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        "uniprot_canonical_ac": "A0ABK0LSL8-1",
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        "protein_name": "G-protein coupled receptors family 1 profile domain-containing protein",
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        "gene_names_uniprotkb": "Or2i1; Olfr94",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "G-protein coupled receptors family 1 profile domain-containing protein",
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        "length": 296,
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        "refseq_name": "hepatic leukemia factor isoform X1",
        "refseq_ac": "XP_006247198",
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        "gene_names_refseq": "Hlf",
        "protein_names_uniprotkb": "HLF transcription factor, PAR bZIP family member",
        "protein_names_refseq": "hepatic leukemia factor isoform X1",
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        "disease": "stomach cancer (Disease Ontology:DOID:10534); acute lymphoblastic leukemia (Disease Ontology:DOID:9952)",
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        "refseq_ac": "",
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    },
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        "gene_names_uniprotkb": "Bag2",
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        "protein_names_uniprotkb": "BAG family molecular chaperone regulator 2; Bcl-2-associated athanogene 2",
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        "function": "Co-chaperone for HSP70 and HSC70 chaperone proteins. Acts as a nucleotide-exchange factor (NEF) promoting the release of ADP from the HSP70 and HSC70 proteins thereby triggering client/substrate protein release., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0042802 identical protein binding;GO:0051087 protein-folding chaperone binding;GO:0031072 heat shock protein binding;GO:0031625 ubiquitin protein ligase binding;GO:0044325 transmembrane transporter binding",
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        "gene_names_refseq": "",
        "protein_names_uniprotkb": "ATP synthase F(0) complex subunit g, mitochondrial; ATPase subunit g",
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        "function": "Subunit g, of the mitochondrial membrane ATP synthase complex (F(1)F(0) ATP synthase or Complex V) that produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. ATP synthase complex consist of a soluble F(1) head domain - the catalytic core - and a membrane F(1) domain - the membrane proton channel. These two domains are linked by a central stalk rotating inside the F(1) region and a stationary peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation. In vivo, can only synthesize ATP although its ATP hydrolase activity can be activated artificially in vitro. Part of the complex F(0) domain., [UniProtKB, UniProtKB]",
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        "protein_names_uniprotkb": "HMG box domain-containing protein",
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        "function": "In the cytoplasm proposed to dissociate the BECN1:BCL2 complex via competitive interaction with BECN1 leading to autophagy activation. Can protect BECN1 and ATG5 from calpain-mediated cleavage and thus proposed to control their proautophagic and proapoptotic functions and to regulate the extent and severity of inflammation-associated cellular injury. In myeloid cells has a protective role against endotoxemia and bacterial infection by promoting autophagy. Involved in endosomal translocation and activation of TLR9 in response to CpG-DNA in macrophages., [UniProtKB, UniProtKB]",
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        "protein_name": "Secondary ossification center-associated regulator of chondrocyte maturation",
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        "protein_names_uniprotkb": "Secondary ossification center-associated regulator of chondrocyte maturation",
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        "protein_name": "Ig-like domain-containing protein",
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        "protein_names_uniprotkb": "Ig-like domain-containing protein",
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        "protein_name": "Olfactory receptor family 13 subfamily P member 4",
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        "gene_names_refseq": "Olr857; Or13p4-ps1; Or13p4",
        "protein_names_uniprotkb": "Olfactory receptor family 13 subfamily P member 4",
        "protein_names_refseq": "olfactory receptor 2A12-like; olfactory receptor 857; olfactory receptor Olr857; olfactory receptor family 13 subfamily P member 4, pseudogene 1; olfactory receptor gene Olr857; olfactory receptor-like protein",
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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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        "protein_name": "Large ribosomal subunit protein eL33",
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        "gene_names_uniprotkb": "LOC103694795",
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        "protein_names_uniprotkb": "Large ribosomal subunit protein eL33; 60S ribosomal protein L35a",
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        "function": "Data showed that lysophosphatidic acid receptors LPA1-3, are phosphoproteins whose phosphorylation state is modulated by the natural agonist, LPA. Publication Status: Online-Only, [RefSeq, PubMed]; These findings identify ATX and LPA2 as radiation-regulated genes that appear to play a physiological role in DNA repair. Erratum:[Cell Signal. 2015 Oct;27(10):2137. Banerje, Souvik [corrected to Banerjee, Souvik]], [RefSeq, PubMed]",
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        "protein_name": "Y-linked testis-specific protein 1-like",
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        "protein_names_refseq": "putative vomeronasal receptor-like protein 4; vomernasal 1 receptor Vom1r68; vomeronasal 1 receptor 68; vomeronasal 1 receptor, C1; vomeronasal V1r-type receptor V1rc1",
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        "length": 439,
        "protein_name": "Ectonucleotide pyrophosphatase/phosphodiesterase family member 7",
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        "protein_names_refseq": "E-NPP7; NPP-7; alk-SMase; alkaline sphingomyelin phosphodiesterase; ectonucleotide pyrophosphatase/phosphodiesterase family member 7 precursor; ectonucleotide pyrophosphatase/phosphodiesterase family member 7; intestinal alkaline sphingomyelinase; sphingomyelinase, intestinal alkaline",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0008081 phosphoric diester hydrolase activity;GO:0004767 sphingomyelin phosphodiesterase activity",
        "go_cellular_component": "GO:0005794 Golgi apparatus;GO:0005886 plasma membrane;GO:0005902 microvillus",
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        "length": 509,
        "protein_name": "non-specific serine/threonine protein kinase",
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        "gene_names_uniprotkb": "LOC134485019; LOC134485067; LOC134485068",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "non-specific serine/threonine protein kinase; 2.7.11.1",
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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",
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    },
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        "protein_names_refseq": "EF-hand protein; centrin, EF-hand protein, 1; centrin-1",
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        "publication_id_list": "15347651",
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        "function": "Cen1 and Cen2 contribute to the centrin-transducin complex and potentially participate in the regulation of transducin translocation through the photoreceptor cilium, [RefSeq, PubMed]",
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        "go_cellular_component": "GO:0042101 T cell receptor complex",
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        "length": 132,
        "protein_name": "40S ribosomal protein S12",
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        "refseq_name": "ribosomal protein S12-like 2",
        "refseq_ac": "NP_001388998",
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        "gene_names_refseq": "Rps12l2",
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        "protein_names_refseq": "40S ribosomal protein S12-like; ribosomal protein S12-like 2",
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        "function": "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. Subunit of the 40S ribosomal complex., [UniProtKB, UniProtKB]",
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        "gene_names_uniprotkb": "Tdpoz2l4",
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        "protein_names_uniprotkb": "TDPOZ2",
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        "length": 834,
        "protein_name": "T-cell activation Rho GTPase-activating protein",
        "gene_name": "LOC120100815",
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        "gene_names_uniprotkb": "LOC120100815",
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        "protein_names_uniprotkb": "T-cell activation Rho GTPase-activating protein",
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        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Pnma8a; Pnmal1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "PNMA family member 8A",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:361515)",
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        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "",
        "predicted_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:0005654 nucleoplasm;GO:0016604 nuclear body",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0LV36-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LVE7-1",
        "uniprot_id": "A0ABK0LVE7_RAT",
        "mass": 55345.0,
        "length": 488,
        "protein_name": "Histone deacetylase 2",
        "gene_name": "Hdac2",
        "organism": "Rat",
        "refseq_name": "histone deacetylase 2",
        "refseq_ac": "NP_445899",
        "gene_names_uniprotkb": "Hdac2",
        "gene_names_refseq": "Hdac2",
        "protein_names_uniprotkb": "Histone deacetylase 2; 3.5.1.98; HD2",
        "protein_names_refseq": "histone deacetylase 2",
        "tax_id": 10116,
        "disease": "fetal alcohol spectrum disorder (Disease Ontology:DOID:0050696); stroke (Disease Ontology:DOID:0051061); prostate carcinoma (Disease Ontology:DOID:10286); stomach cancer (Disease Ontology:DOID:10534); alcohol use disorder (Disease Ontology:DOID:1574); anxiety disorder (Disease Ontology:DOID:2030); asthma (Disease Ontology:DOID:2841); endometriosis (Disease Ontology:DOID:289); chronic obstructive pulmonary disease (Disease Ontology:DOID:3083); temporal lobe epilepsy (Disease Ontology:DOID:3328); bronchitis (Disease Ontology:DOID:6132); pulmonary hypertension (Disease Ontology:DOID:6432); hepatocellular carcinoma (Disease Ontology:DOID:684); Peyronie's disease (Disease Ontology:DOID:8616); cervix uteri carcinoma in situ (Disease Ontology:DOID:8991); pulmonary emphysema (Disease Ontology:DOID:9675); type 1 diabetes mellitus (Disease Ontology:DOID:9744); alopecia areata (Disease Ontology:DOID:986); acute lymphoblastic leukemia (Disease Ontology:DOID:9952)",
        "pathway": " (rno:84577);  (R-RNO-3214815);  (R-RNO-350054);  (R-RNO-4551638);  (R-RNO-6804758);  (R-RNO-73762);  (R-RNO-8943724);  (R-RNO-9022692);  (R-RNO-9701898);  (R-RNO-9764725);  (R-RNO-983231);  (R-RNO-9937850);  (R-RNO-9940951)",
        "pathway_count": 13,
        "publication_count": 6,
        "publication_id_list": "22673903;35902549;35926274;36156740;37021908;39192337",
        "class_list": "",
        "function": "HDAC2 exacerbates rheumatoid arthritis progression via the IL-17-CCL7 signaling pathway., [RefSeq, PubMed]; Histone deacetylase that catalyzes the deacetylation of lysine residues on the N-terminal part of the core histones (H2A, H2B, H3 and H4). Histone deacetylation gives a tag for epigenetic repression and plays an important role in transcriptional regulation, cell cycle progression and developmental events. Histone deacetylases act via the formation of large multiprotein complexes., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Involvement of HDAC2-mediated kcnq2/kcnq3 genes transcription repression activated by EREG/EGFR-ERK-Runx1 signaling in bone cancer pain. Publication Status: Online-Only, [RefSeq, PubMed]; MTOR and HDAC2 are simultaneously activated during electrically induced kindling of seizures., [RefSeq, PubMed]; SCFAs Ameliorate Chronic Postsurgical Pain-Related Cognition Dysfunction via the ACSS2-HDAC2 Axis in Rats., [RefSeq, PubMed]; Selenium-sensitive histone deacetylase 2 is required for forkhead box O3A and regulates extracellular matrix metabolism in cartilage. Erratum:[J Bone Miner Metab. 2023 Jan;41(1):143. doi: 10.1007/s00774-022-01395-7. PMID: 36592235], [RefSeq, PubMed]",
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        "secondary_ac_list": "",
        "ec_number_list": "3.5.1.98;3.5.1.-;2.3.2.-;2.3.1.48;3.6.4.-;3.5.1.48;3.5.1.62",
        "go_molecular_function": "GO:0035851 Krueppel-associated box domain binding;GO:0003682 chromatin binding;GO:0019899 enzyme binding;GO:0046872 metal ion binding;GO:0031072 heat shock protein binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0017053 transcription repressor complex;GO:0005667 transcription regulator complex",
        "go_biological_process": "GO:0051896 regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction;GO:0009913 epidermal cell differentiation;GO:0097305 response to alcohol;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006338 chromatin remodeling",
        "synthesized_glycan_count": 0,
        "hit_score": 0.7,
        "record_id": "A0ABK0LVE7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LVZ9-1",
        "uniprot_id": "A0ABK0LVZ9_RAT",
        "mass": 49908.0,
        "length": 454,
        "protein_name": "Purine nucleoside phosphorylase LACC1",
        "gene_name": "Lacc1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Lacc1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Purine nucleoside phosphorylase LACC1; 2.4.2.1; 2.4.2.28; 3.5.4.4; Adenosine deaminase LACC1; Fatty acid metabolism-immunity nexus; Guanosine phosphorylase LACC1; Isocyanic acid synthase; Laccase domain-containing protein 1; S-methyl-5'-thioadenosine phosphorylase LACC1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "systemic juvenile rheumatoid arthritis (Disease Ontology:DOID:676)",
        "pathway": " (rno:313790)",
        "pathway_count": 1,
        "publication_count": 0,
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        "ec_number_list": "2.4.2.28;3.5.4.4;2.4.2.1",
        "go_molecular_function": "GO:0016787 hydrolase activity;GO:0005507 copper ion binding;GO:0017061 S-methyl-5-thioadenosine phosphorylase activity;GO:0004000 adenosine deaminase activity;GO:0046872 metal ion binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005777 peroxisome;GO:0005783 endoplasmic reticulum",
        "go_biological_process": "GO:0070431 nucleotide-binding oligomerization domain containing 2 signaling pathway;GO:0002221 pattern recognition receptor signaling pathway;GO:0050727 regulation of inflammatory response;GO:0030641 regulation of cellular pH;GO:0002720 positive regulation of cytokine production involved in immune response",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LVZ9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LWA0-1",
        "uniprot_id": "A0ABK0LWA0_RAT",
        "mass": 47246.0,
        "length": 420,
        "protein_name": "Homeobox-containing protein 1",
        "gene_name": "Hmbox1",
        "organism": "Rat",
        "refseq_name": "homeobox-containing protein 1 isoform 1",
        "refseq_ac": "NP_001414030",
        "gene_names_uniprotkb": "Hmbox1",
        "gene_names_refseq": "Hmbox1; RGD1306787",
        "protein_names_uniprotkb": "Homeobox-containing protein 1",
        "protein_names_refseq": "homeobox-containing protein 1 isoform 1; homeobox-containing protein 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 1,
        "publication_id_list": "20822188",
        "class_list": "",
        "function": "Binds directly to 5'-TTAGGG-3' repeats in telomeric DNA. Associates with the telomerase complex at sites of active telomere processing and positively regulates telomere elongation. Important for TERT binding to chromatin, indicating a role in recruitment of the telomerase complex to telomeres. Also plays a role in the alternative lengthening of telomeres (ALT) pathway in telomerase-negative cells where it promotes formation and/or maintenance of ALT-associated promyelocytic leukemia bodies (APBs). Enhances formation of telomere C-circles in ALT cells, suggesting a possible role in telomere recombination. Might also be involved in the DNA damage response at telomeres., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Hmbox1 is a key factor in the differentiation of bone-marrow stromal cells in vascular endothelial cells., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "biomarker_type": "",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0044877 protein-containing complex binding;GO:0003691 double-stranded telomeric DNA binding;GO:0042802 identical protein binding;GO:0042162 telomeric DNA binding;GO:0043565 sequence-specific DNA binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0016605 PML body;GO:0015030 Cajal body;GO:0000781 chromosome, telomeric region;GO:0005634 nucleus",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0045893 positive regulation of DNA-templated transcription;GO:0007004 telomere maintenance via telomerase;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0045892 negative regulation of DNA-templated transcription",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0LWA0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LVF6-1",
        "uniprot_id": "A0ABK0LVF6_RAT",
        "mass": 133161.0,
        "length": 1163,
        "protein_name": "Condensin-2 complex subunit G2",
        "gene_name": "Ncapg2",
        "organism": "Rat",
        "refseq_name": "condensin-2 complex subunit G2 isoform X3",
        "refseq_ac": "XP_038934008",
        "gene_names_uniprotkb": "Ncapg2",
        "gene_names_refseq": "Luzp5; Ncapg2; RGD1308406",
        "protein_names_uniprotkb": "Condensin-2 complex subunit G2; Chromosome-associated protein G2; Leucine zipper protein 5; Non-SMC condensin II complex subunit G2",
        "protein_names_refseq": "condensin-2 complex subunit G2 isoform X3",
        "tax_id": 10116,
        "disease": "autosomal recessive disease (Disease Ontology:DOID:0050737)",
        "pathway": " (rno:362798);  (R-RNO-2299718)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "total_reported_n_glycosites": 0,
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        "go_molecular_function": "GO:0043425 bHLH transcription factor binding;GO:0140117 histone H4K20me1 reader activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0000796 condensin complex;GO:0000794 condensed nuclear chromosome;GO:0005654 nucleoplasm;GO:0016607 nuclear speck",
        "go_biological_process": "GO:0000070 mitotic sister chromatid segregation;GO:1905820 positive regulation of chromosome separation;GO:0051984 positive regulation of chromosome segregation;GO:0021987 cerebral cortex development;GO:0007076 mitotic chromosome condensation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LVF6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LV97-1",
        "uniprot_id": "A0ABK0LV97_RAT",
        "mass": 82333.0,
        "length": 718,
        "protein_name": "non-specific serine/threonine protein kinase",
        "gene_name": "Tlk2",
        "organism": "Rat",
        "refseq_name": "serine/threonine-protein kinase tousled-like 2 isoform X7",
        "refseq_ac": "XP_038942062",
        "gene_names_uniprotkb": "Tlk2",
        "gene_names_refseq": "Tlk2",
        "protein_names_uniprotkb": "non-specific serine/threonine protein kinase; 2.7.11.1",
        "protein_names_refseq": "serine/threonine-protein kinase tousled-like 2 isoform X7",
        "tax_id": 10116,
        "disease": "autosomal dominant intellectual developmental disorder 57 (Disease Ontology:DOID:0061031)",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 1,
        "publication_id_list": "22673903",
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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:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding;GO:0042802 identical protein binding;GO:0044325 transmembrane transporter binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0048471 perinuclear region of cytoplasm;GO:0005882 intermediate filament",
        "go_biological_process": "GO:0006468 protein phosphorylation;GO:0007059 chromosome segregation;GO:0035556 intracellular signal transduction;GO:0006974 DNA damage response;GO:0018105 peptidyl-serine phosphorylation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0LV97-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LX38-1",
        "uniprot_id": "A0ABK0LX38_RAT",
        "mass": 64362.0,
        "length": 565,
        "protein_name": "FERM domain-containing protein 5",
        "gene_name": "Frmd5",
        "organism": "Rat",
        "refseq_name": "FERM domain-containing protein 5 isoform X5",
        "refseq_ac": "XP_008760433",
        "gene_names_uniprotkb": "Frmd5",
        "gene_names_refseq": "Frmd5",
        "protein_names_uniprotkb": "FERM domain-containing protein 5",
        "protein_names_refseq": "FERM domain-containing protein 5 isoform X5",
        "tax_id": 10116,
        "disease": "autism spectrum disorder (Disease Ontology:DOID:0060041); neurodevelopmental disorder with eye movement abnormalities and ataxia (Disease Ontology:DOID:0081275)",
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        "class_list": "",
        "function": "May be involved in regulation of cell migration. May regulate cell-matrix interactions via its interaction with ITGB5 and modifying ITGB5 cytoplasmic tail interactions such as with FERMT2 and TLN1. May regulate ROCK1 kinase activity possibly involved in regulation of actin stress fiber formation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 2,
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        "ec_number_list": "",
        "go_molecular_function": "GO:0008092 cytoskeletal protein binding;GO:0005178 integrin binding;GO:0019901 protein kinase binding",
        "go_cellular_component": "GO:0005856 cytoskeleton;GO:0005912 adherens junction",
        "go_biological_process": "GO:0031032 actomyosin structure organization;GO:0045785 positive regulation of cell adhesion;GO:0030334 regulation of cell migration;GO:2000146 negative regulation of cell motility",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LWX8-1",
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        "length": 411,
        "protein_name": "SUN domain-containing protein 3",
        "gene_name": "Sun3",
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        "refseq_name": "SUN domain-containing protein 3 isoform X1",
        "refseq_ac": "XP_006251533",
        "gene_names_uniprotkb": "Sun3",
        "gene_names_refseq": "Sun3",
        "protein_names_uniprotkb": "SUN domain-containing protein 3; Sad1/unc-84 domain-containing protein 1",
        "protein_names_refseq": "SUN domain-containing protein 3 isoform X1",
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        "disease": "",
        "pathway": " (rno:498412)",
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        "function": "As a probable component of the LINC (LInker of Nucleoskeleton and Cytoskeleton) complex, involved in the connection between the nuclear lamina and the cytoskeleton. The nucleocytoplasmic interactions established by the LINC complex play an important role in the transmission of mechanical forces across the nuclear envelope and in nuclear movement and positioning. May be involved in nuclear remodeling during sperm head formation in spermatogenesis. A probable SUN3:SYNE1 LINC complex may tether spermatid nuclei to posterior cytoskeletal structures such as the manchette., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0043495 protein-membrane adaptor activity",
        "go_cellular_component": "GO:0005635 nuclear envelope;GO:0005637 nuclear inner membrane;GO:0034993 meiotic nuclear membrane microtubule tethering complex",
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        "hit_score": 0.1,
        "record_id": "A0ABK0LWX8-1",
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    {
        "uniprot_canonical_ac": "A0ABK0LX49-1",
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        "length": 214,
        "protein_name": "Sodium/potassium-transporting ATPase subunit beta-1-interacting protein",
        "gene_name": "Nkain1",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Nkain1",
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        "protein_names_uniprotkb": "Sodium/potassium-transporting ATPase subunit beta-1-interacting protein; Na(+)/K(+)-transporting ATPase subunit beta-1-interacting protein",
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        "hit_score": 0.1,
        "record_id": "A0ABK0LX49-1",
        "record_type": "protein"
    },
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        "uniprot_canonical_ac": "A0ABK0LW70-1",
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        "protein_name": "Sterile alpha motif domain containing 12",
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        "protein_names_uniprotkb": "Sterile alpha motif domain containing 12",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "familial adult myoclonic epilepsy 1 (Disease Ontology:DOID:0111690)",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0009898 cytoplasmic side of plasma membrane",
        "go_biological_process": "GO:0007169 cell surface receptor protein tyrosine kinase signaling pathway",
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        "record_id": "A0ABK0LW70-1",
        "record_type": "protein"
    },
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        "uniprot_canonical_ac": "A0ABK0LVZ7-1",
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        "length": 900,
        "protein_name": "Nuclear valosin-containing protein-like",
        "gene_name": "Nvl",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Nvl",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Nuclear valosin-containing protein-like",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:289323)",
