominant polycystic kidney disease (Disease Ontology:DOID:898)",
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        "function": "Positively regulates primary cilium biogenesis. Also involved in autophagy since it is required for trafficking of ATG16L and the expansion of the autophagic compartment., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "tax_id": 10116,
        "disease": "nonsyndromic aplasia cutis congenita (Disease Ontology:DOID:0080661)",
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        "gene_names_refseq": "RGD1566191; Tmem132b",
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        "gene_names_uniprotkb": "Dact2",
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        "protein_names_refseq": "dapper homolog 2, antagonist of beta-catenin; dapper homolog 2; dapper, antagonist of beta-catenin, homolog 2",
        "tax_id": 10116,
        "disease": "retinitis pigmentosa (Disease Ontology:DOID:10584); bile duct carcinoma (Disease Ontology:DOID:4897); pancreatic carcinoma (Disease Ontology:DOID:4905)",
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        "length": 281,
        "protein_name": "BEN domain containing 6",
        "gene_name": "Bend6",
        "organism": "Rat",
        "refseq_name": "BEN domain-containing protein 6",
        "refseq_ac": "NP_001380703",
        "gene_names_uniprotkb": "Bend6",
        "gene_names_refseq": "Bend6; RGD1310392",
        "protein_names_uniprotkb": "BEN domain containing 6",
        "protein_names_refseq": "BEN domain-containing protein 6",
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        "length": 321,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or8h10b; Or8h10c; Or8h10",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr532",
        "refseq_ac": "NP_001000563",
        "gene_names_uniprotkb": "Or8h10b; Or8h10c; Or8h10; Olr526; Olr532; Or8h10b; Or8h10c",
        "gene_names_refseq": "Olr532; Or8h10b; ratchr3-70270952-70269987_ORF",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 532; olfactory receptor Olr532; olfactory receptor gene Olr532",
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        "function": "Odorant receptor., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding",
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        "protein_name": "Small proline rich protein 2B",
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        "go_cellular_component": "GO:0036128 CatSper complex;GO:0097228 sperm principal piece;GO:0031514 motile cilium",
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        "record_type": "protein"
    },
    {
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        "length": 648,
        "protein_name": "Rab11 family-interacting protein 5",
        "gene_name": "Rab11fip5",
        "organism": "Rat",
        "refseq_name": "rab11 family-interacting protein 5",
        "refseq_ac": "NP_001386477",
        "gene_names_uniprotkb": "Rab11fip5",
        "gene_names_refseq": "Rab11fip5",
        "protein_names_uniprotkb": "Rab11 family-interacting protein 5; Rab11-interacting protein Rip11",
        "protein_names_refseq": "RAB11 family interacting protein 5 (class I); rab11 family-interacting protein 5",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:312502)",
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        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Rab effector involved in protein trafficking from apical recycling endosomes to the apical plasma membrane. Involved in insulin granule exocytosis. May regulate V-ATPase intracellular transport in response to extracellular acidosis., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0031267 small GTPase binding;GO:0043015 gamma-tubulin binding",
        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0031966 mitochondrial membrane;GO:0030658 transport vesicle membrane;GO:0031901 early endosome membrane;GO:0055038 recycling endosome membrane",
        "go_biological_process": "GO:0015031 protein transport;GO:0010817 regulation of hormone levels;GO:0070164 negative regulation of adiponectin secretion;GO:0098884 postsynaptic neurotransmitter receptor internalization;GO:0045055 regulated exocytosis",
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        "record_type": "protein"
    },
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        "uniprot_canonical_ac": "G3V8E3-1",
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        "protein_name": "LIM/homeobox protein Lhx3",
        "gene_name": "Lhx3",
        "organism": "Rat",
        "refseq_name": "LIM/homeobox protein Lhx3",
        "refseq_ac": "NP_001413926",
        "gene_names_uniprotkb": "Lhx3",
        "gene_names_refseq": "Lhx3",
        "protein_names_uniprotkb": "LIM/homeobox protein Lhx3",
        "protein_names_refseq": "LIM homeobox protein 3; LIM homeodomain protein 3a; LIM/homeobox protein Lhx3",
        "tax_id": 10116,
        "disease": "combined pituitary hormone deficiency 3 (Disease Ontology:DOID:0061021); hypopituitarism (Disease Ontology:DOID:9406)",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0001228 DNA-binding transcription activator activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005667 transcription regulator complex;GO:0000785 chromatin",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0043066 negative regulation of apoptotic process;GO:0006915 apoptotic process;GO:0001890 placenta development",
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        "hit_score": 0.1,
        "record_id": "G3V8E3-1",
        "record_type": "protein"
    },
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        "length": 198,
        "protein_name": "Proline rich and Gla domain 2",
        "gene_name": "Prrg2",
        "organism": "Rat",
        "refseq_name": "transmembrane gamma-carboxyglutamic acid protein 2 precursor",
        "refseq_ac": "NP_001425060",
        "gene_names_uniprotkb": "Prrg2",
        "gene_names_refseq": "Prrg2",
        "protein_names_uniprotkb": "Proline rich and Gla domain 2",
        "protein_names_refseq": "proline rich Gla (G-carboxyglutamic acid) 2; proline-rich Gla (G-carboxyglutamic acid) polypeptide 2; transmembrane gamma-carboxyglutamic acid protein 2 precursor; transmembrane gamma-carboxyglutamic acid protein 2",
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        "go_molecular_function": "GO:0004252 serine-type endopeptidase activity;GO:0005509 calcium ion binding",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005886 plasma membrane",
        "go_biological_process": "GO:0006508 proteolysis;GO:0007596 blood coagulation;GO:0051239 regulation of multicellular organismal process",
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    },
    {
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        "length": 1031,
        "protein_name": "MORC family CW-type zinc finger 2",
        "gene_name": "Morc2",
        "organism": "Rat",
        "refseq_name": "ATPase MORC2",
        "refseq_ac": "NP_001402037",
        "gene_names_uniprotkb": "Morc2",
        "gene_names_refseq": "Morc2a; Morc2; Zcwcc1",
        "protein_names_uniprotkb": "MORC family CW-type zinc finger 2",
        "protein_names_refseq": "ATPase MORC2; MORC family CW-type zinc finger protein 2; microrchidia 2A; zinc finger, CW-type with coiled-coil domain 1",
        "tax_id": 10116,
        "disease": "Charcot-Marie-Tooth disease axonal type 2Z (Disease Ontology:DOID:0110181)",
        "pathway": " (R-RNO-75105);  (R-RNO-9843970)",
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        "ec_number_list": "5.6.2.3;3.6.4.13;3.6.4.12;2.7.11.1;3.6.1.5;3.6.4.10;3.6.4.-;2.3.2.27;5.6.2.4;3.6.5.-;5.6.2.-;3.1.-.-;2.7.7.7;2.7.7.49;3.1.13.1;4.2.99.18;7.6.2.2;7.6.2.3;7.6.2.-;5.6.1.6;7.2.2.-;3.6.1.15;3.6.4.6;3.1.3.1;3.9.1.1;6.1.1.12;3.6.1.-;2.7.4.3;3.1.4.-;3.4.24.-;3.6.-.-;3.4.21.53;5.6.2.5",
        "go_molecular_function": "GO:0005524 ATP binding;GO:0008270 zinc ion binding;GO:0016787 hydrolase activity;GO:0000287 magnesium ion binding;GO:0003682 chromatin binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0016363 nuclear matrix",
        "go_biological_process": "GO:0006338 chromatin remodeling;GO:0006974 DNA damage response;GO:0140719 constitutive heterochromatin formation;GO:0141005 transposable element silencing by heterochromatin formation",
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        "record_id": "A0A0G2JWF7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7F4B1-1",
        "uniprot_id": "F7F4B1_RAT",
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        "length": 512,
        "protein_name": "MAPK/MAK/MRK overlapping kinase",
        "gene_name": "Mok",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Mok",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "MAPK/MAK/MRK overlapping kinase; 2.7.11.22; MOK protein kinase",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "renal cell carcinoma (Disease Ontology:DOID:4450)",
        "pathway": " (rno:362787)",
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        "publication_id_list": "",
        "class_list": "",
        "function": "Able to phosphorylate several exogenous substrates and to undergo autophosphorylation. Negatively regulates cilium length in a cAMP and mTORC1 signaling-dependent manner., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "ec_number_list": "2.7.11.1;2.7.12.1;2.7.1.153;2.7.1.137;2.7.11.24;2.7.11.25;2.7.11.22;2.7.11.23;2.7.4.6;2.7.1.154;2.7.11.38;2.7.11.17;2.7.11.21;2.7.12.2;2.7.1.40;2.7.11.12;2.7.11.26;2.7.11.34;2.7.10.2;2.7.1.150;2.7.11.13;4.1.1.32;2.7.11.19;2.7.2.3;2.7.11.11;2.7.11.31;3.1.3.16;2.7.11.4;2.3.1.48;3.1.11.-;2.7.13.3;2.7.4.18;3.1.24.-;3.4.19.12;2.7.11.39;2.4.99.18;2.7.11.10",
        "go_molecular_function": "GO:0004672 protein kinase activity;GO:0005524 ATP binding;GO:0004674 protein serine/threonine kinase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005929 cilium;GO:0097546 ciliary base",
        "go_biological_process": "GO:0035556 intracellular signal transduction",
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        "hit_score": 0.1,
        "record_id": "F7F4B1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A0G2K315-1",
        "uniprot_id": "A0A0G2K315_RAT",
        "mass": 181815.0,
        "length": 1650,
        "protein_name": "Centrosomal protein of 170 kDa",
        "gene_name": "Cep170",
        "organism": "Rat",
        "refseq_name": "centrosomal protein of 170 kDa isoform X1",
        "refseq_ac": "XP_063128063",
        "gene_names_uniprotkb": "Cep170",
        "gene_names_refseq": "Cep170; KAB1; Kab; Rhk1",
        "protein_names_uniprotkb": "Centrosomal protein of 170 kDa",
        "protein_names_refseq": "centrosomal protein of 170 kDa isoform X1",
        "tax_id": 10116,
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        "pathway_count": 0,
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        "publication_id_list": "22673903;38843836",
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        "function": "Plays a role in microtubule organization. Required for centriole subdistal appendage assembly., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005813 centrosome;GO:0005814 centriole;GO:0036064 ciliary basal body;GO:0120103 centriolar subdistal appendage;GO:0005819 spindle",
        "go_biological_process": "",
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        "hit_score": 0.5,
        "record_id": "A0A0G2K315-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A0G2K0L0-1",
        "uniprot_id": "A0A0G2K0L0_RAT",
        "mass": 70755.0,
        "length": 624,
        "protein_name": "Bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase 1",
        "gene_name": "Papss1",
        "organism": "Rat",
        "refseq_name": "bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase 1",
        "refseq_ac": "NP_001381988",
        "gene_names_uniprotkb": "Papss1",
        "gene_names_refseq": "Papss1",
        "protein_names_uniprotkb": "Bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase 1; 2.7.1.25; 2.7.7.4; Sulfurylase kinase 1",
        "protein_names_refseq": "bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:295443);  (R-RNO-174362)",
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        "publication_count": 0,
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        "class_list": "",
        "function": "Bifunctional enzyme with both ATP sulfurylase and APS kinase activity, which mediates two steps in the sulfate activation pathway. The first step is the transfer of a sulfate group to ATP to yield adenosine 5'-phosphosulfate (APS), and the second step is the transfer of a phosphate group from ATP to APS yielding 3'-phosphoadenylylsulfate (PAPS: activated sulfate donor used by sulfotransferase). In mammals, PAPS is the sole source of sulfate; APS appears to be only an intermediate in the sulfate-activation pathway. Required for normal biosynthesis of sulfated L-selectin ligands in endothelial cells., [UniProtKB, UniProtKB]",
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        "ec_number_list": "2.7.1.25;2.7.7.4",
        "go_molecular_function": "GO:0005524 ATP binding;GO:0016301 kinase activity;GO:0004781 sulfate adenylyltransferase (ATP) activity;GO:0042803 protein homodimerization activity;GO:0004020 adenylylsulfate kinase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005829 cytosol",
        "go_biological_process": "GO:0000103 sulfate assimilation;GO:0050428 3'-phosphoadenosine 5'-phosphosulfate biosynthetic process;GO:0044272 sulfur compound biosynthetic process",
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    },
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        "uniprot_canonical_ac": "A0A0G2K302-1",
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        "protein_name": "Adaptor related protein complex 3 subunit sigma 2",
        "gene_name": "Ap3s2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ap3s2",
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        "protein_names_uniprotkb": "Adaptor related protein complex 3 subunit sigma 2",
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        "function": "Part of the AP-3 complex, an adaptor-related complex which is not clathrin-associated. The complex is associated with the Golgi region as well as more peripheral structures. It facilitates the budding of vesicles from the Golgi membrane and may be directly involved in trafficking to lysosomes. In concert with the BLOC-1 complex, AP-3 is required to target cargos into vesicles assembled at cell bodies for delivery into neurites and nerve terminals., [UniProtKB, UniProtKB, UniProtKB]",
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        "protein_name": "V-type proton ATPase subunit G",
        "gene_name": "Atp6v1g2",
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        "refseq_name": "V-type proton ATPase subunit G 2",
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        "gene_names_uniprotkb": "Atp6v1g2",
        "gene_names_refseq": "ATP6G; Atp6g2; Atp6v1g2; NG38",
        "protein_names_uniprotkb": "V-type proton ATPase subunit G",
        "protein_names_refseq": "ATPase, H+ transporting, V1 subunit G; ATPase, H+ transporting, lysosomal V1 subunit G2; V-type proton ATPase subunit G 2; lysosomal ATPase; vacuolar ATPase NG38",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:368044);  (R-RNO-1222556);  (R-RNO-77387);  (R-RNO-917977);  (R-RNO-9639288);  (R-RNO-983712)",
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        "publication_id_list": "32165585;38900912",
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        "function": "Subunit of the V1 complex of vacuolar(H+)-ATPase (V-ATPase), a multisubunit enzyme composed of a peripheral complex (V1) that hydrolyzes ATP and a membrane integral complex (V0) that translocates protons. V-ATPase is responsible for acidifying and maintaining the pH of intracellular compartments and in some cell types, is targeted to the plasma membrane, where it is responsible for acidifying the extracellular environment., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0046961 proton-transporting ATPase activity, rotational mechanism;GO:0008553 P-type proton-exporting transporter activity;GO:0016887 ATP hydrolysis activity",
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        "record_id": "Q8R2H0-1",
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        "refseq_name": "peptide chain release factor 1, mitochondrial isoform X2",
        "refseq_ac": "XP_063130713",
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        "gene_names_refseq": "Mtrf1",
        "protein_names_uniprotkb": "Mitochondrial translation release factor 1",
        "protein_names_refseq": "peptide chain release factor 1, mitochondrial isoform X2",
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        "go_molecular_function": "GO:0003747 translation release factor activity;GO:0016149 translation release factor activity, codon specific",
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        "go_biological_process": "GO:0070126 mitochondrial translational termination",
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        "record_id": "M0RDC8-1",
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    },
    {
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        "length": 623,
        "protein_name": "Forkhead box J2",
        "gene_name": "Foxj2",
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        "refseq_name": "forkhead box protein J2 isoform X1",
        "refseq_ac": "XP_006237373",
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        "gene_names_refseq": "Foxj2; RGD1565101",
        "protein_names_uniprotkb": "Forkhead box J2",
        "protein_names_refseq": "forkhead box protein J2 isoform X1",
        "tax_id": 10116,
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        "pathway": " (rno:502886)",
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        "go_molecular_function": "GO:0003700 DNA-binding transcription factor activity;GO:0043565 sequence-specific DNA binding;GO:0042802 identical protein binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0001650 fibrillar center",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0007141 male meiosis I;GO:0110059 negative regulation of blood vessel endothelial cell differentiation;GO:0006357 regulation of transcription by RNA polymerase II;GO:0007283 spermatogenesis",
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    {
        "uniprot_canonical_ac": "Q5EBC0-1",
        "uniprot_id": "Q5EBC0_RAT",
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        "length": 933,
        "protein_name": "Inter-alpha-trypsin inhibitor heavy chain 4",
        "gene_name": "Itih4",
        "organism": "Rat",
        "refseq_name": "inter-alpha-trypsin inhibitor heavy chain H4 precursor",
        "refseq_ac": "NP_062242",
        "gene_names_uniprotkb": "Itih4",
        "gene_names_refseq": "Itih4",
        "protein_names_uniprotkb": "Inter-alpha-trypsin inhibitor heavy chain 4",
        "protein_names_refseq": "inter-alpha-inhibitor H4 heavy chain; inter-alpha-trypsin inhibitor heavy chain H4 precursor; inter-alpha-trypsin inhibitor heavy chain H4; inter-alpha-trypsin inhibitor heavy chain family, member 4",
        "tax_id": 10116,
        "disease": "pulmonary tuberculosis (Disease Ontology:DOID:2957); amyotrophic lateral sclerosis (Disease Ontology:DOID:332); liver cirrhosis (Disease Ontology:DOID:5082); myocardial infarction (Disease Ontology:DOID:5844); hepatocellular carcinoma (Disease Ontology:DOID:684); intermediate coronary syndrome (Disease Ontology:DOID:8805); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (rno:54404);  (R-RNO-114608)",
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        "go_molecular_function": "GO:0004867 serine-type endopeptidase inhibitor activity",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0005615 extracellular space;GO:0005737 cytoplasm;GO:0005886 plasma membrane",
        "go_biological_process": "GO:0006953 acute-phase response;GO:0034097 response to cytokine",
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        "record_id": "Q5EBC0-1",
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    },
    {
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        "uniprot_id": "A0A0G2JVH5_RAT",
        "mass": 113255.0,
        "length": 1003,
        "protein_name": "Helicase-like transcription factor",
        "gene_name": "Hltf",
        "organism": "Rat",
        "refseq_name": "helicase-like transcription factor isoform 2",
        "refseq_ac": "NP_001426369",
        "gene_names_uniprotkb": "Hltf",
        "gene_names_refseq": "Hltf; Smarca3; Snf2l3",
        "protein_names_uniprotkb": "Helicase-like transcription factor",
        "protein_names_refseq": "SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 3; helicase-like transcription factor isoform 2",
        "tax_id": 10116,
        "disease": "gastrointestinal system cancer (Disease Ontology:DOID:3119)",
        "pathway": " (rno:295568);  (R-RNO-8866654)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "21507896",
        "class_list": "",
        "function": "Circadian Prl transcription depended on an interaction between the pituitary-specific transcription factor, PIT-1, and the helicase-like transcription factor (HLTF), a SWI/SNF chromatin remodeler., [RefSeq, PubMed]",
        "predicted_glycosites": 1,
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        "go_molecular_function": "GO:0005524 ATP binding;GO:0008270 zinc ion binding;GO:0003676 nucleic acid binding;GO:0004386 helicase activity;GO:0016818 hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides",
        "go_cellular_component": "GO:0005634 nucleus;GO:0043596 nuclear replication fork;GO:0005654 nucleoplasm;GO:0000785 chromatin;GO:0090575 RNA polymerase II transcription regulator complex",
        "go_biological_process": "GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0006974 DNA damage response;GO:0000209 protein polyubiquitination;GO:0070534 protein K63-linked ubiquitination;GO:0042789 mRNA transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
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        "record_id": "A0A0G2JVH5-1",
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    {
        "uniprot_canonical_ac": "A0A0G2JU45-1",
        "uniprot_id": "A0A0G2JU45_RAT",
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        "length": 496,
        "protein_name": "tRNA (guanine(37)-N1)-methyltransferase",
        "gene_name": "Trmt5",
        "organism": "Rat",
        "refseq_name": "tRNA (guanine(37)-N1)-methyltransferase isoform X1",
        "refseq_ac": "XP_038968435",
        "gene_names_uniprotkb": "Trmt5; TRM5; TRMT5",
        "gene_names_refseq": "RGD1306567; Trmt5",
        "protein_names_uniprotkb": "tRNA (guanine(37)-N1)-methyltransferase; 2.1.1.228; M1G-methyltransferase; tRNA [GM37] methyltransferase; tRNA methyltransferase 5 homolog",
        "protein_names_refseq": "tRNA (guanine(37)-N1)-methyltransferase isoform X1",
        "tax_id": 10116,
        "disease": "mitochondrial complex I deficiency (Disease Ontology:DOID:0060536); mitochondrial complex III deficiency (Disease Ontology:DOID:0111139); combined oxidative phosphorylation deficiency 26 (Disease Ontology:DOID:0111490); hypertrophic cardiomyopathy (Disease Ontology:DOID:11984); hypercalcemia (Disease Ontology:DOID:12678); lactic acidosis (Disease Ontology:DOID:3650); cytochrome-c oxidase deficiency disease (Disease Ontology:DOID:3762); mitochondrial myopathy (Disease Ontology:DOID:699)",
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        "publication_id_list": "",
        "class_list": "",
        "function": "Involved in mitochondrial tRNA methylation. Specifically methylates the N1 position of guanosine-37 in various tRNAs. Methylation is not dependent on the nature of the nucleoside 5' of the target nucleoside. This is the first step in the biosynthesis of wybutosine (yW), a modified base adjacent to the anticodon of tRNAs and required for accurate decoding., [UniProtKB, UniProtKB, UniProtKB]; Specifically methylates the N1 position of guanosine-37 in various cytoplasmic and mitochondrial tRNAs. Methylation is not dependent on the nature of the nucleoside 5' of the target nucleoside. This is the first step in the biosynthesis of wybutosine (yW), a modified base adjacent to the anticodon of tRNAs and required for accurate decoding., [UniProtKB, HAMAP, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
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        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 8,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "2.1.1.228",
        "go_molecular_function": "GO:0052906 tRNA (guanine(37)-N1)-methyltransferase activity;GO:0008175 tRNA methyltransferase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005759 mitochondrial matrix;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0030488 tRNA methylation;GO:0002939 tRNA N1-guanine methylation;GO:0070901 mitochondrial tRNA methylation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A0G2JU45-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q8R490-1",
        "uniprot_id": "Q8R490_RAT",
        "mass": 78086.0,
        "length": 714,
        "protein_name": "Cadherin-13",
        "gene_name": "Cdh13",
        "organism": "Rat",
        "refseq_name": "cadherin-13 precursor",
        "refseq_ac": "NP_620244",
        "gene_names_uniprotkb": "Cdh13",
        "gene_names_refseq": "Cdh13; Cdht; T-cadherin; Tcad",
        "protein_names_uniprotkb": "Cadherin-13",
        "protein_names_refseq": "cadherin-13 precursor",
        "tax_id": 10116,
        "disease": "prostate cancer (Disease Ontology:DOID:10283); urinary bladder cancer (Disease Ontology:DOID:11054); breast cancer (Disease Ontology:DOID:1612); arteriosclerosis (Disease Ontology:DOID:2349); ovarian cancer (Disease Ontology:DOID:2394); endometrial carcinoma (Disease Ontology:DOID:2871); substance-related disorder (Disease Ontology:DOID:303); breast carcinoma (Disease Ontology:DOID:3459); lung non-small cell carcinoma (Disease Ontology:DOID:3908); coronary restenosis (Disease Ontology:DOID:4247); cervical cancer (Disease Ontology:DOID:4362)",
        "pathway": " (rno:192248);  (R-RNO-418990)",
        "pathway_count": 2,
        "publication_count": 5,
        "publication_id_list": "24090084;28387990;28392425;28657654;38843836",
        "class_list": "",
        "function": "Cadherins are calcium-dependent cell adhesion proteins. They preferentially interact with themselves in a homophilic manner in connecting cells; cadherins may thus contribute to the sorting of heterogeneous cell types. May act as a negative regulator of neural cell growth., [UniProtKB, UniProtKB, UniProtKB]; Cdh13 regulates sensitivity to psychomotor stimulants and palatable rewards without producing major changes in other behaviors., [RefSeq, PubMed]; Using rat and murine aortic smooth muscle cells as experimental models, we surveyed the ability of T-cadherin to regulate autophagy in SMCs during serum-starvation stress. Overall our findings have identified T-cadherin as a novel positive regulator of autophagy and survival in smooth muscle cells, [RefSeq, PubMed]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_c_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 2,
        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 2,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
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        "reported_fully_resolved_glycans": 1,
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        "reported_mutagensis": 0,
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        "missing_score": 0,
        "biomarker_type": "",
        "glycan_count": 1,
        "disease_count": 11,
        "glyco_site_count": 2,
        "binding_glycan_count": 0,
        "secondary_ac_list": "A6IZI0",
        "ec_number_list": "",
        "go_molecular_function": "GO:0042802 identical protein binding;GO:0005509 calcium ion binding;GO:0045296 cadherin binding;GO:0071813 lipoprotein particle binding;GO:0030169 low-density lipoprotein particle binding",
        "go_cellular_component": "GO:0098982 GABA-ergic synapse;GO:0005615 extracellular space;GO:0005737 cytoplasm;GO:0005886 plasma membrane;GO:0045202 synapse",
        "go_biological_process": "GO:0007162 negative regulation of cell adhesion;GO:0008285 negative regulation of cell population proliferation;GO:0030100 regulation of endocytosis;GO:0030335 positive regulation of cell migration;GO:0045944 positive regulation of transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
        "hit_score": 0.9,
        "record_id": "Q8R490-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V858-1",
        "uniprot_id": "G3V858_RAT",
        "mass": 128767.0,
        "length": 1125,
        "protein_name": "Exportin-6",
        "gene_name": "Xpo6",
        "organism": "Rat",
        "refseq_name": "exportin-6",
        "refseq_ac": "NP_001011935",
        "gene_names_uniprotkb": "Xpo6; LOC100912006",
        "gene_names_refseq": "Xpo6",
        "protein_names_uniprotkb": "Exportin-6; Ran-binding protein 20",
        "protein_names_refseq": "exportin-6",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:293476)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Mediates the nuclear export of actin and profilin-actin complexes in somatic cells., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