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        "function": "Participates in the assembly of the telomerase holoenzyme and effecting of telomerase activity via its interaction with TERT. Involved in both early and late stages of the pre-rRNA processing pathways. Spatiotemporally regulates 60S ribosomal subunit biogenesis in the nucleolus. Catalyzes the release of specific assembly factors, such as WDR74, from pre-60S ribosomal particles through the ATPase activity., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005524 ATP binding;GO:0016887 ATP hydrolysis activity;GO:1990275 preribosome binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0000176 nuclear exosome (RNase complex);GO:0005697 telomerase holoenzyme complex",
        "go_biological_process": "GO:0042254 ribosome biogenesis;GO:0042273 ribosomal large subunit biogenesis;GO:0006364 rRNA processing;GO:1905323 telomerase holoenzyme complex assembly;GO:0032206 positive regulation of telomere maintenance",
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        "hit_score": 0.2,
        "record_id": "A0ABK0LVZ7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LUQ5-1",
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        "length": 432,
        "protein_name": "Luc7-like protein",
        "gene_name": "Luc7l3",
        "organism": "Rat",
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        "gene_names_uniprotkb": "Luc7l3; Luc7l-ps3; Luc7l3-ps2",
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        "protein_names_uniprotkb": "Luc7-like protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (rno:360602)",
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        "class_list": "",
        "function": "Binds cAMP regulatory element DNA sequence. Plays a role in RNA splicing., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003729 mRNA binding",
        "go_cellular_component": "GO:0005685 U1 snRNP;GO:0005634 nucleus;GO:0016607 nuclear speck;GO:0071004 U2-type prespliceosome",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LUU3-1",
        "uniprot_id": "A0ABK0LUU3_RAT",
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        "length": 492,
        "protein_name": "Sushi domain-containing protein 4",
        "gene_name": "Susd4",
        "organism": "Rat",
        "refseq_name": "sushi domain-containing protein 4 isoform X1",
        "refseq_ac": "XP_063128241",
        "gene_names_uniprotkb": "Susd4",
        "gene_names_refseq": "RGD1564043; Susd4",
        "protein_names_uniprotkb": "Sushi domain-containing protein 4",
        "protein_names_refseq": "sushi domain-containing protein 4 isoform X1",
        "tax_id": 10116,
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        "pathway": " (rno:289335)",
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        "function": "Acts as a complement inhibitor by disrupting the formation of the classical C3 convertase. Isoform 3 inhibits the classical complement pathway, while membrane-bound isoform 1 inhibits deposition of C3b via both the classical and alternative complement pathways., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0016020 membrane;GO:0045211 postsynaptic membrane;GO:0098688 parallel fiber to Purkinje cell synapse",
        "go_biological_process": "GO:0030449 regulation of complement activation;GO:0045959 negative regulation of complement activation, classical pathway;GO:0045957 negative regulation of complement activation, alternative pathway;GO:0099149 regulation of postsynaptic neurotransmitter receptor internalization",
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        "record_id": "A0ABK0LUU3-1",
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    {
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        "protein_name": "Coiled-coil domain containing 12",
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        "gene_names_uniprotkb": "Ccdc12",
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        "protein_names_uniprotkb": "Coiled-coil domain containing 12",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (rno:363151);  (R-RNO-72163)",
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0071014 post-mRNA release spliceosomal complex;GO:0005684 U2-type spliceosomal complex",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LVU1-1",
        "uniprot_id": "A0ABK0LVU1_RAT",
        "mass": 64463.0,
        "length": 575,
        "protein_name": "Copine-4",
        "gene_name": "Cpne4",
        "organism": "Rat",
        "refseq_name": "copine-4 isoform X1",
        "refseq_ac": "XP_017451278",
        "gene_names_uniprotkb": "Cpne4",
        "gene_names_refseq": "Cpne4",
        "protein_names_uniprotkb": "Copine-4; Copine IV",
        "protein_names_refseq": "copine-4 isoform X1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:367160)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Probable calcium-dependent phospholipid-binding protein that may play a role in calcium-mediated intracellular processes., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0046872 metal ion binding;GO:0005544 calcium-dependent phospholipid binding",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0098978 glutamatergic synapse;GO:0045202 synapse",
        "go_biological_process": "GO:0071277 cellular response to calcium ion",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LVU1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LUN9-1",
        "uniprot_id": "A0ABK0LUN9_RAT",
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        "length": 529,
        "protein_name": "spleen exonuclease",
        "gene_name": "Pld4",
        "organism": "Rat",
        "refseq_name": "5'-3' exonuclease PLD4",
        "refseq_ac": "NP_001119760",
        "gene_names_uniprotkb": "Pld4",
        "gene_names_refseq": "Pld4",
        "protein_names_uniprotkb": "spleen exonuclease; 3.1.16.1",
        "protein_names_refseq": "5'-3' exonuclease PLD4; phospholipase D4",
        "tax_id": 10116,
        "disease": "systemic lupus erythematosus (Disease Ontology:DOID:9074)",
        "pathway": " (rno:362792);  (R-RNO-1855204);  (R-RNO-2029485)",
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        "function": "",
        "predicted_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "3.1.16.1;3.1.4.4;2.3.1.-;3.1.4.11",
        "go_molecular_function": "GO:0016788 hydrolase activity, acting on ester bonds;GO:0045145 single-stranded DNA 5'-3' DNA exonuclease activity",
        "go_cellular_component": "GO:0012505 endomembrane system;GO:0005634 nucleus;GO:0005769 early endosome;GO:0005783 endoplasmic reticulum;GO:0032588 trans-Golgi network membrane",
        "go_biological_process": "GO:0006909 phagocytosis;GO:0002244 hematopoietic progenitor cell differentiation;GO:1900015 regulation of cytokine production involved in inflammatory response",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LUN9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LVH6-1",
        "uniprot_id": "A0ABK0LVH6_RAT",
        "mass": 107916.0,
        "length": 974,
        "protein_name": "Zinc finger protein 280D",
        "gene_name": "Zfp280d",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Zfp280d",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger protein 280D",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "autism spectrum disorder (Disease Ontology:DOID:0060041); intellectual disability (Disease Ontology:DOID:1059)",
        "pathway": " (rno:315798)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "May function as a transcription factor., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "predicted_o_glycosites": 1,
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        "biomarker_type": "",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0003677 DNA binding;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_biological_process": "GO:0006351 DNA-templated transcription;GO:0006355 regulation of DNA-templated transcription",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0LVH6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LW29-1",
        "uniprot_id": "A0ABK0LW29_RAT",
        "mass": 64144.0,
        "length": 573,
        "protein_name": "Beta-1,3-glucosyltransferase",
        "gene_name": "B3glct",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "B3glct",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Beta-1,3-glucosyltransferase; Beta 3-glucosyltransferase; Beta-3-glycosyltransferase-like",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "Peters plus syndrome (Disease Ontology:DOID:0080201)",
        "pathway": " (R-RNO-5173214)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "38843836",
        "class_list": "",
        "function": "Beta-1,3-glucosyltransferase involved in one of the two pathways responsible for protein O-linked fucosylation, a unique post-translational modification of cysteine-knotted proteins that regulates various biological processes. This pathway targets proteins with Thrombospondin type-1 (TSP1) repeats (TSR) in the endoplasmic reticulum. It starts with POFUT2, which attaches fucose via an O-glycosidic bond to a conserved serine or threonine residue. B3GLCT extends this modification by transferring a glucose molecule from UDP-glucose to the fucose., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0008375 acetylglucosaminyltransferase activity;GO:0016757 glycosyltransferase activity;GO:0160265 O-fucosylpeptide 3-beta-glucosyltransferase activity",
        "go_cellular_component": "GO:0005789 endoplasmic reticulum membrane;GO:0016020 membrane;GO:0012505 endomembrane system",
        "go_biological_process": "GO:0036066 protein O-linked glycosylation via fucose;GO:0006004 fucose metabolic process;GO:1904888 cranial skeletal system development;GO:0001501 skeletal system development;GO:0007420 brain development",
        "synthesized_glycan_count": 6,
        "hit_score": 0.4,
        "record_id": "A0ABK0LW29-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LV49-1",
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        "mass": 56203.0,
        "length": 486,
        "protein_name": "Leucine-rich repeat-containing protein 6",
        "gene_name": "Dnaaf11",
        "organism": "Rat",
        "refseq_name": "dynein axonemal assembly factor 11 isoform X1",
        "refseq_ac": "XP_038934705",
        "gene_names_uniprotkb": "Dnaaf11",
        "gene_names_refseq": "Dnaaf11; Lrrc6; Lrtp; Tslrp",
        "protein_names_uniprotkb": "Leucine-rich repeat-containing protein 6",
        "protein_names_refseq": "dynein axonemal assembly factor 11 isoform X1",
        "tax_id": 10116,
        "disease": "primary ciliary dyskinesia 19 (Disease Ontology:DOID:0110608)",
        "pathway": " (rno:299920)",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0005737 cytoplasm;GO:0005929 cilium;GO:0005829 cytosol;GO:0090651 apical cytoplasm",
        "go_biological_process": "GO:0030317 flagellated sperm motility;GO:0061512 protein localization to cilium;GO:0036158 outer dynein arm assembly;GO:0061458 reproductive system development;GO:0060287 epithelial cilium movement involved in determination of left/right asymmetry",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LV49-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LWI8-1",
        "uniprot_id": "A0ABK0LWI8_RAT",
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        "length": 193,
        "protein_name": "Membrane integral NOTCH2 associated receptor 2",
        "gene_name": "Minar2",
        "organism": "Rat",
        "refseq_name": "major intrinsically disordered NOTCH2-binding receptor 1-like",
        "refseq_ac": "NP_001099614",
        "gene_names_uniprotkb": "Minar2; RGD1312005",
        "gene_names_refseq": "Minar2; RGD1312005",
        "protein_names_uniprotkb": "Membrane integral NOTCH2 associated receptor 2",
        "protein_names_refseq": "UPF0258 protein KIAA1024-like homolog; major intrinsically disordered NOTCH2-binding receptor 1-like",
        "tax_id": 10116,
        "disease": "autosomal recessive nonsyndromic deafness (Disease Ontology:DOID:0050565); Parkinson's disease (Disease Ontology:DOID:14330)",
        "pathway": " (rno:291580)",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0015485 cholesterol binding",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005765 lysosomal membrane;GO:0032420 stereocilium;GO:0012505 endomembrane system",
        "go_biological_process": "GO:0042491 inner ear auditory receptor cell differentiation;GO:0001525 angiogenesis;GO:0007626 locomotory behavior;GO:0051402 neuron apoptotic process;GO:0006915 apoptotic process",
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        "hit_score": 0.1,
        "record_id": "A0ABK0LWI8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LVH9-1",
        "uniprot_id": "A0ABK0LVH9_RAT",
        "mass": 52489.0,
        "length": 461,
        "protein_name": "Cytokine-dependent hematopoietic cell linker",
        "gene_name": "Clnk",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Clnk",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Cytokine-dependent hematopoietic cell linker",
        "protein_names_refseq": "",
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        "secondary_ac_list": "",
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        "go_molecular_function": "GO:0030674 protein-macromolecule adaptor activity;GO:0044877 protein-containing complex binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0042629 mast cell granule;GO:0032991 protein-containing complex",
        "go_biological_process": "GO:0007169 cell surface receptor protein tyrosine kinase signaling pathway;GO:0035556 intracellular signal transduction;GO:0043303 mast cell degranulation;GO:0002729 positive regulation of natural killer cell cytokine production;GO:0032815 negative regulation of natural killer cell activation",
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        "hit_score": 0.1,
        "record_id": "A0ABK0LVH9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LX88-1",
        "uniprot_id": "A0ABK0LX88_RAT",
        "mass": 36447.0,
        "length": 331,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or6s1",
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        "refseq_name": "olfactory receptor Olr1637",
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        "protein_names_uniprotkb": "Uridylate-specific endoribonuclease; 4.6.1.-",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm",
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    },
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        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Efna3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ephrin-A3; EHK1 ligand; EPH-related receptor tyrosine kinase ligand 3",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "function": "Cell surface GPI-bound ligand for Eph receptors, a family of receptor tyrosine kinases which are crucial for migration, repulsion and adhesion during neuronal, vascular and epithelial development. Binds promiscuously Eph receptors 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., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "disease": "oral squamous cell carcinoma (Disease Ontology:DOID:0050866); myelodysplastic syndrome (Disease Ontology:DOID:0050908); colon adenoma (Disease Ontology:DOID:0050912); chronic myelomonocytic leukemia (Disease Ontology:DOID:0080188); stomach cancer (Disease Ontology:DOID:10534); breast cancer (Disease Ontology:DOID:1612); myeloproliferative neoplasm (Disease Ontology:DOID:2226); colon adenocarcinoma (Disease Ontology:DOID:234); esophagus squamous cell carcinoma (Disease Ontology:DOID:3748); lung non-small cell carcinoma (Disease Ontology:DOID:3908); primary immunodeficiency disease (Disease Ontology:DOID:612); hepatocellular carcinoma (Disease Ontology:DOID:684); acute myeloid leukemia (Disease Ontology:DOID:9119); colorectal cancer (Disease Ontology:DOID:9256); nasopharynx carcinoma (Disease Ontology:DOID:9261)",
        "pathway": " (rno:310859)",
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        "function": "Dioxygenase that catalyzes the conversion of the modified genomic base 5-methylcytosine (5mC) into 5-hydroxymethylcytosine (5hmC) and plays a key role in epigenetic chromatin reprogramming during embryonic development., [UniProtKB, UniProtKB, UniProtKB]",
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        "uniprot_canonical_ac": "A0ABK0LX72-1",
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        "protein_name": "Collagen type IV alpha 3 chain",
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        "gene_names_refseq": "Col4a3",
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        "protein_names_refseq": "collagen alpha-3(IV) chain precursor; collagen alpha-3(IV) chain-like; collagen alpha-3(IV) chain; collagen, type IV, alpha 3 (Goodpasture antigen); procollagen, type IV, alpha 3",
        "tax_id": 10116,
        "disease": "Alport syndrome 3A (Disease Ontology:DOID:0110032); Alport syndrome 2 (Disease Ontology:DOID:0110033); benign familial hematuria (Disease Ontology:DOID:0111365); Alport syndrome (Disease Ontology:DOID:10983); glomerulonephritis (Disease Ontology:DOID:2921); end stage renal disease (Disease Ontology:DOID:783)",
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        "function": "COL4A mutations comprise a frequent cause of Familial microscopic hematuria., [RefSeq, PubMed]; Data show that collagen type III (Col3), collagen type IV (Col4) and p38 mitogen-activated protein kinase (p38 MAPK) are up-regulated in models of diabetic nephropathy., [RefSeq, PubMed]; Glomerular collagen alpha3(IV) protein was higher and more intense in immunofluorescence staining according to diabetic durations., [RefSeq, PubMed]; These findings suggested that artesunate attenuates alveolitis and pulmonary fibrosis by regulating expression of collagen-IV, TIMP-1 and 2, as well as MMP-2 and -9, to reduce ECM accumulation. Publication Status: Online-Only, [RefSeq, PubMed]; Type IV collagen is the major structural component of glomerular basement membranes (GBM), forming a 'chicken-wire' meshwork together with laminins, proteoglycans and entactin/nidogen., [UniProtKB, UniProtKB, UniProtKB]",
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        "protein_names_uniprotkb": "Cilia and flagella associated protein 47",
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        "disease": "X-linked spermatogenic failure 3 (Disease Ontology:DOID:0112274); male infertility (Disease Ontology:DOID:12336)",
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        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005929 cilium;GO:0120212 sperm head-tail coupling apparatus",
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        "record_id": "A0ABK0LW19-1",
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        "gene_names_uniprotkb": "Stap1",
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        "protein_names_uniprotkb": "Signal transducing adaptor family member 1",
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        "refseq_ac": "XP_038951863",
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        "gene_names_refseq": "Plxdc2",
        "protein_names_uniprotkb": "Plexin domain containing 2",
        "protein_names_refseq": "plexin domain-containing protein 2 isoform X1",
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        "protein_names_uniprotkb": "Beta-1,4 N-acetylgalactosaminyltransferase",
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        "gene_names_uniprotkb": "Cyb561",
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        "protein_names_uniprotkb": "Transmembrane ascorbate-dependent reductase CYB561; 7.2.1.3; Cytochrome b-561; Cytochrome b561",
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        "protein_names_uniprotkb": "Tumor protein D54",
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        "gene_names_refseq": "Olr1316; Or8g52",
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        "length": 302,
        "protein_name": "Vomeronasal type-1 receptor",
        "gene_name": "Vom1r69",
        "organism": "Rat",
        "refseq_name": "vomeronasal 1 receptor 69",
        "refseq_ac": "NP_001009531",
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        "gene_names_refseq": "V1rc40; Vom1r69",
        "protein_names_uniprotkb": "Vomeronasal type-1 receptor",
        "protein_names_refseq": "putative vomeronasal receptor-like protein 4; vomernasal 1 receptor Vom1r69; vomeronasal 1 receptor 69; vomeronasal 1 receptor, C40; vomeronasal V1r-type receptor V1rc40",
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        "function": "Putative pheromone receptor implicated in the regulation of social as well as reproductive behavior., [UniProtKB, UniProtKB]",
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        "refseq_name": "guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2",
        "refseq_ac": "NP_001244278",
        "gene_names_uniprotkb": "Gng2",
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        "protein_names_uniprotkb": "Guanine nucleotide-binding protein subunit gamma",
        "protein_names_refseq": "guanine nucleotide binding protein (G protein), gamma 2 subunit; guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2",
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        "function": "Data show that the C-terminus of SNAP-25 is a binding target for Gbetagamma necessary for both transient transmitter-mediated presynaptic inhibition, and the induction of presynaptic LTD., [RefSeq, PubMed]; Guanine nucleotide-binding proteins (G proteins) are involved as a modulator or transducer in various transmembrane signaling systems. The beta and gamma chains are required for the GTPase activity, for replacement of GDP by GTP, and for G protein-effector interaction., [UniProtKB, UniProtKB]; We used matrix-assisted laser desorption ionization-imaging mass spectrometry to reveal a novel protein marker, G-protein gamma2 subunit (Gng2), which is enriched in the claustrum but not adjacent structures of the rat forebrain., [RefSeq, PubMed]",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0031681 G-protein beta-subunit binding",
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        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "A0ABK0LUX3-1",
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        "length": 217,
        "protein_name": "Claudin",
        "gene_name": "Cldn9",
        "organism": "Rat",
        "refseq_name": "claudin-9",
        "refseq_ac": "NP_001011889",
        "gene_names_uniprotkb": "Cldn9",
        "gene_names_refseq": "Cldn9",
        "protein_names_uniprotkb": "Claudin",
        "protein_names_refseq": "claudin-9",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
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        "record_type": "protein"
    },
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        "protein_name": "H/ACA ribonucleoprotein complex subunit 3",
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        "refseq_name": "H/ACA ribonucleoprotein complex subunit 3-like",
        "refseq_ac": "XP_038947335",
        "gene_names_uniprotkb": "Nop10l2",
        "gene_names_refseq": "Nop10l2",
        "protein_names_uniprotkb": "H/ACA ribonucleoprotein complex subunit 3; Nucleolar protein 10; Nucleolar protein family A member 3; snoRNP protein NOP10",
        "protein_names_refseq": "H/ACA ribonucleoprotein complex subunit 3-like",
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        "function": "Required for ribosome biogenesis and telomere maintenance. Part of the H/ACA small nucleolar ribonucleoprotein (H/ACA snoRNP) complex, which catalyzes pseudouridylation of rRNA. This involves the isomerization of uridine such that the ribose is subsequently attached to C5, instead of the normal N1. Each rRNA can contain up to 100 pseudouridine ('psi') residues, which may serve to stabilize the conformation of rRNAs. May also be required for correct processing or intranuclear trafficking of TERC, the RNA component of the telomerase reverse transcriptase (TERT) holoenzyme., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0030515 snoRNA binding",
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        "length": 263,
        "protein_name": "Y-linked testis-specific protein 1-like",
        "gene_name": "LOC103694730",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "LOC103694730",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Y-linked testis-specific protein 1-like",
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    },
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        "protein_name": "Large ribosomal subunit protein eL33",
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        "organism": "Rat",
        "refseq_name": "",
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        "gene_names_uniprotkb": "",
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        "protein_names_uniprotkb": "Large ribosomal subunit protein eL33; 60S ribosomal protein L35a",
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        "function": "Component of the large ribosomal subunit. The ribosome is a large ribonucleoprotein complex responsible for the synthesis of proteins in the cell. Required for the proliferation and viability of hematopoietic cells., [UniProtKB, UniProtKB]",
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        "length": 126,
        "protein_name": "Histone H2B",
        "gene_name": "H2bc27",
        "organism": "Rat",
        "refseq_name": "H2B clustered histone 27",
        "refseq_ac": "NP_001103111",
        "gene_names_uniprotkb": "H2bc27; H2bu1",
        "gene_names_refseq": "H2bc27; H2bu1; Hist3h2bb",
        "protein_names_uniprotkb": "Histone H2B",
        "protein_names_refseq": "H2B clustered histone 27; H2B.U histone 1; histone 3, H2bb; histone cluster 3 H2B family member b; histone cluster 3, H2bb",
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        "length": 185,
        "protein_name": "Uncharacterized protein",
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        "refseq_name": "keratin-associated protein 9-1-like",
        "refseq_ac": "XP_063126083",
        "gene_names_uniprotkb": "Krtap9-1-ps1",
        "gene_names_refseq": "Krtap9-1-ps1",
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        "protein_names_refseq": "keratin-associated protein 9-1-like",
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        "length": 1191,
        "protein_name": "DENN domain containing 2A",
        "gene_name": "Dennd2a",
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        "gene_names_uniprotkb": "Dennd2a",
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        "protein_names_uniprotkb": "DENN domain containing 2A",
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        "protein_name": "Ubiquitin conjugating enzyme E2 V1",
        "gene_name": "Ube2v1l1; Ube2v1",
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        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ube2v1l1; Ube2v1; LOC679539; Ube2v1-ps22; Ube2v1l1; Ube2v1",
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        "protein_names_uniprotkb": "Ubiquitin conjugating enzyme E2 V1",
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        "biomarker_type": "",
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        "disease_count": 6,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0015179 L-amino acid transmembrane transporter activity;GO:0022857 transmembrane transporter activity;GO:0015327 cystine:glutamate antiporter activity;GO:0015252 proton channel activity;GO:0022840 leak channel activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0009986 cell surface;GO:0016020 membrane;GO:0045177 apical part of cell;GO:0097449 astrocyte projection",
        "go_biological_process": "GO:0015804 neutral amino acid transport;GO:0003333 amino acid transmembrane transport;GO:1904717 regulation of AMPA glutamate receptor clustering;GO:0051223 regulation of protein transport;GO:0006979 response to oxidative stress",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LY51-1",
        "uniprot_id": "A0ABK0LY51_RAT",
        "mass": 67390.0,
        "length": 596,
        "protein_name": "Zinc finger protein 8",
        "gene_name": "LOC108348304; Znf8",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "LOC108348304; Znf8; Znf8",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger protein 8",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:120099766)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Transcriptional repressor. May modulate BMP and TGF-beta signal transduction, through its interaction with SMAD proteins., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_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_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0006355 regulation of DNA-templated transcription;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription",
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        "record_type": "protein"
    },
    {
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        "length": 124,
        "protein_name": "Transcription initiation factor TFIID subunit 13",
        "gene_name": "Taf13",
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        "refseq_name": "transcription initiation factor TFIID subunit 13",
        "refseq_ac": "NP_001290545",
        "gene_names_uniprotkb": "Taf13",
        "gene_names_refseq": "Taf13",
        "protein_names_uniprotkb": "Transcription initiation factor TFIID subunit 13; Transcription initiation factor TFIID 18 kDa subunit",
        "protein_names_refseq": "TAF13 RNA polymerase II, TATA box binding protein (TBP)-associated factor; transcription initiation factor TFIID subunit 13",
        "tax_id": 10116,
        "disease": "autosomal recessive intellectual developmental disorder 60 (Disease Ontology:DOID:0081222)",
        "pathway": " (rno:310784);  (R-RNO-674695);  (R-RNO-6804756);  (R-RNO-6807505);  (R-RNO-73776);  (R-RNO-73779);  (R-RNO-75953);  (R-RNO-76042)",
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        "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 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. TAF13, together with TAF11 and TBP, play key roles during promoter binding by the TFIID and TFIIA transcription factor complexes., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0046982 protein heterodimerization activity;GO:0017025 TBP-class protein binding",
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        "record_type": "protein"
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        "protein_name": "protein-tyrosine-phosphatase",
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        "organism": "Rat",
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        "gene_names_uniprotkb": "Ptpn22",
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        "protein_names_uniprotkb": "protein-tyrosine-phosphatase; 3.1.3.48",
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        "disease": "Graves ophthalmopathy (Disease Ontology:DOID:0081120); graft-versus-host disease (Disease Ontology:DOID:0081267); chronic lymphocytic leukemia (Disease Ontology:DOID:1040); vitiligo (Disease Ontology:DOID:12306); Graves' disease (Disease Ontology:DOID:12361); Sjogren's syndrome (Disease Ontology:DOID:12894); Behcet's disease (Disease Ontology:DOID:13241); temporal arteritis (Disease Ontology:DOID:13375); Addison's disease (Disease Ontology:DOID:13774); hypothyroidism (Disease Ontology:DOID:1459); urticaria (Disease Ontology:DOID:1555); endometriosis (Disease Ontology:DOID:289); pulmonary tuberculosis (Disease Ontology:DOID:2957); coronary artery disease (Disease Ontology:DOID:3393); systemic scleroderma (Disease Ontology:DOID:418); myasthenia gravis (Disease Ontology:DOID:437); systemic juvenile rheumatoid arthritis (Disease Ontology:DOID:676); rheumatoid arthritis (Disease Ontology:DOID:7148); autoimmune thyroiditis (Disease Ontology:DOID:7188); Crohn's disease (Disease Ontology:DOID:8778); psoriasis (Disease Ontology:DOID:8893); autoimmune thrombocytopenic purpura (Disease Ontology:DOID:8924); psoriatic arthritis (Disease Ontology:DOID:9008); systemic lupus erythematosus (Disease Ontology:DOID:9074); diabetes mellitus (Disease Ontology:DOID:9351); type 1 diabetes mellitus (Disease Ontology:DOID:9744); Meniere's disease (Disease Ontology:DOID:9849); alopecia areata (Disease Ontology:DOID:986)",
        "pathway": " (rno:295338);  (R-RNO-202427);  (R-RNO-202430)",
        "pathway_count": 3,
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        "protein_name": "Prostate and testis expressed 2",
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        "organism": "Rat",
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        "gene_names_uniprotkb": "Pate2",
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        "protein_names_uniprotkb": "Prostate and testis expressed 2",
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        "gene_names_uniprotkb": "Cwf19l2",
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        "protein_names_uniprotkb": "CWF19-like protein 2",
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        "record_type": "protein"
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        "protein_name": "Acyl-coenzyme A oxidase",
        "gene_name": "Acoxl",
        "organism": "Rat",
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        "gene_names_uniprotkb": "Acoxl",
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        "protein_names_uniprotkb": "Acyl-coenzyme A oxidase",
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        "pathway": " (rno:296138);  (R-RNO-389887)",
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        "go_cellular_component": "GO:0005777 peroxisome;GO:0005829 cytosol",
        "go_biological_process": "GO:0006635 fatty acid beta-oxidation;GO:0033540 fatty acid beta-oxidation using acyl-CoA oxidase",
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        "protein_name": "Inhibitor of carbonic anhydrase",
        "gene_name": "Inhca",
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        "gene_names_uniprotkb": "Inhca; RGD1310507",
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        "protein_names_uniprotkb": "Inhibitor of carbonic anhydrase",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0046872 metal ion binding;GO:0004857 enzyme inhibitor activity",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005576 extracellular region;GO:0005769 early endosome;GO:0005886 plasma membrane;GO:0055037 recycling endosome",
        "go_biological_process": "GO:0019731 antibacterial humoral response;GO:0006826 iron ion transport",
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    },
    {
        "uniprot_canonical_ac": "A0ABK0LYB6-1",
        "uniprot_id": "A0ABK0LYB6_RAT",
        "mass": 175266.0,
        "length": 1554,
        "protein_name": "Lysine-specific demethylase 5C",
        "gene_name": "Kdm5c",
        "organism": "Rat",
        "refseq_name": "lysine-specific demethylase 5C",
        "refseq_ac": "NP_001406701",
        "gene_names_uniprotkb": "Kdm5c",
        "gene_names_refseq": "Kdm5c; RGD1560601",
        "protein_names_uniprotkb": "Lysine-specific demethylase 5C; 1.14.11.67; Histone demethylase JARID1C; Jumonji/ARID domain-containing protein 1C; Protein SmcX; Protein Xe169; [histone H3]-trimethyl-L-lysine(4) demethylase 5C",
        "protein_names_refseq": "lysine (K)-specific demethylase 5C; lysine-specific demethylase 5C",
        "tax_id": 10116,
        "disease": "syndromic intellectual disability (Disease Ontology:DOID:0050888); autism spectrum disorder (Disease Ontology:DOID:0060041); syndromic X-linked intellectual disability Claes-Jensen type (Disease Ontology:DOID:0060809); stomach cancer (Disease Ontology:DOID:10534); intellectual disability (Disease Ontology:DOID:1059); descending colon cancer (Disease Ontology:DOID:12190); Huntington's disease (Disease Ontology:DOID:12858); alcohol use disorder (Disease Ontology:DOID:1574); breast cancer (Disease Ontology:DOID:1612); colon cancer (Disease Ontology:DOID:219); schizophrenia (Disease Ontology:DOID:5419); hepatocellular carcinoma (Disease Ontology:DOID:684); colorectal cancer (Disease Ontology:DOID:9256)",
        "pathway": " (rno:317432);  (R-RNO-3214842)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Histone demethylase that specifically demethylates 'Lys-4' of histone H3, thereby playing a central role in histone code. Does not demethylate histone H3 'Lys-9', H3 'Lys-27', H3 'Lys-36', H3 'Lys-79' or H4 'Lys-20'. Demethylates trimethylated and dimethylated but not monomethylated H3 'Lys-4'. Participates in transcriptional repression of neuronal genes by recruiting histone deacetylases and REST at neuron-restrictive silencer elements. Represses the CLOCK-BMAL1 heterodimer-mediated transcriptional activation of the core clock component PER2., [UniProtKB, UniProtKB, UniProtKB]",
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "1.14.11.67",
        "go_molecular_function": "GO:0034647 histone H3K4me/H3K4me2/H3K4me3 demethylase activity;GO:0003677 DNA binding;GO:0008270 zinc ion binding;GO:0032453 histone H3K4 demethylase activity;GO:0042802 identical protein binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0000785 chromatin;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006338 chromatin remodeling;GO:0006355 regulation of DNA-templated transcription;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0045892 negative regulation of DNA-templated transcription",
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        "record_id": "A0ABK0LYB6-1",
        "record_type": "protein"
    },
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        "length": 226,
        "protein_name": "Cleavage and polyadenylation specificity factor subunit 4",
        "gene_name": "Cpsf4l",
        "organism": "Rat",
        "refseq_name": "putative cleavage and polyadenylation specificity factor subunit 4-like protein isoform X2",
        "refseq_ac": "XP_063126239",
        "gene_names_uniprotkb": "Cpsf4l",
        "gene_names_refseq": "Cpsf4l",
        "protein_names_uniprotkb": "Cleavage and polyadenylation specificity factor subunit 4; CPSF 30 kDa subunit; Cleavage and polyadenylation specificity factor 30 kDa subunit",
        "protein_names_refseq": "putative cleavage and polyadenylation specificity factor subunit 4-like protein isoform X2",
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        "pathway_count": 0,
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        "function": "Component of the cleavage and polyadenylation specificity factor (CPSF) complex that play a key role in pre-mRNA 3'-end formation, recognizing the AAUAAA signal sequence and interacting with poly(A) polymerase and other factors to bring about cleavage and poly(A) addition. CPSF4 binds RNA polymers with a preference for poly(U)., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005847 mRNA cleavage and polyadenylation specificity factor complex",
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        "length": 459,
        "protein_name": "Transcription factor AP-2 beta",
        "gene_name": "Tfap2b",
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        "refseq_name": "transcription factor AP-2-beta isoform 1",
        "refseq_ac": "NP_001400699",
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        "gene_names_refseq": "Tcfap2b; Tfap2b",
        "protein_names_uniprotkb": "Transcription factor AP-2 beta",
        "protein_names_refseq": "transcription factor AP-2-beta isoform 1",
        "tax_id": 10116,
        "disease": "Char syndrome (Disease Ontology:DOID:0060563); angle-closure glaucoma (Disease Ontology:DOID:13550); patent ductus arteriosus (Disease Ontology:DOID:13832); sleep disorder (Disease Ontology:DOID:535)",
        "pathway": " (R-RNO-8866904);  (R-RNO-8866907);  (R-RNO-9834899)",
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        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0007399 nervous system development;GO:0042127 regulation of cell population proliferation;GO:0043066 negative regulation of apoptotic process;GO:0045944 positive regulation of transcription by RNA polymerase II",
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        "protein_names_uniprotkb": "CD164 molecule like 2",
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        "protein_name": "Centrosomal P4.1-associated protein",
        "gene_name": "Cpap",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Cpap",
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        "protein_names_uniprotkb": "Centrosomal P4.1-associated protein; Centromere protein J; Centrosome assembly and centriole elongation protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "Seckel syndrome (Disease Ontology:DOID:0050569); Seckel syndrome 4 (Disease Ontology:DOID:0070010); primary autosomal recessive microcephaly 6 (Disease Ontology:DOID:0070290); autosomal recessive primary microcephaly (Disease Ontology:DOID:0070296); microcephaly (Disease Ontology:DOID:10907)",
        "pathway": " (R-RNO-2565942);  (R-RNO-380259);  (R-RNO-380270);  (R-RNO-380284);  (R-RNO-380320);  (R-RNO-5620912);  (R-RNO-6804115);  (R-RNO-8854518)",
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        "protein_names_uniprotkb": "Transmembrane protein 130",
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        "protein_name": "Similar to human chromosome 10 open reading frame 143",
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        "gene_names_uniprotkb": "C1h10orf143; LOC100362342",
        "gene_names_refseq": "",
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        "protein_name": "ADP/ATP translocase",
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        "refseq_name": "solute carrier family 25 member 31",
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        "protein_names_uniprotkb": "ADP/ATP translocase; ADP,ATP carrier protein",
        "protein_names_refseq": "ADP/ATP translocase 4; adenine nucleotide translocator), member 31-like; adenine nucleotide translocator), member 31; solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 31-like; solute carrier family 25 (mitochondrial carrier; solute carrier family 25 member 31",
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        "disease": "mitochondrial DNA depletion syndrome 12b (Disease Ontology:DOID:0080335); autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 (Disease Ontology:DOID:0111517); hypertrophic cardiomyopathy (Disease Ontology:DOID:11984); mitochondrial metabolism disease (Disease Ontology:DOID:700)",
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        "protein_names_uniprotkb": "DEAH-box helicase 37",
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        "go_biological_process": "GO:0000462 maturation of SSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA);GO:2000020 positive regulation of male gonad development;GO:0007420 brain development;GO:0042254 ribosome biogenesis;GO:0042255 ribosome assembly",
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        "function": "Methionine-sulfoxide reductase that specifically reduces methionine (R)-sulfoxide back to methionine. While in many cases methionine oxidation is the result of random oxidation following oxidative stress, methionine oxidation is also a post-translational modification that takes place on specific residues., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "protein_names_uniprotkb": "Collagen type V alpha 2 chain",
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        "tax_id": 10116,
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        "function": "May influence APP processing, resulting in a decrease in sAPP-alpha production and increased amyloidogenic P3 peptide production. May regulate ITCH and NEDD4 E3 ligase activity and degradation., [UniProtKB, UniProtKB, UniProtKB]",
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    {
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        "protein_name": "Protein HIRA",
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        "organism": "Rat",
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        "gene_names_uniprotkb": "Hira",
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        "protein_names_uniprotkb": "Protein HIRA",
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        "protein_name": "Kelch-like family member 8",
        "gene_name": "Klhl8",
        "organism": "Rat",
        "refseq_name": "kelch-like protein 8",
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        "protein_names_uniprotkb": "Pentraxin-related protein PTX3; Pentaxin-related protein PTX3; Tumor necrosis factor-inducible gene 14 protein",
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        "tax_id": 10116,
        "disease": "invasive aspergillosis (Disease Ontology:DOID:0050073); pulmonary aspergilloma (Disease Ontology:DOID:0050153); obstructive sleep apnea (Disease Ontology:DOID:0050848); pelvic inflammatory disease (Disease Ontology:DOID:1003); toxic shock syndrome (Disease Ontology:DOID:14115); cystic fibrosis (Disease Ontology:DOID:1485); hepatitis C (Disease Ontology:DOID:1883)",
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        "function": "Plays a role in the regulation of innate resistance to pathogens, inflammatory reactions, possibly clearance of self-components and female fertility., [UniProtKB, UniProtKB, UniProtKB]",
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    {
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        "protein_name": "Receptor protein-tyrosine kinase",
        "gene_name": "Egfr",
        "organism": "Rat",
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        "gene_names_uniprotkb": "Egfr",
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        "protein_names_uniprotkb": "Receptor protein-tyrosine kinase; 2.7.10.1",
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        "tax_id": 10116,
        "disease": "cardiomyopathy (Disease Ontology:DOID:0050700); nicotine dependence (Disease Ontology:DOID:0050742); oral squamous cell carcinoma (Disease Ontology:DOID:0050866); neonatal nephrocutaneous inflammatory syndrome (Disease Ontology:DOID:0061191); Coronavirus infectious disease (Disease Ontology:DOID:0080599); Parkinsonism (Disease Ontology:DOID:0080855); intestinal cancer (Disease Ontology:DOID:10155); prostate cancer (Disease Ontology:DOID:10283); hypertension (Disease Ontology:DOID:10763); urinary bladder cancer (Disease Ontology:DOID:11054); Human papillomavirus infectious disease (Disease Ontology:DOID:11166); dilated cardiomyopathy (Disease Ontology:DOID:12930); dementia (Disease Ontology:DOID:1307); lung cancer (Disease Ontology:DOID:1324); peptic esophagitis (Disease Ontology:DOID:13976); Parkinson's disease (Disease Ontology:DOID:14330); alcohol use disorder (Disease Ontology:DOID:1574); breast cancer (Disease Ontology:DOID:1612); cancer (Disease Ontology:DOID:162); pancreatic cancer (Disease Ontology:DOID:1793); transitional cell carcinoma (Disease Ontology:DOID:2671); asthma (Disease Ontology:DOID:2841); laryngeal squamous cell carcinoma (Disease Ontology:DOID:2876); pulmonary tuberculosis (Disease Ontology:DOID:2957); acute kidney failure (Disease Ontology:DOID:3021); carcinoma (Disease Ontology:DOID:305); high grade glioma (Disease Ontology:DOID:3070); chronic obstructive pulmonary disease (Disease Ontology:DOID:3083); breast carcinoma (Disease Ontology:DOID:3459); esophagus squamous cell carcinoma (Disease Ontology:DOID:3748); pulmonary fibrosis (Disease Ontology:DOID:3770); lung non-small cell carcinoma (Disease Ontology:DOID:3908); lung adenocarcinoma (Disease Ontology:DOID:3910); renal cell carcinoma (Disease Ontology:DOID:4450); bronchiolo-alveolar adenocarcinoma (Disease Ontology:DOID:4926); liver cirrhosis (Disease Ontology:DOID:5082); schizophrenia (Disease Ontology:DOID:5419); median neuropathy (Disease Ontology:DOID:571); aortic valve disease (Disease Ontology:DOID:62); pulmonary hypertension (Disease Ontology:DOID:6432); hepatocellular carcinoma (Disease Ontology:DOID:684); lung disease (Disease Ontology:DOID:850); diabetic retinopathy (Disease Ontology:DOID:8947); colorectal cancer (Disease Ontology:DOID:9256); diabetes mellitus (Disease Ontology:DOID:9351); type 1 diabetes mellitus (Disease Ontology:DOID:9744)",
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        "go_molecular_function": "GO:0005524 ATP binding;GO:0004714 transmembrane receptor protein tyrosine kinase activity;GO:0048408 epidermal growth factor binding;GO:0003682 chromatin binding;GO:0004713 protein tyrosine kinase activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0043235 receptor complex;GO:0009925 basal plasma membrane;GO:0016020 membrane;GO:0071944 cell periphery",
        "go_biological_process": "GO:0007611 learning or memory;GO:0043066 negative regulation of apoptotic process;GO:0043410 positive regulation of MAPK cascade;GO:0007173 epidermal growth factor receptor signaling pathway;GO:0030182 neuron differentiation",
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        "hit_score": 0.5,
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        "record_type": "protein"
    },
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        "uniprot_canonical_ac": "A0ABK0LYN5-1",
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        "length": 483,
        "protein_name": "Zinc finger protein 773",
        "gene_name": "Znf773",
        "organism": "Rat",
        "refseq_name": "",
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        "gene_names_uniprotkb": "Znf773; LOC102547412",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger protein 773",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (R-RNO-212436)",
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        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB, UniProtKB]",
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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:0003677 DNA binding",
        "go_cellular_component": "GO:0005634 nucleus",
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    },
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        "protein_name": "KH and NYN domain containing",
        "gene_name": "Khnyn",
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        "refseq_name": "protein KHNYN isoform X1",
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        "gene_names_refseq": "Khnyn-ps1; Khnyn; RGD1565688",
        "protein_names_uniprotkb": "KH and NYN domain containing",
        "protein_names_refseq": "protein KHNYN isoform X1",
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    },
    {
        "uniprot_canonical_ac": "A0ABK0LYP8-1",
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        "length": 1193,
        "protein_name": "Tyrosine-protein kinase",
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        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Tyk2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Tyrosine-protein kinase; 2.7.10.2",
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        "pathway": " (rno:100361294);  (R-RNO-1059683);  (R-RNO-110056);  (R-RNO-112411);  (R-RNO-6783783);  (R-RNO-6785807);  (R-RNO-6788467);  (R-RNO-8854691);  (R-RNO-8984722);  (R-RNO-9020591);  (R-RNO-9020933);  (R-RNO-9020956);  (R-RNO-909733);  (R-RNO-912694);  (R-RNO-9674555);  (R-RNO-9705462);  (R-RNO-9958825)",
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        "go_molecular_function": "GO:0004715 non-membrane spanning protein tyrosine kinase activity;GO:0005524 ATP binding;GO:0005131 growth hormone receptor binding;GO:0004713 protein tyrosine kinase activity;GO:0031702 type 1 angiotensin receptor binding",
        "go_cellular_component": "GO:0005829 cytosol;GO:0005856 cytoskeleton;GO:0016020 membrane;GO:0005634 nucleus;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0030154 cell differentiation;GO:0035556 intracellular signal transduction;GO:0022407 regulation of cell-cell adhesion;GO:0019221 cytokine-mediated signaling pathway;GO:0060397 growth hormone receptor signaling pathway via JAK-STAT",
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        "record_type": "protein"
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    {
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        "length": 290,
        "protein_name": "Solute carrier family 25 member 14",
        "gene_name": "Slc25a14",
        "organism": "Rat",
        "refseq_name": "brain mitochondrial carrier protein 1 isoform X3",
        "refseq_ac": "XP_006257597",
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        "gene_names_refseq": "Bmcp1; Slc25a14",
        "protein_names_uniprotkb": "Solute carrier family 25 member 14",
        "protein_names_refseq": "brain mitochondrial carrier protein 1 isoform X3",
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        "go_molecular_function": "GO:0042803 protein homodimerization activity;GO:0015078 proton transmembrane transporter activity;GO:0005452 solute:inorganic anion antiporter activity;GO:0015108 chloride transmembrane transporter activity",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005740 mitochondrial envelope;GO:0005743 mitochondrial inner membrane",
        "go_biological_process": "GO:1900407 regulation of cellular response to oxidative stress;GO:0015698 inorganic anion transport;GO:0055085 transmembrane transport",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0M030-1",