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        "reported_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0031267 small GTPase binding;GO:0005049 nuclear export signal receptor activity",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005829 cytosol;GO:0032991 protein-containing complex;GO:0005634 nucleus",
        "go_biological_process": "GO:0006611 protein export from nucleus",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "G3V858-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V896-1",
        "uniprot_id": "G3V896_RAT",
        "mass": 15038.0,
        "length": 135,
        "protein_name": "C-C motif chemokine",
        "gene_name": "Ccl28",
        "organism": "Rat",
        "refseq_name": "C-C motif chemokine 28 precursor",
        "refseq_ac": "NP_446152",
        "gene_names_uniprotkb": "Ccl28",
        "gene_names_refseq": "Ccl28; Scya28",
        "protein_names_uniprotkb": "C-C motif chemokine",
        "protein_names_refseq": "C-C motif chemokine 28 precursor; C-C motif chemokine 28; CC chemokine CCL28; chemokine (C-C motif) ligand 28",
        "tax_id": 10116,
        "disease": "hypertension (Disease Ontology:DOID:10763); atopic dermatitis (Disease Ontology:DOID:3310); lymphopenia (Disease Ontology:DOID:614)",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 3,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008009 chemokine activity",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0030141 secretory granule",
        "go_biological_process": "GO:0007204 positive regulation of cytosolic calcium ion concentration;GO:0007584 response to nutrient;GO:0061844 antimicrobial humoral immune response mediated by antimicrobial peptide;GO:0060326 cell chemotaxis;GO:0001954 positive regulation of cell-matrix adhesion",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "G3V896-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V8C7-1",
        "uniprot_id": "G3V8C7_RAT",
        "mass": 22043.0,
        "length": 204,
        "protein_name": "Msh homeobox 3",
        "gene_name": "Msx3",
        "organism": "Rat",
        "refseq_name": "homeo box, msh-like 3",
        "refseq_ac": "NP_446164",
        "gene_names_uniprotkb": "Msx3",
        "gene_names_refseq": "Msx3",
        "protein_names_uniprotkb": "Msh homeobox 3",
        "protein_names_refseq": "homeo box, msh-like 3",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:114504)",
        "pathway_count": 1,
        "publication_count": 0,
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        "class_list": "",
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        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0035034 histone acetyltransferase regulator activity;GO:0035035 histone acetyltransferase binding",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0048598 embryonic morphogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "G3V8C7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V8L4-1",
        "uniprot_id": "G3V8L4_RAT",
        "mass": 40186.0,
        "length": 392,
        "protein_name": "Single stranded DNA binding protein 4",
        "gene_name": "Ssbp4",
        "organism": "Rat",
        "refseq_name": "single-stranded DNA-binding protein 4 isoform X2",
        "refseq_ac": "XP_038950642",
        "gene_names_uniprotkb": "Ssbp4",
        "gene_names_refseq": "Ssbp4",
        "protein_names_uniprotkb": "Single stranded DNA binding protein 4",
        "protein_names_refseq": "single-stranded DNA-binding protein 4 isoform X2",
        "tax_id": 10116,
        "disease": "autism spectrum disorder (Disease Ontology:DOID:0060041)",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 2,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 2,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003713 transcription coactivator activity;GO:0003697 single-stranded DNA binding",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0045944 positive regulation of transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "G3V8L4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V8Q8-1",
        "uniprot_id": "G3V8Q8_RAT",
        "mass": 110943.0,
        "length": 999,
        "protein_name": "SEC23-interacting protein",
        "gene_name": "Sec23ip",
        "organism": "Rat",
        "refseq_name": "SEC23-interacting protein",
        "refseq_ac": "NP_001128331",
        "gene_names_uniprotkb": "Sec23ip",
        "gene_names_refseq": "Sec23ip",
        "protein_names_uniprotkb": "SEC23-interacting protein",
        "protein_names_refseq": "SEC23-interacting protein",
        "tax_id": 10116,
        "disease": "hereditary spastic paraplegia 28 (Disease Ontology:DOID:0110779); hereditary spastic paraplegia 54 (Disease Ontology:DOID:0110806); hereditary spastic paraplegia (Disease Ontology:DOID:2476)",
        "pathway": " (rno:309010);  (R-RNO-204005)",
        "pathway_count": 2,
        "publication_count": 2,
        "publication_id_list": "18683930;22673903",
        "class_list": "",
        "function": "Plays a role in the organization of endoplasmic reticulum exit sites. Specifically binds to phosphatidylinositol 3-phosphate (PI(3)P), phosphatidylinositol 4-phosphate (PI(4)P) and phosphatidylinositol 5-phosphate (PI(5)P)., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "reported_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 1,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 1,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 1,
        "total_c_glycosites": 0,
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        "reported_fully_resolved_glycans": 1,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
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        "missing_score": 0,
        "biomarker_type": "",
        "glycan_count": 1,
        "disease_count": 3,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0046872 metal ion binding;GO:0004620 phospholipase activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005794 Golgi apparatus;GO:0030134 COPII-coated ER to Golgi transport vesicle;GO:0048471 perinuclear region of cytoplasm;GO:0097038 perinuclear endoplasmic reticulum",
        "go_biological_process": "GO:0007286 spermatid development;GO:0007338 single fertilization;GO:0001675 acrosome assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.5,
        "record_id": "G3V8Q8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V8R8-1",
        "uniprot_id": "KCNK6_RAT",
        "mass": 34183.0,
        "length": 313,
        "protein_name": "Potassium channel subfamily K member 6",
        "gene_name": "Kcnk6",
        "organism": "Rat",
        "refseq_name": "potassium channel subfamily K member 6",
        "refseq_ac": "NP_446258",
        "gene_names_uniprotkb": "Kcnk6",
        "gene_names_refseq": "Kcnk6; Twik-2; Twik2",
        "protein_names_uniprotkb": "Potassium channel subfamily K member 6",
        "protein_names_refseq": "potassium channel subfamily K member 6-like; potassium channel subfamily K member 6; potassium channel, subfamily K, member 6; potassium channel, two pore domain subfamily K, member 6; potassium inwardly-rectifying channel, subfamily K, member 6",
        "tax_id": 10116,
        "disease": "brain infarction (Disease Ontology:DOID:3454)",
        "pathway": " (rno:116491);  (R-RNO-1299308);  (R-RNO-5576886)",
        "pathway_count": 3,
        "publication_count": 5,
        "publication_id_list": "10887187;18838117;19363137;28381826;29393594",
        "class_list": "",
        "function": "Although K(2P) channels are highly expressed, K(2P) currents are not activated via the NO/cGMP pathway in rat middle cerebral artery smooth muscle, despite the presence of numerous putative PKG phosphorylation sites, [RefSeq, PubMed]; Does not display channel activity., [UniProtKB, PubMed]; K(+) channel that conducts outward rectifying currents at the membranes of the endolysosomal system (PubMed:10887187, PubMed:28381826). Active in lysosomes where it regulates lysosome numbers and size (PubMed:28381826). In macrophages, enables K(+) efflux coupled to ATP-induced NLRP3 inflammasome activation upon bacterial infection. Cooperates with ATP-gated P2RX7 channels to activate NLRP3 inflammasome, with P2RX7 conducting Ca(2+) and Na(+) influx that sets the membrane potential for K(+) efflux (By similarity)., [UniProtKB, UniProtKB, PubMed, PubMed]; K(2P)6.1 (TWIK 2) immunoreactivity was detected in nerve terminals, blood vessels hair cells and transitional cells of the crista ampullaris and in the somata and neuron fibers of Scarpa's ganglia., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "binding_glycan_count": 0,
        "secondary_ac_list": "Q9ERU4;Q9ERU5",
        "ec_number_list": "1.8.-.-",
        "go_molecular_function": "GO:0015271 outward rectifier potassium channel activity;GO:0022841 potassium ion leak channel activity;GO:0046872 metal ion binding;GO:0005267 potassium channel activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0005765 lysosomal membrane;GO:0031902 late endosome membrane",
        "go_biological_process": "GO:0003085 negative regulation of systemic arterial blood pressure;GO:0003073 regulation of systemic arterial blood pressure;GO:0060075 regulation of resting membrane potential;GO:0071805 potassium ion transmembrane transport;GO:1900227 positive regulation of NLRP3 inflammasome complex assembly",
        "synthesized_glycan_count": 0,
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        "record_id": "G3V8R8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V8S6-1",
        "uniprot_id": "G3V8S6_RAT",
        "mass": 86503.0,
        "length": 754,
        "protein_name": "Histidine rich calcium binding protein",
        "gene_name": "Hrc",
        "organism": "Rat",
        "refseq_name": "sarcoplasmic reticulum histidine-rich calcium-binding protein precursor",
        "refseq_ac": "NP_852034",
        "gene_names_uniprotkb": "Hrc",
        "gene_names_refseq": "Hrc",
        "protein_names_uniprotkb": "Histidine rich calcium binding protein",
        "protein_names_refseq": "sarcoplasmic reticulum histidine-rich calcium-binding protein precursor; sarcoplasmic reticulum histidine-rich calcium-binding protein",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:292905);  (R-RNO-381426);  (R-RNO-8957275)",
        "pathway_count": 3,
        "publication_count": 2,
        "publication_id_list": "15777620;22673903",
        "class_list": "",
        "function": "Structure and expression of the mammalian HRC gene, together with the comparative expression data of the related sarcoplasmic reticulum genes., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "ec_number_list": "",
        "go_molecular_function": "GO:0051117 ATPase binding;GO:0044325 transmembrane transporter binding;GO:0005509 calcium ion binding;GO:0140314 calcium ion sequestering activity",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0030018 Z disc;GO:0016529 sarcoplasmic reticulum;GO:0033017 sarcoplasmic reticulum membrane",
        "go_biological_process": "GO:0051480 regulation of cytosolic calcium ion concentration;GO:0008016 regulation of heart contraction;GO:0010460 positive regulation of heart rate;GO:0010880 regulation of release of sequestered calcium ion into cytosol by sarcoplasmic reticulum;GO:0002027 regulation of heart rate",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "G3V8S6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V8X9-1",
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        "length": 415,
        "protein_name": "Serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 16",
        "gene_name": "Serpina16",
        "organism": "Rat",
        "refseq_name": "serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 16 precursor",
        "refseq_ac": "NP_853661",
        "gene_names_uniprotkb": "Serpina16",
        "gene_names_refseq": "Serpina16",
        "protein_names_uniprotkb": "Serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 16",
        "protein_names_refseq": "serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 16 precursor; serine proteinase inhibitor HongrES1; serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 16",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:299271)",
        "pathway_count": 1,
        "publication_count": 2,
        "publication_id_list": "16641100;19116669",
        "class_list": "",
        "function": "HongrES1 as a novel and critical molecule in the regulation of sperm capacitation and male fertility., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004867 serine-type endopeptidase inhibitor activity",
        "go_cellular_component": "GO:0005615 extracellular space",
        "go_biological_process": "GO:0034097 response to cytokine",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "G3V8X9-1",
        "record_type": "protein"
    },
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        "length": 336,
        "protein_name": "Thioredoxin-related transmembrane protein 4",
        "gene_name": "Tmx4",
        "organism": "Rat",
        "refseq_name": "thioredoxin-related transmembrane protein 4 precursor",
        "refseq_ac": "NP_001093999",
        "gene_names_uniprotkb": "Tmx4",
        "gene_names_refseq": "RGD1305146; Tmx4; Txndc13",
        "protein_names_uniprotkb": "Thioredoxin-related transmembrane protein 4",
        "protein_names_refseq": "thioredoxin domain containing 13; thioredoxin-related transmembrane protein 4 precursor",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:296182)",
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        "publication_count": 1,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0015036 disulfide oxidoreductase activity",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005789 endoplasmic reticulum membrane;GO:0012505 endomembrane system;GO:0005637 nuclear inner membrane",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "G3V912-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V920-1",
        "uniprot_id": "G3V920_RAT",
        "mass": 74806.0,
        "length": 674,
        "protein_name": "WD repeat-containing protein 43",
        "gene_name": "Wdr43",
        "organism": "Rat",
        "refseq_name": "WD repeat-containing protein 43",
        "refseq_ac": "NP_001032880",
        "gene_names_uniprotkb": "Wdr43",
        "gene_names_refseq": "Wdr43",
        "protein_names_uniprotkb": "WD repeat-containing protein 43",
        "protein_names_refseq": "WD repeat-containing protein 43",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:362703);  (R-RNO-6791226)",
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        "go_molecular_function": "GO:0003723 RNA binding;GO:0000993 RNA polymerase II complex binding;GO:0003711 transcription elongation factor activity",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0001650 fibrillar center;GO:0000785 chromatin;GO:0032040 small-subunit processome",
        "go_biological_process": "GO:2000234 positive regulation of rRNA processing;GO:0034243 regulation of transcription elongation by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0045943 positive regulation of transcription by RNA polymerase I;GO:2000036 regulation of stem cell population maintenance",
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        "hit_score": 0.2,
        "record_id": "G3V920-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "G3V925-1",
        "uniprot_id": "G3V925_RAT",
        "mass": 42998.0,
        "length": 380,
        "protein_name": "Pregnancy-specific beta 1-glycoprotein",
        "gene_name": "Psgb1",
        "organism": "Rat",
        "refseq_name": "pregnancy-specific beta 1-glycoprotein",
        "refseq_ac": "NP_067709",
        "gene_names_uniprotkb": "Psgb1",
        "gene_names_refseq": "Psgb1; Psg",
        "protein_names_uniprotkb": "Pregnancy-specific beta 1-glycoprotein",
        "protein_names_refseq": "pregnancy-specific beta 1-glycoprotein",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:59313);  (R-RNO-163125);  (R-RNO-6798695)",
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        "go_molecular_function": "GO:1990782 protein tyrosine kinase binding",
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        "go_biological_process": "GO:0007165 signal transduction;GO:0002682 regulation of immune system process",
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        "hit_score": 0.1,
        "record_id": "G3V925-1",
        "record_type": "protein"
    },
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        "uniprot_id": "G3V955_RAT",
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        "length": 1139,
        "protein_name": "Membrane spanning 4-domains A14",
        "gene_name": "Ms4a14",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ms4a14",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Membrane spanning 4-domains A14",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "length": 501,
        "protein_name": "Transcription factor CP2",
        "gene_name": "Tfcp2",
        "organism": "Rat",
        "refseq_name": "alpha-globin transcription factor CP2 isoform X1",
        "refseq_ac": "XP_006242403",
        "gene_names_uniprotkb": "Tfcp2; Tcfcp2",
        "gene_names_refseq": "Tcfcp2; Tfcp2",
        "protein_names_uniprotkb": "Transcription factor CP2",
        "protein_names_refseq": "alpha-globin transcription factor CP2 isoform X1",
        "tax_id": 10116,
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0032991 protein-containing complex",
        "go_biological_process": "GO:0006357 regulation of transcription by RNA polymerase II;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0042789 mRNA transcription by RNA polymerase II;GO:0006351 DNA-templated transcription",
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    },
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        "length": 248,
        "protein_name": "Stratifin",
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        "protein_names_refseq": "14-3-3 protein sigma",
        "tax_id": 10116,
        "disease": "intellectual disability (Disease Ontology:DOID:1059); urinary bladder cancer (Disease Ontology:DOID:11054); vulva squamous cell carcinoma (Disease Ontology:DOID:2101); ovarian cancer (Disease Ontology:DOID:2394); transitional cell carcinoma (Disease Ontology:DOID:2671); endometrial carcinoma (Disease Ontology:DOID:2871); in situ carcinoma (Disease Ontology:DOID:8719)",
        "pathway": " (rno:313017);  (R-RNO-111447);  (R-RNO-5625740);  (R-RNO-5628897);  (R-RNO-6804114);  (R-RNO-75035);  (R-RNO-9614399);  (R-RNO-9968551)",
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        "go_molecular_function": "GO:0019901 protein kinase binding;GO:0042802 identical protein binding;GO:0050815 phosphoserine residue binding;GO:0051219 phosphoprotein binding;GO:0140311 protein sequestering activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0007165 signal transduction;GO:0030307 positive regulation of cell growth;GO:0031424 keratinization;GO:0045785 positive regulation of cell adhesion;GO:0061436 establishment of skin barrier",
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    },
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        "protein_name": "Zinc finger protein 111",
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        "gene_names_uniprotkb": "Zfp111",
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        "protein_names_uniprotkb": "Zinc finger protein 111",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (R-RNO-212436)",
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0008270 zinc ion binding;GO:0000976 transcription cis-regulatory region binding",
        "go_cellular_component": "GO:0005634 nucleus",
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    },
    {
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        "length": 345,
        "protein_name": "Leucine-rich repeat-containing protein 23",
        "gene_name": "Lrrc23",
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        "refseq_name": "leucine-rich repeat-containing protein 23",
        "refseq_ac": "NP_001381276",
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        "protein_names_uniprotkb": "Leucine-rich repeat-containing protein 23; Leucine-rich protein B7",
        "protein_names_refseq": "leucine rich protein, B7; leucine-rich repeat-containing protein 23-like; leucine-rich repeat-containing protein 23; neuron-specific enolase",
        "tax_id": 10116,
        "disease": "spermatogenic failure 92 (Disease Ontology:DOID:0070591)",
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        "publication_id_list": "18569155;22673903",
        "class_list": "",
        "function": "Essential for sperm motility and male fertility. Plays an important role in the proper assembly of the third radial spoke (RS3) head and the bridge structure between RS2 and RS3 in the sperm flagella., [UniProtKB, UniProtKB, UniProtKB]; The results suggest that NSE immunoreactivity may be a valuable marker for determination of the number of metabolically active neurons in different brain regions after single and repeated experimental seizures., [RefSeq, PubMed]",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0036126 sperm flagellum",
        "go_biological_process": "GO:0030317 flagellated sperm motility;GO:0062177 radial spoke assembly",
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        "record_id": "G3V9K7-1",
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        "protein_name": "Centrin 2",
        "gene_name": "Cetn2",
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        "gene_names_uniprotkb": "Cetn2",
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        "protein_names_uniprotkb": "Centrin 2",
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        "tax_id": 10116,
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        "pathway": " (rno:84593);  (R-RNO-2565942);  (R-RNO-3108214);  (R-RNO-380259);  (R-RNO-380270);  (R-RNO-380284);  (R-RNO-380320);  (R-RNO-5620912);  (R-RNO-5696394);  (R-RNO-5696395);  (R-RNO-8854518)",
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        "go_molecular_function": "GO:0008017 microtubule binding;GO:0031683 G-protein beta/gamma-subunit complex binding;GO:0032795 heterotrimeric G-protein binding;GO:0005509 calcium ion binding",
        "go_cellular_component": "GO:0044615 nuclear pore nuclear basket;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005813 centrosome;GO:0005929 cilium",
        "go_biological_process": "GO:0007283 spermatogenesis;GO:0000226 microtubule cytoskeleton organization;GO:0006289 nucleotide-excision repair;GO:0032465 regulation of cytokinesis;GO:0007099 centriole replication",
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        "record_id": "G3V9W0-1",
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    },
    {
        "uniprot_canonical_ac": "G3V9W2-1",
        "uniprot_id": "G3V9W2_RAT",
        "mass": 133261.0,
        "length": 1153,
        "protein_name": "Tyrosine-protein kinase",
        "gene_name": "Jak1",
        "organism": "Rat",
        "refseq_name": "tyrosine-protein kinase JAK1",
        "refseq_ac": "NP_445918",
        "gene_names_uniprotkb": "Jak1",
        "gene_names_refseq": "Jak1",
        "protein_names_uniprotkb": "Tyrosine-protein kinase; 2.7.10.2",
        "protein_names_refseq": "Janus protein tyrosine kinase 1; tyrosine-protein kinase JAK1",
        "tax_id": 10116,
        "disease": "prostate cancer (Disease Ontology:DOID:10283); stomach cancer (Disease Ontology:DOID:10534); sciatic neuropathy (Disease Ontology:DOID:11446); endometrial cancer (Disease Ontology:DOID:1380); disease of cellular proliferation (Disease Ontology:DOID:14566); cancer (Disease Ontology:DOID:162); transient cerebral ischemia (Disease Ontology:DOID:224); ovarian cancer (Disease Ontology:DOID:2394); hematologic cancer (Disease Ontology:DOID:2531); pancreatic ductal adenocarcinoma (Disease Ontology:DOID:3498); lung non-small cell carcinoma (Disease Ontology:DOID:3908); pancreatic adenocarcinoma (Disease Ontology:DOID:4074); T-cell acute lymphoblastic leukemia (Disease Ontology:DOID:5603); hepatocellular carcinoma (Disease Ontology:DOID:684); systemic lupus erythematosus (Disease Ontology:DOID:9074); colorectal cancer (Disease Ontology:DOID:9256)",
        "pathway": " (rno:84598)",
        "pathway_count": 1,
        "publication_count": 2,
        "publication_id_list": "30664158;36794521",
        "class_list": "",
        "function": "Folic acid deficiency exacerbates the inflammatory response of astrocytes after ischemia-reperfusion by enhancing the interaction between IL-6 and JAK-1/pSTAT3., [RefSeq, PubMed]; Treatment downregulated the expression of JAK1, JAK3 and STAT3, and upregulated cytosolic nuclear factor (NF)kappaB p65 and IkappaB. In conclusion, the results of the present study indicated that curculigoside exhibited significant antiarthritic effects in vivo and in vitro, and the molecular mechanism may be associated with the JAK/STAT/NFkappaB signaling pathway., [RefSeq, PubMed]; Tyrosine kinase of the non-receptor type, involved in the IFN-alpha/beta/gamma signal pathway. Kinase partner for the interleukin (IL)-2 receptor as well as interleukin (IL)-10 receptor. Kinase partner for the type I interferon receptor IFNAR2. In response to interferon-binding to IFNAR1-IFNAR2 heterodimer, phosphorylates and activates its binding partner IFNAR2, creating docking sites for STAT proteins. Directly phosphorylates STAT proteins but also activates STAT signaling through the transactivation of other JAK kinases associated with signaling receptors., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 2,
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        "ec_number_list": "2.7.12.1;2.7.10.1;2.7.10.2;2.7.12.2;2.7.1.40;2.7.11.1;2.7.11.13;2.7.10.4;2.7.1.32;2.7.1.82;2.7.11.23",
        "go_molecular_function": "GO:0004713 protein tyrosine kinase activity;GO:0004715 non-membrane spanning protein tyrosine kinase activity;GO:0005524 ATP binding;GO:0046872 metal ion binding;GO:0031625 ubiquitin protein ligase binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005856 cytoskeleton;GO:0031234 extrinsic component of cytoplasmic side of plasma membrane;GO:0012505 endomembrane system",
        "go_biological_process": "GO:0035771 interleukin-4-mediated signaling pathway;GO:0038110 interleukin-2-mediated signaling pathway;GO:1903672 positive regulation of sprouting angiogenesis;GO:0150105 protein localization to cell-cell junction;GO:0006468 protein phosphorylation",
        "synthesized_glycan_count": 0,
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        "record_id": "G3V9W2-1",
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    {
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        "protein_name": "HOXA11 antisense RNA",
        "gene_name": "Hoxa11-as",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Hoxa11-as",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "HOXA11 antisense RNA",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "congestive heart failure (Disease Ontology:DOID:6000)",
        "pathway": "",
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        "record_id": "G3V9W7-1",
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    },
    {
        "uniprot_canonical_ac": "G3V9W8-1",
        "uniprot_id": "G3V9W8_RAT",
        "mass": 220978.0,
        "length": 1980,
        "protein_name": "Voltage-dependent L-type calcium channel subunit alpha",
        "gene_name": "Cacna1f",
        "organism": "Rat",
        "refseq_name": "voltage-dependent L-type calcium channel subunit alpha-1F",
        "refseq_ac": "NP_446153",
        "gene_names_uniprotkb": "Cacna1f",
        "gene_names_refseq": "Cacna1f",
        "protein_names_uniprotkb": "Voltage-dependent L-type calcium channel subunit alpha",
        "protein_names_refseq": "calcium channel, voltage-dependent, L type, alpha 1F subunit; calcium channel, voltage-dependent, alpha 1F subunit; voltage-dependent L-type calcium channel subunit alpha-1F",
        "tax_id": 10116,
        "disease": "congenital stationary night blindness (Disease Ontology:DOID:0050534); Aland Island eye disease (Disease Ontology:DOID:0050630); Timothy syndrome (Disease Ontology:DOID:0060173); congenital stationary night blindness 2A (Disease Ontology:DOID:0110871); X-linked cone-rod dystrophy 3 (Disease Ontology:DOID:0111007); Duchenne muscular dystrophy (Disease Ontology:DOID:11723)",
        "pathway": " (rno:114493)",
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        "go_biological_process": "GO:0036265 RNA (guanine-N7)-methylation;GO:0006400 tRNA modification;GO:0030488 tRNA methylation;GO:0033554 cellular response to stress;GO:0106004 tRNA (guanine-N7)-methylation",
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        "refseq_name": "coiled-coil domain-containing protein 179",
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        "gene_names_uniprotkb": "Ccdc179; RGD1559980",
        "gene_names_refseq": "Ccdc179; RGD1559980",
        "protein_names_uniprotkb": "Coiled-coil domain containing 179",
        "protein_names_refseq": "coiled-coil domain-containing protein 179",
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    },