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        "length": 620,
        "protein_name": "Meiosis initiator",
        "gene_name": "Meiosin",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Meiosin",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Meiosis initiator",
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0046983 protein dimerization activity",
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        "go_biological_process": "GO:0006357 regulation of transcription by RNA polymerase II;GO:0007283 spermatogenesis;GO:0071300 cellular response to retinoic acid;GO:0048477 oogenesis;GO:0051321 meiotic cell cycle",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LYY3-1",
        "uniprot_id": "A0ABK0LYY3_RAT",
        "mass": 549953.0,
        "length": 4999,
        "protein_name": "Histone-lysine N-methyltransferase 2C",
        "gene_name": "Kmt2c",
        "organism": "Rat",
        "refseq_name": "histone-lysine N-methyltransferase 2C isoform X7",
        "refseq_ac": "XP_038964897",
        "gene_names_uniprotkb": "Kmt2c",
        "gene_names_refseq": "Kmt2c",
        "protein_names_uniprotkb": "Histone-lysine N-methyltransferase 2C; 2.1.1.364",
        "protein_names_refseq": "histone-lysine N-methyltransferase 2C isoform X7",
        "tax_id": 10116,
        "disease": "adenoid cystic carcinoma (Disease Ontology:DOID:0080202); Kleefstra syndrome 2 (Disease Ontology:DOID:0080598); prostate cancer (Disease Ontology:DOID:10283); stomach cancer (Disease Ontology:DOID:10534); congenital heart disease (Disease Ontology:DOID:1682); squamous cell carcinoma (Disease Ontology:DOID:1749); laryngeal carcinoma (Disease Ontology:DOID:2600); esophagus squamous cell carcinoma (Disease Ontology:DOID:3748); lung non-small cell carcinoma (Disease Ontology:DOID:3908); lung adenocarcinoma (Disease Ontology:DOID:3910); Klatskin's tumor (Disease Ontology:DOID:4927); primary ovarian insufficiency (Disease Ontology:DOID:5426); stomach carcinoma (Disease Ontology:DOID:5517); rheumatoid arthritis (Disease Ontology:DOID:7148); nasopharynx carcinoma (Disease Ontology:DOID:9261)",
        "pathway": " (R-RNO-3214841);  (R-RNO-8936459);  (R-RNO-9772755);  (R-RNO-9909649)",
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        "function": "Histone methyltransferase that catalyzes methyl group transfer from S-adenosyl-L-methionine to the epsilon-amino group of 'Lys-4' of histone H3 (H3K4). Part of chromatin remodeling machinery predominantly forms H3K4me1 methylation marks at active chromatin sites where transcription and DNA repair take place. Likely plays a redundant role with KMT2D in enriching H3K4me1 mark on primed and active enhancer elements., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "2.1.1.364;2.1.1.370;2.1.1.371;2.3.1.48;2.1.1.-;2.1.1.85;2.1.1.359;2.1.1.355;2.1.1.354;2.1.1.362;2.1.1.361;2.1.1.319",
        "go_molecular_function": "GO:0003713 transcription coactivator activity;GO:0008270 zinc ion binding;GO:0140945 histone H3K4 monomethyltransferase activity;GO:0042054 histone methyltransferase activity;GO:0042800 histone H3K4 methyltransferase activity",
        "go_cellular_component": "GO:0044666 MLL3/4 complex;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0035097 histone methyltransferase complex",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0032259 methylation;GO:0006355 regulation of DNA-templated transcription;GO:0007338 single fertilization",
        "synthesized_glycan_count": 0,
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    {
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        "protein_name": "GPRIN family member 3",
        "gene_name": "Gprin3",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Gprin3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "GPRIN family member 3",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:502784)",
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        "publication_id_list": "22673903",
        "class_list": "",
        "function": "May be involved in neurite outgrowth., [UniProtKB, UniProtKB, UniProtKB]",
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        "protein_names_uniprotkb": "Large ribosomal subunit protein uL23; 60S ribosomal protein L23a",
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        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:299190)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "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. Binds a specific region on the 26S rRNA. May promote p53/TP53 degradation possibly through the stimulation of MDM2-mediated TP53 polyubiquitination., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "missing_score": 10000,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003735 structural constituent of ribosome",
        "go_cellular_component": "GO:0044391 ribosomal subunit;GO:0022626 cytosolic ribosome",
        "go_biological_process": "GO:0006412 translation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LXH7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LYZ4-1",
        "uniprot_id": "A0ABK0LYZ4_RAT",
        "mass": 26563.0,
        "length": 240,
        "protein_name": "Glial cell line-derived neurotrophic factor",
        "gene_name": "Gdnf",
        "organism": "Rat",
        "refseq_name": "glial cell line-derived neurotrophic factor isoform 1 precursor",
        "refseq_ac": "NP_062012",
        "gene_names_uniprotkb": "Gdnf",
        "gene_names_refseq": "Gdnf; gndf",
        "protein_names_uniprotkb": "Glial cell line-derived neurotrophic factor",
        "protein_names_refseq": "ATF; Glial cell line derived neutrophic factor; astrocyte-derived trophic factor; glial cell line-derived neurotrophic factor isoform 1 precursor; glial cell line-derived neurotrophic factor",
        "tax_id": 10116,
        "disease": "alcohol dependence (Disease Ontology:DOID:0050741); nicotine dependence (Disease Ontology:DOID:0050742); Kennedy's disease (Disease Ontology:DOID:0060161); alcohol-associated liver disease (Disease Ontology:DOID:0070658); Parkinsonism (Disease Ontology:DOID:0080855); Hirschsprung's disease (Disease Ontology:DOID:10487); Alzheimer's disease (Disease Ontology:DOID:10652); obsessive-compulsive disorder (Disease Ontology:DOID:10933); sciatic neuropathy (Disease Ontology:DOID:11446); acoustic neuroma (Disease Ontology:DOID:12689); hyperprolactinemia (Disease Ontology:DOID:12700); Guillain-Barre syndrome (Disease Ontology:DOID:12842); Sjogren's syndrome (Disease Ontology:DOID:12894); Parkinson's disease (Disease Ontology:DOID:14330); alcohol use disorder (Disease Ontology:DOID:1574); depressive disorder (Disease Ontology:DOID:1596); pancreatic cancer (Disease Ontology:DOID:1793); epilepsy (Disease Ontology:DOID:1826); anxiety disorder (Disease Ontology:DOID:2030); glomerulonephritis (Disease Ontology:DOID:2921); Churg-Strauss syndrome (Disease Ontology:DOID:3049); amyotrophic lateral sclerosis (Disease Ontology:DOID:332); temporal lobe epilepsy (Disease Ontology:DOID:3328); middle cerebral artery infarction (Disease Ontology:DOID:3525); neuromuscular disease (Disease Ontology:DOID:440); amphetamine abuse (Disease Ontology:DOID:670); irritable bowel syndrome (Disease Ontology:DOID:9778); polyarteritis nodosa (Disease Ontology:DOID:9810); heroin dependence (Disease Ontology:DOID:9976)",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 2,
        "publication_id_list": "37178997;38219812",
        "class_list": "",
        "function": "Differential expression of RET and GDNF family receptor, GFR-alpha1, between striatum and substantia nigra following nigrostriatal lesion: A case for diminished GDNF-signaling., [RefSeq, PubMed]; Neurotrophic factor that enhances survival and morphological differentiation of dopaminergic neurons and increases their high-affinity dopamine uptake., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; The effects of induced type I diabetes on developmental regulation of GDNF, NRTN, and NCAM proteins in the dentate gyrus of male rat offspring., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 29,
        "glyco_site_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0030971 receptor tyrosine kinase binding;GO:0008083 growth factor activity;GO:0030116 glial cell-derived neurotrophic factor receptor binding;GO:0042803 protein homodimerization activity",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0005615 extracellular space;GO:0005794 Golgi apparatus;GO:0043235 receptor complex",
        "go_biological_process": "GO:0048731 system development;GO:0001759 organ induction;GO:0030432 peristalsis;GO:0051584 regulation of dopamine uptake involved in synaptic transmission;GO:0048484 enteric nervous system development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "A0ABK0LYZ4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LYM1-1",
        "uniprot_id": "A0ABK0LYM1_RAT",
        "mass": 22260.0,
        "length": 197,
        "protein_name": "Murine leukemia virus integrase C-terminal domain-containing protein",
        "gene_name": "",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Murine leukemia virus integrase C-terminal domain-containing protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
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        "pathway_count": 0,
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        "publication_id_list": "",
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        "function": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0016787 hydrolase activity;GO:0004519 endonuclease activity;GO:0016779 nucleotidyltransferase activity",
        "go_cellular_component": "",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LYM1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LY74-1",
        "uniprot_id": "A0ABK0LY74_RAT",
        "mass": 29329.0,
        "length": 269,
        "protein_name": "Regulating synaptic membrane exocytosis 4",
        "gene_name": "Rims4",
        "organism": "Rat",
        "refseq_name": "regulating synaptic membrane exocytosis protein 4",
        "refseq_ac": "NP_733766",
        "gene_names_uniprotkb": "Rims4",
        "gene_names_refseq": "RIM 4; Rim4gamma; Rims4",
        "protein_names_uniprotkb": "Regulating synaptic membrane exocytosis 4",
        "protein_names_refseq": "rab3-interacting molecule 4; regulating synaptic membrane exocytosis protein 4; synaptic regulatory protein RIM4gamma",
        "tax_id": 10116,
        "disease": "autism spectrum disorder (Disease Ontology:DOID:0060041); schizophrenia (Disease Ontology:DOID:5419)",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 1,
        "publication_id_list": "23303958",
        "class_list": "",
        "function": "Gamma-RIMs are involved in cell biological functions distinct from the regulation of synaptic vesicle exocytosis and play a role in the molecular mechanisms controlling the establishment of dendritic complexity and axonal outgrowth, [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "total_reported_n_glycosites": 0,
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        "missing_score": 10000,
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        "go_molecular_function": "GO:0031267 small GTPase binding;GO:0044325 transmembrane transporter binding",
        "go_cellular_component": "GO:0016020 membrane;GO:0045202 synapse;GO:0098978 glutamatergic synapse;GO:0097060 synaptic membrane;GO:0098793 presynapse",
        "go_biological_process": "GO:0006887 exocytosis;GO:0006836 neurotransmitter transport;GO:0042391 regulation of membrane potential;GO:0007269 neurotransmitter secretion;GO:0050807 regulation of synapse organization",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0LY74-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LZD4-1",
        "uniprot_id": "A0ABK0LZD4_RAT",
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        "length": 417,
        "protein_name": "Carbohydrate sulfotransferase",
        "gene_name": "Chst8",
        "organism": "Rat",
        "refseq_name": "carbohydrate sulfotransferase 8",
        "refseq_ac": "NP_001100974",
        "gene_names_uniprotkb": "Chst8",
        "gene_names_refseq": "Chst8",
        "protein_names_uniprotkb": "Carbohydrate sulfotransferase; 2.8.2.-",
        "protein_names_refseq": "carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 8; carbohydrate sulfotransferase 8",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:308511)",
        "pathway_count": 1,
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        "class_list": "glycan-modifying enzyme;glycogene",
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        "go_molecular_function": "GO:0008146 sulfotransferase activity;GO:0001537 dermatan 4-sulfotransferase activity",
        "go_cellular_component": "GO:0000139 Golgi membrane",
        "go_biological_process": "GO:0016051 carbohydrate biosynthetic process;GO:0042446 hormone biosynthetic process;GO:0006790 sulfur compound metabolic process;GO:0030166 proteoglycan biosynthetic process",
        "synthesized_glycan_count": 139,
        "hit_score": 0.1,
        "record_id": "A0ABK0LZD4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LX97-1",
        "uniprot_id": "A0ABK0LX97_RAT",
        "mass": 15062.0,
        "length": 128,
        "protein_name": "Disks large homolog 5 N-terminal domain-containing protein",
        "gene_name": "LOC134483442",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "LOC134483442",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Disks large homolog 5 N-terminal domain-containing protein",
        "protein_names_refseq": "",
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    {
        "uniprot_canonical_ac": "A0ABK0LXA2-1",
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        "length": 162,
        "protein_name": "Murine leukemia virus integrase C-terminal domain-containing protein",
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        "organism": "Rat",
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        "protein_names_uniprotkb": "Murine leukemia virus integrase C-terminal domain-containing protein",
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        "go_molecular_function": "GO:0016787 hydrolase activity;GO:0004519 endonuclease activity;GO:0016779 nucleotidyltransferase activity",
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        "record_id": "A0ABK0LXA2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LXA5-1",
        "uniprot_id": "A0ABK0LXA5_RAT",
        "mass": 48845.0,
        "length": 412,
        "protein_name": "Uncharacterized protein",
        "gene_name": "Zfp950l6",
        "organism": "Rat",
        "refseq_name": "zinc finger protein 431-like",
        "refseq_ac": "XP_017453250",
        "gene_names_uniprotkb": "Zfp950l6",
        "gene_names_refseq": "Zfp950l6",
        "protein_names_uniprotkb": "Uncharacterized protein",
        "protein_names_refseq": "zinc finger protein 431-like",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:102551882)",
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        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB]",
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        "gene_names_refseq": "LOC103690904",
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        "protein_names_refseq": "high mobility group protein B4-like",
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        "disease": "stomach cancer (Disease Ontology:DOID:10534); pre-eclampsia (Disease Ontology:DOID:10591)",
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        "protein_names_refseq": "proline rich protein 2 precursor; salivary proline-rich protein",
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        "protein_name": "Ribonucleoside-diphosphate reductase subunit M2",
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        "refseq_name": "ribonucleoside-diphosphate reductase subunit M2-like",
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        "uniprot_id": "A0ABK0LYU5_RAT",
        "mass": 21162.0,
        "length": 184,
        "protein_name": "Large ribosomal subunit protein uL6",
        "gene_name": "Rpl9-ps31",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Rpl9-ps31",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Large ribosomal subunit protein uL6; 60S ribosomal protein L9",
        "protein_names_refseq": "",
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        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "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]",
        "predicted_glycosites": 0,
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        "biomarker_type": "",
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        "go_molecular_function": "GO:0019843 rRNA binding;GO:0003735 structural constituent of ribosome",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005840 ribosome;GO:1990904 ribonucleoprotein complex",
        "go_biological_process": "GO:0006412 translation",
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        "hit_score": 0.1,
        "record_id": "A0ABK0LYU5-1",
        "record_type": "protein"
    },
    {
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        "mass": 57969.0,
        "length": 514,
        "protein_name": "non-specific serine/threonine protein kinase",
        "gene_name": "LOC134482835",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "LOC134482835; LOC134484874",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "non-specific serine/threonine protein kinase; 2.7.11.1",
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        "class_list": "",
        "function": "May play a role in sperm motility, especially in the regulation of flagellar function., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "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:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding",
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    },
    {
        "uniprot_canonical_ac": "A0ABK0LYV7-1",
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        "length": 108,
        "protein_name": "Small ubiquitin-related modifier",
        "gene_name": "LOC120095693",
        "organism": "Rat",
        "refseq_name": "small ubiquitin-related modifier 2-like",
        "refseq_ac": "XP_038944880",
        "gene_names_uniprotkb": "LOC120095693",
        "gene_names_refseq": "LOC120095693",
        "protein_names_uniprotkb": "Small ubiquitin-related modifier; SUMO",
        "protein_names_refseq": "small ubiquitin-related modifier 2-like",
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        "disease": "type 1 diabetes mellitus 5 (Disease Ontology:DOID:0110744)",
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        "function": "Ubiquitin-like protein which can be covalently attached to target lysines either as a monomer or as a lysine-linked polymer. Does not seem to be involved in protein degradation and may function as an antagonist of ubiquitin in the degradation process. Plays a role in a number of cellular processes such as nuclear transport, DNA replication and repair, mitosis and signal transduction. Covalent attachment to its substrates requires prior activation by the E1 complex SAE1-SAE2 and linkage to the E2 enzyme UBE2I, and can be promoted by an E3 ligase such as PIAS1-4, RANBP2 or CBX4. Plays a role in the regulation of sumoylation status of SETX., [UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0016604 nuclear body;GO:0016605 PML body;GO:0106068 SUMO ligase complex",
        "go_biological_process": "GO:0016925 protein sumoylation;GO:0045892 negative regulation of DNA-templated transcription;GO:0034599 cellular response to oxidative stress;GO:0043122 regulation of canonical NF-kappaB signal transduction;GO:1900180 regulation of protein localization to nucleus",
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        "record_type": "protein"
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    {
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        "length": 310,
        "protein_name": "Olfactory receptor",
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        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr1248",
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        "gene_names_uniprotkb": "Or8b46",
        "gene_names_refseq": "Olr1248; Or8b46",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 1248; olfactory receptor Olr1248; olfactory receptor gene Olr1248",
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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",
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        "record_type": "protein"
    },
    {
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        "mass": 15179.0,
        "length": 128,
        "protein_name": "Disks large homolog 5 N-terminal domain-containing protein",
        "gene_name": "",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Disks large homolog 5 N-terminal domain-containing protein",
        "protein_names_refseq": "",
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        "record_id": "A0ABK0LYW3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LYW6-1",
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        "length": 121,
        "protein_name": "Ig-like domain-containing protein",
        "gene_name": "",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ig-like domain-containing protein",
        "protein_names_refseq": "",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0019814 immunoglobulin complex",
        "go_biological_process": "GO:0002250 adaptive immune response",
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        "hit_score": 0.1,
        "record_id": "A0ABK0LYW6-1",
        "record_type": "protein"
    },
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        "length": 64,
        "protein_name": "Coiled-coil domain-containing protein 72",
        "gene_name": "Tma7b",
        "organism": "Rat",
        "refseq_name": "translation machinery-associated protein 7-like",
        "refseq_ac": "XP_038964599",
        "gene_names_uniprotkb": "Tma7b",
        "gene_names_refseq": "Tma7b",
        "protein_names_uniprotkb": "Coiled-coil domain-containing protein 72",
        "protein_names_refseq": "translation machinery-associated protein 7-like",
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        "record_id": "A0ABK0LYW7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LYX5-1",
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        "mass": 52582.0,
        "length": 495,
        "protein_name": "Insulinoma-associated protein 2",
        "gene_name": "Insm2",
        "organism": "Rat",
        "refseq_name": "insulinoma-associated protein 2",
        "refseq_ac": "NP_001385718",
        "gene_names_uniprotkb": "Insm2",
        "gene_names_refseq": "Insm2",
        "protein_names_uniprotkb": "Insulinoma-associated protein 2",
        "protein_names_refseq": "insulinoma-associated 2; insulinoma-associated protein 2",
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        "function": "May function as a growth suppressor or tumor suppressor in liver cells and in certain neurons., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "length": 311,
        "protein_name": "Olfactory receptor",
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        "protein_name": "H/ACA ribonucleoprotein complex subunit DKC1",
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        "protein_names_uniprotkb": "H/ACA ribonucleoprotein complex subunit DKC1; Dyskerin; Nopp140-associated protein of 57 kDa; Nucleolar protein NAP57; Nucleolar protein family A member 4; snoRNP protein DKC1",
        "protein_names_refseq": "",
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        "disease": "X-linked dyskeratosis congenita (Disease Ontology:DOID:0070025); aplastic anemia (Disease Ontology:DOID:12449); dyskeratosis congenita (Disease Ontology:DOID:2729)",
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        "function": "Catalytic subunit of H/ACA small nucleolar ribonucleoprotein (H/ACA snoRNP) complex, which catalyzes pseudouridylation of rRNA. This involves the isomerization of uridine such that the ribose is subsequently attached to C5, instead of the normal N1. Each rRNA can contain up to 100 pseudouridine ('psi') residues, which may serve to stabilize the conformation of rRNAs. Required for ribosome biogenesis and telomere maintenance. Also required for correct processing or intranuclear trafficking of TERC, the RNA component of the telomerase reverse transcriptase (TERT) holoenzyme., [UniProtKB, UniProtKB]",
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        "go_biological_process": "GO:0000455 enzyme-directed rRNA pseudouridine synthesis;GO:0090666 scaRNA localization to Cajal body;GO:0008284 positive regulation of cell population proliferation;GO:0032212 positive regulation of telomere maintenance via telomerase;GO:0031118 rRNA pseudouridine synthesis",
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        "length": 374,
        "protein_name": "Forkhead box protein L2",
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        "protein_names_uniprotkb": "Forkhead box protein L2",
        "protein_names_refseq": "forkhead box protein L2",
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        "disease": "primary ovarian insufficiency 3 (Disease Ontology:DOID:0080860); blepharophimosis, ptosis, and epicanthus inversus syndrome (Disease Ontology:DOID:14778); laryngeal squamous cell carcinoma (Disease Ontology:DOID:2876); granulosa cell tumor (Disease Ontology:DOID:2999); lung non-small cell carcinoma (Disease Ontology:DOID:3908)",
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        "protein_names_uniprotkb": "Ubiquitin carboxyl-terminal hydrolase 3; 3.4.19.12; Deubiquitinating enzyme 3; Ubiquitin thioesterase 3; Ubiquitin-specific-processing protease 3",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-5689880)",
        "pathway_count": 1,
        "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, 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": "3.4.19.12;2.3.1.48",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0004843 cysteine-type deubiquitinase activity;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0042393 histone binding;GO:1990841 promoter-specific chromatin binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005654 nucleoplasm;GO:0000785 chromatin",
        "go_biological_process": "GO:0006508 proteolysis;GO:0016579 protein deubiquitination;GO:0006974 DNA damage response;GO:0006325 chromatin organization;GO:0000122 negative regulation of transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0M0Z8-1",
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        "length": 538,