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        "protein_name": "Transmembrane protein 247",
        "gene_name": "Tmem247",
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        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Transmembrane protein 247",
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    },
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        "uniprot_canonical_ac": "M0R933-1",
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        "length": 168,
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        "gene_name": "Krtap14",
        "organism": "Rat",
        "refseq_name": "keratin-associated protein 14",
        "refseq_ac": "NP_001102796",
        "gene_names_uniprotkb": "Krtap14",
        "gene_names_refseq": "Krtap14; RGD1564302",
        "protein_names_uniprotkb": "Keratin-associated protein",
        "protein_names_refseq": "keratin-associated protein 14",
        "tax_id": 10116,
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        "function": "In the hair cortex, hair keratin intermediate filaments are embedded in an interfilamentous matrix, consisting of hair keratin-associated proteins (KRTAP), which are essential for the formation of a rigid and resistant hair shaft through their extensive disulfide bond cross-linking with abundant cysteine residues of hair keratins. The matrix proteins include the high-sulfur and high-glycine-tyrosine keratins., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "predicted_c_glycosites": 0,
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005829 cytosol;GO:0045095 keratin filament",
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    },
    {
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        "length": 475,
        "protein_name": "E3 ubiquitin-protein ligase TRIM62",
        "gene_name": "Trim62",
        "organism": "Rat",
        "refseq_name": "E3 ubiquitin-protein ligase TRIM62",
        "refseq_ac": "NP_001414601",
        "gene_names_uniprotkb": "Trim62",
        "gene_names_refseq": "Trim62",
        "protein_names_uniprotkb": "E3 ubiquitin-protein ligase TRIM62; 2.3.2.27; Tripartite motif-containing protein 62",
        "protein_names_refseq": "E3 ubiquitin-protein ligase TRIM62; tripartite motif-containing protein 62",
        "tax_id": 10116,
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        "pathway": " (rno:313045)",
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        "function": "E3 ubiquitin ligase that plays a role in antifungal immunity by mediating 'Lys-27'-linked ubiquitination of CARD9 downstream of C-type lectin receptors; leading to CARD9 activation, followed by activation of NF-kappa-B and MAP kinase p38 pathways. E3 ubiquitin ligase activity is dependent on E2 ubiquitin-conjugating enzyme UBE2D2., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0061630 ubiquitin protein ligase activity;GO:0003713 transcription coactivator activity;GO:0042802 identical protein binding;GO:0004842 ubiquitin-protein transferase activity",
        "go_cellular_component": "GO:0005737 cytoplasm",
        "go_biological_process": "GO:0045087 innate immune response;GO:0043123 positive regulation of canonical NF-kappaB signal transduction;GO:1905036 positive regulation of antifungal innate immune response;GO:0046596 regulation of viral entry into host cell;GO:0032897 negative regulation of viral transcription",
        "synthesized_glycan_count": 0,
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        "uniprot_canonical_ac": "M0R966-1",
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        "length": 302,
        "protein_name": "Transmembrane epididymal protein 1B",
        "gene_name": "Teddm1b",
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        "refseq_name": "similar to putative membrane protein Re9",
        "refseq_ac": "NP_001395943",
        "gene_names_uniprotkb": "Teddm1b; LOC684709",
        "gene_names_refseq": "Teddm1b",
        "protein_names_uniprotkb": "Transmembrane epididymal protein 1B",
        "protein_names_refseq": "similar to putative membrane protein Re9; transmembrane epididymal protein 1",
        "tax_id": 10116,
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    },
    {
        "uniprot_canonical_ac": "M0RAA8-1",
        "uniprot_id": "M0RAA8_RAT",
        "mass": 116717.0,
        "length": 1032,
        "protein_name": "Toll-like receptor 9",
        "gene_name": "Tlr9",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Tlr9",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Toll-like receptor 9",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "sinusitis (Disease Ontology:DOID:0050127); lupus nephritis (Disease Ontology:DOID:0080162); metabolic dysfunction-associated steatotic liver disease (Disease Ontology:DOID:0080208); acute necrotizing pancreatitis (Disease Ontology:DOID:0080998); dermatomyositis (Disease Ontology:DOID:10223); viral pneumonia (Disease Ontology:DOID:10533); mastitis (Disease Ontology:DOID:10690); Human papillomavirus infectious disease (Disease Ontology:DOID:11166); anogenital venereal wart (Disease Ontology:DOID:11168); allergic conjunctivitis (Disease Ontology:DOID:11204); primary biliary cholangitis (Disease Ontology:DOID:12236); cardiovascular system disease (Disease Ontology:DOID:1287); allergic bronchopulmonary aspergillosis (Disease Ontology:DOID:13166); alcoholic liver cirrhosis (Disease Ontology:DOID:14018); cystic fibrosis (Disease Ontology:DOID:1485); alcohol use disorder (Disease Ontology:DOID:1574); breast cancer (Disease Ontology:DOID:1612); squamous cell carcinoma (Disease Ontology:DOID:1749); hepatitis C (Disease Ontology:DOID:1883); hepatitis B (Disease Ontology:DOID:2043); bronchiolitis obliterans (Disease Ontology:DOID:2799); asthma (Disease Ontology:DOID:2841); pulmonary tuberculosis (Disease Ontology:DOID:2957); IgA glomerulonephritis (Disease Ontology:DOID:2986); interstitial lung disease (Disease Ontology:DOID:3082); chronic granulomatous disease (Disease Ontology:DOID:3265); pulmonary fibrosis (Disease Ontology:DOID:3770); lung non-small cell carcinoma (Disease Ontology:DOID:3908); renal cell carcinoma (Disease Ontology:DOID:4450); allergic rhinitis (Disease Ontology:DOID:4481); proteinuria (Disease Ontology:DOID:576); hepatocellular carcinoma (Disease Ontology:DOID:684); chronic kidney disease (Disease Ontology:DOID:784); perinatal necrotizing enterocolitis (Disease Ontology:DOID:8677); cervix uteri carcinoma in situ (Disease Ontology:DOID:8991); systemic lupus erythematosus (Disease Ontology:DOID:9074); cutaneous leishmaniasis (Disease Ontology:DOID:9111)",
        "pathway": " (R-RNO-109704);  (R-RNO-1679131);  (R-RNO-168138)",
        "pathway_count": 3,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Key component of innate and adaptive immunity. TLRs (Toll-like receptors) control host immune response against pathogens through recognition of molecular patterns specific to microorganisms. TLR9 is a nucleotide-sensing TLR which is activated by unmethylated cytidine-phosphate-guanosine (CpG) dinucleotides. Acts via MYD88 and TRAF6, leading to NF-kappa-B activation, cytokine secretion and the inflammatory response. Also acts via ADCY7, leading to cyclic di-AMP (c-di-AMP) synthesis and activation of the NLRP3 inflammasome. Plays a role in defense against systemic mouse cytomegalovirus infection. Controls lymphocyte response to Helicobacter infection. Upon CpG stimulation, induces B-cell proliferation, activation, survival and antibody production., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0035197 siRNA binding;GO:0045322 unmethylated CpG binding;GO:0005149 interleukin-1 receptor binding;GO:0038187 pattern recognition receptor activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005768 endosome;GO:0005783 endoplasmic reticulum;GO:0005886 plasma membrane;GO:0016323 basolateral plasma membrane",
        "go_biological_process": "GO:0045577 regulation of B cell differentiation;GO:0032727 positive regulation of interferon-alpha production;GO:0032741 positive regulation of interleukin-18 production;GO:1901895 negative regulation of ATPase-coupled calcium transmembrane transporter activity;GO:0002730 regulation of dendritic cell cytokine production",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "M0RAA8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "M0RAG0-1",
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        "length": 694,
        "protein_name": "Transmembrane protein 151A",
        "gene_name": "Tmem151a",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Tmem151a",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Transmembrane protein 151A",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "episodic kinesigenic dyskinesia 3 (Disease Ontology:DOID:0060944)",
        "pathway": " (rno:309158)",
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        "publication_id_list": "22673903",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0016020 membrane",
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    },
    {
        "uniprot_canonical_ac": "M0RAH8-1",
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        "protein_name": "Ly6/PLAUR domain containing 10 like 1",
        "gene_name": "Lypd10l1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Lypd10l1; LOC681077",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ly6/PLAUR domain containing 10 like 1",
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        "disease": "congenital malabsorptive diarrhea 4 (Disease Ontology:DOID:0060779); glucose intolerance (Disease Ontology:DOID:10603); type 2 diabetes mellitus (Disease Ontology:DOID:9352)",
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        "length": 414,
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        "gene_name": "Dusp9",
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        "protein_names_uniprotkb": "Dual specificity protein phosphatase; 3.1.3.16; 3.1.3.48",
        "protein_names_refseq": "dual specificity protein phosphatase 9",
        "tax_id": 10116,
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        "pathway": " (rno:293847);  (R-RNO-112409);  (R-RNO-5675221)",
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        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol",
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        "protein_name": "Melanoma-associated antigen D1",
        "gene_name": "Maged2",
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        "refseq_name": "melanoma-associated antigen D2",
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        "gene_names_refseq": "Maged2",
        "protein_names_uniprotkb": "Melanoma-associated antigen D1; MAGE-D1 antigen; Neurotrophin receptor-interacting MAGE homolog",
        "protein_names_refseq": "melanoma antigen, family D, 2; melanoma-associated antigen D2",
        "tax_id": 10116,
        "disease": "Bartter disease type 5 (Disease Ontology:DOID:0110147)",
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        "function": "Expression pattern and further characterization of human MAGED2 and identification of rodent orthologues, [RefSeq, PubMed]",
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        "protein_name": "Kazal-type serine peptidase inhibitor domain 1",
        "gene_name": "Kazald1",
        "organism": "Rat",
        "refseq_name": "kazal-type serine protease inhibitor domain-containing protein 1 precursor",
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        "gene_names_uniprotkb": "Kazald1",
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        "protein_names_refseq": "Kazal-type serine protease inhibitor domain 1; kazal-type serine protease inhibitor domain-containing protein 1 precursor; kazal-type serine protease inhibitor domain-containing protein 1",
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        "record_id": "Q3ZAU4-1",
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    },
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        "uniprot_canonical_ac": "Q498S0-1",
        "uniprot_id": "Q498S0_RAT",
        "mass": 49255.0,
        "length": 419,
        "protein_name": "Carbohydrate sulfotransferase",
        "gene_name": "Chst12",
        "organism": "Rat",
        "refseq_name": "carbohydrate sulfotransferase 12",
        "refseq_ac": "NP_001032864",
        "gene_names_uniprotkb": "Chst12",
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        "protein_names_uniprotkb": "Carbohydrate sulfotransferase; 2.8.2.-",
        "protein_names_refseq": "carbohydrate (chondroitin 4) sulfotransferase 12; carbohydrate sulfotransferase 12",
        "tax_id": 10116,
        "disease": "hypertension (Disease Ontology:DOID:10763)",
        "pathway": " (rno:304322);  (R-RNO-2022870)",
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        "ec_number_list": "2.8.2.-;2.8.2.5",
        "go_molecular_function": "GO:0008146 sulfotransferase activity;GO:0047756 chondroitin 4-sulfotransferase activity",
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        "go_biological_process": "GO:0016051 carbohydrate biosynthetic process;GO:0050650 chondroitin sulfate proteoglycan biosynthetic process;GO:0050651 dermatan sulfate proteoglycan biosynthetic process;GO:0030166 proteoglycan biosynthetic process",
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    {
        "uniprot_canonical_ac": "Q4JEI9-1",
        "uniprot_id": "Q4JEI9_RAT",
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        "length": 93,
        "protein_name": "Defensin alpha 24",
        "gene_name": "Defa24",
        "organism": "Rat",
        "refseq_name": "defensin 5 precursor",
        "refseq_ac": "NP_001013071",
        "gene_names_uniprotkb": "Defa24",
        "gene_names_refseq": "Defa24; Defcr24; Defcr4; Rd5; defensin 6; defensin 7; defensin-5",
        "protein_names_uniprotkb": "Defensin alpha 24",
        "protein_names_refseq": "RD-5; alpha-defensin, 24; defensin 5 precursor; defensin 5; defensin related cryptdin 24; defensin related cryptdin 4; enteric defensin alpha 5",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:290856);  (R-RNO-1461973);  (R-RNO-1462054);  (R-RNO-6798695)",
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        "publication_id_list": "17878170",
        "class_list": "",
        "function": "CRP4 mediates cGMP/PKG stimulation of SM-specific gene expression, and PKG plays an important role in regulating the phenotype of VSMCs, [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0140911 pore-forming activity",
        "go_cellular_component": "GO:0005615 extracellular space",
        "go_biological_process": "GO:0019731 antibacterial humoral response;GO:0045087 innate immune response;GO:0050829 defense response to Gram-negative bacterium;GO:0050830 defense response to Gram-positive bacterium;GO:0061844 antimicrobial humoral immune response mediated by antimicrobial peptide",
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    {
        "uniprot_canonical_ac": "Q4KLN5-1",
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        "length": 287,
        "protein_name": "Phospholipase A and acyltransferase 5",
        "gene_name": "Plaat5",
        "organism": "Rat",
        "refseq_name": "phospholipase A and acyltransferase 5",
        "refseq_ac": "NP_001034096",
        "gene_names_uniprotkb": "Plaat5; Hrasls5; Hrlp5; Rlp-1",
        "gene_names_refseq": "HRSL5; Hrasls5; Plaat5; RGD1308376; RLP-1; iNAT",
        "protein_names_uniprotkb": "Phospholipase A and acyltransferase 5; 2.3.1.-; 3.1.1.32; 3.1.1.4; Ca(2+)-independent N-acyltransferase; H-rev107-like protein 5; HRAS-like suppressor 5; HRSL5; RLP-1; Rat LRAT-like protein-1; iNAT",
        "protein_names_refseq": "Ca(2+)-independent N-acyltransferase; H-rev107-like protein 5; HRAS-like suppressor 5; HRAS-like suppressor family, member 5; LRAT-like protein-1; phospholipase A and acyltransferase 5",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:293711);  (R-RNO-1482839)",
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        "publication_count": 2,
        "publication_id_list": "17158102;18460797",
        "class_list": "",
        "function": "Exhibits both phospholipase A1/2 and acyltransferase activities (By similarity). Shows phospholipase A1 (PLA1) and A2 (PLA2) activity, catalyzing the calcium-independent release of fatty acids from the sn-1 or sn-2 position of glycerophospholipids (By similarity). Shows N-acyltransferase activity, catalyzing the calcium-independent transfer of a fatty acyl group at the sn-1 position of phosphatidylcholine (PC) and other glycerophospholipids to the primary amine of phosphatidylethanolamine (PE), forming N-acylphosphatidylethanolamine (NAPE), which serves as precursor for N-acylethanolamines (NAEs) (PubMed:17158102)., [UniProtKB, UniProtKB, UniProtKB, PubMed]; Expression was detected primarily in the spermatocytes in the maturing rat testis. The Hrasls5 gene product might function as a tumor suppressor as well as in spermatogenesis, as deduced from its amino acid sequence., [RefSeq, PubMed]",
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        "secondary_ac_list": "",
        "ec_number_list": "3.1.1.4;3.1.1.32;2.3.1.-;2.3.1.51;3.1.1.3;3.1.1.-;3.1.1.5;1.11.1.27;2.3.1.23;3.1.2.2;3.1.1.34",
        "go_molecular_function": "GO:0004623 phospholipase A2 activity;GO:0008970 phospholipase A1 activity;GO:0016410 N-acyltransferase activity;GO:0016787 hydrolase activity;GO:0016740 transferase activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0070292 N-acylphosphatidylethanolamine metabolic process;GO:0006629 lipid metabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "Q4KLN5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q4V7C2-1",
        "uniprot_id": "Q4V7C2_RAT",
        "mass": 35517.0,
        "length": 327,
        "protein_name": "E3 ubiquitin-protein ligase ZNRF4",
        "gene_name": "Znrf4",
        "organism": "Rat",
        "refseq_name": "E3 ubiquitin-protein ligase ZNRF4 precursor",
        "refseq_ac": "NP_001020049",
        "gene_names_uniprotkb": "Znrf4",
        "gene_names_refseq": "Znrf4",
        "protein_names_uniprotkb": "E3 ubiquitin-protein ligase ZNRF4; 2.3.2.27; RING-type E3 ubiquitin transferase ZNRF4; Zinc/RING finger protein 4",
        "protein_names_refseq": "E3 ubiquitin-protein ligase ZNRF4 precursor; E3 ubiquitin-protein ligase ZNRF4; zinc/RING finger protein 4",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:301127)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "E3 ubiquitin-protein ligase that acts as a negative regulator of NOD2 signaling by mediating ubiquitination and degradation of RIPK2. Also catalyzes ubiquitination and proteasomal degradation of CANX within the endoplasmic reticulum. Could have a role in spermatogenesis., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0061630 ubiquitin protein ligase activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005783 endoplasmic reticulum;GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process;GO:0006511 ubiquitin-dependent protein catabolic process;GO:0045786 negative regulation of cell cycle;GO:0070433 negative regulation of nucleotide-binding oligomerization domain containing 2 signaling pathway",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "Q4V7C2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q505J7-1",
        "uniprot_id": "Q505J7_RAT",
        "mass": 49295.0,
        "length": 432,
        "protein_name": "Galactose-3-O-sulfotransferase 3",
        "gene_name": "Gal3st3",
        "organism": "Rat",
        "refseq_name": "galactose-3-O-sulfotransferase 3",
        "refseq_ac": "NP_001019461",
        "gene_names_uniprotkb": "Gal3st3",
        "gene_names_refseq": "Gal3st3",
        "protein_names_uniprotkb": "Galactose-3-O-sulfotransferase 3; Beta-galactose-3-O-sulfotransferase 3; Gal-beta-1, 3-GalNAc 3'-sulfotransferase 3",
        "protein_names_refseq": "galactose-3-O-sulfotransferase 3",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:499302)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "38843836",
        "class_list": "",
        "function": "Catalyzes the transfer of a sulfate group from 3'-phosphoadenylyl sulfate (PAPS) to the C-3 hydroxyl group of terminal non-reducing beta-1,4-linked galactose residues in both N-glycans and O-glycans. It acts efficiently on type 2 chains (Gal-beta-1,4-GlcNAc-R) found in N-glycans and core 2-branched O-glycans (Gal-beta-1,4-GlcNAc-beta-1,6(Gal-beta-1,3)GalNAc-R). In contrast, it shows poor activity on type 1 chains (Gal-beta-1,3-GlcNAc-R) and intermediate activity on core 1 structures (Gal-beta-1,3-GalNAc-R). Participates in the glycoconjugates sulfation namely the 3'-sulfated Lewis X epitope (Gal-beta-1,4(Fuc-alpha-1,3)GlcNAc), by sulfating N-acetyllactosamine (Gal-beta-1,4-GlcNAc) at the 3' position; then the resulting modification is fucosylated by FUT5., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 1,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 1,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 1,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 1,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 0,
        "biomarker_type": "",
        "glycan_count": 1,
        "disease_count": 0,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0050694 galactose 3-O-sulfotransferase activity;GO:0001733 galactosylceramide sulfotransferase activity",
        "go_cellular_component": "GO:0032580 Golgi cisterna membrane",
        "go_biological_process": "GO:0009247 glycolipid biosynthetic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "Q505J7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q568Z3-1",
        "uniprot_id": "Q568Z3_RAT",
        "mass": 29206.0,
        "length": 273,
        "protein_name": "Progestin and adipoQ receptor family member 4",
        "gene_name": "Paqr4",
        "organism": "Rat",
        "refseq_name": "progestin and adipoQ receptor family member 4",
        "refseq_ac": "NP_001017377",
        "gene_names_uniprotkb": "Paqr4",
        "gene_names_refseq": "Paqr4",
        "protein_names_uniprotkb": "Progestin and adipoQ receptor family member 4",
        "protein_names_refseq": "progestin and adipoQ receptor family member 4; progestin and adipoQ receptor family member IV",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:302967)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
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        "total_c_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0060090 molecular adaptor activity;GO:0046872 metal ion binding",
        "go_cellular_component": "GO:0000139 Golgi membrane",
        "go_biological_process": "GO:2000303 regulation of ceramide biosynthetic process;GO:0050821 protein stabilization",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "Q568Z3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q5BJU0-1",
        "uniprot_id": "Q5BJU0_RAT",
        "mass": 23400.0,
        "length": 204,
        "protein_name": "RAS related 2",
        "gene_name": "Rras2",
        "organism": "Rat",
        "refseq_name": "ras-related protein R-Ras2",
        "refseq_ac": "NP_001013452",
        "gene_names_uniprotkb": "Rras2",
        "gene_names_refseq": "Rras2",
        "protein_names_uniprotkb": "RAS related 2",
        "protein_names_refseq": "ras-related protein R-Ras2; related RAS viral (r-ras) oncogene homolog 2",
        "tax_id": 10116,
        "disease": "Costello syndrome (Disease Ontology:DOID:0050469); RASopathy (Disease Ontology:DOID:0080690); Noonan syndrome 12 (Disease Ontology:DOID:0112170); urinary bladder cancer (Disease Ontology:DOID:11054)",
        "pathway": " (rno:365355);  (R-RNO-9696273)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
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        "mined_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 4,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003924 GTPase activity;GO:0005525 GTP binding",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0030335 positive regulation of cell migration;GO:0007265 Ras protein signal transduction;GO:0007163 establishment or maintenance of cell polarity",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "Q5BJU0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q5BJY8-1",
        "uniprot_id": "Q5BJY8_RAT",
        "mass": 9468.0,
        "length": 85,
        "protein_name": "Mannosidase beta like",
        "gene_name": "Manbal",
        "organism": "Rat",
        "refseq_name": "protein MANBAL",
        "refseq_ac": "NP_001166851",
        "gene_names_uniprotkb": "Manbal",
        "gene_names_refseq": "Manbal",
        "protein_names_uniprotkb": "Mannosidase beta like",
        "protein_names_refseq": "mannosidase beta A like; mannosidase, beta A, lysosomal-like; protein MANBAL",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:499934)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
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        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0016020 membrane",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "Q5BJY8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q5BK16-1",
        "uniprot_id": "Q5BK16_RAT",
        "mass": 33604.0,
        "length": 316,
        "protein_name": "exodeoxyribonuclease III",
        "gene_name": "Trex1",
        "organism": "Rat",
        "refseq_name": "three-prime repair exonuclease 1",
        "refseq_ac": "NP_001020160",
        "gene_names_uniprotkb": "Trex1",
        "gene_names_refseq": "RGD1309596; Trex1",
        "protein_names_uniprotkb": "exodeoxyribonuclease III; 3.1.11.2",
        "protein_names_refseq": "three-prime repair exonuclease 1",
        "tax_id": 10116,
        "disease": "cutaneous lupus erythematosus (Disease Ontology:DOID:0050169); Aicardi-Goutieres syndrome (Disease Ontology:DOID:0050629); Chilblain lupus (Disease Ontology:DOID:0060386); retinal vasculopathy with cerebral leukodystrophy (Disease Ontology:DOID:0111567); systemic lupus erythematosus (Disease Ontology:DOID:9074)",
        "pathway": " (rno:100049583)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "29393594",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 5,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008301 DNA binding, bending;GO:0008296 3'-5'-DNA exonuclease activity;GO:0000287 magnesium ion binding;GO:0003677 DNA binding;GO:0042802 identical protein binding",
        "go_cellular_component": "GO:0043596 nuclear replication fork;GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005783 endoplasmic reticulum;GO:0005829 cytosol",
        "go_biological_process": "GO:0071357 cellular response to type I interferon;GO:0043457 regulation of cellular respiration;GO:0002637 regulation of immunoglobulin production;GO:0002253 activation of immune response;GO:0002457 T cell antigen processing and presentation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "Q5BK16-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q5G5D4-1",
        "uniprot_id": "Q5G5D4_RAT",
        "mass": 68830.0,
        "length": 618,
        "protein_name": "Endogenous retrovirus group FRD member 1, envelope",
        "gene_name": "Ervfrd-1",
        "organism": "Rat",
        "refseq_name": "envelope glycoprotein syncytin-A precursor",
        "refseq_ac": "NP_001014771",
        "gene_names_uniprotkb": "Ervfrd-1; Syna",
        "gene_names_refseq": "Ervfrd-1; Gm52; Syna",
        "protein_names_uniprotkb": "Endogenous retrovirus group FRD member 1, envelope",
        "protein_names_refseq": "envelope glycoprotein syncytin-A precursor; envelope glycoprotein syncytin-A; syncytin a",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:288602)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Many different endogenous retrovirus families are expressed in normal placental tissue at high levels, suggesting that endogenous retroviruses are functionally important in reproduction. This gene is part of a endogenous retrovirus provirus on rat chromosome 12 that has inactivating mutations in the gag and pol genes. This gene is the envelope glycoprotein gene which appears to have been selectively preserved. The gene's protein product plays a major role in placental development and trophoblast fusion. The protein has the characteristics of a typical retroviral envelope protein, including a cleavage site that separates the surface (SU) and transmembrane (TM) proteins which form a heterodimer. [provided by RefSeq, Apr 2015]., [RefSeq]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_o_glycosites": 0,
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        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "glyco_site_count": 4,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0046703 natural killer cell lectin-like receptor binding;GO:0048018 receptor ligand activity",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005886 plasma membrane;GO:0009986 cell surface;GO:0009897 external side of plasma membrane",
        "go_biological_process": "GO:0002418 immune response to tumor cell;GO:0006955 immune response;GO:0051607 defense response to virus;GO:0006974 DNA damage response;GO:0042742 defense response to bacterium",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "Q60I18-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q642B5-1",
        "uniprot_id": "Q642B5_RAT",
        "mass": 79853.0,
        "length": 770,
        "protein_name": "Armadillo repeat containing, X-linked 2",
        "gene_name": "Armcx2",
        "organism": "Rat",
        "refseq_name": "armadillo repeat-containing X-linked protein 2",
        "refseq_ac": "NP_001014296",
        "gene_names_uniprotkb": "Armcx2",
        "gene_names_refseq": "Armcx2",
        "protein_names_uniprotkb": "Armadillo repeat containing, X-linked 2",
        "protein_names_refseq": "ALEX2 protein; armadillo repeat-containing X-linked protein 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:367903)",
        "pathway_count": 1,
        "publication_count": 0,
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        "class_list": "",
        "function": "",
        "predicted_glycosites": 3,
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        "predicted_c_glycosites": 0,
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        "total_reported_n_glycosites": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "D4A765",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005741 mitochondrial outer membrane;GO:1904115 axon cytoplasm",
        "go_biological_process": "GO:0019896 axonal transport of mitochondrion",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "Q642B5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q66H09-1",
        "uniprot_id": "Q66H09_RAT",
        "mass": 33310.0,
        "length": 292,
        "protein_name": "Tetratricopeptide repeat protein 1",
        "gene_name": "Ttc1",
        "organism": "Rat",
        "refseq_name": "tetratricopeptide repeat protein 1",
        "refseq_ac": "NP_001005529",
        "gene_names_uniprotkb": "Ttc1",
        "gene_names_refseq": "Ttc1",
        "protein_names_uniprotkb": "Tetratricopeptide repeat protein 1",
        "protein_names_refseq": "tetratricopeptide repeat protein 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:287208)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Adapter protein that plays a role downstream of GNA15 to stimulate Ras activation and subsequent phosphorylation of ERK1/2 independently of phospholipase Cbeta signaling. Mechanistically, interacts with GNA15 and SOS2 to form a macromolecular signaling complex which has a high affinity for HRAS. Additionally, participates in signaling via other G-alpha proteins like GNA14, activating NF-kappa-B through Ras and ERK pathways. Beyond signaling, supports protein homeostasis by cooperating with HSP40 in the HSP70 chaperone cycle, promoting protein folding through the regulated dissociation of the HSP70 inhibitor HSPBP1., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "total_reported_n_glycosites": 0,
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        "biomarker_type": "",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0030674 protein-macromolecule adaptor activity",
        "go_cellular_component": "GO:0005829 cytosol",
        "go_biological_process": "GO:0150078 positive regulation of neuroinflammatory response",
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        "hit_score": 0.2,
        "record_id": "Q66H09-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q66H91-1",
        "uniprot_id": "GIT2_RAT",
        "mass": 84525.0,
        "length": 759,
        "protein_name": "ARF GTPase-activating protein GIT2",
        "gene_name": "Git2",
        "organism": "Rat",
        "refseq_name": "ARF GTPase-activating protein GIT2",
        "refseq_ac": "NP_001005553",
        "gene_names_uniprotkb": "Git2",
        "gene_names_refseq": "CAT-2; CAT2; Git2",
        "protein_names_uniprotkb": "ARF GTPase-activating protein GIT2; ARF GAP GIT2; CAT-2; CAT2; Cool-interacting tyrosine-phosphorylated protein 2; G protein-coupled receptor kinase-interactor 2; GRK-interacting protein 2",
        "protein_names_refseq": "ARF GAP GIT2; ARF GTPase-activating protein GIT2; G protein-coupled receptor kinase interacting ArfGAP 2; G protein-coupled receptor kinase-interactor 2; GRK-interacting protein 2; cool-interacting tyrosine-phosphorylated protein 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:304546);  (R-RNO-9013149);  (R-RNO-9013404);  (R-RNO-9013406);  (R-RNO-9013420);  (R-RNO-9013423);  (R-RNO-9013424)",
        "pathway_count": 7,
        "publication_count": 6,
        "publication_id_list": "12473661;12629171;19912111;22606319;22673903;29393594",
        "class_list": "",
        "function": "GTPase-activating protein for ADP ribosylation factor family members, including ARF1., [UniProtKB, UniProtKB]; Potentially identified the G protein-coupled receptor/cytoskeletal-associated protein GIT2 as a vital integrator and modulator of the normal aging process, [RefSeq, PubMed]; Rat basophilic leukaemia RBL-2H3 cells stably transfected with the chemoattractant receptor expressed both GIT1-p21-activated kinase and GIT2-p21-activated kinase endogenous complexes. Publication Status: Online-Only, [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "predicted_c_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005096 GTPase activator activity;GO:0008270 zinc ion binding;GO:0044877 protein-containing complex binding;GO:0031267 small GTPase binding",
        "go_cellular_component": "GO:0044305 calyx of Held;GO:0005654 nucleoplasm;GO:0045202 synapse;GO:0098793 presynapse;GO:0150034 distal axon",
        "go_biological_process": "GO:0007420 brain development;GO:0036465 synaptic vesicle recycling;GO:0048266 behavioral response to pain;GO:0032012 regulation of ARF protein signal transduction;GO:2000300 regulation of synaptic vesicle exocytosis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.7,
        "record_id": "Q66H91-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q67ES8-1",
        "uniprot_id": "Q67ES8_RAT",
        "mass": 35192.0,
        "length": 303,
        "protein_name": "Taste receptor type 2",
        "gene_name": "Tas2r7l",
        "organism": "Rat",
        "refseq_name": "taste receptor type 2 member 7-like",
        "refseq_ac": "NP_001019490",
        "gene_names_uniprotkb": "Tas2r7l; RGD1564521",
        "gene_names_refseq": "RGD1564521; Tas2r7l",
        "protein_names_uniprotkb": "Taste receptor type 2",
        "protein_names_refseq": "putative taste receptor T2R22; taste receptor type 2 member 7-like",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:500033)",
        "pathway_count": 1,
        "publication_count": 0,
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        "class_list": "",
        "function": "",
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0033038 bitter taste receptor activity",
        "go_cellular_component": "GO:0016020 membrane",
        "go_biological_process": "GO:0001580 detection of chemical stimulus involved in sensory perception of bitter taste",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "Q67ES8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q6AYB9-1",
        "uniprot_id": "Q6AYB9_RAT",
        "mass": 52508.0,
        "length": 463,
        "protein_name": "Protein arginine N-methyltransferase 2",
        "gene_name": "Prmt2",
        "organism": "Rat",
        "refseq_name": "protein arginine N-methyltransferase 2 isoform X1",
        "refseq_ac": "XP_063135531",
        "gene_names_uniprotkb": "Prmt2",
        "gene_names_refseq": "Hrmt1l1; Prmt2",
        "protein_names_uniprotkb": "Protein arginine N-methyltransferase 2; 2.1.1.319; Histone-arginine N-methyltransferase PRMT2",
        "protein_names_refseq": "protein arginine N-methyltransferase 2 isoform X1",
        "tax_id": 10116,
        "disease": "asthma (Disease Ontology:DOID:2841)",
        "pathway": " (rno:499420)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "binding_glycan_count": 0,
        "secondary_ac_list": "F1LMD8",
        "ec_number_list": "2.1.1.319",
        "go_molecular_function": "GO:0003713 transcription coactivator activity;GO:0042803 protein homodimerization activity;GO:0044877 protein-containing complex binding;GO:0008013 beta-catenin binding;GO:0016274 protein-arginine N-methyltransferase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0006338 chromatin remodeling;GO:0043065 positive regulation of apoptotic process;GO:0001666 response to hypoxia;GO:0006355 regulation of DNA-templated transcription;GO:0045892 negative regulation of DNA-templated transcription",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "Q6AYB9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q6AYD0-1",
        "uniprot_id": "Q6AYD0_RAT",
        "mass": 52141.0,
        "length": 446,
        "protein_name": "Leucine-rich repeat-containing protein 17",
        "gene_name": "Lrrc17",
        "organism": "Rat",
        "refseq_name": "leucine-rich repeat-containing protein 17 precursor",
        "refseq_ac": "NP_001020326",
        "gene_names_uniprotkb": "Lrrc17",
        "gene_names_refseq": "Lrrc17",
        "protein_names_uniprotkb": "Leucine-rich repeat-containing protein 17",
        "protein_names_refseq": "leucine-rich repeat-containing protein 17 precursor; leucine-rich repeat-containing protein 17",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:502715)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Involved in bone homeostasis. Acts as a negative regulator of RANKL-induced osteoclast precursor differentiation from bone marrow precursors., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "predicted_c_glycosites": 0,
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        "reported_phosphosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0038023 signaling receptor activity",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005886 plasma membrane",
        "go_biological_process": "GO:0001503 ossification;GO:0045671 negative regulation of osteoclast differentiation;GO:0048539 bone marrow development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "Q6AYD0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q6AYG1-1",
        "uniprot_id": "MS3L2_RAT",
        "mass": 41420.0,
        "length": 371,
        "protein_name": "MSL complex subunit 3B",
        "gene_name": "Msl3b",
        "organism": "Rat",
        "refseq_name": "MSL complex subunit 3B",
        "refseq_ac": "NP_001014054",
        "gene_names_uniprotkb": "Msl3b; Msl3l2",
        "gene_names_refseq": "Msl3b; Msl3l2; RGD1308699",
        "protein_names_uniprotkb": "MSL complex subunit 3B; MSL3-like 2; Male-specific lethal-3 homolog 2; Male-specific lethal-3 protein-like 2",
        "protein_names_refseq": "MSL complex subunit 3B; MSL3-like 2; male-specific lethal-3 homolog 2; male-specific lethal-3 protein-like 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:309790)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Probable non-catalytic component of the MSL histone acetyltransferase complex, a multiprotein complex that mediates the majority of histone H4 acetylation at 'Lys-16' (H4K16ac), an epigenetic mark that prevents chromatin compaction., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "missing_score": 10000,
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        "ec_number_list": "2.7.11.1;2.7.12.1;2.7.1.153;2.7.1.137;2.7.11.24;2.7.11.25;2.7.11.22;2.7.11.23;2.7.4.6;2.7.1.154;2.7.11.38;2.7.11.17;2.7.11.21;2.7.12.2;2.7.1.40;2.7.11.12;2.7.11.26;2.7.11.34;2.7.10.2;2.7.1.150;2.7.11.13;4.1.1.32;2.7.11.19;2.7.2.3;2.7.11.11;2.7.11.31;3.1.3.16;2.7.11.4;2.3.1.48;3.1.11.-;2.7.13.3;2.7.4.18;3.1.24.-;3.4.19.12;2.7.11.39;2.4.99.18;2.7.11.10",
        "go_molecular_function": "GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding;GO:0042803 protein homodimerization activity;GO:0046872 metal ion binding",
        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005737 cytoplasm;GO:0005794 Golgi apparatus;GO:0090443 FAR/SIN/STRIPAK complex",
        "go_biological_process": "GO:0006468 protein phosphorylation;GO:0035556 intracellular signal transduction;GO:0046777 protein autophosphorylation;GO:0034599 cellular response to oxidative stress;GO:0051683 establishment of Golgi localization",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
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    },
    {
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        "mass": 41420.0,
        "length": 365,
        "protein_name": "non-specific serine/threonine protein kinase",
        "gene_name": "Tssk1b",
        "organism": "Rat",
        "refseq_name": "testis-specific serine/threonine-protein kinase 1",
        "refseq_ac": "NP_001011900",
        "gene_names_uniprotkb": "Tssk1b",
        "gene_names_refseq": "Stk22a; Tssk1b; Tssk1",
        "protein_names_uniprotkb": "non-specific serine/threonine protein kinase; 2.7.11.1",
        "protein_names_refseq": "serine/threonine kinase 22A (spermiogenesis associated); spermiogenesis associated; testis-specific serine kinase 1; testis-specific serine/threonine-protein kinase 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:288358)",
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        "missing_score": 10000,
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        "ec_number_list": "2.7.11.1;2.7.12.1;2.7.1.153;2.7.1.137;2.7.11.24;2.7.11.25;2.7.11.22;2.7.11.23;2.7.4.6;2.7.1.154;2.7.11.38;2.7.11.17;2.7.11.21;2.7.12.2;2.7.1.40;2.7.11.12;2.7.11.26;2.7.11.34;2.7.10.2;2.7.1.150;2.7.11.13;4.1.1.32;2.7.11.19;2.7.2.3;2.7.11.11;2.7.11.31;3.1.3.16;2.7.11.4;2.3.1.48;3.1.11.-;2.7.13.3;2.7.4.18;3.1.24.-;3.4.19.12;2.7.11.39;2.4.99.18;2.7.11.10",
        "go_molecular_function": "GO:0000287 magnesium ion binding;GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding;GO:0044877 protein-containing complex binding",
        "go_cellular_component": "GO:0001669 acrosomal vesicle;GO:0031514 motile cilium",
        "go_biological_process": "GO:0007286 spermatid development;GO:0006468 protein phosphorylation;GO:0018105 peptidyl-serine phosphorylation;GO:0007283 spermatogenesis;GO:0030154 cell differentiation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
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    },
    {
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        "length": 268,
        "protein_name": "Testis-specific serine/threonine-protein kinase 3",
        "gene_name": "Tssk3",
        "organism": "Rat",
        "refseq_name": "testis-specific serine/threonine-protein kinase 3",
        "refseq_ac": "NP_001007651",
        "gene_names_uniprotkb": "Tssk3",
        "gene_names_refseq": "Stk22c; Tssk-3; Tssk3",
        "protein_names_uniprotkb": "Testis-specific serine/threonine-protein kinase 3; 2.7.11.1; Serine/threonine-protein kinase 22C",
        "protein_names_refseq": "serine/threonine kinase 22C; spermiogenesis associated; testis-specific serine/threonine-protein kinase 3",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:297891)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Serine/threonine protein kinase required for spermatid development and male fertility., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "ec_number_list": "2.7.11.1;2.7.12.1;2.7.1.153;2.7.1.137;2.7.11.24;2.7.11.25;2.7.11.22;2.7.11.23;2.7.4.6;2.7.1.154;2.7.11.38;2.7.11.17;2.7.11.21;2.7.12.2;2.7.1.40;2.7.11.12;2.7.11.26;2.7.11.34;2.7.10.2;2.7.1.150;2.7.11.13;4.1.1.32;2.7.11.19;2.7.2.3;2.7.11.11;2.7.11.31;3.1.3.16;2.7.11.4;2.3.1.48;3.1.11.-;2.7.13.3;2.7.4.18;3.1.24.-;3.4.19.12;2.7.11.39;2.4.99.18;2.7.11.10",
        "go_molecular_function": "GO:0000287 magnesium ion binding;GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding;GO:0030145 manganese ion binding",
        "go_cellular_component": "GO:0036126 sperm flagellum",
        "go_biological_process": "GO:0007283 spermatogenesis;GO:0007286 spermatid development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "Q6V9Y3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q6W9J5-1",
        "uniprot_id": "Q6W9J5_RAT",
        "mass": 39293.0,
        "length": 344,
        "protein_name": "RT1 class Ib, locus M2",
        "gene_name": "RT1-M2",
        "organism": "Rat",
        "refseq_name": "RT1 class Ib, locus M2 precursor",
        "refseq_ac": "NP_001001717",
        "gene_names_uniprotkb": "RT1-M2",
        "gene_names_refseq": "RT1-M2",
        "protein_names_uniprotkb": "RT1 class Ib, locus M2",
        "protein_names_refseq": "RT1 class Ib, locus M2 precursor",
        "tax_id": 10116,
        "disease": "Stevens-Johnson syndrome (Disease Ontology:DOID:0050426); colitis (Disease Ontology:DOID:0060180); Cytomegalovirus retinitis (Disease Ontology:DOID:0080160); COVID-19 (Disease Ontology:DOID:0080600); ankylosing spondylitis 1 (Disease Ontology:DOID:0080603); erythema nodosum (Disease Ontology:DOID:0080750); occupational asthma (Disease Ontology:DOID:0080820); birdshot chorioretinopathy (Disease Ontology:DOID:0111079); psoriasis 1 (Disease Ontology:DOID:0111286); sensorineural hearing loss (Disease Ontology:DOID:10003); spondyloarthropathy (Disease Ontology:DOID:1123); trachoma (Disease Ontology:DOID:11265); sarcoidosis (Disease Ontology:DOID:11335); retinal vasculitis (Disease Ontology:DOID:11563); otosclerosis (Disease Ontology:DOID:12185); Graves' disease (Disease Ontology:DOID:12361); retinopathy of prematurity (Disease Ontology:DOID:13025); uveitis (Disease Ontology:DOID:13141); Behcet's disease (Disease Ontology:DOID:13241); anterior uveitis (Disease Ontology:DOID:1407); Takayasu's arteritis (Disease Ontology:DOID:2508); synovitis (Disease Ontology:DOID:2703); dermatitis (Disease Ontology:DOID:2723); asthma (Disease Ontology:DOID:2841); severe acute respiratory syndrome (Disease Ontology:DOID:2945); bipolar disorder (Disease Ontology:DOID:3312); cerebral infarction (Disease Ontology:DOID:3526); acute retinal necrosis syndrome (Disease Ontology:DOID:3611); thrombophlebitis (Disease Ontology:DOID:3875); tuberculosis (Disease Ontology:DOID:399); cervical cancer (Disease Ontology:DOID:4362); human immunodeficiency virus infectious disease (Disease Ontology:DOID:526); uveal melanoma (Disease Ontology:DOID:6039); reactive arthritis (Disease Ontology:DOID:6196); ankylosing spondylitis (Disease Ontology:DOID:7147); diabetic retinopathy (Disease Ontology:DOID:8947); allergic asthma (Disease Ontology:DOID:9415); Meniere's disease (Disease Ontology:DOID:9849); alopecia (Disease Ontology:DOID:987); mitral valve prolapse (Disease Ontology:DOID:988); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (rno:24988);  (R-RNO-1236974);  (R-RNO-1236977);  (R-RNO-198933);  (R-RNO-6798695);  (R-RNO-983170)",
        "pathway_count": 6,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Involved in the presentation of foreign antigens to the immune system., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "predicted_c_glycosites": 0,
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        "total_reported_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 41,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "F1LW75",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005102 signaling receptor binding;GO:0030881 beta-2-microglobulin binding;GO:0042605 peptide antigen binding",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0009897 external side of plasma membrane;GO:0030670 phagocytic vesicle membrane;GO:0042612 MHC class I protein complex;GO:0098553 lumenal side of endoplasmic reticulum membrane",
        "go_biological_process": "GO:0002476 antigen processing and presentation of endogenous peptide antigen via MHC class Ib;GO:0006955 immune response;GO:0002486 antigen processing and presentation of endogenous peptide antigen via MHC class I via ER pathway, TAP-independent;GO:0001916 positive regulation of T cell mediated cytotoxicity",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "Q6W9J5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q6WN19-1",
        "uniprot_id": "RTN2_RAT",
        "mass": 50967.0,
        "length": 469,
        "protein_name": "Reticulon-2",
        "gene_name": "Rtn2",
        "organism": "Rat",
        "refseq_name": "reticulon-2",
        "refseq_ac": "NP_963856",
        "gene_names_uniprotkb": "Rtn2; Nspl1",
        "gene_names_refseq": "NSPLI; RTN2-B; Rtn2",
        "protein_names_uniprotkb": "Reticulon-2; NSP-like protein 1; NSP-like protein I; NSPLI; Neuroendocrine-specific protein-like 1; Neuroendocrine-specific protein-like I",
        "protein_names_refseq": "NSP-like 1; NSP-like protein 1; NSP-like protein I; formerly RTN2w; neuroendocrine-specific protein-like 1; neuroendocrine-specific protein-like I; reticulon 2 (Z-band associated protein); reticulon-2",
        "tax_id": 10116,
        "disease": "hereditary spastic paraplegia 12 (Disease Ontology:DOID:0110765)",
        "pathway": " (rno:308410)",
        "pathway_count": 1,
        "publication_count": 3,
        "publication_id_list": "12832288;18096700;22673903",
        "class_list": "",
        "function": "Inhibits amyloid precursor protein processing, probably by blocking BACE1 activity (By similarity). Enhances trafficking of the glutamate transporter SLC1A1/EAAC1 from the endoplasmic reticulum to the cell surface (PubMed:18096700). Plays a role in the translocation of SLC2A4/GLUT4 from intracellular membranes to the cell membrane which facilitates the uptake of glucose into the cell (By similarity)., [UniProtKB, UniProtKB, PubMed, UniProtKB]; RTN2B functions as a positive regulator in the delivery of EAAC1 from the ER to the cell surface., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "mined_c_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "reported_phosphosites": 1,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "F1LM00",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0009986 cell surface;GO:0014069 postsynaptic density;GO:0005789 endoplasmic reticulum membrane;GO:0005882 intermediate filament",
        "go_biological_process": "GO:0015031 protein transport;GO:0046324 regulation of D-glucose import;GO:1902430 negative regulation of amyloid-beta formation;GO:0007420 brain development;GO:0030182 neuron differentiation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "Q6WN19-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q6XCE7-1",
        "uniprot_id": "Q6XCE7_RAT",
        "mass": 42843.0,
        "length": 373,
        "protein_name": "Probable G-protein coupled receptor 34",
        "gene_name": "Gpr34",
        "organism": "Rat",
        "refseq_name": "probable G-protein coupled receptor 34",
        "refseq_ac": "NP_001020096",
        "gene_names_uniprotkb": "Gpr34",
        "gene_names_refseq": "Gpr34",
        "protein_names_uniprotkb": "Probable G-protein coupled receptor 34",
        "protein_names_refseq": "probable G-protein coupled receptor 34",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:554353)",
        "pathway_count": 1,
        "publication_count": 2,
        "publication_id_list": "16460680;22343749",
        "class_list": "",
        "function": "G-protein-coupled receptor of lysophosphatidylserine (LysoPS) that plays different roles in immune response. Acts a damage-sensing receptor that triggers tissue repair upon recognition of dying neutrophils. Mechanistically, apoptotic neutrophils release lysophosphatydilserine that are recognized by type 3 innate lymphoid cells (ILC3s) via GPR34, which activates downstream PI3K-AKT and RAS-ERK signaling pathways leading to STAT3 activation and IL-22 production. Plays an important role in microglial function, controlling morphology and phagocytosis., [UniProtKB, UniProtKB]; Results suggest that GPR34 is the functional mast cell lysophosphatidylserine receptor, [RefSeq, PubMed]; The present studies confirm that GPR34 is a cellular receptor for LysoPS, especially with a fatty acid at the sn-2 position., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
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        "reported_c_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "A6JZX9",
        "ec_number_list": "",
        "go_molecular_function": "GO:0045028 G protein-coupled purinergic nucleotide receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "Q6XCE7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q71FD8-1",
        "uniprot_id": "Q71FD8_RAT",
        "mass": 18633.0,
        "length": 170,
        "protein_name": "Potassium voltage-gated channel subfamily E regulatory subunit 4",
        "gene_name": "Kcne4",
        "organism": "Rat",
        "refseq_name": "potassium voltage-gated channel subfamily E member 4",
        "refseq_ac": "NP_997691",
        "gene_names_uniprotkb": "Kcne4",
        "gene_names_refseq": "Kcne4",
        "protein_names_uniprotkb": "Potassium voltage-gated channel subfamily E regulatory subunit 4",
        "protein_names_refseq": "minK-related peptide 3; potassium channel, voltage gated subfamily E regulatory beta subunit 4; potassium channel, voltage-gated Isk-related subfamily E regulatory beta subunit 4; potassium voltage-gated channel subfamily E member 4; potassium voltage-gated channel, Isk-related family, member 4; potassium voltage-gated channel, Isk-related subfamily, gene 4",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:367302);  (R-RNO-5576890);  (R-RNO-5576893)",
        "pathway_count": 3,
        "publication_count": 4,
        "publication_id_list": "12944270;18463315;26503181;30969795",
        "class_list": "",
        "function": "Experimental data and the in silico structure suggest that the KCNE4 interaction hides a forward-trafficking motif within Kv1.3 in addition to adding a strong endoplasmic reticulum retention signature to the Kv1.3-KCNE4 complex., [RefSeq, PubMed]; Knockdown of KCNE4 leads to reduced Kv7.4 membrane abundance, a depolarized membrane potential and an augmented response to vasoconstrictors., [RefSeq, PubMed]; MiRP3 (encoded by the KCNE4 gene) plays a role in modulation of BK-dependent urinary potassium excretion. GeneRIF: Apparent association with BK channel in renal collecting duct, [RefSeq, PubMed]; Mouse studies regarding function of mouse Kcne4 protein, [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0019870 potassium channel inhibitor activity;GO:0015459 potassium channel regulator activity;GO:0044325 transmembrane transporter binding;GO:0005249 voltage-gated potassium channel activity",
        "go_cellular_component": "GO:0016324 apical plasma membrane;GO:0008076 voltage-gated potassium channel complex",
        "go_biological_process": "GO:0086011 membrane repolarization during action potential;GO:0098915 membrane repolarization during ventricular cardiac muscle cell action potential;GO:0086091 regulation of heart rate by cardiac conduction;GO:0060307 regulation of ventricular cardiac muscle cell membrane repolarization;GO:0086005 ventricular cardiac muscle cell action potential",
        "synthesized_glycan_count": 0,
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        "record_id": "Q71FD8-1",
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    },
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        "length": 93,
        "protein_name": "Antisense paternally expressed gene 3",
        "gene_name": "Apeg3",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Apeg3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Antisense paternally expressed gene 3",
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    },
    {
        "uniprot_canonical_ac": "Q8CGQ0-1",
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        "length": 197,
        "protein_name": "Beta-crystallin A2",
        "gene_name": "Cryba2",
        "organism": "Rat",
        "refseq_name": "beta-crystallin A2",
        "refseq_ac": "NP_775163",
        "gene_names_uniprotkb": "Cryba2",
        "gene_names_refseq": "Cryba2",
        "protein_names_uniprotkb": "Beta-crystallin A2; Beta-A2 crystallin",
        "protein_names_refseq": "beta-crystallin A2; betaA2-crystallin",
        "tax_id": 10116,
        "disease": "cataract 42 (Disease Ontology:DOID:0110237)",
        "pathway": " (rno:286925)",
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        "publication_count": 0,
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        "class_list": "",
        "function": "Crystallins are the dominant structural components of the vertebrate eye lens., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "ec_number_list": "",
        "go_molecular_function": "GO:0042802 identical protein binding;GO:0005212 structural constituent of eye lens",
        "go_cellular_component": "",
        "go_biological_process": "GO:0007601 visual perception;GO:0002088 lens development in camera-type eye",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "Q8CGQ0-1",
        "record_type": "protein"
    },
    {
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        "uniprot_id": "Q8R3Z7_RAT",
        "mass": 62480.0,
        "length": 549,
        "protein_name": "EH-domain containing 4",
        "gene_name": "Ehd4",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ehd4",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "EH-domain containing 4",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:192204)",
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        "class_list": "",
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        "go_molecular_function": "GO:0005524 ATP binding;GO:0005525 GTP binding;GO:0030674 protein-macromolecule adaptor activity;GO:0005509 calcium ion binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005769 early endosome;GO:0005783 endoplasmic reticulum;GO:0005886 plasma membrane;GO:0005912 adherens junction",