        "protein_name": "BAR/IMD domain containing adaptor protein 2 like 2",
        "gene_name": "Baiap2l2",
        "organism": "Rat",
        "refseq_name": "brain-specific angiogenesis inhibitor 1-associated protein 2-like protein 2 isoform 1",
        "refseq_ac": "NP_001389081",
        "gene_names_uniprotkb": "Baiap2l2",
        "gene_names_refseq": "Baiap2l2; RGD1308786",
        "protein_names_uniprotkb": "BAR/IMD domain containing adaptor protein 2 like 2",
        "protein_names_refseq": "BAI1-associated protein 2-like 2; brain-specific angiogenesis inhibitor 1-associated protein 2-like protein 2 isoform 1; brain-specific angiogenesis inhibitor 1-associated protein 2-like protein 2; rCG60233-like",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:685357);  (R-RNO-9035034)",
        "pathway_count": 2,
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        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Phosphoinositides-binding protein that induces the formation of planar or gently curved membrane structures. Binds to phosphoinositides, including to phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2) headgroups. There seems to be no clear preference for a specific phosphoinositide., [UniProtKB, 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:0008289 lipid binding;GO:0005543 phospholipid binding;GO:0042802 identical protein binding",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0030659 cytoplasmic vesicle membrane;GO:0070161 anchoring junction",
        "go_biological_process": "GO:0007009 plasma membrane organization;GO:0051017 actin filament bundle assembly;GO:0051764 actin crosslink formation;GO:0030838 positive regulation of actin filament polymerization;GO:0061024 membrane organization",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0M0Z8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0M2A2-1",
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        "length": 1242,
        "protein_name": "non-specific serine/threonine protein kinase",
        "gene_name": "Ttbk2",
        "organism": "Rat",
        "refseq_name": "tau-tubulin kinase 2",
        "refseq_ac": "NP_001402630",
        "gene_names_uniprotkb": "Ttbk2",
        "gene_names_refseq": "Ttbk2",
        "protein_names_uniprotkb": "non-specific serine/threonine protein kinase; 2.7.11.1",
        "protein_names_refseq": "tau-tubulin kinase 2",
        "tax_id": 10116,
        "disease": "spinocerebellar ataxia 11 (Disease Ontology:DOID:0050961)",
        "pathway": " (rno:311349);  (R-RNO-5620912)",
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        "biomarker_type": "",
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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;3.6.5.2;2.7.11.31;3.1.3.16;3.6.5.-;3.6.4.10;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:0019894 kinesin binding;GO:0004672 protein kinase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005829 cytosol;GO:0005814 centriole;GO:0036064 ciliary basal body;GO:0097546 ciliary base",
        "go_biological_process": "GO:0021681 cerebellar granular layer development;GO:0060271 cilium assembly;GO:0016055 Wnt signaling pathway;GO:0030334 regulation of cell migration;GO:0007026 negative regulation of microtubule depolymerization",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0M2A2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0M0C0-1",
        "uniprot_id": "A0ABK0M0C0_RAT",
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        "length": 1400,
        "protein_name": "non-specific serine/threonine protein kinase",
        "gene_name": "Aatk",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Aatk",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "non-specific serine/threonine protein kinase; 2.7.11.1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:690853)",
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        "publication_id_list": "22673903",
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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:0004713 protein tyrosine kinase activity;GO:0005524 ATP binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0016020 membrane;GO:0030425 dendrite;GO:0012505 endomembrane system;GO:0005783 endoplasmic reticulum",
        "go_biological_process": "GO:0051402 neuron apoptotic process;GO:0007420 brain development;GO:0038083 peptidyl-tyrosine autophosphorylation;GO:0006915 apoptotic process;GO:0046777 protein autophosphorylation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0M0C0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0M2F5-1",
        "uniprot_id": "A0ABK0M2F5_RAT",
        "mass": 102429.0,
        "length": 935,
        "protein_name": "IQ domain-containing protein E",
        "gene_name": "Iqce",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Iqce",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "IQ domain-containing protein E",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
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        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Component of the EvC complex that positively regulates ciliary Hedgehog (Hh) signaling. Required for proper limb morphogenesis., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0031514 motile cilium;GO:0060170 ciliary membrane;GO:0009898 cytoplasmic side of plasma membrane;GO:0098797 plasma membrane protein complex",
        "go_biological_process": "GO:0120229 protein localization to motile cilium;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0008589 regulation of smoothened signaling pathway;GO:0035108 limb morphogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0M2F5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0M2N2-1",
        "uniprot_id": "A0ABK0M2N2_RAT",
        "mass": 53913.0,
        "length": 494,
        "protein_name": "Uridine 5'-monophosphate synthase",
        "gene_name": "Umps",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Umps",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Uridine 5'-monophosphate synthase; 2.4.2.10; 4.1.1.23",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "orotic aciduria (Disease Ontology:DOID:0050833); purine-pyrimidine metabolic disorder (Disease Ontology:DOID:653)",
        "pathway": "",
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        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Bifunctional enzyme catalyzing the last two steps of de novo pyrimidine biosynthesis, orotate phosphoribosyltransferase (OPRT), which converts orotate to orotidine-5'-monophosphate (OMP), and orotidine-5'-monophosphate decarboxylase (ODC), the terminal enzymatic reaction that decarboxylates OMP to uridine monophosphate (UMP)., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "ec_number_list": "2.4.2.10;4.1.1.23",
        "go_molecular_function": "GO:0004588 orotate phosphoribosyltransferase activity;GO:0004590 orotidine-5'-phosphate decarboxylase activity;GO:0042802 identical protein binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0006207 'de novo' pyrimidine nucleobase biosynthetic process;GO:0044205 'de novo' UMP biosynthetic process;GO:0071466 cellular response to xenobiotic stimulus;GO:0007565 female pregnancy;GO:0007595 lactation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0M2N2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0M279-1",
        "uniprot_id": "A0ABK0M279_RAT",
        "mass": 47959.0,
        "length": 432,
        "protein_name": "Thioredoxin domain-containing protein 5",
        "gene_name": "Txndc5",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Txndc5",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Thioredoxin domain-containing protein 5; 5.3.4.1; Endoplasmic reticulum resident protein 46; Thioredoxin-like protein p46",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:100362805);  (R-RNO-432720);  (R-RNO-432722);  (R-RNO-6798695)",
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        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Protein disulfide isomerase of the endoplasmic reticulum lumen involved in the formation of disulfide bonds in proteins. Can reduce insulin disulfide bonds., [UniProtKB, UniProtKB, UniProtKB]",
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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": "1.11.2.2;3.4.21.4;3.4.16.-;3.2.1.-;5.3.4.1;2.3.1.-;1.1.1.205;3.2.1.23;5.3.99.3;1.11.1.27;3.1.1.4;2.3.1.23;3.2.1.17;3.2.1.31;3.5.3.1;2.7.11.13;2.3.3.8;3.2.1.51;3.4.21.20;1.6.2.2;3.5.3.15;3.5.1.26;3.6.5.5;3.6.4.6;3.1.6.12;2.4.1.1;3.6.4.10;2.7.11.24;3.1.27.-;3.4.14.1;3.6.5.2;3.1.6.4;3.1.6.8;1.6.5.5;3.6.1.-;2.7.10.2;3.4.19.9;3.1.3.16;3.2.1.52;6.3.4.21;3.4.14.2;3.1.22.1;3.4.18.1",
        "go_molecular_function": "GO:0016491 oxidoreductase activity;GO:0003756 protein disulfide isomerase activity;GO:0015035 protein-disulfide reductase activity",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005788 endoplasmic reticulum lumen",
        "go_biological_process": "GO:0006457 protein folding",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0M279-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0M0X7-1",
        "uniprot_id": "A0ABK0M0X7_RAT",
        "mass": 33797.0,
        "length": 292,
        "protein_name": "DNA repair protein complementing XP-A cells homolog",
        "gene_name": "Xpa",
        "organism": "Rat",
        "refseq_name": "DNA repair protein complementing XP-A cells isoform X1",
        "refseq_ac": "XP_006238097",
        "gene_names_uniprotkb": "Xpa",
        "gene_names_refseq": "Xpa",
        "protein_names_uniprotkb": "DNA repair protein complementing XP-A cells homolog; Xeroderma pigmentosum group A-complementing protein homolog",
        "protein_names_refseq": "DNA repair protein complementing XP-A cells isoform X1",
        "tax_id": 10116,
        "disease": "xeroderma pigmentosum (Disease Ontology:DOID:0050427); xeroderma pigmentosum group A (Disease Ontology:DOID:0110843)",
        "pathway": " (rno:298074);  (R-RNO-5696395);  (R-RNO-5696400);  (R-RNO-6781823);  (R-RNO-6782135)",
        "pathway_count": 5,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Involved in DNA excision repair. Initiates repair by binding to damaged sites with various affinities, depending on the photoproduct and the transcriptional state of the region. Required for UV-induced CHEK1 phosphorylation and the recruitment of CEP164 to cyclobutane pyrimidine dimmers (CPD), sites of DNA damage after UV irradiation., [UniProtKB, UniProtKB, UniProtKB, 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,
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        "reported_o_glycosites": 0,
        "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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        "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:0008270 zinc ion binding;GO:0003684 damaged DNA binding;GO:0019904 protein domain specific binding;GO:0042803 protein homodimerization activity;GO:1990837 sequence-specific double-stranded DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0000110 nucleotide-excision repair factor 1 complex;GO:0005654 nucleoplasm;GO:0016604 nuclear body;GO:0005662 DNA replication factor A complex",
        "go_biological_process": "GO:0006289 nucleotide-excision repair;GO:0006284 base-excision repair;GO:0070914 UV-damage excision repair;GO:0000715 nucleotide-excision repair, DNA damage recognition;GO:1901255 nucleotide-excision repair involved in interstrand cross-link repair",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0M0X7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0M1F0-1",
        "uniprot_id": "A0ABK0M1F0_RAT",
        "mass": 29741.0,
        "length": 264,
        "protein_name": "Lysosomal protein transmembrane 5",
        "gene_name": "Laptm5",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Laptm5",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Lysosomal protein transmembrane 5",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:89783)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_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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        "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:0140311 protein sequestering activity;GO:0019899 enzyme binding;GO:0031625 ubiquitin protein ligase binding",
        "go_cellular_component": "GO:0005764 lysosome;GO:0005765 lysosomal membrane;GO:0012505 endomembrane system;GO:0016020 membrane;GO:0005829 cytosol",
        "go_biological_process": "GO:0097213 regulation of lysosomal membrane permeability;GO:2000646 positive regulation of receptor catabolic process;GO:0032703 negative regulation of interleukin-2 production;GO:0097214 positive regulation of lysosomal membrane permeability;GO:0006886 intracellular protein transport",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0M1F0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0M197-1",
        "uniprot_id": "A0ABK0M197_RAT",
        "mass": 44644.0,
        "length": 393,
        "protein_name": "RT1 class Ib, locus M3, gene 1",
        "gene_name": "RT1-M3-1",
        "organism": "Rat",
        "refseq_name": "RT1 class Ib, locus M3-1 isoform X1",
        "refseq_ac": "XP_063135029",
        "gene_names_uniprotkb": "RT1-M3-1",
        "gene_names_refseq": "4B2/3.7; H2-M3; RT1-M3-1; RT1-M3; RanoM301; RanoM302; RanoM3",
        "protein_names_uniprotkb": "RT1 class Ib, locus M3, gene 1",
        "protein_names_refseq": "RT1 class Ib, locus M3-1 isoform X1",
        "tax_id": 10116,
        "disease": "respiratory syncytial virus infectious disease (Disease Ontology:DOID:1273); cystic fibrosis (Disease Ontology:DOID:1485); hepatitis C (Disease Ontology:DOID:1883); asthma (Disease Ontology:DOID:2841); bipolar disorder (Disease Ontology:DOID:3312); allergic rhinitis (Disease Ontology:DOID:4481); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (rno:24747)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "29393594",
        "class_list": "",
        "function": "Involved in the presentation of foreign antigens to the immune system., [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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        "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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        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005102 signaling receptor binding;GO:0042802 identical protein binding;GO:0042803 protein homodimerization activity;GO:0042605 peptide antigen binding;GO:0042610 CD8 receptor binding",
        "go_cellular_component": "GO:0030670 phagocytic vesicle membrane;GO:0042612 MHC class I protein complex;GO:0098553 lumenal side of endoplasmic reticulum membrane;GO:0032398 MHC class Ib protein complex;GO:0005769 early endosome",
        "go_biological_process": "GO:0002474 antigen processing and presentation of peptide antigen via MHC class I;GO:0002476 antigen processing and presentation of endogenous peptide antigen via MHC class Ib;GO:0002645 positive regulation of tolerance induction;GO:0002666 positive regulation of T cell tolerance induction;GO:0002767 immune response-inhibiting cell surface receptor signaling pathway",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0M197-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0M1V5-1",
        "uniprot_id": "A0ABK0M1V5_RAT",
        "mass": 150838.0,
        "length": 1383,
        "protein_name": "Zinc finger protein 536",
        "gene_name": "Zfp536",
        "organism": "Rat",
        "refseq_name": "zinc finger protein 536",
        "refseq_ac": "NP_001414064",
        "gene_names_uniprotkb": "Zfp536",
        "gene_names_refseq": "RGD1563363; Zfp536; Znf536",
        "protein_names_uniprotkb": "Zinc finger protein 536",
        "protein_names_refseq": "zinc finger protein 536",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:292820)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "17065439",
        "class_list": "",
        "function": "Transcriptional repressor that negatively regulates neuron differentiation by repressing retinoic acid-induced gene transcription. Binds and interrupts RARA from binding to retinoic acid response elements (RARE) composed of tandem 5'-AGGTCA-3' sites known as DR1-DR5. Recognizes and binds 2 copies of the core DNA sequence 5'-CCCCCA-3'., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; ZFP536 promotes the late phase of oligodendrocyte differentiation, [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_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,
        "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: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:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006355 regulation of DNA-templated transcription;GO:0000122 negative regulation of transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0M1V5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0M285-1",
        "uniprot_id": "A0ABK0M285_RAT",
        "mass": 84324.0,
        "length": 752,
        "protein_name": "DNA replication licensing factor MCM5",
        "gene_name": "Mcm5",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Mcm5",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "DNA replication licensing factor MCM5; 3.6.4.12",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "Meier-Gorlin syndrome (Disease Ontology:DOID:0060306); Meier-Gorlin syndrome 8 (Disease Ontology:DOID:0080255); alcohol use disorder (Disease Ontology:DOID:1574)",
        "pathway": " (R-RNO-176187);  (R-RNO-68867);  (R-RNO-68949);  (R-RNO-68962)",
        "pathway_count": 4,
        "publication_count": 0,
        "publication_id_list": "",
        "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, 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, 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_c_glycosites_with_glycan": 0,
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        "total_reported_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": 3,
        "glyco_site_count": 0,
        "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:0003688 DNA replication origin binding;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:0005694 chromosome;GO:0042555 MCM complex",
        "go_biological_process": "GO:0006270 DNA replication initiation;GO:0000727 double-strand break repair via break-induced replication",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0M285-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0M2X6-1",
        "uniprot_id": "A0ABK0M2X6_RAT",
        "mass": 132909.0,
        "length": 1203,
        "protein_name": "Partitioning defective 3 homolog B",
        "gene_name": "Pard3b",
        "organism": "Rat",
        "refseq_name": "partitioning defective 3 homolog B",
        "refseq_ac": "NP_001178737",
        "gene_names_uniprotkb": "Pard3b",
        "gene_names_refseq": "Pard3b",
        "protein_names_uniprotkb": "Partitioning defective 3 homolog B; PAR3-beta; Partitioning defective 3-like protein",
        "protein_names_refseq": "par-3 partitioning defective 3 homolog B; partitioning defective 3 homolog B",
        "tax_id": 10116,
        "disease": "developmental disorder of mental health (Disease Ontology:DOID:0060037)",
        "pathway": " (rno:301455)",
        "pathway_count": 1,
        "publication_count": 2,
        "publication_id_list": "16641100;22673903",
        "class_list": "",
        "function": "Putative adapter protein involved in asymmetrical cell division and cell polarization processes. May play a role in the formation of epithelial tight junctions., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
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        "predicted_s_glycosites": 0,
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        "protein_names_uniprotkb": "Serine protease 37",
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        "protein_name": "Tryptophan--tRNA ligase, mitochondrial",
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        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005759 mitochondrial matrix",
        "go_biological_process": "GO:0001570 vasculogenesis;GO:0045766 positive regulation of angiogenesis;GO:0070183 mitochondrial tryptophanyl-tRNA aminoacylation;GO:0006436 tryptophanyl-tRNA aminoacylation;GO:0006418 tRNA aminoacylation for protein translation",
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    },
    {
        "uniprot_canonical_ac": "A0ABK0M2G4-1",
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        "length": 359,
        "protein_name": "Phospholipid scramblase",
        "gene_name": "Plscr4",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Plscr4",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Phospholipid scramblase",
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        "publication_id_list": "22673903",
        "class_list": "",
        "function": "May mediate accelerated ATP-independent bidirectional transbilayer migration of phospholipids upon binding calcium ions that results in a loss of phospholipid asymmetry in the plasma membrane., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0017128 phospholipid scramblase activity;GO:0019899 enzyme binding;GO:0042609 CD4 receptor binding",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0005634 nucleus",
        "go_biological_process": "GO:0017121 plasma membrane phospholipid scrambling;GO:0071222 cellular response to lipopolysaccharide;GO:0061589 calcium activated phosphatidylserine scrambling;GO:0061590 calcium activated phosphatidylcholine scrambling",
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    },
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        "length": 514,
        "protein_name": "Histone H4 transcription factor",
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        "protein_names_uniprotkb": "Histone H4 transcription factor; Histone nuclear factor P; MBD2-interacting zinc finger protein; Methyl-CpG-binding protein 2-interacting zinc finger protein",
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        "function": "Transcriptional repressor that binds to the consensus sequence 5'-CGGACGTT-3' and to the RB1 promoter. Transcriptional activator that promotes histone H4 gene transcription at the G1/S phase transition in conjunction with NPAT. Also activates transcription of the ATM and PRKDC genes. Autoregulates its expression by associating with its own promoter., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0015030 Cajal body",
        "go_biological_process": "GO:0006357 regulation of transcription by RNA polymerase II;GO:0045892 negative regulation of DNA-templated transcription;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0001701 in utero embryonic development;GO:0006281 DNA repair",
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        "protein_names_uniprotkb": "PAX-interacting protein 1; PAX transactivation activation domain-interacting protein",
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        "protein_names_uniprotkb": "E3 ubiquitin-protein ligase TRIM33; 2.3.2.27; Ectodermin homolog; RING-type E3 ubiquitin transferase TRIM33; Transcription intermediary factor 1-gamma; Tripartite motif-containing protein 33",
        "protein_names_refseq": "E3 ubiquitin-protein ligase TRIM33; tripartite motif protein 33",
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        "protein_name": "pre-mRNA 3' end processing protein WDR33",
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        "gene_names_refseq": "Wdr33",
        "protein_names_uniprotkb": "pre-mRNA 3' end processing protein WDR33; WD repeat-containing protein 33; WD repeat-containing protein of 146 kDa",
        "protein_names_refseq": "pre-mRNA 3' end processing protein WDR33 isoform X1",
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        "disease": "primary ovarian insufficiency (Disease Ontology:DOID:5426)",
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        "function": "Essential for both cleavage and polyadenylation of pre-mRNA 3' ends., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "length": 356,
        "protein_name": "Similar to human chromosome 20 open reading frame 96",
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        "organism": "Rat",
        "refseq_name": "uncharacterized protein C20orf96 homolog",
        "refseq_ac": "NP_001382549",
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        "gene_names_refseq": "C3h20orf96",
        "protein_names_uniprotkb": "Similar to human chromosome 20 open reading frame 96",
        "protein_names_refseq": "uncharacterized protein C20orf96 homolog",
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        "uniprot_id": "A0ABK0M1U7_RAT",
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        "length": 1392,
        "protein_name": "S-phase cyclin A-associated protein in the ER",
        "gene_name": "Scaper",
        "organism": "Rat",
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        "gene_names_uniprotkb": "Scaper",
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        "protein_names_uniprotkb": "S-phase cyclin A-associated protein in the ER",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "azoospermia (Disease Ontology:DOID:14227); Bardet-Biedl syndrome (Disease Ontology:DOID:1935)",
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        "protein_names_uniprotkb": "24-hydroxycholesterol 7-alpha-hydroxylase; 1.14.14.26; Cytochrome P450 39A1; Oxysterol 7-alpha-hydroxylase",
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        "function": "A cytochrome P450 monooxygenase involved in neural cholesterol clearance through bile acid synthesis. Catalyzes 7-alpha hydroxylation of (24S)-hydroxycholesterol, a neural oxysterol that is metabolized to bile acids in the liver. Mechanistically, uses molecular oxygen inserting one oxygen atom into a substrate, and reducing the second into a water molecule, with two electrons provided by NADPH via cytochrome P450 reductase (CPR; NADPH-ferrihemoprotein reductase)., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005506 iron ion binding;GO:0020037 heme binding;GO:0008395 steroid hydroxylase activity;GO:0016705 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen;GO:0004497 monooxygenase activity",
        "go_cellular_component": "GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0006699 bile acid biosynthetic process;GO:0042632 cholesterol homeostasis;GO:0016125 sterol metabolic process;GO:0044281 small molecule metabolic process;GO:0008202 steroid metabolic process",
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        "protein_name": "Similar to chromosome 2 open reading frame 76",
        "gene_name": "C13h2orf76",
        "organism": "Rat",
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        "gene_names_uniprotkb": "C13h2orf76; LOC288978",
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        "protein_names_uniprotkb": "Similar to chromosome 2 open reading frame 76",