        "go_biological_process": "GO:0006897 endocytosis;GO:0030100 regulation of endocytosis;GO:0051260 protein homooligomerization;GO:0072659 protein localization to plasma membrane;GO:0071363 cellular response to growth factor stimulus",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "Q8R3Z7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q923V7-1",
        "uniprot_id": "Q923V7_RAT",
        "mass": 51722.0,
        "length": 482,
        "protein_name": "KLF transcription factor 4",
        "gene_name": "Klf4",
        "organism": "Rat",
        "refseq_name": "Krueppel-like factor 4",
        "refseq_ac": "NP_446165",
        "gene_names_uniprotkb": "Klf4",
        "gene_names_refseq": "GKLF; Klf4",
        "protein_names_uniprotkb": "KLF transcription factor 4",
        "protein_names_refseq": "Krueppel-like factor 4; Kruppel like factor 4; Kruppel-like factor 4 (gut)",
        "tax_id": 10116,
        "disease": "hepatocellular carcinoma (Disease Ontology:DOID:684)",
        "pathway": " (rno:114505)",
        "pathway_count": 1,
        "publication_count": 6,
        "publication_id_list": "22673903;37441941;38084712;38085146;38774964;38866991",
        "class_list": "",
        "function": "Hypoxia-inducible factor-1alpha attenuates renal podocyte injury in male rats in a simulated high-altitude environment by upregulating Kruppel-like factor 4 expression., [RefSeq, PubMed]; MicroRNA-29a-3p Accelerates Inflammatory Damage in Neonatal Pneumonia Via Targeting Kruppel-like Factor 4. Publication Status: Online-Only, [RefSeq, PubMed]; N6-methyladenosine-driven miR-143/145-KLF4 circuit orchestrates the phenotypic switch of pulmonary artery smooth muscle cells. Publication Status: Online-Only, [RefSeq, PubMed]; Ovarian Tumor Domain-Containing 7B Attenuates Pathological Cardiac Hypertrophy by Inhibiting Ubiquitination and Degradation of Kruppel-Like Factor 4., [RefSeq, PubMed]; Protective effects of KLF4 on blood-brain barrier and oxidative stress after cerebral ischemia-reperfusion in rats through the Nrf2/Trx1 pathway., [RefSeq, PubMed]",
        "predicted_glycosites": 2,
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        "go_molecular_function": "GO:0001010 RNA polymerase II sequence-specific DNA-binding transcription factor recruiting activity;GO:0003700 DNA-binding transcription factor activity;GO:0008270 zinc ion binding;GO:0042826 histone deacetylase binding;GO:0003690 double-stranded DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005667 transcription regulator complex;GO:0000785 chromatin",
        "go_biological_process": "GO:1903672 positive regulation of sprouting angiogenesis;GO:0009913 epidermal cell differentiation;GO:0014740 negative regulation of muscle hyperplasia;GO:0048679 regulation of axon regeneration;GO:1904998 negative regulation of leukocyte adhesion to arterial endothelial cell",
        "synthesized_glycan_count": 0,
        "hit_score": 0.7,
        "record_id": "Q923V7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q924H6-1",
        "uniprot_id": "Q924H6_RAT",
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        "length": 748,
        "protein_name": "Solute carrier organic anion transporter family member",
        "gene_name": "Slco6b1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Slco6b1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Solute carrier organic anion transporter family member",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "biomarker_type": "",
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        "secondary_ac_list": "F1MA40",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0016323 basolateral plasma membrane",
        "go_biological_process": "GO:0006811 monoatomic ion transport;GO:0055085 transmembrane transport;GO:0043252 sodium-independent organic anion transport",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "Q924H6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q99MA1-1",
        "uniprot_id": "Q99MA1_RAT",
        "mass": 28291.0,
        "length": 269,
        "protein_name": "Cbp/p300-interacting transactivator 2",
        "gene_name": "Cited2",
        "organism": "Rat",
        "refseq_name": "cbp/p300-interacting transactivator 2",
        "refseq_ac": "NP_446150",
        "gene_names_uniprotkb": "Cited2",
        "gene_names_refseq": "Cited2; Mrg1",
        "protein_names_uniprotkb": "Cbp/p300-interacting transactivator 2",
        "protein_names_refseq": "Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2; cbp/p300-interacting transactivator 2",
        "tax_id": 10116,
        "disease": "atrial heart septal defect 8 (Disease Ontology:DOID:0110113); ventricular septal defect (Disease Ontology:DOID:1657); congenital heart disease (Disease Ontology:DOID:1682); brain ischemia (Disease Ontology:DOID:2316); osteosarcoma (Disease Ontology:DOID:3347); tetralogy of Fallot (Disease Ontology:DOID:6419)",
        "pathway": " (rno:114490);  (R-RNO-1234158);  (R-RNO-8866907)",
        "pathway_count": 3,
        "publication_count": 5,
        "publication_id_list": "26240138;27680315;36626551;38291157;38922923",
        "class_list": "",
        "function": "CITED2 is a conserved regulator of the uterine-placental interface., [RefSeq, PubMed]; Cited2 is a key regulator of placental development and plasticity. Review article, [RefSeq, PubMed]; Dysregulation of CITED2 in abnormal lung development in the nitrofen rat model. Publication Status: Online-Only, [RefSeq, PubMed]; Gestational diabetes mellitus is a risk factor for abnormal heart development. Cited2 expression decreased in the heart tissues of diabetic-exposed embryos comparing with the control., [RefSeq, PubMed]; MicroRNAs in the Myocyte Enhancer Factor 2 (MEF2)-regulated Gtl2-Dio3 Noncoding RNA Locus Promote Cardiomyocyte Proliferation by Targeting the Transcriptional Coactivator Cited2., [RefSeq, PubMed]",
        "predicted_glycosites": 2,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0050693 LBD domain binding;GO:0003682 chromatin binding;GO:0003713 transcription coactivator activity;GO:0019904 protein domain specific binding;GO:0003714 transcription corepressor activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0000785 chromatin;GO:0032991 protein-containing complex",
        "go_biological_process": "GO:0003156 regulation of animal organ formation;GO:0007530 sex determination;GO:0022409 positive regulation of cell-cell adhesion;GO:0035802 adrenal cortex formation;GO:0060971 embryonic heart tube left/right pattern formation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.6,
        "record_id": "Q99MA1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q99N82-1",
        "uniprot_id": "Q99N82_RAT",
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        "length": 145,
        "protein_name": "Prolactin-inducible protein homolog",
        "gene_name": "Sval1",
        "organism": "Rat",
        "refseq_name": "seminal vesicle antigen-like 1 precursor",
        "refseq_ac": "NP_579826",
        "gene_names_uniprotkb": "Sval1",
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        "protein_names_refseq": "seminal vesicle antigen-like 1 precursor",
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        "disease": "Alzheimer's disease (Disease Ontology:DOID:10652)",
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        "length": 1478,
        "protein_name": "Shortage in chiasmata 1",
        "gene_name": "Shoc1",
        "organism": "Rat",
        "refseq_name": "protein shortage in chiasmata 1 ortholog isoform X1",
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        "protein_names_refseq": "protein shortage in chiasmata 1 ortholog isoform X1",
        "tax_id": 10116,
        "disease": "spermatogenic failure 75 (Disease Ontology:DOID:0070574)",
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        "go_molecular_function": "GO:0016887 ATP hydrolysis activity;GO:0003697 single-stranded DNA binding",
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    {
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        "protein_name": "V-type proton ATPase subunit S1",
        "gene_name": "Atp6ap1l",
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        "gene_names_uniprotkb": "Atp6ap1l",
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        "protein_names_uniprotkb": "V-type proton ATPase subunit S1; V-ATPase Ac45 subunit; V-ATPase S1 accessory protein; Vacuolar proton pump subunit S1",
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        "function": "Accessory subunit of the proton-transporting vacuolar (V)-ATPase protein pump, which is required for luminal acidification of secretory vesicles. Guides the V-type ATPase into specialized subcellular compartments, such as neuroendocrine regulated secretory vesicles or the ruffled border of the osteoclast, thereby regulating its activity. Involved in membrane trafficking and Ca(2+)-dependent membrane fusion. May play a role in the assembly of the V-type ATPase complex. In aerobic conditions, involved in intracellular iron homeostasis, thus triggering the activity of Fe(2+) prolyl hydroxylase (PHD) enzymes, and leading to HIF1A hydroxylation and subsequent proteasomal degradation. In islets of Langerhans cells, may regulate the acidification of dense-core secretory granules., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0033176 proton-transporting V-type ATPase complex;GO:0016020 membrane",
        "go_biological_process": "GO:0030641 regulation of cellular pH",
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        "record_id": "D3ZA00-1",
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        "gene_name": "4933400A11Rik",
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        "gene_names_uniprotkb": "4933400A11Rik",
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        "protein_names_uniprotkb": "F-actin-capping protein subunit alpha",
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        "function": "F-actin-capping proteins bind in a Ca(2+)-independent manner to the fast growing ends of actin filaments (barbed end) thereby blocking the exchange of subunits at these ends. Unlike other capping proteins (such as gelsolin and severin), these proteins do not sever actin filaments., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0051015 actin filament binding",
        "go_cellular_component": "GO:0008290 F-actin capping protein complex;GO:0030863 cortical cytoskeleton",
        "go_biological_process": "GO:0030036 actin cytoskeleton organization;GO:0051016 barbed-end actin filament capping",
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        "record_id": "D3ZVN8-1",
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        "length": 869,
        "protein_name": "Rho guanine nucleotide exchange factor 26",
        "gene_name": "Arhgef26",
        "organism": "Rat",
        "refseq_name": "rho guanine nucleotide exchange factor 26",
        "refseq_ac": "NP_001414611",
        "gene_names_uniprotkb": "Arhgef26",
        "gene_names_refseq": "Arhgef26; RGD1562559; Sgef",
        "protein_names_uniprotkb": "Rho guanine nucleotide exchange factor 26",
        "protein_names_refseq": "Rho guanine nucleotide exchange factor (GEF) 26; Src homology 3 domain-containing guanine nucleotide exchange factor; rho guanine nucleotide exchange factor 26",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:310460);  (R-RNO-193648);  (R-RNO-416482);  (R-RNO-9013148);  (R-RNO-9013408)",
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        "go_molecular_function": "GO:0005085 guanyl-nucleotide exchange factor activity",
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        "go_biological_process": "GO:0032956 regulation of actin cytoskeleton organization;GO:0097178 ruffle assembly;GO:0001886 endothelial cell morphogenesis",
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    {
        "uniprot_canonical_ac": "D4A624-1",
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        "length": 516,
        "protein_name": "Shugoshin 1",
        "gene_name": "Sgo1",
        "organism": "Rat",
        "refseq_name": "shugoshin 1",
        "refseq_ac": "NP_001386273",
        "gene_names_uniprotkb": "Sgo1",
        "gene_names_refseq": "Sgo1; Sgol1",
        "protein_names_uniprotkb": "Shugoshin 1; Shugoshin-like 1",
        "protein_names_refseq": "shugoshin 1; shugoshin-like 1",
        "tax_id": 10116,
        "disease": "chronic atrial and intestinal dysrhythmia (Disease Ontology:DOID:0060339)",
        "pathway": " (rno:363174);  (R-RNO-141430);  (R-RNO-141444);  (R-RNO-2467813);  (R-RNO-2500257);  (R-RNO-5663220);  (R-RNO-68877);  (R-RNO-69273);  (R-RNO-9648025)",
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        "publication_id_list": "33953173",
        "class_list": "",
        "function": "Cohesin-protein Shugoshin-1 controls cardiac automaticity via HCN4 pacemaker channel. Publication Status: Online-Only, [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0019900 kinase binding",
        "go_cellular_component": "GO:0030892 mitotic cohesin complex;GO:0000922 spindle pole;GO:0005654 nucleoplasm;GO:0005813 centrosome;GO:0016607 nuclear speck",
        "go_biological_process": "GO:0045143 homologous chromosome segregation;GO:0007059 chromosome segregation;GO:0008608 attachment of spindle microtubules to kinetochore;GO:0051301 cell division;GO:0071962 mitotic sister chromatid cohesion, centromeric",
        "synthesized_glycan_count": 0,
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        "record_id": "D4A624-1",
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    },
    {
        "uniprot_canonical_ac": "D4AAK5-1",
        "uniprot_id": "D4AAK5_RAT",
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        "length": 786,
        "protein_name": "Receptor-interacting serine/threonine-protein kinase 4",
        "gene_name": "Ripk4",
        "organism": "Rat",
        "refseq_name": "receptor-interacting serine/threonine-protein kinase 4 isoform 1",
        "refseq_ac": "NP_001100573",
        "gene_names_uniprotkb": "Ripk4",
        "gene_names_refseq": "Ripk4",
        "protein_names_uniprotkb": "Receptor-interacting serine/threonine-protein kinase 4; 2.7.11.1; Ankyrin repeat domain-containing protein 3",
        "protein_names_refseq": "receptor-interacting serine/threonine-protein kinase 4 isoform 1; receptor-interacting serine/threonine-protein kinase 4",
        "tax_id": 10116,
        "disease": "popliteal pterygium syndrome (Disease Ontology:DOID:0060055)",
        "pathway": " (rno:304053)",
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        "publication_id_list": "",
        "class_list": "",
        "function": "Serine/threonine protein kinase. Required for embryonic skin development and correct skin homeostasis in adults, via phosphorylation of PKP1 and subsequent promotion of keratinocyte differentiation and cell adhesion. It is a direct transcriptional target of TP63. Plays a role in NF-kappa-B activation., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "ec_number_list": "2.7.11.1;2.7.12.1;2.7.1.153;2.7.1.137;2.7.11.24;2.7.11.25;2.7.11.22;2.7.11.23;2.7.4.6;2.7.1.154;2.7.11.38;2.7.11.17;2.7.11.21;2.7.12.2;2.7.1.40;2.7.11.12;2.7.11.26;2.7.11.34;2.7.10.2;2.7.1.150;2.7.11.13;4.1.1.32;2.7.11.19;2.7.2.3;2.7.11.11;2.7.11.31;3.1.3.16;2.7.11.4;2.3.1.48;3.1.11.-;2.7.13.3;2.7.4.18;3.1.24.-;3.4.19.12;2.7.11.39;2.4.99.18;2.7.11.10",
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        "length": 195,
        "protein_name": "Factor in the germline alpha",
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        "refseq_name": "factor in the germline alpha",
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        "protein_names_uniprotkb": "Factor in the germline alpha; Transcription factor FIGa",
        "protein_names_refseq": "factor in the germline alpha",
        "tax_id": 10116,
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        "refseq_name": "RAD21 cohesin complex component like 1",
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        "gene_names_refseq": "Rad21l1",
        "protein_names_uniprotkb": "RAD21 cohesin complex component like 1",
        "protein_names_refseq": "RAD21 cohesin complex component like 1; RAD21-like 1; double-strand-break repair protein rad21-like protein 1",
        "tax_id": 10116,
        "disease": "Cornelia de Lange syndrome 4 (Disease Ontology:DOID:0080508)",
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        "protein_name": "Ig-like domain-containing protein",
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        "gene_names_uniprotkb": "ENSRNOG00000070366",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ig-like domain-containing protein",
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        "go_cellular_component": "GO:0042101 T cell receptor complex;GO:0019814 immunoglobulin complex",
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        "record_id": "M0R8N3-1",
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    },
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        "length": 314,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or5g28",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr445",
        "refseq_ac": "NP_001001049",
        "gene_names_uniprotkb": "Or5g28",
        "gene_names_refseq": "Olr445; Or5g28",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 445; olfactory receptor Olr445; olfactory receptor gene Olr445",
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        "pathway": " (rno:405936)",
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        "function": "Odorant receptor., [UniProtKB, UniProtKB]; Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding",
        "go_cellular_component": "GO:0005886 plasma membrane",
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        "length": 941,
        "protein_name": "MORC family CW-type zinc finger 3",
        "gene_name": "Morc3",
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        "refseq_name": "MORC family CW-type zinc finger protein 3",
        "refseq_ac": "NP_001382557",
        "gene_names_uniprotkb": "Morc3",
        "gene_names_refseq": "Morc3; Zcwcc3",
        "protein_names_uniprotkb": "MORC family CW-type zinc finger 3",
        "protein_names_refseq": "MORC family CW-type zinc finger protein 3; microrchidia 3; zinc finger, CW-type with coiled-coil domain 3",
        "tax_id": 10116,
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        "publication_id_list": "22673903",
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0008270 zinc ion binding;GO:0030674 protein-macromolecule adaptor activity;GO:0016887 ATP hydrolysis activity;GO:0140002 histone H3K4me3 reader activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0016605 PML body;GO:0000785 chromatin",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006468 protein phosphorylation;GO:0050821 protein stabilization;GO:0009791 post-embryonic development;GO:0048147 negative regulation of fibroblast proliferation",
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        "hit_score": 0.2,
        "record_id": "A0A096MIX0-1",
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    {
        "uniprot_canonical_ac": "A0A096MIY3-1",
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        "length": 410,
        "protein_name": "G/T mismatch-specific thymine DNA glycosylase",
        "gene_name": "Tdg",
        "organism": "Rat",
        "refseq_name": "G/T mismatch-specific thymine DNA glycosylase isoform 1",
        "refseq_ac": "NP_001375432",
        "gene_names_uniprotkb": "Tdg",
        "gene_names_refseq": "Tdg",
        "protein_names_uniprotkb": "G/T mismatch-specific thymine DNA glycosylase; 3.2.2.29; Thymine-DNA glycosylase",
        "protein_names_refseq": "G/T mismatch-specific thymine DNA glycosylase isoform 1; G/T mismatch-specific thymine DNA glycosylase",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:114521);  (R-RNO-110329);  (R-RNO-110357);  (R-RNO-3108214);  (R-RNO-5221030)",
        "pathway_count": 5,
        "publication_count": 1,
        "publication_id_list": "31518169",
        "class_list": "",
        "function": "Thymine DNA glycosylase plays a key role in regulating CaMKIIgamma expression in vascular smooth muscle cells through promoter cytosine methylation/demethylation., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "ec_number_list": "3.2.2.29;3.1.11.2;3.1.21.-;2.3.2.-",
        "go_molecular_function": "GO:0043739 G/U mismatch-specific uracil-DNA glycosylase activity;GO:0000287 magnesium ion binding;GO:0003677 DNA binding;GO:0005524 ATP binding;GO:0019904 protein domain specific binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0016605 PML body",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0006284 base-excision repair;GO:0040029 epigenetic regulation of gene expression;GO:0045995 regulation of embryonic development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A096MIY3-1",
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    {
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        "length": 674,
        "protein_name": "Testis-specific Y-encoded-like protein 2",
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        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Tspyl2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Testis-specific Y-encoded-like protein 2; Differentially-expressed nucleolar TGF-beta1 target protein",
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        "disease": "",
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        "pathway_count": 0,
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        "publication_id_list": "",
        "class_list": "",
        "function": "Part of the CASK/TBR1/TSPYL2 transcriptional complex which modulates gene expression in response to neuronal synaptic activity, probably by facilitating nucleosome assembly. May inhibit cell proliferation by inducing p53-dependent CDKN1A expression., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0030308 negative regulation of cell growth;GO:0006334 nucleosome assembly;GO:0008156 negative regulation of DNA replication;GO:0045859 regulation of protein kinase activity",
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        "length": 409,
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        "refseq_name": "homeobox protein engrailed-1",
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        "protein_names_uniprotkb": "Homeobox protein engrailed-like",
        "protein_names_refseq": "engrailed 1; homeobox protein engrailed-1",
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        "disease": "Parkinson's disease (Disease Ontology:DOID:14330)",
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        "publication_id_list": "20042388",
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        "protein_names_uniprotkb": "Lactase-like protein; Klotho/lactase-phlorizin hydrolase-related protein",
        "protein_names_refseq": "lactase-like protein precursor; lactase-like protein",
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        "disease": "kidney disease (Disease Ontology:DOID:557)",
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        "protein_names_refseq": "regulation of nuclear pre-mRNA domain-containing protein 2 isoform X1",
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        "protein_name": "Dermatan sulfate epimerase",
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        "protein_names_refseq": "dermatan-sulfate epimerase isoform X1",
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        "length": 323,
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        "refseq_ac": "NP_001388548",
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        "protein_names_uniprotkb": "HORMA domain containing 2",
        "protein_names_refseq": "HORMA domain-containing protein 2 isoform 1; HORMA domain-containing protein 2",
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        "protein_names_uniprotkb": "Olfactory receptor family 5 subfamily B member 95 like 1",
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        "protein_names_refseq": "SPATA31 subfamily D, member 3; golgi phosphoprotein 2; spermatogenesis-associated protein 31D1",
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    },
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        "protein_name": "Olfactory receptor",
        "gene_name": "Or12e13b",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr594",
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        "gene_names_uniprotkb": "Or12e13b",
        "gene_names_refseq": "Olr594; Or12e13b",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 594; olfactory receptor Olr594; olfactory receptor gene Olr594",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "protein_names_uniprotkb": "Polycystin-1-like protein 3; PC1-like 3 protein; Polycystic kidney disease protein 1-like 3",
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        "function": "Pore-forming subunit of a heterotetrameric, non-selective cation channel that is permeable to Ca(2+). Also shows permeability towards NA(1+), K(+) and Mg(2+). Heterotetrameric complex channel is activated by external low pH and Ca(2+), but opens only when the extracellular pH rises again and after the removal of acid stimulus. May act as a sour taste receptor in gustatory cells; however, its contribution to sour taste perception is unclear in vivo and may be indirect., [UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "2.7.11.1;1.8.-.-",
        "go_molecular_function": "GO:0005509 calcium ion binding;GO:0005262 calcium channel activity;GO:0044325 transmembrane transporter binding;GO:0030246 carbohydrate binding;GO:0005227 calcium-activated cation channel activity",
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        "go_biological_process": "GO:0098655 monoatomic cation transmembrane transport;GO:0006812 monoatomic cation transport;GO:0070588 calcium ion transmembrane transport;GO:0050915 sensory perception of sour taste;GO:0050982 detection of mechanical stimulus",
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        "refseq_name": "coiled-coil domain-containing protein 27",
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        "gene_names_refseq": "Ccdc27",
        "protein_names_uniprotkb": "Coiled-coil domain containing 27",
        "protein_names_refseq": "coiled-coil domain-containing protein 27",
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        "length": 1859,
        "protein_name": "Zinc finger protein 142",
        "gene_name": "Zfp142",
        "organism": "Rat",
        "refseq_name": "zinc finger protein 142 isoform 1",
        "refseq_ac": "NP_001418925",
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        "gene_names_refseq": "Zfp142; Znf142",
        "protein_names_uniprotkb": "Zinc finger protein 142",
        "protein_names_refseq": "zinc finger protein 142 (clone pHZ-49); zinc finger protein 142 isoform 1",
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        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003700 DNA-binding transcription factor activity;GO:0008270 zinc ion binding;GO:0000976 transcription cis-regulatory region binding;GO:0003677 DNA binding",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006355 regulation of DNA-templated transcription;GO:0010468 regulation of gene expression",
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        "record_id": "A0A0G2JVD5-1",
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    {
        "uniprot_canonical_ac": "A0A0G2JVJ7-1",
        "uniprot_id": "A0A0G2JVJ7_RAT",
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        "length": 489,
        "protein_name": "Limb development membrane protein 1-like",
        "gene_name": "Lmbr1l",
        "organism": "Rat",
        "refseq_name": "protein LMBR1L isoform 1",
        "refseq_ac": "NP_001382658",
        "gene_names_uniprotkb": "Lmbr1l",
        "gene_names_refseq": "Lmbr1l; RGD1309631",
        "protein_names_uniprotkb": "Limb development membrane protein 1-like",
        "protein_names_refseq": "limb region 1 like; limb region 1-like homolog; protein LMBR1L isoform 1",
        "tax_id": 10116,
        "disease": "bone development disease (Disease Ontology:DOID:0080006)",
        "pathway": " (rno:300215)",
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        "go_molecular_function": "GO:0004888 transmembrane signaling receptor activity",
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        "go_biological_process": "GO:0007165 signal transduction;GO:0090090 negative regulation of canonical Wnt signaling pathway;GO:0060218 hematopoietic stem cell differentiation;GO:0006898 receptor-mediated endocytosis;GO:0016055 Wnt signaling pathway",
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    },
    {
        "uniprot_canonical_ac": "A0A0G2JVU1-1",
        "uniprot_id": "A0A0G2JVU1_RAT",
        "mass": 84415.0,
        "length": 767,
        "protein_name": "Integrin beta",
        "gene_name": "Itgb8",
        "organism": "Rat",
        "refseq_name": "integrin beta-8",
        "refseq_ac": "NP_001388746",
        "gene_names_uniprotkb": "Itgb8",
        "gene_names_refseq": "Itgb8",
        "protein_names_uniprotkb": "Integrin beta",
        "protein_names_refseq": "integrin beta-8; integrin, beta 8",
        "tax_id": 10116,
        "disease": "cancer (Disease Ontology:DOID:162)",
        "pathway": " (rno:362800);  (R-RNO-2129379);  (R-RNO-216083);  (R-RNO-2173789)",