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        "pathway": " (rno:288978)",
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    },
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        "length": 314,
        "protein_name": "Coiled-coil domain containing 92",
        "gene_name": "Ccdc92",
        "organism": "Rat",
        "refseq_name": "coiled-coil domain-containing protein 92",
        "refseq_ac": "NP_001077367",
        "gene_names_uniprotkb": "Ccdc92",
        "gene_names_refseq": "Ccdc92",
        "protein_names_uniprotkb": "Coiled-coil domain containing 92",
        "protein_names_refseq": "coiled-coil domain-containing protein 92",
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        "go_molecular_function": "GO:0042802 identical protein binding",
        "go_cellular_component": "GO:0005814 centriole;GO:0005813 centrosome",
        "go_biological_process": "GO:0044546 NLRP3 inflammasome complex assembly;GO:0001889 liver development;GO:0006631 fatty acid metabolic process;GO:0006954 inflammatory response;GO:0060612 adipose tissue development",
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        "hit_score": 0.2,
        "record_id": "A0ABK0M299-1",
        "record_type": "protein"
    },
    {
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        "protein_name": "E3 ubiquitin-protein ligase RNF144B",
        "gene_name": "Rnf144b",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Rnf144b",
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        "protein_names_uniprotkb": "E3 ubiquitin-protein ligase RNF144B; 2.3.2.31; IBR domain-containing protein 2; RING finger protein 144B",
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        "pathway": " (rno:364681);  (R-RNO-983168)",
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        "function": "E3 ubiquitin-protein ligase which accepts ubiquitin from E2 ubiquitin-conjugating enzymes UBE2L3 and UBE2L6 in the form of a thioester and then directly transfers the ubiquitin to targeted substrates such as LCMT2, thereby promoting their degradation. Induces apoptosis via a p53/TP53-dependent but caspase-independent mechanism. Plays a crucial role in maintaining the genomic stability by controlling the degradation of multiple proteins involved in mitotic progression and DNA damage. Regulates epithelial homeostasis by mediating degradation of CDKN1A and isoform 2 of TP63. Plays a regulatory role in innate immunity by negatively regulating IRF3 activation and IFN-beta production. Mechanistically, inhibits TBK1 phosphorylation and 'Lys-63'-linked polyubiquitination independently of its E3 ligase activity. Alternatively, promotes 'Lys-27' and 'Lys-33'-linked ubiquitination of IFIH1/MDA5, promoting selective autophagic degradation of IFIH1/MDA5 to inhibit antiviral response., [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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        "refseq_name": "tyrosine-protein kinase transmembrane receptor ROR2 isoform X1",
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        "protein_names_uniprotkb": "Receptor tyrosine kinase-like orphan receptor 2",
        "protein_names_refseq": "tyrosine-protein kinase transmembrane receptor ROR2 isoform X1",
        "tax_id": 10116,
        "disease": "autosomal recessive Robinow syndrome (Disease Ontology:DOID:0060764); brachydactyly type B1 (Disease Ontology:DOID:0110969); cleft palate (Disease Ontology:DOID:674)",
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        "go_molecular_function": "GO:0005524 ATP binding;GO:0017147 Wnt-protein binding;GO:0004714 transmembrane receptor protein tyrosine kinase activity;GO:0004672 protein kinase activity;GO:0038023 signaling receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0030424 axon;GO:0043235 receptor complex;GO:0016020 membrane;GO:0098978 glutamatergic synapse",
        "go_biological_process": "GO:0007169 cell surface receptor protein tyrosine kinase signaling pathway;GO:0016055 Wnt signaling pathway;GO:0048839 inner ear development;GO:0007165 signal transduction;GO:0030154 cell differentiation",
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        "length": 2255,
        "protein_name": "Zinc finger protein 407",
        "gene_name": "Zfp407",
        "organism": "Rat",
        "refseq_name": "zinc finger protein 407 isoform X1",
        "refseq_ac": "XP_008770443",
        "gene_names_uniprotkb": "Zfp407",
        "gene_names_refseq": "RGD1310645; Zfp407",
        "protein_names_uniprotkb": "Zinc finger protein 407",
        "protein_names_refseq": "zinc finger protein 407 isoform X1",
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        "disease": "",
        "pathway": " (rno:307213)",
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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:0003676 nucleic acid binding",
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        "length": 389,
        "protein_name": "Gamma-parvin",
        "gene_name": "Parvg",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Parvg",
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        "protein_names_uniprotkb": "Gamma-parvin",
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        "tax_id": 10116,
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        "pathway": " (rno:689069)",
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        "function": "Plays a role with ILK in promoting the cell adhesion and spreading of leukocytes., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003779 actin binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005886 plasma membrane;GO:0005925 focal adhesion;GO:0015629 actin cytoskeleton;GO:0005856 cytoskeleton",
        "go_biological_process": "GO:0030036 actin cytoskeleton organization;GO:0034446 substrate adhesion-dependent cell spreading;GO:0071963 establishment or maintenance of cell polarity regulating cell shape;GO:0030031 cell projection assembly;GO:0007155 cell adhesion",
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        "record_id": "A0ABK0M1T9-1",
        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "A0ABK0M1S8-1",
        "uniprot_id": "A0ABK0M1S8_RAT",
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        "length": 297,
        "protein_name": "Chloride intracellular channel 3",
        "gene_name": "Clic3",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Clic3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Chloride intracellular channel 3",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "alcohol use disorder (Disease Ontology:DOID:1574)",
        "pathway": " (rno:296566)",
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        "function": "In the soluble state, catalyzes glutaredoxin-like thiol disulfide exchange reactions with reduced glutathione as electron donor. Reduced in a glutathione-dependent way and secreted into the extracellular matrix where it activates TGM2 and promotes blood vessel growth during tissue remodeling as occurs in tumorigenesis. Can reduce specific cysteines in TGM2 and regulate cofactor binding. Can insert into membranes and form outwardly rectifying chloride ion channels. May participate in cellular growth control., [UniProtKB, UniProtKB]",
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        "gene_names_uniprotkb": "Prl3d1l1; Rpl-1",
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        "gene_names_uniprotkb": "Vom1r79",
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        "function": "Putative pheromone receptor implicated in the regulation of social as well as reproductive behavior., [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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        "function": "Core component of the CTLH E3 ubiquitin-protein ligase complex that selectively accepts ubiquitin from UBE2H and mediates ubiquitination and subsequent proteasomal degradation of the transcription factor HBP1. MAEA and RMND5A are both required for catalytic activity of the CTLH E3 ubiquitin-protein ligase complex. Catalytic activity of the complex is required for normal cell proliferation. The CTLH E3 ubiquitin-protein ligase complex is not required for the degradation of enzymes involved in gluconeogenesis, such as FBP1., [UniProtKB, UniProtKB]",
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        "length": 266,
        "protein_name": "Immunoreceptor Ly49si3",
        "gene_name": "Ly49si3",
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        "gene_names_uniprotkb": "Ly49si3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Immunoreceptor Ly49si3",
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        "go_molecular_function": "GO:0030246 carbohydrate binding",
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    {
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        "length": 310,
        "protein_name": "Olfactory receptor",
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        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr1201",
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        "gene_names_uniprotkb": "Or8b8",
        "gene_names_refseq": "Olr1201; Or8b8",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 1201; olfactory receptor Olr1201; olfactory receptor gene Olr1201",
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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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    },
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        "length": 273,
        "protein_name": "L-xylulose reductase",
        "gene_name": "Dcxr",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Dcxr",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "L-xylulose reductase; 1.1.1.10; Dicarbonyl/L-xylulose reductase",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "pentosuria (Disease Ontology:DOID:0111258)",
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        "function": "Catalyzes the NADPH-dependent reduction of several pentoses, tetroses, trioses, alpha-dicarbonyl compounds and L-xylulose. Can use both NAD and NADP as cosubstrate but shows higher activity with NADP. Participates in the uronate cycle of glucose metabolism. May play a role in the water absorption and cellular osmoregulation in the proximal renal tubules by producing xylitol, an osmolyte, thereby preventing osmolytic stress from occurring in the renal tubules., [UniProtKB, UniProtKB]",
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        "ec_number_list": "1.1.1.10",
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        "go_cellular_component": "GO:0005829 cytosol;GO:0005903 brush border;GO:0016020 membrane;GO:0005902 microvillus;GO:0005881 cytoplasmic microtubule",
        "go_biological_process": "GO:0005997 xylulose metabolic process;GO:0006739 NADP+ metabolic process;GO:0042732 D-xylose metabolic process;GO:0006006 glucose metabolic process;GO:2000379 positive regulation of reactive oxygen species metabolic process",
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        "protein_names_uniprotkb": "Uncharacterized protein",
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        "record_id": "A0ABK0M244-1",
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    },
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        "length": 127,
        "protein_name": "Ig-like domain-containing protein",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ig-like domain-containing protein",
        "protein_names_refseq": "",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0042101 T cell receptor complex",
        "go_biological_process": "GO:0002250 adaptive immune response",
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        "record_id": "A0ABK0M246-1",
        "record_type": "protein"
    },
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        "mass": 35979.0,
        "length": 315,
        "protein_name": "Vomeronasal type-1 receptor",
        "gene_name": "Vom1r23",
        "organism": "Rat",
        "refseq_name": "vomeronasal 1 receptor 23",
        "refseq_ac": "NP_001008941",
        "gene_names_uniprotkb": "Vom1r23",
        "gene_names_refseq": "V1rf5; Vom1r23",
        "protein_names_uniprotkb": "Vomeronasal type-1 receptor",
        "protein_names_refseq": "vomernasal 1 receptor Vom1r23; vomeronasal 1 receptor 23; vomeronasal 1 receptor, F5; vomeronasal V1r-type receptor V1rf5; vomeronasal type-1 receptor 4",
        "tax_id": 10116,
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        "pathway": " (rno:494288)",
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        "function": "Putative pheromone receptor implicated in the regulation of social as well as reproductive behavior., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0016503 pheromone receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
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        "hit_score": 0.1,
        "record_id": "A0ABK0M256-1",
        "record_type": "protein"
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        "uniprot_canonical_ac": "A0ABK0M267-1",
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        "protein_name": "S100 calcium binding protein A7A",
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        "refseq_name": "protein S100-A15A",
        "refseq_ac": "NP_001102941",
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        "gene_names_refseq": "S100a15; S100a7a",
        "protein_names_uniprotkb": "S100 calcium binding protein A7A",
        "protein_names_refseq": "S100 calcium binding protein A15; protein S100-A15A",
        "tax_id": 10116,
        "disease": "psoriasis (Disease Ontology:DOID:8893)",
        "pathway": " (rno:685479)",
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        "go_molecular_function": "GO:0042802 identical protein binding;GO:0046914 transition metal ion binding;GO:0005509 calcium ion binding",
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    },
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        "uniprot_canonical_ac": "A0ABK0M293-1",
        "uniprot_id": "A0ABK0M293_RAT",
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        "length": 436,
        "protein_name": "Septin",
        "gene_name": "",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Septin",
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        "function": "Filament-forming cytoskeletal GTPase. Required for normal organization of the actin cytoskeleton. Required for normal progress through mitosis. Involved in cytokinesis. Required for normal association of CENPE with the kinetochore. Plays a role in ciliogenesis and collective cell movements. Forms a filamentous structure with SEPTIN12, SEPTIN6, SEPTIN2 and probably SEPTIN4 at the sperm annulus which is required for the structural integrity and motility of the sperm tail during postmeiotic differentiation., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005525 GTP binding",
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        "record_id": "A0ABK0M293-1",
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    },
    {
        "uniprot_canonical_ac": "A0ABK0M2A6-1",
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        "length": 53,
        "protein_name": "Photoreceptor disc component",
        "gene_name": "Prcd",
        "organism": "Rat",
        "refseq_name": "photoreceptor disk component PRCD isoform X1",
        "refseq_ac": "XP_017453237",
        "gene_names_uniprotkb": "Prcd",
        "gene_names_refseq": "Prcd",
        "protein_names_uniprotkb": "Photoreceptor disc component",
        "protein_names_refseq": "photoreceptor disk component PRCD isoform X1",
        "tax_id": 10116,
        "disease": "retinitis pigmentosa 36 (Disease Ontology:DOID:0110405)",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0002046 opsin binding",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0005737 cytoplasm;GO:0005783 endoplasmic reticulum;GO:0005794 Golgi apparatus;GO:0001750 photoreceptor outer segment",
        "go_biological_process": "GO:0050908 detection of light stimulus involved in visual perception",
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        "hit_score": 0.1,
        "record_id": "A0ABK0M2A6-1",
        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "A0ABK0M2B2-1",
        "uniprot_id": "A0ABK0M2B2_RAT",
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        "length": 114,
        "protein_name": "DNA-directed RNA polymerase III subunit RPC10",
        "gene_name": "Polr3k",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Polr3k",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "DNA-directed RNA polymerase III subunit RPC10; DNA-directed RNA polymerase III subunit K; RNA polymerase III subunit C11",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "hypomyelinating leukodystrophy (Disease Ontology:DOID:0060786); hypomyelinating leukodystrophy 21 (Disease Ontology:DOID:0070407)",
        "pathway": "",
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        "function": "Core component of RNA polymerase III (Pol III) which synthesizes small non-coding RNAs using the four ribonucleoside triphosphates as substrates. Can mediate Pol I proofreading of the nascent RNA transcript. Anchors into the Pol III active site to constantly monitor transcription fidelity, cleaves mis-incorporated 5'-ribonucleotides and restarts the transcription process. Once Pol III reaches the poly(dT) termination signal, can induce Pol III clamp opening and transcription termination. Pol III plays an important role in sensing and limiting infection by intracellular bacteria and DNA viruses. Acts as a nuclear and cytosolic DNA sensor involved in innate immune response. Can sense non-self dsDNA that serves as template for transcription into dsRNA. The non-self RNA polymerase III transcripts, such as Epstein-Barr virus-encoded RNAs (EBERs) induce type I interferon and NF-kappa-B through the RIG-I pathway., [UniProtKB, UniProtKB]",
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        "gene_name": "Ptges",
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        "refseq_ac": "",
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        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Prostaglandin E synthase; 2.5.1.18; 5.3.99.3; Glutathione peroxidase PTGES; Glutathione transferase PTGES; Microsomal prostaglandin E synthase 1",
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        "disease": "ductal carcinoma in situ (Disease Ontology:DOID:0060074); penile benign neoplasm (Disease Ontology:DOID:11624); peptic esophagitis (Disease Ontology:DOID:13976); ovary epithelial cancer (Disease Ontology:DOID:2152); papilloma (Disease Ontology:DOID:2615); transitional cell carcinoma (Disease Ontology:DOID:2671); endometrial adenocarcinoma (Disease Ontology:DOID:2870); endometriosis (Disease Ontology:DOID:289); ischemia (Disease Ontology:DOID:326); lung non-small cell carcinoma (Disease Ontology:DOID:3908); in situ carcinoma (Disease Ontology:DOID:8719); Barrett's esophagus (Disease Ontology:DOID:9206)",
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        "protein_name": "Y-linked testis-specific protein 1-like",
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        "go_molecular_function": "GO:0003723 RNA binding",
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        "length": 123,
        "protein_name": "Thioredoxin domain-containing protein 17",
        "gene_name": "Txndc17",
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        "refseq_name": "thioredoxin domain-containing protein 17",
        "refseq_ac": "NP_001099275",
        "gene_names_uniprotkb": "Txndc17",
        "gene_names_refseq": "Txndc17; Txnl5",
        "protein_names_uniprotkb": "Thioredoxin domain-containing protein 17; Thioredoxin-like protein 5",
        "protein_names_refseq": "thioredoxin domain-containing protein 17; thioredoxin-like 5",
        "tax_id": 10116,
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        "go_molecular_function": "GO:0004601 peroxidase activity;GO:0047134 protein-disulfide reductase [NAD(P)H] activity",
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        "protein_name": "Murine leukemia virus integrase C-terminal domain-containing protein",
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        "protein_names_uniprotkb": "Murine leukemia virus integrase C-terminal domain-containing protein",
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        "go_molecular_function": "GO:0003824 catalytic activity",
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    },
    {
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        "length": 286,
        "protein_name": "Prohibitin",
        "gene_name": "AABR07037878.1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "AABR07037878.1; Phb1l1; RGD1566197",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Prohibitin",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "In the nucleus, acts as a transcription coregulator, enhances promoter binding by TP53, a transcription factor it activates, but reduces the promoter binding by E2F1, a transcription factor it represses. Interacts with STAT3 to affect IL17 secretion in T-helper Th17 cells., [UniProtKB, UniProtKB, UniProtKB]; In the plasma membrane, cooperates with CD86 to mediate CD86-signaling in B lymphocytes that regulates the level of IgG1 produced through the activation of distal signaling intermediates. Upon CD40 engagement, required to activate NF-kappa-B signaling pathway via phospholipase C and protein kinase C activation., [UniProtKB, UniProtKB, UniProtKB]; Protein with pleiotropic attributes mediated in a cell-compartment- and tissue-specific manner, which include the plasma membrane-associated cell signaling functions, mitochondrial chaperone, and transcriptional co-regulator of transcription factors in the nucleus. Plays a role in adipose tissue and glucose homeostasis in a sex-specific manner. Contributes to pulmonary vascular remodeling by accelerating proliferation of pulmonary arterial smooth muscle cells., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005743 mitochondrial inner membrane",
        "go_biological_process": "GO:0071897 DNA biosynthetic process;GO:0007005 mitochondrion organization",
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        "record_id": "A0ABK0M6C3-1",
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    },
    {
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        "length": 267,
        "protein_name": "Centromere protein K",
        "gene_name": "Cenpk",
        "organism": "Rat",
        "refseq_name": "centromere protein K isoform 1",
        "refseq_ac": "NP_001386127",
        "gene_names_uniprotkb": "Cenpk",
        "gene_names_refseq": "Cenpk; Solt",
        "protein_names_uniprotkb": "Centromere protein K",
        "protein_names_refseq": "SoxLZ/Sox6 leucine zipper binding protein in testis; centromere protein K isoform 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-141430);  (R-RNO-141444);  (R-RNO-2467813);  (R-RNO-2500257);  (R-RNO-5663220);  (R-RNO-606279);  (R-RNO-68877);  (R-RNO-9648025)",
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        "function": "",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005634 nucleus;GO:0000775 chromosome, centromeric region;GO:0000939 inner kinetochore",
        "go_biological_process": "GO:0051382 kinetochore assembly;GO:0000070 mitotic sister chromatid segregation;GO:0045944 positive regulation of transcription by RNA polymerase II",
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        "record_type": "protein"
    },
    {
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        "length": 300,
        "protein_name": "XIAP associated factor 1",
        "gene_name": "Xaf1",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Xaf1; XAF1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "XIAP associated factor 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (rno:679600)",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0140313 molecular sequestering activity",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005654 nucleoplasm",
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        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0M5E1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0M6W4-1",
        "uniprot_id": "A0ABK0M6W4_RAT",
        "mass": 68558.0,
        "length": 623,
        "protein_name": "Ubiquitin carboxyl-terminal hydrolase",
        "gene_name": "Mindy2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Mindy2; Fam63b",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ubiquitin carboxyl-terminal hydrolase; 3.4.19.12",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:363089)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Hydrolase that can specifically remove 'Lys-48'-linked conjugated ubiquitin from proteins. Has exodeubiquitinase activity and has a preference for long polyubiquitin chains. May play a regulatory role at the level of protein turnover., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "ec_number_list": "",
        "go_molecular_function": "GO:0036435 K48-linked polyubiquitin modification-dependent protein binding;GO:0004843 cysteine-type deubiquitinase activity;GO:1990380 K48-linked deubiquitinase activity;GO:0140934 histone deubiquitinase activity;GO:0016807 cysteine-type carboxypeptidase activity",
        "go_cellular_component": "GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0006508 proteolysis",
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        "hit_score": 0.2,
        "record_id": "A0ABK0M6W4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0M3M5-1",
        "uniprot_id": "A0ABK0M3M5_RAT",
        "mass": 65795.0,
        "length": 586,
        "protein_name": "Protein NNX3",
        "gene_name": "Uri1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Uri1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Protein NNX3; Protein phosphatase 1 regulatory subunit 19; RNA polymerase II subunit 5-mediating protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:308537)",
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        "publication_count": 1,
        "publication_id_list": "22673903",