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        "publication_id_list": "24090084;24461183;37931653;38843836",
        "class_list": "",
        "function": "Integrin alpha-V:beta-8 (ITGAV:ITGB8) is a receptor for fibronectin. It recognizes the sequence R-G-D in its ligands. Integrin alpha-V:beta-6 (ITGAV:ITGB6) mediates R-G-D-dependent release of transforming growth factor beta-1 (TGF-beta-1) from regulatory Latency-associated peptide (LAP), thereby playing a key role in TGF-beta-1 activation on the surface of activated regulatory T-cells (Tregs). Required during vasculogenesis., [UniProtKB, UniProtKB, UniProtKB]; Integrin beta8 prevents pericyte-myofibroblast transition and renal fibrosis through inhibiting the TGF-beta1/TGFBR1/Smad3 pathway in diabetic kidney disease., [RefSeq, PubMed]; The highly expressed beta8 plays important roles in the regulation of TGF-beta1 activation in neonatal rats with hypoxic-ischemic brain damage., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0005178 integrin binding;GO:0046872 metal ion binding;GO:1990430 extracellular matrix protein binding;GO:0005102 signaling receptor binding",
        "go_cellular_component": "GO:0005925 focal adhesion;GO:0009986 cell surface;GO:0008305 integrin complex;GO:0034686 integrin alphav-beta8 complex;GO:0005886 plasma membrane",
        "go_biological_process": "GO:0007229 integrin-mediated signaling pathway;GO:0016477 cell migration;GO:0030154 cell differentiation;GO:0045785 positive regulation of cell adhesion;GO:0033627 cell adhesion mediated by integrin",
        "synthesized_glycan_count": 0,
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        "record_id": "A0A0G2JVU1-1",
        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "A0A0G2JVW6-1",
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        "length": 1593,
        "protein_name": "Sterile alpha motif domain containing 9",
        "gene_name": "Samd9",
        "organism": "Rat",
        "refseq_name": "sterile alpha motif domain-containing protein 9",
        "refseq_ac": "NP_001386282",
        "gene_names_uniprotkb": "Samd9; RGD1563091",
        "gene_names_refseq": "RGD1563091; Samd9",
        "protein_names_uniprotkb": "Sterile alpha motif domain containing 9",
        "protein_names_refseq": "sterile alpha motif domain-containing protein 9",
        "tax_id": 10116,
        "disease": "normophosphatemic familial tumoral calcinosis (Disease Ontology:DOID:0080170)",
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        "protein_name": "Phospholipid-transporting ATPase",
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        "refseq_name": "phospholipid-transporting ATPase VA",
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        "gene_names_refseq": "Atp10a",
        "protein_names_uniprotkb": "Phospholipid-transporting ATPase; 7.6.2.1",
        "protein_names_refseq": "ATPase, class V, type 10A; phospholipid-transporting ATPase VA; probable phospholipid-transporting ATPase VA",
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        "refseq_ac": "NP_001414557",
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        "gene_names_refseq": "Ccdc113; Cfap263; RGD1565763",
        "protein_names_uniprotkb": "Cilia- and flagella-associated protein 263",
        "protein_names_refseq": "coiled-coil domain containing 113; coiled-coil domain-containing protein 113",
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        "refseq_name": "serine/threonine-protein kinase 32B",
        "refseq_ac": "NP_001100694",
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        "gene_names_refseq": "Stk32b",
        "protein_names_uniprotkb": "Serine/threonine-protein kinase 32B; 2.7.11.1",
        "protein_names_refseq": "serine/threonine-protein kinase 32B",
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        "secondary_ac_list": "F1M3G9",
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        "protein_name": "Zinc finger protein 420-like",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "LOC108348215",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger protein 420-like",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:108348215)",
        "pathway_count": 1,
        "publication_count": 0,
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        "class_list": "",
        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000976 transcription cis-regulatory region binding",
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        "record_id": "A0A0G2JX65-1",
        "record_type": "protein"
    },
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        "length": 496,
        "protein_name": "Loricrin cornified envelope precursor protein",
        "gene_name": "Loricrin",
        "organism": "Rat",
        "refseq_name": "loricrin",
        "refseq_ac": "NP_001386436",
        "gene_names_uniprotkb": "Loricrin",
        "gene_names_refseq": "Loricrin; Lor; RGD1559993",
        "protein_names_uniprotkb": "Loricrin cornified envelope precursor protein",
        "protein_names_refseq": "loricrin",
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        "biomarker_type": "",
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        "secondary_ac_list": "",
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        "go_molecular_function": "GO:0005200 structural constituent of cytoskeleton;GO:0030280 structural constituent of skin epidermis",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0009898 cytoplasmic side of plasma membrane;GO:0001533 cornified envelope",
        "go_biological_process": "GO:0030216 keratinocyte differentiation;GO:0018149 peptide cross-linking",
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        "record_id": "A0A0G2JXL7-1",
        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "A0A0G2JXR8-1",
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        "length": 654,
        "protein_name": "non-specific serine/threonine protein kinase",
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        "refseq_name": "sperm motility kinase-like",
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        "protein_names_uniprotkb": "non-specific serine/threonine protein kinase; 2.7.11.1",
        "protein_names_refseq": "sperm motility kinase-like",
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        "function": "May play a role in sperm motility, especially in the regulation of flagellar function., [UniProtKB, UniProtKB]",
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        "ec_number_list": "2.7.11.1;2.7.12.1;2.7.1.153;2.7.1.137;2.7.11.24;2.7.11.25;2.7.11.22;2.7.11.23;2.7.4.6;2.7.1.154;2.7.11.38;2.7.11.17;2.7.11.21;2.7.12.2;2.7.1.40;2.7.11.12;2.7.11.26;2.7.11.34;2.7.10.2;2.7.1.150;2.7.11.13;4.1.1.32;2.7.11.19;2.7.2.3;2.7.11.11;2.7.11.31;3.1.3.16;2.7.11.4;2.3.1.48;3.1.11.-;2.7.13.3;2.7.4.18;3.1.24.-;3.4.19.12;2.7.11.39;2.4.99.18;2.7.11.10",
        "go_molecular_function": "GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding",
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        "go_biological_process": "GO:0042149 cellular response to glucose starvation",
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        "hit_score": 0.1,
        "record_id": "A0A0G2JXR8-1",
        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "A0A0G2JYE1-1",
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        "mass": 60250.0,
        "length": 514,
        "protein_name": "Tripartite motif-containing 30C",
        "gene_name": "Trim30c",
        "organism": "Rat",
        "refseq_name": "tripartite motif-containing protein 30A",
        "refseq_ac": "XP_006229977",
        "gene_names_uniprotkb": "Trim30c",
        "gene_names_refseq": "Trim30c",
        "protein_names_uniprotkb": "Tripartite motif-containing 30C",
        "protein_names_refseq": "tripartite motif-containing protein 30A",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0019901 protein kinase binding;GO:0042803 protein homodimerization activity;GO:0061630 ubiquitin protein ligase activity",
        "go_cellular_component": "GO:0005737 cytoplasm",
        "go_biological_process": "GO:0046596 regulation of viral entry into host cell;GO:0045087 innate immune response;GO:0032880 regulation of protein localization;GO:0043123 positive regulation of canonical NF-kappaB signal transduction;GO:0010468 regulation of gene expression",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A0G2JYE1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A0G2JYL5-1",
        "uniprot_id": "A0A0G2JYL5_RAT",
        "mass": 517774.0,
        "length": 4508,
        "protein_name": "Dynein axonemal heavy chain 2",
        "gene_name": "Dnah2",
        "organism": "Rat",
        "refseq_name": "dynein axonemal heavy chain 2",
        "refseq_ac": "NP_001094146",
        "gene_names_uniprotkb": "Dnah2",
        "gene_names_refseq": "DLP2; Dnah2; Dnahc2; axo f",
        "protein_names_uniprotkb": "Dynein axonemal heavy chain 2; Axonemal beta dynein heavy chain 2; Ciliary dynein heavy chain 2",
        "protein_names_refseq": "axonemal dynein heavy chain; dynein axonemal heavy chain 2; dynein heavy chain 2, axonemal-like; dynein heavy chain 2, axonemal; dynein-like protein 2",
        "tax_id": 10116,
        "disease": "spermatogenic failure 45 (Disease Ontology:DOID:0112163)",
        "pathway": " (rno:303242)",
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        "publication_id_list": "",
        "class_list": "",
        "function": "As part of the axonemal inner dynein arm complex plays a central role in ciliary beat. Expressed in sperm flagellum, it is required for sperm motility. Dyneins are microtubule-based molecular motors possessing ATPase activities that can convert the chemical energy of ATP into relative sliding between adjacent microtubule doublets to generate ciliary bending., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 3,
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        "go_molecular_function": "GO:0005524 ATP binding;GO:0008569 minus-end-directed microtubule motor activity;GO:0051959 dynein light intermediate chain binding;GO:0045505 dynein intermediate chain binding",
        "go_cellular_component": "GO:0097229 sperm end piece;GO:0005874 microtubule;GO:0005929 cilium;GO:0031514 motile cilium;GO:0036126 sperm flagellum",
        "go_biological_process": "GO:0060294 cilium movement involved in cell motility;GO:0003341 cilium movement;GO:0036159 inner dynein arm assembly;GO:0060285 cilium-dependent cell motility",
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        "hit_score": 0.1,
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        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "A0A0G2JYZ7-1",
        "uniprot_id": "A0A0G2JYZ7_RAT",
        "mass": 35232.0,
        "length": 312,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or6c69e",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr956",
        "refseq_ac": "NP_001001381",
        "gene_names_uniprotkb": "Or6c69e",
        "gene_names_refseq": "Olr956; Or6c69e",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 956; olfactory receptor Olr956; olfactory receptor gene Olr956",
        "tax_id": 10116,
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        "pathway": " (rno:302041)",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
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        "go_molecular_function": "GO:0019901 protein kinase binding",
        "go_cellular_component": "GO:0005730 nucleolus;GO:0005737 cytoplasm;GO:0005783 endoplasmic reticulum;GO:0005829 cytosol;GO:0005886 plasma membrane",
        "go_biological_process": "GO:0006886 intracellular protein transport;GO:0007409 axonogenesis;GO:0007528 neuromuscular junction development;GO:0007613 memory;GO:0008088 axo-dendritic transport",
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        "protein_name": "Histone-lysine N-methyltransferase NSD3",
        "gene_name": "Nsd3",
        "organism": "Rat",
        "refseq_name": "histone-lysine N-methyltransferase NSD3 isoform X1",
        "refseq_ac": "XP_038950324",
        "gene_names_uniprotkb": "Nsd3; Whsc1l1",
        "gene_names_refseq": "Nsd3; Whsc1l1",
        "protein_names_uniprotkb": "Histone-lysine N-methyltransferase NSD3; 2.1.1.370; 2.1.1.371; Nuclear SET domain-containing protein 3",
        "protein_names_refseq": "histone-lysine N-methyltransferase NSD3 isoform X1",
        "tax_id": 10116,
        "disease": "Sotos syndrome 1 (Disease Ontology:DOID:0112103); syndrome (Disease Ontology:DOID:225); myeloid leukemia (Disease Ontology:DOID:8692)",
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        "function": "Histone methyltransferase. Preferentially dimethylates 'Lys-4' and 'Lys-27' of histone H3 forming H3K4me2 and H3K27me2. H3 'Lys-4' methylation represents a specific tag for epigenetic transcriptional activation, while 'Lys-27' is a mark for transcriptional repression., [UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "2.1.1.364;2.1.1.370;2.1.1.371;2.1.1.357;2.1.1.-;2.1.1.85",
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        "length": 2798,
        "protein_name": "Nipped-B protein",
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        "protein_names_refseq": "Nipped-B homolog; delangin; nipped-B-like protein isoform 1; nipped-B-like protein",
        "tax_id": 10116,
        "disease": "Cornelia de Lange syndrome 1 (Disease Ontology:DOID:0080505); Cornelia de Lange syndrome (Disease Ontology:DOID:11725); cancer (Disease Ontology:DOID:162)",
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        "protein_names_uniprotkb": "Zinc finger protein 160",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0001228 DNA-binding transcription activator activity, RNA polymerase II-specific",
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        "length": 225,
        "protein_name": "TMF1-regulated nuclear protein 1",
        "gene_name": "Trnp1",
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        "refseq_name": "TMF-regulated nuclear protein 1",
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        "protein_names_uniprotkb": "TMF1-regulated nuclear protein 1",
        "protein_names_refseq": "TMF-regulated nuclear protein 1",
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        "pathway": " (rno:688990)",
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        "go_molecular_function": "GO:0003677 DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0000791 euchromatin",
        "go_biological_process": "GO:0021696 cerebellar cortex morphogenesis;GO:0042127 regulation of cell population proliferation;GO:0061351 neural precursor cell proliferation;GO:0051726 regulation of cell cycle",
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        "record_id": "A0A0G2K0Y1-1",
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        "length": 188,
        "protein_name": "Similar to human chromosome 1 open reading frame 230",
        "gene_name": "C5h1orf232",
        "organism": "Rat",
        "refseq_name": "uncharacterized protein C1orf232 homolog",
        "refseq_ac": "NP_001406535",
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        "gene_names_refseq": "C5h1orf232",
        "protein_names_uniprotkb": "Similar to human chromosome 1 open reading frame 230",
        "protein_names_refseq": "uncharacterized protein C1orf232 homolog",
        "tax_id": 10116,
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    {
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        "length": 317,
        "protein_name": "Olfactory receptor family 8 subfamily K member 25",
        "gene_name": "Or8k25",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr500",
        "refseq_ac": "NP_001000680",
        "gene_names_uniprotkb": "Or8k25",
        "gene_names_refseq": "Olr500; Or8k25",
        "protein_names_uniprotkb": "Olfactory receptor family 8 subfamily K member 25",
        "protein_names_refseq": "olfactory receptor 500; olfactory receptor Olr500; olfactory receptor gene Olr500",
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        "pathway": " (rno:404884)",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
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    {
        "uniprot_canonical_ac": "A0A0G2K1C4-1",
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        "length": 649,
        "protein_name": "Zinc finger protein 799",
        "gene_name": "Zfp799",
        "organism": "Rat",
        "refseq_name": "zinc finger protein 799",
        "refseq_ac": "NP_001009537",
        "gene_names_uniprotkb": "Zfp799",
        "gene_names_refseq": "Zfp799; Zpf799",
        "protein_names_uniprotkb": "Zinc finger protein 799",
        "protein_names_refseq": "zinc finger protein 799",
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        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0061630 ubiquitin protein ligase activity;GO:0004842 ubiquitin-protein transferase activity;GO:0031491 nucleosome binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0035861 site of double-strand break",
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    },
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        "length": 382,
        "protein_name": "Zinc finger CW-type and PWWP domain containing 2",
        "gene_name": "Zcwpw2",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Zcwpw2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger CW-type and PWWP domain containing 2",
        "protein_names_refseq": "",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0140002 histone H3K4me3 reader activity",
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    },
    {
        "uniprot_canonical_ac": "A0A0G2K4C0-1",
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        "length": 381,
        "protein_name": "Beta-1,4-galactosyltransferase",
        "gene_name": "B4galt7",
        "organism": "Rat",
        "refseq_name": "beta-1,4-galactosyltransferase 7 isoform X1",
        "refseq_ac": "XP_008769723",
        "gene_names_uniprotkb": "B4galt7",
        "gene_names_refseq": "B4galt7",
        "protein_names_uniprotkb": "Beta-1,4-galactosyltransferase; 2.4.1.-; Beta-1,4-GalTase",
        "protein_names_refseq": "beta-1,4-galactosyltransferase 7 isoform X1",
        "tax_id": 10116,
        "disease": "Ehlers-Danlos syndrome spondylodysplastic type 1 (Disease Ontology:DOID:0080738); Ehlers-Danlos syndrome (Disease Ontology:DOID:13359)",
        "pathway": " (R-RNO-1971475)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Required for the biosynthesis of the tetrasaccharide linkage region of proteoglycans, especially for small proteoglycans in skin fibroblasts., [UniProtKB, UniProtKB]; Responsible for the synthesis of complex-type N-linked oligosaccharides in many glycoproteins as well as the carbohydrate moieties of glycolipids., [UniProtKB, UniProtKB]",
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        "ec_number_list": "2.4.1.-",
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        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0032580 Golgi cisterna membrane;GO:0005794 Golgi apparatus;GO:0016020 membrane",
        "go_biological_process": "GO:0005975 carbohydrate metabolic process;GO:0009101 glycoprotein biosynthetic process;GO:0006024 glycosaminoglycan biosynthetic process;GO:0048147 negative regulation of fibroblast proliferation;GO:0006487 protein N-linked glycosylation",
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        "length": 238,
        "protein_name": "Proline rich 23 domain containing 1",
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        "refseq_name": "proline rich 23 domain containing 1",
        "refseq_ac": "NP_001395721",
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        "gene_names_refseq": "Prr23d1",
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        "protein_names_refseq": "proline rich 23 domain containing 1; proline-rich protein 23A3-like",
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    },
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        "length": 210,
        "protein_name": "Glutathione S-transferase",
        "gene_name": "Gstp3",
        "organism": "Rat",
        "refseq_name": "Glutathione S-transferase P-like isoform 1",
        "refseq_ac": "NP_001385709",
        "gene_names_uniprotkb": "Gstp3; RGD1307603",
        "gene_names_refseq": "Gstp3; RGD1307603",
        "protein_names_uniprotkb": "Glutathione S-transferase; 2.5.1.18; GST class-pi",
        "protein_names_refseq": "Glutathione S-transferase P-like isoform 1; Glutathione S-transferase P-like",
        "tax_id": 10116,
        "disease": "obesity (Disease Ontology:DOID:9970)",
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        "function": "Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0004364 glutathione transferase activity",
        "go_cellular_component": "GO:0005829 cytosol;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0006749 glutathione metabolic process",
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        "hit_score": 0.1,
        "record_id": "A0A0G2K4Q5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A0G2K4R1-1",
        "uniprot_id": "A0A0G2K4R1_RAT",
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        "length": 784,
        "protein_name": "Protein phosphatase 1 regulatory subunit",
        "gene_name": "Ppp1r12c",
        "organism": "Rat",
        "refseq_name": "protein phosphatase 1 regulatory subunit 12C",
        "refseq_ac": "NP_001178875",
        "gene_names_uniprotkb": "Ppp1r12c",
        "gene_names_refseq": "Ppp1r12c",
        "protein_names_uniprotkb": "Protein phosphatase 1 regulatory subunit",
        "protein_names_refseq": "protein phosphatase 1 regulatory subunit 12C; protein phosphatase 1, regulatory (inhibitor) subunit 12C",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:499076)",
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        "function": "Regulates myosin phosphatase activity., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0017020 myosin phosphatase regulator activity;GO:0004857 enzyme inhibitor activity;GO:0019901 protein kinase binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0001725 stress fiber",
        "go_biological_process": "GO:0007165 signal transduction;GO:0048812 neuron projection morphogenesis",
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        "hit_score": 0.2,
        "record_id": "A0A0G2K4R1-1",
        "record_type": "protein"
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    {
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        "uniprot_id": "A0A0G2K4Y6_RAT",
        "mass": 104763.0,
        "length": 929,
        "protein_name": "HAUS augmin like complex subunit 6",
        "gene_name": "Haus6",
        "organism": "Rat",
        "refseq_name": "HAUS augmin-like complex subunit 6",
        "refseq_ac": "NP_001388801",
        "gene_names_uniprotkb": "Haus6",
        "gene_names_refseq": "Fam29a; Haus6",
        "protein_names_uniprotkb": "HAUS augmin like complex subunit 6",
        "protein_names_refseq": "HAUS augmin-like complex subunit 6; family with sequence similarity 29, member A",
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        "disease": "",
        "pathway": " (rno:366403);  (R-RNO-2565942);  (R-RNO-380259);  (R-RNO-380270);  (R-RNO-380284);  (R-RNO-380320);  (R-RNO-5620912);  (R-RNO-8854518)",
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        "go_molecular_function": "GO:0008017 microtubule binding",
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        "go_biological_process": "GO:0000226 microtubule cytoskeleton organization;GO:0007098 centrosome cycle;GO:0051225 spindle assembly",
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    },
    {
        "uniprot_canonical_ac": "A0A0G2K5T4-1",
        "uniprot_id": "A0A0G2K5T4_RAT",
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        "length": 1711,
        "protein_name": "Chromodomain helicase DNA binding protein 1",
        "gene_name": "Chd1",
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        "gene_names_uniprotkb": "Chd1",
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        "protein_names_uniprotkb": "Chromodomain helicase DNA binding protein 1",
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        "disease": "autism spectrum disorder (Disease Ontology:DOID:0060041); castration-resistant prostate carcinoma (Disease Ontology:DOID:0080909); prostate cancer (Disease Ontology:DOID:10283)",
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        "protein_name": "[histone H3]-lysine(4) N-methyltransferase",
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        "protein_names_refseq": "histone-lysine N-methyltransferase SETD1A",
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        "protein_name": "SIX homeobox 5",
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        "refseq_name": "homeobox protein SIX5",
        "refseq_ac": "NP_001359006",
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        "gene_names_refseq": "Six5",
        "protein_names_uniprotkb": "SIX homeobox 5",
        "protein_names_refseq": "homeobox protein SIX5; sine oculis-related homeobox 5 homolog",
        "tax_id": 10116,
        "disease": "branchiootorenal syndrome 2 (Disease Ontology:DOID:0111424); myotonic dystrophy type 1 (Disease Ontology:DOID:11722); branchiootorenal syndrome (Disease Ontology:DOID:14702)",
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        "protein_names_refseq": "ANTXR like 1 precursor; anthrax toxin receptor-like",
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        "go_molecular_function": "GO:0004888 transmembrane signaling receptor activity;GO:0046872 metal ion binding",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0009986 cell surface",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
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        "record_type": "protein"
    },
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        "mass": 41001.0,
        "length": 372,
        "protein_name": "MHC class I-like protein MILL2",
        "gene_name": "Micb; Mill2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Micb; Mill2; Micb",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "MHC class I-like protein MILL2; MHC class I polypeptide-related sequence B; MHC class I-like located near the leukocyte receptor complex 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:365212)",
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        "publication_count": 1,
        "publication_id_list": "15162429",
        "class_list": "",
        "function": "Binds to heparan sulfate proteoglycans on the surface of fibroblast cells., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 3,
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        "secondary_ac_list": "Q60I19",
        "ec_number_list": "",
        "go_molecular_function": "GO:0046703 natural killer cell lectin-like receptor binding",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0009897 external side of plasma membrane",
        "go_biological_process": "GO:0006955 immune response;GO:0006979 response to oxidative stress;GO:0032526 response to retinoic acid;GO:0009408 response to heat;GO:0002429 immune response-activating cell surface receptor signaling pathway",
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        "record_type": "protein"
    },
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        "length": 165,
        "protein_name": "Large ribosomal subunit protein uL15",
        "gene_name": "LOC102547604",
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        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "LOC102547604; Rpl27al3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Large ribosomal subunit protein uL15; 60S ribosomal protein L27a",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "intrinsic cardiomyopathy (Disease Ontology:DOID:0060036)",
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        "class_list": "",
        "function": "Component of the large ribosomal subunit. The ribosome is a large ribonucleoprotein complex responsible for the synthesis of proteins in the cell., [UniProtKB, UniProtKB, UniProtKB]",
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    },
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        "mass": 69205.0,
        "length": 610,
        "protein_name": "TNF receptor-associated factor",
        "gene_name": "Traf3",
        "organism": "Rat",
        "refseq_name": "TNF receptor-associated factor 3 isoform X1",
        "refseq_ac": "XP_038968511",
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        "gene_names_refseq": "Traf3",
        "protein_names_uniprotkb": "TNF receptor-associated factor; 2.3.2.27",
        "protein_names_refseq": "TNF receptor-associated factor 3 isoform X1",
        "tax_id": 10116,
        "disease": "immunodeficiency 132B (Disease Ontology:DOID:0061097); immunodeficiency 132A (Disease Ontology:DOID:0061101)",
        "pathway": " (rno:362788);  (R-RNO-5668541);  (R-RNO-5676594);  (R-RNO-5689896);  (R-RNO-936964);  (R-RNO-9824878)",
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        "ec_number_list": "2.3.2.27;3.4.19.12;2.7.11.10;2.7.11.25;3.2.2.-;3.2.2.6;2.7.11.1;3.4.25.1;3.1.3.48;3.6.5.2",