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        "function": "Plays a central role in maintaining S6K1 signaling and BAD phosphorylation under normal growth conditions thereby protecting cells from potential deleterious effects of sustained S6K1 signaling. The URI1-PPP1CC complex acts as a central component of a negative feedback mechanism that counteracts excessive S6K1 survival signaling to BAD in response to growth factors. Mediates inhibition of PPP1CC phosphatase activity in mitochondria. Coordinates the regulation of nutrient-sensitive gene expression availability in a mTOR-dependent manner. Seems to be a scaffolding protein able to assemble a prefoldin-like complex that contains PFDs and proteins with roles in transcription and ubiquitination., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0004864 protein phosphatase inhibitor activity;GO:0003682 chromatin binding;GO:0003714 transcription corepressor activity;GO:0019212 phosphatase inhibitor activity;GO:0051219 phosphoprotein binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005739 mitochondrion;GO:0030425 dendrite;GO:0005654 nucleoplasm;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0042771 intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator;GO:2001243 negative regulation of intrinsic apoptotic signaling pathway;GO:0006357 regulation of transcription by RNA polymerase II",
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    },
    {
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        "length": 516,
        "protein_name": "Na(+)/H(+) exchange regulatory cofactor NHE-RF4",
        "gene_name": "Nherf4",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Nherf4; Pdzd3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Na(+)/H(+) exchange regulatory cofactor NHE-RF4; Natrium-phosphate cotransporter IIa C-terminal-associated protein 2; PDZ domain-containing protein 2; PDZ domain-containing protein 3; Sodium-hydrogen exchanger regulatory factor 4",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "hypophosphatemic nephrolithiasis/osteoporosis 2 (Disease Ontology:DOID:0080078)",
        "pathway": " (rno:500986)",
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        "publication_id_list": "",
        "class_list": "",
        "function": "Acts as a regulatory protein that associates with GUCY2C and negatively modulates its heat-stable enterotoxin-mediated activation. Stimulates SLC9A3 activity in the presence of elevated calcium ions., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005102 signaling receptor binding;GO:0043495 protein-membrane adaptor activity;GO:1990381 ubiquitin-specific protease binding;GO:0030251 guanylate cyclase inhibitor activity",
        "go_cellular_component": "GO:0016324 apical plasma membrane;GO:0005886 plasma membrane;GO:0045177 apical part of cell;GO:0005737 cytoplasm;GO:0005903 brush border",
        "go_biological_process": "GO:0072659 protein localization to plasma membrane",
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        "record_id": "A0ABK0M3S3-1",
        "record_type": "protein"
    },
    {
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        "length": 911,
        "protein_name": "Family with sequence similarity 171, member A1",
        "gene_name": "Fam171a1",
        "organism": "Rat",
        "refseq_name": "protein FAM171A1 isoform X1",
        "refseq_ac": "XP_038952338",
        "gene_names_uniprotkb": "Fam171a1",
        "gene_names_refseq": "Fam171a1",
        "protein_names_uniprotkb": "Family with sequence similarity 171, member A1",
        "protein_names_refseq": "protein FAM171A1 isoform X1",
        "tax_id": 10116,
        "disease": "",
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        "pathway_count": 0,
        "publication_count": 2,
        "publication_id_list": "22673903;38843836",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
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    },
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        "protein_name": "Platelet glycoprotein Ib alpha chain",
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        "gene_names_uniprotkb": "Gp1ba",
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        "protein_names_uniprotkb": "Platelet glycoprotein Ib alpha chain",
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        "tax_id": 10116,
        "disease": "non-arteritic anterior ischemic optic neuropathy (Disease Ontology:DOID:0050864); platelet-type bleeding disorder 3 (Disease Ontology:DOID:0111056); Bernard-Soulier syndrome type A2 (Disease Ontology:DOID:0111059); diabetic angiopathy (Disease Ontology:DOID:11713); nephrotic syndrome (Disease Ontology:DOID:1184); peritoneum cancer (Disease Ontology:DOID:1725); Bernard-Soulier syndrome (Disease Ontology:DOID:2217); liver cirrhosis (Disease Ontology:DOID:5082); myocardial infarction (Disease Ontology:DOID:5844); chronic kidney disease (Disease Ontology:DOID:784)",
        "pathway": " (rno:691992);  (R-RNO-430116);  (R-RNO-9769739);  (R-RNO-9769743);  (R-RNO-9935598)",
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        "function": "GP-Ib, a surface membrane protein of platelets, participates in the formation of platelet plugs by binding to the A1 domain of vWF, which is already bound to the subendothelium., [UniProtKB, UniProtKB, UniProtKB]",
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    },
    {
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        "protein_names_uniprotkb": "Uroplakin 3A",
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        "tax_id": 10116,
        "disease": "vesicoureteral reflux (Disease Ontology:DOID:9620)",
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        "go_cellular_component": "GO:0005886 plasma membrane;GO:0120001 apical plasma membrane urothelial plaque;GO:0016324 apical plasma membrane",
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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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        "protein_names_uniprotkb": "BICD family like cargo adaptor 1",
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        "protein_name": "Ecto-NOX disulfide-thiol exchanger 2",
        "gene_name": "Enox2",
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        "refseq_name": "ecto-NOX disulfide-thiol exchanger 2 isoform X1",
        "refseq_ac": "XP_017457884",
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        "gene_names_refseq": "Cova1; Enox2; RGD1563643",
        "protein_names_uniprotkb": "Ecto-NOX disulfide-thiol exchanger 2",
        "protein_names_refseq": "ecto-NOX disulfide-thiol exchanger 2 isoform X1",
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        "go_molecular_function": "GO:0003723 RNA binding;GO:0016491 oxidoreductase activity",
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    {
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        "protein_name": "Calponin",
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        "protein_names_uniprotkb": "Calponin",
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        "protein_name": "Diacylglycerol kinase",
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        "protein_names_uniprotkb": "Diacylglycerol kinase; 2.7.1.107; DAG kinase",
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        "ec_number_list": "2.7.1.107;2.7.1.94;2.7.1.138;2.7.1.93",
        "go_molecular_function": "GO:0004143 ATP-dependent diacylglycerol kinase activity;GO:0005524 ATP binding;GO:0008270 zinc ion binding;GO:0042803 protein homodimerization activity;GO:0046982 protein heterodimerization activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005905 clathrin-coated pit;GO:0031410 cytoplasmic vesicle",
        "go_biological_process": "GO:0046339 diacylglycerol metabolic process;GO:0006654 phosphatidic acid biosynthetic process;GO:0035556 intracellular signal transduction;GO:0007200 phospholipase C-activating G protein-coupled receptor signaling pathway;GO:0046486 glycerolipid metabolic process",
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    },
    {
        "uniprot_canonical_ac": "A0ABK0M5C7-1",
        "uniprot_id": "A0ABK0M5C7_RAT",
        "mass": 216890.0,
        "length": 1918,
        "protein_name": "Endoribonuclease Dicer",
        "gene_name": "Dicer1",
        "organism": "Rat",
        "refseq_name": "endoribonuclease Dicer",
        "refseq_ac": "NP_001414144",
        "gene_names_uniprotkb": "Dicer1",
        "gene_names_refseq": "Dicer1",
        "protein_names_uniprotkb": "Endoribonuclease Dicer; 3.1.26.3",
        "protein_names_refseq": "Dicer1, Dcr-1 homolog; dicer 1, ribonuclease type III; endoribonuclease Dicer",
        "tax_id": 10116,
        "disease": "multinodular goiter (Disease Ontology:DOID:0050489); diffuse large B-cell lymphoma (Disease Ontology:DOID:0050745); nephroma (Disease Ontology:DOID:0080615); DICER1 syndrome (Disease Ontology:DOID:0081063); stomach cancer (Disease Ontology:DOID:10534); DiGeorge syndrome (Disease Ontology:DOID:11198); dilated cardiomyopathy (Disease Ontology:DOID:12930); middle cerebral artery infarction (Disease Ontology:DOID:3525); pleuropulmonary blastoma (Disease Ontology:DOID:4769); hepatocellular carcinoma (Disease Ontology:DOID:684); colorectal cancer (Disease Ontology:DOID:9256)",
        "pathway": " (rno:299284);  (R-RNO-203927);  (R-RNO-426486)",
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        "function": "Double-stranded RNA (dsRNA) endoribonuclease playing a central role in short dsRNA-mediated post-transcriptional gene silencing. Cleaves naturally occurring long dsRNAs and short hairpin pre-microRNAs (miRNA) into fragments of twenty-one to twenty-three nucleotides with 3' overhang of two nucleotides, producing respectively short interfering RNAs (siRNA) and mature microRNAs. SiRNAs and miRNAs serve as guide to direct the RNA-induced silencing complex (RISC) to complementary RNAs to degrade them or prevent their translation. Gene silencing mediated by siRNAs, also called RNA interference, controls the elimination of transcripts from mobile and repetitive DNA elements of the genome but also the degradation of exogenous RNA of viral origin for instance. The miRNA pathway on the other side is a mean to specifically regulate the expression of target genes., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Granulosa cells (GCs) of PCOS, the expression of miR-9119, and targeted NFkappaB/p65-DICER axis are upregulated in order to maintain cell viability and prevent apoptosis, thereby promoting Anti-Mullerian hormone production in GCs., [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]",
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        "ec_number_list": "3.1.26.3;3.1.26.n2",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0003723 RNA binding;GO:0005524 ATP binding;GO:0046872 metal ion binding;GO:0004386 helicase activity",
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        "go_biological_process": "GO:0031054 pre-miRNA processing;GO:0030422 siRNA processing;GO:0006309 apoptotic DNA fragmentation;GO:0006396 RNA processing;GO:0031047 regulatory ncRNA-mediated gene silencing",
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    },
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        "protein_name": "Actin binding LIM protein family, member 3",
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        "gene_names_uniprotkb": "Ablim3",
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        "protein_names_uniprotkb": "Actin binding LIM protein family, member 3",
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        "go_molecular_function": "GO:0046872 metal ion binding;GO:0051015 actin filament binding;GO:0003779 actin binding",
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    },
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        "protein_name": "Sialic acid binding Ig-like lectin 5",
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        "gene_names_uniprotkb": "Siglec5",
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        "protein_names_uniprotkb": "Sialic acid binding Ig-like lectin 5",
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        "pathway": " (R-RNO-198933);  (R-RNO-6798695)",
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        "go_molecular_function": "GO:0030246 carbohydrate binding;GO:0033691 sialic acid binding",
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    },
    {
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        "protein_name": "CBFA2/RUNX1 partner transcriptional co-repressor 2",
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    {
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        "length": 534,
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        "function": "Skin-specific kinase that plays a key role in glycerol metabolism, catalyzing its phosphorylation to produce sn-glycerol 3-phosphate. Involved in skin-specific regulation of sterol regulatory element-binding protein (SREBP) processing and lipid biosynthesis., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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    {
        "uniprot_canonical_ac": "A0ABK0M5D5-1",
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        "protein_name": "Proteasome activator complex subunit 1",
        "gene_name": "Psme1-ps1",
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        "gene_names_uniprotkb": "Psme1-ps1",
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        "protein_names_uniprotkb": "Proteasome activator complex subunit 1; 11S regulator complex subunit alpha; Activator of multicatalytic protease subunit 1; Proteasome activator 28 subunit alpha",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0061133 endopeptidase activator activity",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0008537 proteasome activator complex",
        "go_biological_process": "GO:2000045 regulation of G1/S transition of mitotic cell cycle;GO:0061136 regulation of proteasomal protein catabolic process",
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    },
    {
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        "protein_name": "Mimecan",
        "gene_name": "Ogn",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ogn; LOC100910855",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Mimecan; Osteoglycin",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:291015);  (R-RNO-2022854);  (R-RNO-2022857)",
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        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Induces bone formation in conjunction with TGF-beta-1 or TGF-beta-2., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0008083 growth factor activity",
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    },
    {
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        "protein_name": "KLF transcription factor 13",
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        "refseq_name": "Krueppel-like factor 13",
        "refseq_ac": "NP_001425194",
        "gene_names_uniprotkb": "Klf13",
        "gene_names_refseq": "Klf13; RGD1565099",
        "protein_names_uniprotkb": "KLF transcription factor 13",
        "protein_names_refseq": "Krueppel-like factor 13; Kruppel-like factor 13",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:499171)",
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        "publication_count": 2,
        "publication_id_list": "29122578;29377979",
        "class_list": "",
        "function": "Data show that Kruppel-like factor 1 (KLF13) was a downstream target of miR-147b., [RefSeq, PubMed]; The improvement of cardiac function and structure elicited by miR-125b-5p is in part attributed to repression of the pro-apoptotic genes Bak1 and Klf13 in cardiomyocytes., [RefSeq, PubMed]",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0003677 DNA binding;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;GO:1990837 sequence-specific double-stranded DNA binding",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:1990859 cellular response to endothelin;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0008285 negative regulation of cell population proliferation;GO:0045944 positive regulation of transcription by RNA polymerase II",
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        "record_type": "protein"
    },
    {
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        "protein_name": "Leucine rich repeat and Ig domain containing 3",
        "gene_name": "Lingo3",
        "organism": "Rat",
        "refseq_name": "leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 3 precursor",
        "refseq_ac": "NP_001103079",
        "gene_names_uniprotkb": "Lingo3",
        "gene_names_refseq": "Lingo3",
        "protein_names_uniprotkb": "Leucine rich repeat and Ig domain containing 3",
        "protein_names_refseq": "leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 3 precursor; leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 3",
        "tax_id": 10116,
        "disease": "",
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        "go_molecular_function": "GO:0038023 signaling receptor activity",
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        "record_type": "protein"
    },
    {
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        "protein_name": "NADP-dependent oxidoreductase domain-containing protein 1",
        "gene_name": "Noxred1",
        "organism": "Rat",
        "refseq_name": "NADP-dependent oxidoreductase domain containing 1 isoform 1",
        "refseq_ac": "NP_001419050",
        "gene_names_uniprotkb": "Noxred1; LOC681924",
        "gene_names_refseq": "Noxred1",
        "protein_names_uniprotkb": "NADP-dependent oxidoreductase domain-containing protein 1",
        "protein_names_refseq": "NADP-dependent oxidoreductase domain containing 1 isoform 1; NADP-dependent oxidoreductase domain-containing protein 1",
        "tax_id": 10116,
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        "function": "Probable oxidoreductase., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_biological_process": "GO:0055129 L-proline biosynthetic process",
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        "record_type": "protein"
    },
    {
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        "protein_name": "Zic family member 2",
        "gene_name": "Zic2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Zic2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zic family member 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
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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:0003677 DNA binding;GO:0003700 DNA-binding transcription factor activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0016604 nuclear body",
        "go_biological_process": "GO:0006357 regulation of transcription by RNA polymerase II;GO:0007417 central nervous system development;GO:0007399 nervous system development;GO:0030154 cell differentiation;GO:0045944 positive regulation of transcription by RNA polymerase II",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0M462-1",
        "uniprot_id": "A0ABK0M462_RAT",
        "mass": 168179.0,
        "length": 1728,
        "protein_name": "Collagen type IV alpha 6 chain",
        "gene_name": "Col4a6",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Col4a6",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Collagen type IV alpha 6 chain",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "X-linked deafness 6 (Disease Ontology:DOID:0111740)",
        "pathway": " (rno:363458);  (R-RNO-1442490);  (R-RNO-1566977);  (R-RNO-1650814);  (R-RNO-2022090);  (R-RNO-216083);  (R-RNO-2243919);  (R-RNO-3000157);  (R-RNO-3000171)",
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        "class_list": "",
        "function": "Type IV collagen is the major structural component of glomerular basement membranes (GBM), forming a 'chicken-wire' meshwork together with laminins, proteoglycans and entactin/nidogen., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 4,
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        "go_molecular_function": "GO:0030020 extracellular matrix structural constituent conferring tensile strength;GO:0005201 extracellular matrix structural constituent",
        "go_cellular_component": "GO:0031012 extracellular matrix;GO:0005587 collagen type IV trimer;GO:0005604 basement membrane;GO:0005581 collagen trimer",
        "go_biological_process": "GO:0030198 extracellular matrix organization;GO:0038063 collagen-activated tyrosine kinase receptor signaling pathway;GO:0071230 cellular response to amino acid stimulus",
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        "record_id": "A0ABK0M462-1",
        "record_type": "protein"
    },
    {
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        "protein_name": "Ubiquitin carboxyl-terminal hydrolase MINDY",
        "gene_name": "Mindy4",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Mindy4; Fam188b",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ubiquitin carboxyl-terminal hydrolase MINDY; 3.4.19.12",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
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        "publication_id_list": "",
        "class_list": "",
        "function": "Hydrolase that can remove 'Lys-48'-linked conjugated ubiquitin from proteins., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Probable hydrolase that can remove 'Lys-48'-linked conjugated ubiquitin from proteins., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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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:0005829 cytosol",
        "go_biological_process": "GO:0006508 proteolysis;GO:0071108 protein K48-linked deubiquitination",
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    {
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        "length": 578,
        "protein_name": "Six6 opposite strand transcript 1",
        "gene_name": "Six6os1",
        "organism": "Rat",
        "refseq_name": "protein SIX6OS1 isoform X1",
        "refseq_ac": "XP_063118738",
        "gene_names_uniprotkb": "Six6os1",
        "gene_names_refseq": "Six6os1",
        "protein_names_uniprotkb": "Six6 opposite strand transcript 1",
        "protein_names_refseq": "protein SIX6OS1 isoform X1",
        "tax_id": 10116,
        "disease": "primary ovarian insufficiency 18 (Disease Ontology:DOID:0112269); spermatogenic failure 52 (Disease Ontology:DOID:0112270)",
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0000801 central element;GO:0005694 chromosome",
        "go_biological_process": "GO:0007283 spermatogenesis;GO:0048477 oogenesis;GO:0007129 homologous chromosome pairing at meiosis;GO:0010705 meiotic DNA double-strand break processing involved in reciprocal meiotic recombination;GO:0007130 synaptonemal complex assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0M7U0-1",
        "uniprot_id": "A0ABK0M7U0_RAT",
        "mass": 88612.0,
        "length": 777,
        "protein_name": "Inactive carboxypeptidase-like protein X2",
        "gene_name": "Cpxm2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Cpxm2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Inactive carboxypeptidase-like protein X2",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (rno:293566)",
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        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "May be involved in cell-cell interactions., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0004181 metallocarboxypeptidase activity",
        "go_cellular_component": "GO:0005576 extracellular region",
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        "hit_score": 0.1,
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    },
    {
        "uniprot_canonical_ac": "A0ABK0M6J6-1",
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        "length": 2375,
        "protein_name": "AT-rich interaction domain 1B",
        "gene_name": "Arid1b",
        "organism": "Rat",
        "refseq_name": "AT-rich interactive domain-containing protein 1B",
        "refseq_ac": "NP_001406731",
        "gene_names_uniprotkb": "Arid1b",
        "gene_names_refseq": "6A3-5; Arid1b; Smcf1; smcf-1",
        "protein_names_uniprotkb": "AT-rich interaction domain 1B",
        "protein_names_refseq": "AT rich interactive domain 1B (Swi1 like); AT-rich interactive domain-containing protein 1B; transcription factor 1",
        "tax_id": 10116,
        "disease": "autism spectrum disorder (Disease Ontology:DOID:0060041); Coffin-Siris syndrome 1 (Disease Ontology:DOID:0070042); Coffin-Siris syndrome 2 (Disease Ontology:DOID:0070044); intellectual disability (Disease Ontology:DOID:1059); hypertension (Disease Ontology:DOID:10763); alcohol use disorder (Disease Ontology:DOID:1574); cancer (Disease Ontology:DOID:162); Coffin-Siris syndrome (Disease Ontology:DOID:1925); ischemia (Disease Ontology:DOID:326); lung non-small cell carcinoma (Disease Ontology:DOID:3908); kidney disease (Disease Ontology:DOID:557); neuroblastoma (Disease Ontology:DOID:769)",
        "pathway": " (rno:282546);  (R-RNO-3214858);  (R-RNO-8939243);  (R-RNO-9933937);  (R-RNO-9934037)",
        "pathway_count": 5,
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        "publication_id_list": "14633620;16641100;34620277",
        "class_list": "",
        "function": "6A3-5 expression is associated with alpha-smooth muscle cell actin in mesangial cells, arteriolar smooth muscle cells, and interstitial myofibroblasts. could potentially be a novel early vascular marker of acute and chronic renal ischemic stress, [RefSeq, PubMed]; The molecular mechanism of the transcriptional activator SWI regulating gene ARID1B affecting swallowing dysfunction after stroke in rats., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0003700 DNA-binding transcription factor activity",
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        "go_biological_process": "GO:0006338 chromatin remodeling;GO:0006351 DNA-templated transcription;GO:0007399 nervous system development;GO:0006357 regulation of transcription by RNA polymerase II;GO:0045893 positive regulation of DNA-templated transcription",
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    },
    {
        "uniprot_canonical_ac": "A0ABK0M7R6-1",
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        "length": 317,
        "protein_name": "Zinc finger protein 330",
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        "organism": "Rat",
        "refseq_name": "zinc finger protein 330",
        "refseq_ac": "NP_001101913",
        "gene_names_uniprotkb": "Zfp330",
        "gene_names_refseq": "Zfp330",
        "protein_names_uniprotkb": "Zinc finger protein 330; Nucleolar autoantigen 36",
        "protein_names_refseq": "zinc finger protein 330",
        "tax_id": 10116,
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        "pathway": " (rno:361387)",
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        "go_molecular_function": "GO:0008270 zinc ion binding",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0M411-1",
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        "length": 415,
        "protein_name": "TNF receptor superfamily member 25",