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        "go_biological_process": "GO:0032648 regulation of interferon-beta production;GO:0007166 cell surface receptor signaling pathway;GO:0045087 innate immune response;GO:0006915 apoptotic process;GO:0030162 regulation of proteolysis",
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        "length": 416,
        "protein_name": "Phakinin",
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        "protein_names_refseq": "49 kDa cytoskeletal protein; beaded filament structural protein 2, phakinin; lens fiber cell beaded filament protein CP 47; lens fiber cell beaded filament protein CP 49; lens intermediate filament-like light; phakinin",
        "tax_id": 10116,
        "disease": "cataract 12 multiple types (Disease Ontology:DOID:0110239); cataract (Disease Ontology:DOID:83)",
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        "go_biological_process": "GO:0007010 cytoskeleton organization;GO:0007601 visual perception;GO:0045109 intermediate filament organization;GO:0048469 cell maturation;GO:0045104 intermediate filament cytoskeleton organization",
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        "refseq_name": "protein SSXT",
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        "gene_names_refseq": "Ss18",
        "protein_names_uniprotkb": "SS18 subunit of BAF chromatin remodeling complex",
        "protein_names_refseq": "SS18, nBAF chromatin remodeling complex subunit; protein SSXT; synovial sarcoma translocation, Chromosome 18",
        "tax_id": 10116,
        "disease": "synovial sarcoma (Disease Ontology:DOID:5485)",
        "pathway": " (rno:361295);  (R-RNO-9933937);  (R-RNO-9933946);  (R-RNO-9933947);  (R-RNO-9934037)",
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        "go_molecular_function": "GO:0003713 transcription coactivator activity",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005634 nucleus;GO:0016514 SWI/SNF complex;GO:0071564 npBAF complex;GO:0015630 microtubule cytoskeleton",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0035556 intracellular signal transduction;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0048013 ephrin receptor signaling pathway;GO:0000902 cell morphogenesis",
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        "length": 381,
        "protein_name": "RALY heterogeneous nuclear ribonucleoprotein",
        "gene_name": "Raly",
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        "gene_names_uniprotkb": "Raly",
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        "protein_names_uniprotkb": "RALY heterogeneous nuclear ribonucleoprotein",
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        "protein_names_uniprotkb": "Pleckstrin homology-like domain, family B, member 2",
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        "go_cellular_component": "GO:0045180 basal cortex;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0005925 focal adhesion;GO:0005938 cell cortex",
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        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "E9PTG1-1",
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        "protein_name": "SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2",
        "gene_name": "Smarca2",
        "organism": "Rat",
        "refseq_name": "probable global transcription activator SNF2L2 isoform 1",
        "refseq_ac": "NP_001004446",
        "gene_names_uniprotkb": "Smarca2",
        "gene_names_refseq": "Smarca2",
        "protein_names_uniprotkb": "SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2",
        "protein_names_refseq": "SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2; probable global transcription activator SNF2L2 isoform 1; probable global transcription activator SNF2L2",
        "tax_id": 10116,
        "disease": "opportunistic bacterial infectious disease (Disease Ontology:DOID:0050340); Nicolaides-Baraitser syndrome (Disease Ontology:DOID:0081441); blepharophimosis-impaired intellectual development syndrome (Disease Ontology:DOID:0081442); prostate cancer (Disease Ontology:DOID:10283); alcohol use disorder (Disease Ontology:DOID:1574); cancer (Disease Ontology:DOID:162)",
        "pathway": " (rno:361745);  (R-RNO-3214858);  (R-RNO-8939243);  (R-RNO-9933937);  (R-RNO-9933939);  (R-RNO-9933947);  (R-RNO-9934037)",
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        "ec_number_list": "5.6.2.3;3.6.4.13;3.6.4.12;2.7.11.1;3.6.1.5;3.6.4.10;3.6.4.-;2.3.2.27;5.6.2.4;3.6.5.-;5.6.2.-;3.1.-.-;2.7.7.7;2.7.7.49;3.1.13.1;4.2.99.18;7.6.2.2;7.6.2.3;7.6.2.-;5.6.1.6;7.2.2.-;3.6.1.15;3.6.4.6;3.1.3.1;3.9.1.1;6.1.1.12;3.6.1.-;2.7.4.3;3.1.4.-;3.4.24.-;3.6.-.-;3.4.21.53;5.6.2.5",
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        "protein_names_uniprotkb": "Zinc finger protein 654",
        "protein_names_refseq": "zinc finger protein 654 isoform 1",
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        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB, UniProtKB]",
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        "refseq_name": "U2 small nuclear ribonucleoprotein A'",
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        "gene_names_refseq": "Snrpa1",
        "protein_names_uniprotkb": "Small nuclear ribonucleoprotein polypeptide A'",
        "protein_names_refseq": "U2 small nuclear ribonucleoprotein A'; U2 small nuclear ribonucleoprotein polypeptide A'",
        "tax_id": 10116,
        "disease": "azoospermia (Disease Ontology:DOID:14227); connective tissue disease (Disease Ontology:DOID:65)",
        "pathway": " (rno:100361269);  (R-RNO-72163);  (R-RNO-9770562);  (R-RNO-9943411)",
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        "function": "Involved in pre-mRNA splicing as component of the spliceosome. Associated with sn-RNP U2, where it contributes to the binding of stem loop IV of U2 snRNA., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "gene_names_refseq": "Ercc4",
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        "disease": "xeroderma pigmentosum (Disease Ontology:DOID:0050427); XFE progeroid syndrome (Disease Ontology:DOID:0060590); xeroderma pigmentosum group A (Disease Ontology:DOID:0110843); xeroderma pigmentosum group F (Disease Ontology:DOID:0110848); Fanconi anemia complementation group Q (Disease Ontology:DOID:0111093); Fanconi anemia (Disease Ontology:DOID:13636); polyneuropathy due to drug (Disease Ontology:DOID:14184); cancer (Disease Ontology:DOID:162); pancreatic cancer (Disease Ontology:DOID:1793); Cockayne syndrome (Disease Ontology:DOID:2962); colorectal cancer (Disease Ontology:DOID:9256)",
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        "function": "Catalytic component of a structure-specific DNA repair endonuclease responsible for the 5-prime incision during DNA repair, and which is essential for nucleotide excision repair (NER) and interstrand cross-link (ICL) repair., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "protein_names_uniprotkb": "PR domain zinc finger protein 15; PR domain-containing protein 15",
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        "go_biological_process": "GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0090263 positive regulation of canonical Wnt signaling pathway;GO:0010468 regulation of gene expression;GO:0043409 negative regulation of MAPK cascade;GO:2000035 regulation of stem cell division",
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    {
        "uniprot_canonical_ac": "D3ZDT7-1",
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        "length": 2109,
        "protein_name": "separase",
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        "protein_names_uniprotkb": "separase; 3.4.22.49",
        "protein_names_refseq": "extra spindle pole bodies 1, separase; extra spindle pole bodies homolog 1; extra spindle poles like 1; separin-like; separin",
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        "disease": "breast cancer (Disease Ontology:DOID:1612)",
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        "go_molecular_function": "GO:0004197 cysteine-type endopeptidase activity;GO:0008233 peptidase activity;GO:0008234 cysteine-type peptidase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005813 centrosome;GO:0072686 mitotic spindle;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0051307 meiotic chromosome separation;GO:0006508 proteolysis;GO:0045143 homologous chromosome segregation;GO:0000278 mitotic cell cycle;GO:0007059 chromosome segregation",
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    {
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        "refseq_name": "serine/threonine-protein kinase ULK2",
        "refseq_ac": "NP_001178574",
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        "gene_names_refseq": "Ulk2",
        "protein_names_uniprotkb": "non-specific serine/threonine protein kinase; 2.7.11.1",
        "protein_names_refseq": "Unc-51 like kinase 2; serine/threonine-protein kinase ULK2",
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        "ec_number_list": "2.7.11.1;2.7.12.1;2.7.1.153;2.7.1.137;2.7.11.24;2.7.11.25;2.7.11.22;2.7.11.23;2.7.4.6;2.7.1.154;2.7.11.38;2.7.11.17;2.7.12.2;2.7.11.12;2.7.11.26;2.7.11.21;2.7.11.34;2.7.1.150;2.7.10.2;2.7.11.13;2.7.11.19;2.7.2.3;2.7.11.11;2.7.11.31;3.1.3.16;2.7.11.4;2.3.1.48;3.1.11.-;2.7.13.3;2.7.4.18;3.1.24.-;3.4.19.12;2.7.11.39;2.4.99.18;2.7.11.10",
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        "go_cellular_component": "GO:0034045 phagophore assembly site membrane;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005776 autophagosome;GO:0000407 phagophore assembly site",
        "go_biological_process": "GO:0010506 regulation of autophagy;GO:0042594 response to starvation;GO:0006914 autophagy;GO:0048668 collateral sprouting;GO:0048675 axon extension",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZQN7-1",
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        "mass": 197392.0,
        "length": 1786,
        "protein_name": "Laminin subunit beta-1",
        "gene_name": "Lamb1",
        "organism": "Rat",
        "refseq_name": "laminin subunit beta-1 precursor",
        "refseq_ac": "NP_001100191",
        "gene_names_uniprotkb": "Lamb1",
        "gene_names_refseq": "Lamb1-1; Lamb1",
        "protein_names_uniprotkb": "Laminin subunit beta-1; Laminin B1 chain; Laminin-1 subunit beta; Laminin-10 subunit beta; Laminin-12 subunit beta; Laminin-2 subunit beta; Laminin-6 subunit beta; Laminin-8 subunit beta",
        "protein_names_refseq": "laminin B1 subunit 1; laminin subunit beta-1 precursor; laminin, beta 1",
        "tax_id": 10116,
        "disease": "leukoencephalopathy with variable cortical brain malformations and/or hydrocephalus (Disease Ontology:DOID:0112230); coloboma (Disease Ontology:DOID:12270); autistic disorder (Disease Ontology:DOID:12849)",
        "pathway": " (rno:298941)",
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        "publication_id_list": "38843836",
        "class_list": "",
        "function": "Binding to cells via a high affinity receptor, laminin is thought to mediate the attachment, migration and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components. Involved in the organization of the laminar architecture of the cerebral cortex. It is probably required for the integrity of the basement membrane/glia limitans that serves as an anchor point for the endfeet of radial glial cells and as a physical barrier to migrating neurons. Radial glial cells play a central role in cerebral cortical development, where they act both as the proliferative unit of the cerebral cortex and a scaffold for neurons migrating toward the pial surface. As a subunit of laminin-1 (also known as laminin-111 or EHS laminin), it is involved in the stimulation of agrin-induced receptor clustering through a MuSK-independent pathway., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005178 integrin binding;GO:0043208 glycosphingolipid binding;GO:0019899 enzyme binding;GO:0048018 receptor ligand activity;GO:0005201 extracellular matrix structural constituent",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0005737 cytoplasm;GO:0005606 laminin-1 complex;GO:0043259 laminin-10 complex;GO:0005615 extracellular space",
        "go_biological_process": "GO:0007155 cell adhesion;GO:0031175 neuron projection development;GO:1904395 positive regulation of skeletal muscle acetylcholine-gated channel clustering;GO:0007162 negative regulation of cell adhesion;GO:0030335 positive regulation of cell migration",
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        "hit_score": 0.4,
        "record_id": "D3ZQN7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4AAH9-1",
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        "length": 699,
        "protein_name": "TBC1 domain family member 23",
        "gene_name": "Tbc1d23",
        "organism": "Rat",
        "refseq_name": "TBC1 domain family member 23 isoform 1",
        "refseq_ac": "NP_001358824",
        "gene_names_uniprotkb": "Tbc1d23",
        "gene_names_refseq": "RGD1307925; Tbc1d23",
        "protein_names_uniprotkb": "TBC1 domain family member 23",
        "protein_names_refseq": "TBC1 domain family member 23 isoform 1",
        "tax_id": 10116,
        "disease": "pontocerebellar hypoplasia (Disease Ontology:DOID:0060264); pontocerebellar hypoplasia type 11 (Disease Ontology:DOID:0112324)",
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        "go_cellular_component": "GO:0005794 Golgi apparatus;GO:0005829 cytosol;GO:0031410 cytoplasmic vesicle;GO:0005802 trans-Golgi network;GO:0071203 WASH complex",
        "go_biological_process": "GO:0007399 nervous system development;GO:0042147 retrograde transport, endosome to Golgi;GO:0048513 animal organ development;GO:0031175 neuron projection development;GO:0032755 positive regulation of interleukin-6 production",
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    },
    {
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Dntt",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "DNA nucleotidylexotransferase; 2.7.7.31",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "acute lymphoblastic leukemia (Disease Ontology:DOID:9952)",
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        "publication_id_list": "",
        "class_list": "",
        "function": "Template-independent DNA polymerase which catalyzes the random addition of deoxynucleoside 5'-triphosphate to the 3'-end of a DNA initiator., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "2.7.7.7;2.7.7.102;2.7.7.49;3.6.4.12;2.7.7.31;3.1.11.-;4.2.99.18;4.2.99.-",
        "go_molecular_function": "GO:0003887 DNA-directed DNA polymerase activity;GO:0003677 DNA binding;GO:0046872 metal ion binding;GO:0003912 DNA nucleotidylexotransferase activity",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005829 cytosol;GO:0005634 nucleus;GO:0016363 nuclear matrix;GO:0000785 chromatin",
        "go_biological_process": "GO:0006281 DNA repair;GO:0006304 DNA modification;GO:0006259 DNA metabolic process;GO:0006303 double-strand break repair via nonhomologous end joining;GO:0033198 response to ATP",
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        "protein_name": "Nuclear exosome regulator NRDE2",
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        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Nrde2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Nuclear exosome regulator NRDE2; Protein NRDE2 homolog",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": "",
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        "class_list": "",
        "function": "Protein of the nuclear speckles that regulates RNA degradation and export from the nucleus through its interaction with MTREX an essential factor directing various RNAs to exosomal degradation. Changes the conformation of MTREX, precluding its association with the nuclear exosome and interaction with proteins required for its function in RNA exosomal degradation. Negatively regulates, for instance, the degradation of mRNAs and lncRNAs by inhibiting their MTREX-mediated recruitment to nuclear exosome. By preventing the degradation of RNAs in the nucleus, it promotes their export to the cytoplasm. U5 snRNP-associated RNA splicing factor which is required for efficient splicing of CEP131 pre-mRNA and plays an important role in centrosome maturation, integrity and function during mitosis. Suppresses intron retention in a subset of pre-mRNAs containing short, GC-rich introns with relatively weak 5' and 3' splice sites. Plays a role in DNA damage response., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005739 mitochondrion;GO:0016607 nuclear speck",
        "go_biological_process": "GO:0031048 regulatory ncRNA-mediated heterochromatin formation;GO:1902369 negative regulation of RNA catabolic process;GO:0046833 positive regulation of RNA export from nucleus;GO:0000278 mitotic cell cycle;GO:0048255 mRNA stabilization",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D3ZDR9-1",
        "record_type": "protein"
    },
    {
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        "length": 2376,
        "protein_name": "Zinc finger, DBF-type containing 2",
        "gene_name": "Zdbf2",
        "organism": "Rat",
        "refseq_name": "DBF4-type zinc finger-containing protein 2",
        "refseq_ac": "NP_001414608",
        "gene_names_uniprotkb": "Zdbf2",
        "gene_names_refseq": "RGD1560005; Zdbf2",
        "protein_names_uniprotkb": "Zinc finger, DBF-type containing 2",
        "protein_names_refseq": "DBF4-type zinc finger-containing protein 2",
        "tax_id": 10116,
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        "pathway": " (rno:501153)",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0003676 nucleic acid binding",
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        "go_biological_process": "GO:0043045 epigenetic programming of gene expression;GO:0071514 genomic imprinting",
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        "record_id": "D4A582-1",
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    {
        "uniprot_canonical_ac": "D3ZCM7-1",
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        "length": 769,
        "protein_name": "TLE family member 1, transcriptional corepressor",
        "gene_name": "Tle1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Tle1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "TLE family member 1, transcriptional corepressor",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (R-RNO-201722);  (R-RNO-3769402);  (R-RNO-4641265);  (R-RNO-9764725)",
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        "go_molecular_function": "GO:0003682 chromatin binding;GO:0042802 identical protein binding;GO:0003714 transcription corepressor activity;GO:0140297 DNA-binding transcription factor binding",
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        "go_biological_process": "GO:0006355 regulation of DNA-templated transcription;GO:0016055 Wnt signaling pathway;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006357 regulation of transcription by RNA polymerase II;GO:0010628 positive regulation of gene expression",
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    {
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        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Fam193a",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Family with sequence similarity 193, member A",
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        "tax_id": 10116,
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        "go_biological_process": "GO:0010766 negative regulation of sodium ion transport;GO:0035556 intracellular signal transduction;GO:1903288 positive regulation of potassium ion import across plasma membrane;GO:0050801 monoatomic ion homeostasis;GO:0006468 protein phosphorylation",
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    {
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        "length": 1684,
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        "protein_names_uniprotkb": "Alpha-protein kinase 3; 2.7.11.1",
        "protein_names_refseq": "alpha-protein kinase 3",
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        "disease": "hypertrophic cardiomyopathy 27 (Disease Ontology:DOID:0061102)",
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        "publication_id_list": "22673903",
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        "function": "Involved in cardiomyocyte differentiation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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    },
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        "protein_names_uniprotkb": "Solute carrier family 75 member 1; Major facilitator superfamily domain-containing protein 10; Tetracycline transporter-like protein",
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        "function": "Probable organic anion transporter which may serve as a transporter for some non-steroidal anti-inflammatory drugs (NSAIDs) as well as other organic anions across the luminal membranes of renal proximal tubules at the final excretion step into the urine., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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    },
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        "tax_id": 10116,
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        "function": "Processive microtubule plus-end directed motor protein involved in neuronal axon guidance. Is recruited by KANK1 to cortical microtubule stabilizing complexes (CMSCs) at focal adhesions (FAs) rims where it promotes microtubule capture and stability. Controls microtubule polymerization rate at axonal growth cones and suppresses microtubule growth without inducing microtubule disassembly once it reaches the cell cortex., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005524 ATP binding;GO:0008017 microtubule binding;GO:0003777 microtubule motor activity;GO:0016887 ATP hydrolysis activity;GO:0008574 plus-end-directed microtubule motor activity",
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        "go_biological_process": "GO:0007018 microtubule-based movement;GO:1902667 regulation of axon guidance;GO:0031113 regulation of microtubule polymerization;GO:0008089 anterograde axonal transport;GO:0043622 cortical microtubule organization",
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        "protein_names_uniprotkb": "PH and SEC7 domain-containing protein 4; Exchange factor for ADP-ribosylation factor guanine nucleotide factor 6 B; Pleckstrin homology and SEC7 domain-containing protein 4",
        "protein_names_refseq": "PH and SEC7 domain-containing protein 4",
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        "disease": "alcohol use disorder (Disease Ontology:DOID:1574)",
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        "function": "Guanine nucleotide exchange factor for ARF6 and ARL14/ARF7. Through ARL14 activation, controls the movement of MHC class II-containing vesicles along the actin cytoskeleton in dendritic cells. Involved in membrane recycling. Interacts with several phosphatidylinositol phosphate species, including phosphatidylinositol 3,4-bisphosphate, phosphatidylinositol 3,5-bisphosphate and phosphatidylinositol 4,5-bisphosphate., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005543 phospholipid binding;GO:0005085 guanyl-nucleotide exchange factor activity",
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    {
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        "protein_name": "Stathmin domain containing 1",
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        "refseq_name": "stathmin domain containing 1",
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        "gene_names_uniprotkb": "Stmnd1",
        "gene_names_refseq": "RGD1564013; Stmnd1",
        "protein_names_uniprotkb": "Stathmin domain containing 1",
        "protein_names_refseq": "stathmin domain containing 1; stathmin domain-containing protein 1-like",
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        "pathway": " (rno:102554838)",
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        "go_molecular_function": "GO:0015631 tubulin binding",
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        "hit_score": 0.1,
        "record_id": "D3ZHF4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZZM7-1",
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        "length": 850,
        "protein_name": "Solute carrier organic anion transporter family member",
        "gene_name": "Slco5a1",
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        "refseq_name": "solute carrier organic anion transporter family member 5A1 isoform 1",
        "refseq_ac": "NP_001423667",
        "gene_names_uniprotkb": "Slco5a1",
        "gene_names_refseq": "Slco5a1",
        "protein_names_uniprotkb": "Solute carrier organic anion transporter family member",
        "protein_names_refseq": "solute carrier organic anion transporter family member 5A1 isoform 1",
        "tax_id": 10116,
        "disease": "epilepsy (Disease Ontology:DOID:1826)",
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        "go_molecular_function": "GO:0022857 transmembrane transporter activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0016323 basolateral plasma membrane;GO:0016020 membrane",
        "go_biological_process": "GO:0006811 monoatomic ion transport;GO:0043252 sodium-independent organic anion transport;GO:0055085 transmembrane transport",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZZ94-1",
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        "length": 954,
        "protein_name": "Poly [ADP-ribose] polymerase",
        "gene_name": "Parp10",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Parp10; LOC102548778",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Poly [ADP-ribose] polymerase; 2.4.2.-; PARP",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "function": "ADP-ribosyltransferase that mediates mono-ADP-ribosylation of glutamate and aspartate residues on target proteins. In contrast to PARP1 and PARP2, it is not able to mediate poly-ADP-ribosylation. Catalyzes mono-ADP-ribosylation of GSK3B, leading to negatively regulate GSK3B kinase activity. Involved in translesion DNA synthesis in response to DNA damage via its interaction with PCNA., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:1990404 NAD+-protein mono-ADP-ribosyltransferase activity;GO:0003714 transcription corepressor activity;GO:0070530 K63-linked polyubiquitin modification-dependent protein binding;GO:0016779 nucleotidyltransferase activity;GO:0003950 NAD+ poly-ADP-ribosyltransferase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005730 nucleolus;GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0070213 protein auto-ADP-ribosylation;GO:0006281 DNA repair;GO:0010629 negative regulation of gene expression;GO:0043124 negative regulation of canonical NF-kappaB signal transduction;GO:0048147 negative regulation of fibroblast proliferation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D3ZZ94-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A0G2KA38-1",
        "uniprot_id": "A0A0G2KA38_RAT",
        "mass": 21586.0,
        "length": 191,
        "protein_name": "Interferon stimulated exonuclease gene 20",
        "gene_name": "Isg20",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Isg20",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Interferon stimulated exonuclease gene 20",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
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        "reported_o_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
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        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003676 nucleic acid binding;GO:0004527 exonuclease activity;GO:0008310 single-stranded DNA 3'-5' DNA exonuclease activity;GO:0030620 U2 snRNA binding;GO:0000175 3'-5'-RNA exonuclease activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005730 nucleolus;GO:0005737 cytoplasm;GO:0016605 PML body;GO:0015030 Cajal body",
        "go_biological_process": "GO:0051607 defense response to virus;GO:0045071 negative regulation of viral genome replication;GO:0009615 response to virus;GO:0006308 DNA catabolic process;GO:0006401 RNA catabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A0G2KA38-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A1D3-1",
        "uniprot_id": "D4A1D3_RAT",
        "mass": 521482.0,
        "length": 4590,
        "protein_name": "Sacsin",
        "gene_name": "Sacs",
        "organism": "Rat",
        "refseq_name": "sacsin isoform X1",
        "refseq_ac": "XP_006252229",
        "gene_names_uniprotkb": "Sacs",
        "gene_names_refseq": "RGD1305416; Sacs",
        "protein_names_uniprotkb": "Sacsin; DnaJ homolog subfamily C member 29",
        "protein_names_refseq": "sacsin isoform X1",
        "tax_id": 10116,
        "disease": "Charlevoix-Saguenay spastic ataxia (Disease Ontology:DOID:0050946)",
        "pathway": " (rno:305940)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Co-chaperone which acts as a regulator of the Hsp70 chaperone machinery and may be involved in the processing of other ataxia-linked proteins., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0042802 identical protein binding;GO:0050750 low-density lipoprotein particle receptor binding;GO:0051087 protein-folding chaperone binding;GO:0070628 proteasome binding;GO:0030544 Hsp70 protein binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005739 mitochondrion",
        "go_biological_process": "GO:0090084 negative regulation of inclusion body assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D4A1D3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZRG1-1",
        "uniprot_id": "D3ZRG1_RAT",
        "mass": 175957.0,
        "length": 1596,
        "protein_name": "Transmembrane protein 131-like",
        "gene_name": "Tmem131l",
        "organism": "Rat",
        "refseq_name": "transmembrane protein 131-like isoform 1 precursor",
        "refseq_ac": "NP_001386453",
        "gene_names_uniprotkb": "Tmem131l; LOC679811",
        "gene_names_refseq": "RGD1305449; Tmem131l",
        "protein_names_uniprotkb": "Transmembrane protein 131-like",
        "protein_names_refseq": "transmembrane protein 131-like isoform 1 precursor; transmembrane protein 131-like",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:679811)",
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        "publication_count": 1,
        "publication_id_list": "29393594",
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        "function": "",
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        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
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        "total_n_glycosites": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0016020 membrane;GO:0005737 cytoplasm;GO:0005886 plasma membrane",
        "go_biological_process": "GO:0090090 negative regulation of canonical Wnt signaling pathway;GO:0033088 negative regulation of immature T cell proliferation in thymus",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "D3ZRG1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZGJ2-1",
        "uniprot_id": "D3ZGJ2_RAT",
        "mass": 108387.0,
        "length": 999,
        "protein_name": "Espin-like protein",
        "gene_name": "Espnl",
        "organism": "Rat",
        "refseq_name": "espin-like protein",
        "refseq_ac": "NP_001178741",
        "gene_names_uniprotkb": "Espnl",
        "gene_names_refseq": "Espnl; RGD1562432",
        "protein_names_uniprotkb": "Espin-like protein",
        "protein_names_refseq": "espin-like protein",
        "tax_id": 10116,
        "disease": "autosomal recessive nonsyndromic deafness 36 (Disease Ontology:DOID:0110494)",
        "pathway": " (rno:301606)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Binds to but does not cross-link actin. Required for the formation and maintenance of inner ear hair cell stereocilia and staircase formation. Essential for normal hearing., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 0,
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        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0051015 actin filament binding",
        "go_cellular_component": "GO:0032420 stereocilium;GO:0005737 cytoplasm;GO:0032426 stereocilium tip",
        "go_biological_process": "GO:0007605 sensory perception of sound;GO:0051017 actin filament bundle assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZGJ2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A9K4-1",
        "uniprot_id": "S18B1_RAT",
        "mass": 48385.0,
        "length": 455,
        "protein_name": "MFS-type transporter SLC18B1",
        "gene_name": "Slc18b1",
        "organism": "Rat",
        "refseq_name": "MFS-type transporter SLC18B1",
        "refseq_ac": "NP_001387757",
        "gene_names_uniprotkb": "Slc18b1",
        "gene_names_refseq": "RGD1306962; Slc18b1; VPAT",
        "protein_names_uniprotkb": "MFS-type transporter SLC18B1; Solute carrier family 18 member B1; VPAT; Vesicular polyamine transporter",
        "protein_names_refseq": "MFS-type transporter SLC18B1; solute carrier family 18, subfamily B, member 1; vesicular polyamine transporter",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:309570)",
        "pathway_count": 1,
        "publication_count": 2,
        "publication_id_list": "25355561;28082679",
        "class_list": "",
        "function": "Proton-coupled polyamine antiporter involved in the translocation of polyamines from cytosol into secretory vesicles prior to their release via exocytosis. Uses the electrochemical proton gradient generated by a V-type proton-pumping ATPase to couple the efflux of protons with the uptake of a polyamine molecule (By similarity) (PubMed:25355561). Facilitates vesicular storage of spermine and spermidine in astrocytes with an impact on glutamatergic neuronal transmission and memory formation (By similarity) (PubMed:25355561). Upon antigen stimulation, regulates polyamine accumulation and release in mast cell secretory granules, which in turn potentiates mast cell degranulation and histamine secretion (By similarity)., [UniProtKB, PubMed, UniProtKB, UniProtKB]; VPAT is expressed and is responsible for vesicular storage of spermine and spermidine in novel secretory granules that differ from histamine- and serotonin-containing granules and is involved in vesicular release of these polyamines from mast cells, [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_s_glycosites": 0,
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        "reported_c_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "total_n_glycosites": 0,
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        "reported_phosphosites": 1,
        "reported_mutagensis": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0022857 transmembrane transporter activity;GO:0015311 monoamine:proton antiporter activity;GO:0015312 polyamine:proton antiporter activity",
        "go_cellular_component": "GO:0030667 secretory granule membrane;GO:0030672 synaptic vesicle membrane",
        "go_biological_process": "GO:0000296 spermine transport;GO:0051610 serotonin uptake;GO:0015848 spermidine transport",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "D4A9K4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D4A5S9-1",
        "uniprot_id": "D4A5S9_RAT",
        "mass": 77938.0,
        "length": 664,
        "protein_name": "Pre-mRNA-processing factor 39",
        "gene_name": "Prpf39",
        "organism": "Rat",
        "refseq_name": "pre-mRNA-processing factor 39",
        "refseq_ac": "NP_001101496",
        "gene_names_uniprotkb": "Prpf39",
        "gene_names_refseq": "Prpf39",
        "protein_names_uniprotkb": "Pre-mRNA-processing factor 39; PRP39 homolog",
        "protein_names_refseq": "PRP39 pre-mRNA processing factor 39 homolog; pre-mRNA-processing factor 39",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:314171)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Involved in pre-mRNA splicing., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "reported_o_glycosites": 0,
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        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005685 U1 snRNP;GO:0000243 commitment complex;GO:0071004 U2-type prespliceosome",
        "go_biological_process": "GO:0006397 mRNA processing;GO:0008380 RNA splicing;GO:0000395 mRNA 5'-splice site recognition",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D4A5S9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZN95-1",
        "uniprot_id": "HCFC1_RAT",
        "mass": 209153.0,
        "length": 2034,
        "protein_name": "Host cell factor 1",
        "gene_name": "Hcfc1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Hcfc1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Host cell factor 1; C1 factor; HCF-1; HCF",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "methylmalonic acidemia and homocysteinemia cblX type (Disease Ontology:DOID:0111814); congenital heart disease (Disease Ontology:DOID:1682)",
        "pathway": " (R-RNO-3214847);  (R-RNO-5689603);  (R-RNO-9772755)",
        "pathway_count": 3,
        "publication_count": 12,
        "publication_id_list": "15340146;16641100;17496889;18683930;19322778;19692427;21909281;22673903;24250814;29393594;38843836;41549750",
        "class_list": "",
        "function": "Transcriptional coregulator (PubMed:24250814). Serves as a scaffold protein, bridging interactions between transcription factors, including THAP11 and ZNF143, and transcriptional coregulators (By similarity). Involved in control of the cell cycle (By similarity). Also antagonizes transactivation by ZBTB17 and GABP2; represses ZBTB17 activation of the p15(INK4b) promoter and inhibits its ability to recruit p300 (By similarity). Coactivator for EGR2 and GABP2 (By similarity). Tethers the chromatin modifying Set1/Ash2 histone H3 'Lys-4' methyltransferase (H3K4me) and Sin3 histone deacetylase (HDAC) complexes (involved in the activation and repression of transcription, respectively) together (By similarity). Component of a THAP1/THAP3-HCFC1-OGT complex that is required for the regulation of the transcriptional activity of RRM1 (By similarity). As part of the NSL complex it may be involved in acetylation of nucleosomal histone H4 on several lysine residues (By similarity). Recruits KMT2E/MLL5 to E2F1 responsive promoters promoting transcriptional activation and thereby facilitates G1 to S phase transition (By similarity). Modulates expression of homeobox protein PDX1, perhaps acting in concert with transcription factor E2F1, thereby regulating pancreatic beta-cell growth and glucose-stimulated insulin secretion (PubMed:24250814). May negatively modulate transcriptional activity of FOXO3 (PubMed:21909281)., [UniProtKB, UniProtKB, PubMed, PubMed]",
        "predicted_glycosites": 3,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 3,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
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        "refseq_name": "zinc finger protein 28 homolog isoform X2",
        "refseq_ac": "XP_006228267",
        "gene_names_uniprotkb": "Zfp28; Zfp78; Zfp78",
        "gene_names_refseq": "Zfp28l; Zfp28",
        "protein_names_uniprotkb": "Zinc finger protein 28",
        "protein_names_refseq": "zinc finger protein 28 homolog isoform X2",
        "tax_id": 10116,
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        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; May be involved in transcriptional regulation. May have a role in embryonic development., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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    },
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        "gene_names_uniprotkb": "Ermap; Zfp691; Ermap; Zfp691",
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        "protein_names_uniprotkb": "Erythroblast membrane associated protein (Scianna blood group); Zinc finger protein 691",
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        "gene_name": "Larp4b",
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        "refseq_name": "la-related protein 4B isoform X3",
        "refseq_ac": "XP_038951686",
        "gene_names_uniprotkb": "Larp4b",
        "gene_names_refseq": "Larp4b; Larp5; RGD1310713",
        "protein_names_uniprotkb": "La ribonucleoprotein 4B",
        "protein_names_refseq": "la-related protein 4B isoform X3",
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    },
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        "protein_name": "VPS39 subunit of HOPS complex",
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        "gene_names_uniprotkb": "Vps39",
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        "protein_names_uniprotkb": "VPS39 subunit of HOPS complex",
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        "gene_name": "Bbs9",
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        "refseq_name": "protein PTHB1 isoform X2",
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        "gene_names_refseq": "Bbs9; RGD1308472",
        "protein_names_uniprotkb": "Bardet-Biedl syndrome 9",
        "protein_names_refseq": "protein PTHB1 isoform X2",
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        "disease": "Bardet-Biedl syndrome 9 (Disease Ontology:DOID:0110131); Bardet-Biedl syndrome (Disease Ontology:DOID:1935); craniosynostosis (Disease Ontology:DOID:2340); primary ovarian insufficiency (Disease Ontology:DOID:5426)",
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        "record_type": "protein"
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        "gene_names_uniprotkb": "Fbxw10; Trim16",
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        "protein_names_uniprotkb": "Tripartite motif-containing 16",
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        "go_biological_process": "GO:0006954 inflammatory response;GO:0009611 response to wounding;GO:0010508 positive regulation of autophagy;GO:0042246 tissue regeneration;GO:0032526 response to retinoic acid",
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    {
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        "protein_names_refseq": "olfactory receptor 122; olfactory receptor Olr122; olfactory receptor gene Olr122",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
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    {
        "uniprot_canonical_ac": "D3ZCZ1-1",
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        "protein_name": "Olfactory receptor",
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        "gene_names_refseq": "Olr137; Or51q1d",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 137; olfactory receptor Olr137; olfactory receptor gene Olr137",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Pi16",
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        "protein_names_uniprotkb": "Peptidase inhibitor 16",
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        "function": "May inhibit cardiomyocyte growth., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "length": 1088,
        "protein_name": "Protocadherin 10",
        "gene_name": "Pcdh10",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Pcdh10",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Protocadherin 10",
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        "go_molecular_function": "GO:0005509 calcium ion binding;GO:0050839 cell adhesion molecule binding",
        "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0045211 postsynaptic membrane;GO:0005886 plasma membrane",
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        "length": 382,
        "protein_name": "Spindlin interactor and repressor of chromatin binding",
        "gene_name": "Spindoc",
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        "gene_names_refseq": "RGD1308106; Spindoc",
        "protein_names_uniprotkb": "Spindlin interactor and repressor of chromatin binding",
        "protein_names_refseq": "spindlin interactor and repressor of chromatin-binding protein; uncharacterized protein C11orf84 homolog",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0090734 site of DNA damage",
        "go_biological_process": "GO:0045892 negative regulation of DNA-templated transcription;GO:0006974 DNA damage response",
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        "length": 1045,
        "protein_name": "Ribosomal protein S6 kinase delta-1",
        "gene_name": "Rps6kc1",
        "organism": "Rat",
        "refseq_name": "ribosomal protein S6 kinase delta-1 isoform 2",
        "refseq_ac": "NP_001402719",
        "gene_names_uniprotkb": "Rps6kc1",
        "gene_names_refseq": "Rps6kc1",
        "protein_names_uniprotkb": "Ribosomal protein S6 kinase delta-1; 2.7.11.1; 52 kDa ribosomal protein S6 kinase",
        "protein_names_refseq": "ribosomal protein S6 kinase delta-1 isoform 2; ribosomal protein S6 kinase delta-1; ribosomal protein S6 kinase, 52kDa, polypeptide 1; ribosomal protein S6 kinase, polypeptide 1; ribosomal protein S6 kinase, polypeptide C1",
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        "disease": "Parkinson's disease (Disease Ontology:DOID:14330)",
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        "function": "May be involved in transmitting sphingosine-1 phosphate (SPP)-mediated signaling into the cell. Plays a role in the recruitment of PRDX3 to early endosomes., [UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "2.7.11.1;2.7.12.1;2.7.1.153;2.7.1.137;2.7.11.24;2.7.11.25;2.7.11.22;2.7.11.23;2.7.4.6;2.7.1.154;2.7.11.38;2.7.11.17;2.7.11.21;2.7.12.2;2.7.1.40;2.7.11.12;2.7.11.26;2.7.11.34;2.7.10.2;2.7.1.150;2.7.11.13;4.1.1.32;2.7.11.19;2.7.2.3;2.7.11.11;2.7.11.31;3.1.3.16;2.7.11.4;2.3.1.48;3.1.11.-;2.7.13.3;2.7.4.18;3.1.24.-;3.4.19.12;2.7.11.39;2.4.99.18;2.7.11.10",
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        "protein_name": "Transcription factor RelB",
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        "gene_names_uniprotkb": "Relb",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Transcription factor RelB",
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        "disease": "immunodeficiency 53 (Disease Ontology:DOID:0111992); bacterial infectious disease (Disease Ontology:DOID:104); prediabetes syndrome (Disease Ontology:DOID:11716); breast cancer (Disease Ontology:DOID:1612); transitional cell carcinoma (Disease Ontology:DOID:2671); atopic dermatitis (Disease Ontology:DOID:3310); ureteral obstruction (Disease Ontology:DOID:5199); kidney disease (Disease Ontology:DOID:557); muscular atrophy (Disease Ontology:DOID:767)",
        "pathway": " (rno:100360982);  (R-RNO-5607761);  (R-RNO-5621575);  (R-RNO-5676590)",
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0003700 DNA-binding transcription factor activity;GO:0019901 protein kinase binding;GO:0042802 identical protein binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding",
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZU09-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A1W2Q671-1",
        "uniprot_id": "A0A1W2Q671_RAT",
        "mass": 191758.0,
        "length": 1745,
        "protein_name": "Serine/threonine-protein kinase WNK3",
        "gene_name": "Wnk3",
        "organism": "Rat",
        "refseq_name": "serine/threonine-protein kinase WNK3 isoform 1",
        "refseq_ac": "NP_001398747",
        "gene_names_uniprotkb": "Wnk3",
        "gene_names_refseq": "RGD1563131; Wnk3",
        "protein_names_uniprotkb": "Serine/threonine-protein kinase WNK3; 2.7.11.1; Protein kinase lysine-deficient 3; Protein kinase with no lysine 3",
        "protein_names_refseq": "serine/threonine-protein kinase WNK3 isoform 1; serine/threonine-protein kinase WNK3",
        "tax_id": 10116,
        "disease": "Prieto syndrome (Disease Ontology:DOID:0060805); pseudohypoaldosteronism (Disease Ontology:DOID:4479)",
        "pathway": " (rno:317420)",
        "pathway_count": 1,
        "publication_count": 4,
        "publication_id_list": "23482566;32589890;34626749;38843836",
        "class_list": "",
        "function": "Activated WNK3 induced by intracerebral hemorrhage deteriorates brain injury maybe via WNK3/SPAK/NKCC1 pathway., [RefSeq, PubMed]; LINGO-1 potentiates neuronal apoptosis, likely by inhibiting WNK3 kinase activity., [RefSeq, PubMed]; WNK3 Promotes Neuronal Survival after Traumatic Brain Injury in Rats., [RefSeq, PubMed]",
        "predicted_glycosites": 2,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 2,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 1,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
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        "total_reported_o_glycosites": 1,
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        "reported_phosphosites": 0,
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        "missing_score": 0,
        "biomarker_type": "",
        "glycan_count": 1,
        "disease_count": 2,
        "glyco_site_count": 2,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "2.7.11.1;2.7.12.1;2.7.1.153;2.7.1.137;2.7.11.24;2.7.11.25;2.7.11.22;2.7.11.23;2.7.4.6;2.7.1.154;2.7.11.38;2.7.11.17;2.7.11.21;2.7.12.2;2.7.1.40;2.7.11.12;2.7.11.26;2.7.11.34;2.7.10.2;2.7.1.150;2.7.11.13;4.1.1.32;2.7.11.19;2.7.2.3;2.7.11.11;2.7.11.31;3.1.3.16;2.7.11.4;2.3.1.48;3.1.11.-;2.7.13.3;2.7.4.18;3.1.24.-;3.4.19.12;2.7.11.39;2.4.99.18;2.7.11.10",
        "go_molecular_function": "GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding;GO:0019870 potassium channel inhibitor activity;GO:0004672 protein kinase activity;GO:0044325 transmembrane transporter binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005912 adherens junction;GO:0005923 bicellular tight junction",
        "go_biological_process": "GO:0006884 cell volume homeostasis;GO:0010766 negative regulation of sodium ion transport;GO:1904062 regulation of monoatomic cation transmembrane transport;GO:0090279 regulation of calcium ion import;GO:0007231 osmosensory signaling pathway",
        "synthesized_glycan_count": 0,
        "hit_score": 0.7,
        "record_id": "A0A1W2Q671-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZYW5-1",
        "uniprot_id": "D3ZYW5_RAT",
        "mass": 65168.0,
        "length": 578,
        "protein_name": "Zinc finger, imprinted 1",
        "gene_name": "Zim1",
        "organism": "Rat",
        "refseq_name": "zinc finger, imprinted 1",
        "refseq_ac": "NP_001100943",
        "gene_names_uniprotkb": "Zim1",
        "gene_names_refseq": "Zim1",
        "protein_names_uniprotkb": "Zinc finger, imprinted 1",
        "protein_names_refseq": "zinc finger, imprinted 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:308322);  (R-RNO-212436)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "binding_glycan_count": 0,
        "secondary_ac_list": "A0A0G2KA26",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0045944 positive regulation of transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZYW5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A1B0GWW4-1",
        "uniprot_id": "A0A1B0GWW4_RAT",
        "mass": 126668.0,
        "length": 1125,
        "protein_name": "Cytosolic carboxypeptidase 4",
        "gene_name": "Agbl1",
        "organism": "Rat",
        "refseq_name": "AGBL carboxypeptidase 1 isoform 1",
        "refseq_ac": "NP_001419181",
        "gene_names_uniprotkb": "Agbl1",
        "gene_names_refseq": "Agbl1; RGD1560280",
        "protein_names_uniprotkb": "Cytosolic carboxypeptidase 4; 3.4.17.24; ATP/GTP-binding protein-like 1; Protein deglutamylase CCP4",
        "protein_names_refseq": "AGBL carboxypeptidase 1 isoform 1; ATP/GTP binding protein-like 1; cytosolic carboxypeptidase 4",
        "tax_id": 10116,
        "disease": "Fuchs' endothelial dystrophy (Disease Ontology:DOID:11555)",
        "pathway": " (rno:308724)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Metallocarboxypeptidase that mediates deglutamylation of tubulin and non-tubulin target proteins. Catalyzes the removal of polyglutamate side chains present on the gamma-carboxyl group of glutamate residues within the C-terminal tail of tubulin protein. Specifically cleaves tubulin long-side-chains, while it is not able to remove the branching point glutamate. Also catalyzes the removal of polyglutamate residues from the carboxy-terminus of non-tubulin proteins such as MYLK., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "3.4.17.24;3.4.17.-",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0004181 metallocarboxypeptidase activity;GO:0015631 tubulin binding",
        "go_cellular_component": "GO:0005829 cytosol;GO:0005737 cytoplasm;GO:0015630 microtubule cytoskeleton",
        "go_biological_process": "GO:0006508 proteolysis;GO:0035610 protein side chain deglutamylation;GO:0035609 C-terminal protein deglutamylation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A1B0GWW4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "D3ZZL1-1",
        "uniprot_id": "D3ZZL1_RAT",
        "mass": 48097.0,
        "length": 434,
        "protein_name": "DNA repair protein RAD52 homolog",
        "gene_name": "Rad52",
        "organism": "Rat",
        "refseq_name": "DNA repair protein RAD52 homolog isoform X1",
        "refseq_ac": "XP_008761454",
        "gene_names_uniprotkb": "Rad52",
        "gene_names_refseq": "Rad52",
        "protein_names_uniprotkb": "DNA repair protein RAD52 homolog",
        "protein_names_refseq": "DNA repair protein RAD52 homolog isoform X1",
        "tax_id": 10116,
        "disease": "nicotine dependence (Disease Ontology:DOID:0050742); salivary gland carcinoma (Disease Ontology:DOID:0050904); lung cancer (Disease Ontology:DOID:1324); colon cancer (Disease Ontology:DOID:219); lung squamous cell carcinoma (Disease Ontology:DOID:3907); lung non-small cell carcinoma (Disease Ontology:DOID:3908); mucoepidermoid carcinoma (Disease Ontology:DOID:4531); lung small cell carcinoma (Disease Ontology:DOID:5409); hepatocellular carcinoma (Disease Ontology:DOID:684); colorectal cancer (Disease Ontology:DOID:9256); nasopharynx carcinoma (Disease Ontology:DOID:9261)",
        "pathway": " (R-RNO-3108214);  (R-RNO-5685938);  (R-RNO-5685939)",
        "pathway_count": 3,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Involved in double-stranded break repair. Plays a central role in genetic recombination and DNA repair by promoting the annealing of complementary single-stranded DNA and by stimulation of the RAD51 recombinase., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 11,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0042802 identical protein binding;GO:0003697 single-stranded DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0032993 protein-DNA complex;GO:0032991 protein-containing complex",
        "go_biological_process": "GO:0045002 double-strand break repair via single-strand annealing;GO:0000730 DNA recombinase assembly;GO:0006312 mitotic recombination;GO:2000819 regulation of nucleotide-excision repair;GO:0006310 DNA recombination",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "D3ZZL1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A0G2K8V0-1",
        "uniprot_id": "A0A0G2K8V0_RAT",
        "mass": 167670.0,
        "length": 1490,
        "protein_name": "protein-tyrosine-phosphatase",
        "gene_name": "Ptprm",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ptprm",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "protein-tyrosine-phosphatase; 3.1.3.48",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "pancreatic ductal adenocarcinoma (Disease Ontology:DOID:3498)",
        "pathway": " (rno:29616)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "38843836",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "missing_score": 0,
        "biomarker_type": "",
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        "glyco_site_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "3.1.3.48;2.7.10.1;3.1.3.16;3.1.3.2;3.1.3.21;3.1.3.18;3.1.3.67;3.1.3.-;3.1.3.27;3.1.3.5",
        "go_molecular_function": "GO:0042802 identical protein binding;GO:0045296 cadherin binding;GO:0005001 transmembrane receptor protein tyrosine phosphatase activity;GO:0016791 phosphatase activity;GO:0004725 protein tyrosine phosphatase activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005886 plasma membrane;GO:0005911 cell-cell junction;GO:0005912 adherens junction;GO:0030027 lamellipodium",
        "go_biological_process": "GO:0007165 signal transduction;GO:0031175 neuron projection development;GO:0042311 vasodilation;GO:0001937 negative regulation of endothelial cell proliferation;GO:0016525 negative regulation of angiogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "A0A0G2K8V0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A0G2K994-1",
        "uniprot_id": "A0A0G2K994_RAT",
        "mass": 57306.0,
        "length": 532,
        "protein_name": "V-set and immunoglobulin domain containing 10",
        "gene_name": "Vsig10",
        "organism": "Rat",
        "refseq_name": "V-set and immunoglobulin domain-containing protein 10 isoform X2",
        "refseq_ac": "XP_006249499",
        "gene_names_uniprotkb": "Vsig10",
        "gene_names_refseq": "RGD1565800; Vsig10",
        "protein_names_uniprotkb": "V-set and immunoglobulin domain containing 10",
        "protein_names_refseq": "V-set and immunoglobulin domain-containing protein 10 isoform X2",
        "tax_id": 10116,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0030424 axon",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A0G2K994-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A0G2K9D3-1",
        "uniprot_id": "A0A0G2K9D3_RAT",
        "mass": 35452.0,
        "length": 319,
        "protein_name": "Olfactory receptor family 8 subfamily G member 34B",
        "gene_name": "Or8g34b",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr1286",
        "refseq_ac": "NP_001000799",
        "gene_names_uniprotkb": "Or8g34b",
        "gene_names_refseq": "Olr1286; Or8g34b",
        "protein_names_uniprotkb": "Olfactory receptor family 8 subfamily G member 34B",
        "protein_names_refseq": "olfactory receptor 1286; olfactory receptor Olr1286; olfactory receptor gene Olr1286",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:405084)",
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        "publication_id_list": "",
        "class_list": "",
        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
        "predicted_glycosites": 0,
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