        "gene_name": "Tnfrsf25",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Tnfrsf25",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "TNF receptor superfamily member 25",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:500592);  (R-RNO-5669034)",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0007165 signal transduction;GO:0006915 apoptotic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0M411-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0M5M7-1",
        "uniprot_id": "A0ABK0M5M7_RAT",
        "mass": 50352.0,
        "length": 463,
        "protein_name": "RCC1-like G exchanging factor-like protein",
        "gene_name": "Rcc1l",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Rcc1l; Wbscr16",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "RCC1-like G exchanging factor-like protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "Williams-Beuren syndrome (Disease Ontology:DOID:1928)",
        "pathway": " (rno:360796)",
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        "class_list": "",
        "function": "Guanine nucleotide exchange factor (GEF) for mitochondrial dynamin-related GTPase OPA1. Activates OPA1, by exchanging bound GDP for free GTP, and drives OPA1 and MFN1-dependent mitochondrial fusion. Plays an essential role in mitochondrial ribosome biogenesis. As a component of a functional protein-RNA module, consisting of RCC1L, NGRN, RPUSD3, RPUSD4, TRUB2, FASTKD2 and 16S mitochondrial ribosomal RNA (16S mt-rRNA), controls 16S mt-rRNA abundance and is required for intra-mitochondrial translation of core subunits of the oxidative phosphorylation system., [UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0005085 guanyl-nucleotide exchange factor activity;GO:0019843 rRNA binding",
        "go_cellular_component": "GO:0005743 mitochondrial inner membrane;GO:0005759 mitochondrial matrix;GO:0031966 mitochondrial membrane",
        "go_biological_process": "GO:0008053 mitochondrial fusion;GO:0061668 mitochondrial ribosome assembly;GO:1902775 mitochondrial large ribosomal subunit assembly;GO:0180026 mitochondrial small ribosomal subunit assembly",
        "synthesized_glycan_count": 0,
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        "record_id": "A0ABK0M5M7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0M5B7-1",
        "uniprot_id": "A0ABK0M5B7_RAT",
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        "length": 210,
        "protein_name": "B-cell CLL/lymphoma 7 protein family member A",
        "gene_name": "Bcl7a",
        "organism": "Rat",
        "refseq_name": "B-cell CLL/lymphoma 7 protein family member A",
        "refseq_ac": "NP_001385885",
        "gene_names_uniprotkb": "Bcl7a",
        "gene_names_refseq": "Bcl7a",
        "protein_names_uniprotkb": "B-cell CLL/lymphoma 7 protein family member A",
        "protein_names_refseq": "B-cell CLL/lymphoma 7 protein family member A; B-cell CLL/lymphoma 7A; BCL tumor suppressor 7A; BCL7A, BAF complex component",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-9933937);  (R-RNO-9933939);  (R-RNO-9933946);  (R-RNO-9933947);  (R-RNO-9934037)",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0016514 SWI/SNF complex",
        "go_biological_process": "GO:0007219 Notch signaling pathway;GO:0050890 cognition;GO:0097009 energy homeostasis;GO:0016055 Wnt signaling pathway;GO:0048168 regulation of neuronal synaptic plasticity",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0M5B7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0M8C7-1",
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        "length": 873,
        "protein_name": "F-box only protein 41",
        "gene_name": "Fbxo41",
        "organism": "Rat",
        "refseq_name": "F-box only protein 41",
        "refseq_ac": "NP_001101341",
        "gene_names_uniprotkb": "Fbxo41",
        "gene_names_refseq": "Fbxo41; RGD1566130",
        "protein_names_uniprotkb": "F-box only protein 41",
        "protein_names_refseq": "F-box only protein 41",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:312504);  (R-RNO-8951664);  (R-RNO-983168)",
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        "publication_id_list": "16641100;22673903;38843836",
        "class_list": "",
        "function": "Substrate-recognition component of the SCF (SKP1-CUL1-F-box protein)-type E3 ubiquitin ligase complex., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "protein_names_uniprotkb": "Zinc finger protein 709 like",
        "protein_names_refseq": "",
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        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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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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    },
    {
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        "length": 1754,
        "protein_name": "Centrosomal protein 152",
        "gene_name": "Cep152",
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        "gene_names_uniprotkb": "Cep152",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Centrosomal protein 152",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "Seckel syndrome 5 (Disease Ontology:DOID:0070012); primary autosomal recessive microcephaly 9 (Disease Ontology:DOID:0070292)",
        "pathway": " (rno:311391);  (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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    },
    {
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        "protein_name": "Cerebellar degeneration-related antigen 1",
        "gene_name": "ENSRNOG00000063675",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "ENSRNOG00000063675",
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        "protein_names_uniprotkb": "Cerebellar degeneration-related antigen 1",
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    },
    {
        "uniprot_canonical_ac": "A0ABK0M4M7-1",
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        "length": 389,
        "protein_name": "26S proteasome non-ATPase regulatory subunit 6",
        "gene_name": "Psmd6",
        "organism": "Rat",
        "refseq_name": "26S proteasome non-ATPase regulatory subunit 6",
        "refseq_ac": "NP_942025",
        "gene_names_uniprotkb": "Psmd6",
        "gene_names_refseq": "P44s10; Psmd6",
        "protein_names_uniprotkb": "26S proteasome non-ATPase regulatory subunit 6; 26S proteasome regulatory subunit RPN7; 26S proteasome regulatory subunit S10; p42A",
        "protein_names_refseq": "26S proteasome non-ATPase regulatory subunit 6; proteasome (prosome, macropain) 26S subunit, non-ATPase, 6; proteasome regulatory particle subunit p44S10; proteasome, 26S, non-ATPase regulatory subunit 6",
        "tax_id": 10116,
        "disease": "neurodegenerative disease (Disease Ontology:DOID:1289)",
        "pathway": " (rno:289924);  (R-RNO-1169091);  (R-RNO-1234176);  (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-6798695);  (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-9929356);  (R-RNO-9929491);  (R-RNO-9931269);  (R-RNO-9932298);  (R-RNO-9954709)",
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        "function": "Component of the 26S proteasome, a multiprotein complex involved in the ATP-dependent degradation of ubiquitinated proteins. This complex plays a key role in the maintenance of protein homeostasis by removing misfolded or damaged proteins, which could impair cellular functions, and by removing proteins whose functions are no longer required. Therefore, the proteasome participates in numerous cellular processes, including cell cycle progression, apoptosis, or DNA damage repair., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005838 proteasome regulatory particle;GO:0022624 proteasome accessory complex;GO:0000502 proteasome complex",
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    },
    {
        "uniprot_canonical_ac": "A0ABK0M3P9-1",
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        "mass": 27241.0,
        "length": 255,
        "protein_name": "Ring finger protein 223",
        "gene_name": "Rnf223",
        "organism": "Rat",
        "refseq_name": "RING finger protein 223",
        "refseq_ac": "NP_001385896",
        "gene_names_uniprotkb": "Rnf223",
        "gene_names_refseq": "Rnf223",
        "protein_names_uniprotkb": "Ring finger protein 223",
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        "tax_id": 10116,
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        "pathway": " (rno:680874)",
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    {
        "uniprot_canonical_ac": "A0ABK0M635-1",
        "uniprot_id": "A0ABK0M635_RAT",
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        "length": 930,
        "protein_name": "Transient receptor potential cation channel, subfamily C, member 6",
        "gene_name": "Trpc6",
        "organism": "Rat",
        "refseq_name": "short transient receptor potential channel 6",
        "refseq_ac": "NP_446011",
        "gene_names_uniprotkb": "Trpc6",
        "gene_names_refseq": "Trpc6; Trrp6",
        "protein_names_uniprotkb": "Transient receptor potential cation channel, subfamily C, member 6",
        "protein_names_refseq": "short transient receptor potential channel 6; transient receptor protein 6",
        "tax_id": 10116,
        "disease": "nephrotic syndrome type 2 (Disease Ontology:DOID:0080379); focal segmental glomerulosclerosis 2 (Disease Ontology:DOID:0111129); focal segmental glomerulosclerosis (Disease Ontology:DOID:1312); transient cerebral ischemia (Disease Ontology:DOID:224); kidney disease (Disease Ontology:DOID:557); proteinuria (Disease Ontology:DOID:576); pulmonary hypertension (Disease Ontology:DOID:6432); chronic fatigue syndrome (Disease Ontology:DOID:8544); type 2 diabetes mellitus (Disease Ontology:DOID:9352)",
        "pathway": " (rno:89823)",
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        "publication_id_list": "22673903;37002575;37093422;37178933;37980653;38330925",
        "class_list": "",
        "function": "Alpha1-Adrenergic Stimulation Increases Platelet Adhesion to Endothelial Cells Mediated by TRPC6., [RefSeq, PubMed]; Interruption of TRPC6-NFATC1 signaling inhibits NADPH oxidase 4 and VSMCs phenotypic switch in intracranial aneurysm., [RefSeq, PubMed]; Klotho Stabilizes the Podocyte Actin Cytoskeleton in Idiopathic Membranous Nephropathy through Regulating the TRPC6/CatL Pathway., [RefSeq, PubMed]; Renal ischaemia-reperfusion injury is promoted by transcription factor NF-kB p65, which inhibits TRPC6 expression by activating miR-150., [RefSeq, PubMed]; TRPC6 promotes daunorubicin-induced mitochondrial fission and cell death in rat cardiomyocytes with the involvement of ERK1/2-DRP1 activation., [RefSeq, PubMed]",
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        "go_biological_process": "GO:0007204 positive regulation of cytosolic calcium ion concentration;GO:0010800 positive regulation of peptidyl-threonine phosphorylation;GO:0045666 positive regulation of neuron differentiation;GO:0071456 cellular response to hypoxia;GO:0050774 negative regulation of dendrite morphogenesis",
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        "protein_name": "Myelin oligodendrocyte glycoprotein",
        "gene_name": "Mog",
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        "gene_names_uniprotkb": "Mog",
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        "protein_names_uniprotkb": "Myelin oligodendrocyte glycoprotein",
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        "pathway": "",
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        "function": "Minor component of the myelin sheath. May be involved in completion and/or maintenance of the myelin sheath and in cell-cell communication. Mediates homophilic cell-cell adhesion., [UniProtKB, UniProtKB]",
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        "protein_name": "Hyaluronidase",
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        "gene_names_uniprotkb": "Hyal3",
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        "protein_names_uniprotkb": "Hyaluronidase; 3.2.1.35",
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        "tax_id": 10116,
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        "function": "Facilitates sperm penetration into the layer of cumulus cells surrounding the egg by digesting hyaluronic acid. Involved in induction of the acrosome reaction in the sperm. Involved in follicular atresia, the breakdown of immature ovarian follicles that are not selected to ovulate. Induces ovarian granulosa cell apoptosis, possibly via apoptotic signaling pathway involving CASP8 and CASP3 activation, and poly(ADP-ribose) polymerase (PARP) cleavage. Has no hyaluronidase activity in embryonic fibroblasts in vitro. Has no hyaluronidase activity in granulosa cells in vitro., [UniProtKB, UniProtKB]",
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        "go_biological_process": "GO:0005975 carbohydrate metabolic process;GO:0007338 single fertilization;GO:0030214 hyaluronan catabolic process;GO:0071493 cellular response to UV-B;GO:2000355 negative regulation of ovarian follicle development",
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    {
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        "length": 251,
        "protein_name": "Apoptosis regulator Bcl-2",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Bcl2",
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        "protein_names_uniprotkb": "Apoptosis regulator Bcl-2",
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        "tax_id": 10116,
        "disease": "tongue squamous cell carcinoma (Disease Ontology:DOID:0050865); follicular lymphoma (Disease Ontology:DOID:0050873); ductal carcinoma in situ (Disease Ontology:DOID:0060074); brain glioma (Disease Ontology:DOID:0060108); oligomeganephronia (Disease Ontology:DOID:0111142); prostate cancer (Disease Ontology:DOID:10283); stomach cancer (Disease Ontology:DOID:10534); Alzheimer's disease (Disease Ontology:DOID:10652); hypertension (Disease Ontology:DOID:10763); gastric ulcer (Disease Ontology:DOID:10808); intracranial aneurysm (Disease Ontology:DOID:10941); urinary bladder cancer (Disease Ontology:DOID:11054); osteoporosis (Disease Ontology:DOID:11476); polycystic ovary syndrome (Disease Ontology:DOID:11612); hypertrophic cardiomyopathy (Disease Ontology:DOID:11984); leiomyoma (Disease Ontology:DOID:127); Huntington's disease (Disease Ontology:DOID:12858); dilated cardiomyopathy (Disease Ontology:DOID:12930); dementia (Disease Ontology:DOID:1307); abdominal obesity-metabolic syndrome 1 (Disease Ontology:DOID:14221); glaucoma (Disease Ontology:DOID:1686); squamous cell carcinoma (Disease Ontology:DOID:1749); status epilepticus (Disease Ontology:DOID:1824); impotence (Disease Ontology:DOID:1875); melanoma (Disease Ontology:DOID:1909); atherosclerosis (Disease Ontology:DOID:1936); post-traumatic stress disorder (Disease Ontology:DOID:2055); colon cancer (Disease Ontology:DOID:219); transient cerebral ischemia (Disease Ontology:DOID:224); brain ischemia (Disease Ontology:DOID:2316); colon adenocarcinoma (Disease Ontology:DOID:234); morphine dependence (Disease Ontology:DOID:2560); transitional cell carcinoma (Disease Ontology:DOID:2671); bilirubin metabolic disorder (Disease Ontology:DOID:2741); endometriosis (Disease Ontology:DOID:289); acute kidney failure (Disease Ontology:DOID:3021); middle cerebral artery infarction (Disease Ontology:DOID:3525); plasmacytoma (Disease Ontology:DOID:3721); renal cell carcinoma (Disease Ontology:DOID:4450); allergic rhinitis (Disease Ontology:DOID:4481); anti-basement membrane glomerulonephritis (Disease Ontology:DOID:4780); esophagus adenocarcinoma (Disease Ontology:DOID:4914); intestinal disease (Disease Ontology:DOID:5295); lung small cell carcinoma (Disease Ontology:DOID:5409); congestive heart failure (Disease Ontology:DOID:6000); pulmonary hypertension (Disease Ontology:DOID:6432); hepatocellular carcinoma (Disease Ontology:DOID:684); end stage renal disease (Disease Ontology:DOID:783); osteoarthritis (Disease Ontology:DOID:8398); retinal degeneration (Disease Ontology:DOID:8466); cervix uteri carcinoma in situ (Disease Ontology:DOID:8991); acute myeloid leukemia (Disease Ontology:DOID:9119); nasopharynx carcinoma (Disease Ontology:DOID:9261); priapism (Disease Ontology:DOID:9286); type 2 diabetes mellitus (Disease Ontology:DOID:9352); oral mucosa leukoplakia (Disease Ontology:DOID:9655); acute lymphoblastic leukemia (Disease Ontology:DOID:9952); obesity (Disease Ontology:DOID:9970)",
        "pathway": "",
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        "class_list": "",
        "function": "Suppresses apoptosis in a variety of cell systems including factor-dependent lymphohematopoietic and neural cells. Regulates cell death by controlling the mitochondrial membrane permeability. Appears to function in a feedback loop system with caspases. Inhibits caspase activity either by preventing the release of cytochrome c from the mitochondria and/or by binding to the apoptosis-activating factor (APAF-1). Also acts as an inhibitor of autophagy: interacts with BECN1 and AMBRA1 during non-starvation conditions and inhibits their autophagy function. May attenuate inflammation by impairing NLRP1-inflammasome activation, hence CASP1 activation and IL1B release., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "go_molecular_function": "GO:0060090 molecular adaptor activity;GO:0002020 protease binding;GO:0042802 identical protein binding;GO:0046982 protein heterodimerization activity;GO:0031625 ubiquitin protein ligase binding",
        "go_cellular_component": "GO:0005741 mitochondrial outer membrane;GO:0031965 nuclear membrane;GO:0005789 endoplasmic reticulum membrane;GO:0005634 nucleus;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0043066 negative regulation of apoptotic process;GO:0006915 apoptotic process;GO:0008406 gonad development;GO:0002260 lymphocyte homeostasis;GO:0002360 T cell lineage commitment",
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        "hit_score": 0.1,
        "record_id": "A0ABK0M473-1",
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    },
    {
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        "length": 570,
        "protein_name": "Nuclear factor 1",
        "gene_name": "Nfib",
        "organism": "Rat",
        "refseq_name": "nuclear factor 1 B-type isoform 4",
        "refseq_ac": "NP_001416496",
        "gene_names_uniprotkb": "Nfib",
        "gene_names_refseq": "Nfib",
        "protein_names_uniprotkb": "Nuclear factor 1",
        "protein_names_refseq": "nuclear factor 1 B-type isoform 4; nuclear factor 1 B-type; olfactory epithelium nuclear factor I-B",
        "tax_id": 10116,
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        "publication_id_list": "33275244;33506922",
        "class_list": "",
        "function": "Inhibition of microRNA-346 inhibits myocardial inflammation and apoptosis after myocardial infarction via targeting NFIB., [RefSeq, PubMed]; Inhibition of microRNA-495 inhibits hypoxia-induced apoptosis in H9c2 cells via targeting NFIB., [RefSeq, PubMed]; 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]",
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0003700 DNA-binding transcription factor activity;GO:0003690 double-stranded 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:0001650 fibrillar center;GO:0044300 cerebellar mossy fiber",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006260 DNA replication;GO:0045893 positive regulation of DNA-templated transcription;GO:0031099 regeneration;GO:0000122 negative regulation of transcription by RNA polymerase II",
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    {
        "uniprot_canonical_ac": "A0ABK0M440-1",
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        "length": 184,
        "protein_name": "Lipocalin 3",
        "gene_name": "Lcn3",
        "organism": "Rat",
        "refseq_name": "lipocalin 3 precursor",
        "refseq_ac": "NP_001417738",
        "gene_names_uniprotkb": "Lcn3",
        "gene_names_refseq": "Lcn3; RGD1562745",
        "protein_names_uniprotkb": "Lipocalin 3",
        "protein_names_refseq": "lipocalin 3 precursor; vomeronasal secretory protein 1",
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        "protein_name": "Vomeronasal type-1 receptor",
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        "disease": "biliary tract benign neoplasm (Disease Ontology:DOID:0050625); mucositis (Disease Ontology:DOID:0080178); Coronavirus infectious disease (Disease Ontology:DOID:0080599); otitis media (Disease Ontology:DOID:10754); allergic conjunctivitis (Disease Ontology:DOID:11204); corneal neovascularization (Disease Ontology:DOID:11382); pancreatic cancer (Disease Ontology:DOID:1793); mucinous adenocarcinoma (Disease Ontology:DOID:3030); pancreatic ductal carcinoma (Disease Ontology:DOID:3587); lung carcinoma (Disease Ontology:DOID:3905); lung adenocarcinoma (Disease Ontology:DOID:3910); common bile duct neoplasm (Disease Ontology:DOID:4608); cholangiocarcinoma (Disease Ontology:DOID:4947)",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 1,
        "publication_id_list": "20054827",
        "class_list": "",
        "function": "Muc4 precursor is synthesized in all layers of the corneal epithelium, but Muc4 is degraded in basal and intermediate layers by a proteosomal mechanism at least partly dependent on TGF-beta inhibition of Muc4 processing., [RefSeq, PubMed]",
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        "go_cellular_component": "GO:0005615 extracellular space;GO:0016324 apical plasma membrane;GO:0032991 protein-containing complex;GO:0031528 microvillus membrane",
        "go_biological_process": "GO:0032869 cellular response to insulin stimulus;GO:0043066 negative regulation of apoptotic process;GO:0030277 maintenance of gastrointestinal epithelium;GO:0007160 cell-matrix adhesion;GO:0001953 negative regulation of cell-matrix adhesion",
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        "protein_name": "Disks large homolog 5 N-terminal domain-containing protein",
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        "protein_names_uniprotkb": "Disks large homolog 5 N-terminal domain-containing protein",
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        "length": 306,
        "protein_name": "Olfactory receptor",
        "gene_name": "Olfr1277",
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        "gene_names_uniprotkb": "Olfr1277",
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        "protein_names_uniprotkb": "Olfactory receptor",
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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": "",
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        "hit_score": 0.1,
        "record_id": "A0ABK0M451-1",
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    },
    {
        "uniprot_canonical_ac": "A0ABK0M454-1",
        "uniprot_id": "A0ABK0M454_RAT",
        "mass": 33815.0,
        "length": 296,
        "protein_name": "Adrenocorticotropic hormone receptor",
        "gene_name": "Mc2r",
        "organism": "Rat",
        "refseq_name": "adrenocorticotropic hormone receptor",
        "refseq_ac": "NP_001093961",
        "gene_names_uniprotkb": "Mc2r",
        "gene_names_refseq": "Mc2r",
        "protein_names_uniprotkb": "Adrenocorticotropic hormone receptor; Adrenocorticotropin receptor; Melanocortin receptor 2",
        "protein_names_refseq": "adrenocorticotropic hormone receptor; melanocortin 2 receptor (adrenocorticotropic hormone)",
        "tax_id": 10116,
        "disease": "West syndrome (Disease Ontology:DOID:0050562); glucocorticoid deficiency 1 (Disease Ontology:DOID:0080621); toxic shock syndrome (Disease Ontology:DOID:14115)",
        "pathway": " (rno:282839)",
        "pathway_count": 1,
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        "publication_id_list": "26868281;29140411;29943847",
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        "function": "Data suggest that increases in adrenal blood flow induced by Ang II (angiotensin II)/Agtr2 signaling are mediated by release of nitric oxide and EETs (epoxyeicosatrienoic acids); increases in adrenal blood flow with ACTH (adrenocorticotropic hormone)/Mc2r receptor signaling are mediated by EETs only. (Agtr2 = angiotensin II receptor; Mc2r = ACTH receptor), [RefSeq, PubMed]; G protein-coupled receptor for corticotropin/ACTH, primarily expressed in adrenal cortex where it plays a key role in the regulation of adrenocortical function. Upon activation, couples to G(s) protein, stimulating adenylate cyclase and activating the cAMP-dependent signaling pathway, the MAPK cascade as well as the PKA pathway, leading to steroidogenic factor 1/NR5A1-mediated transcriptional activation. Activation by ACTH facilitates the release of adrenal glucocorticoids, including cortisol and corticosterone. In addition, MC2R is required for fetal and neonatal adrenal gland development., [UniProtKB, UniProtKB]; Overfeeding during a critical postnatal period exacerbates hypothalamic-pituitary-adrenal axis responses to immune challenge: a role for adrenal melanocortin 2 receptors. Publication Status: Online-Only, [RefSeq, PubMed]; The data demonstrated that the abnormal proliferation of vascular smooth muscle cells induced by conditions of high cyclic strain is in part attributed to ACTH and its receptor MC2R., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0004978 corticotropin receptor activity",
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        "record_id": "A0ABK0M454-1",
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        "protein_name": "Ig-like domain-containing protein",
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        "protein_name": "Ig-like domain-containing protein",
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        "length": 661,
        "protein_name": "Signal recognition particle subunit SRP72",
        "gene_name": "AABR07002546.1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "AABR07002546.1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Signal recognition particle subunit SRP72",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "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). The SRP complex interacts with the signal sequence in nascent secretory and membrane proteins and directs them to the membrane of the ER. The SRP complex targets the ribosome-nascent chain complex to the SRP receptor (SR), which is anchored in the ER, where SR compaction and GTPase rearrangement drive cotranslational protein translocation into the ER. Binds the signal recognition particle RNA (7SL RNA) in presence of SRP68. Can bind 7SL RNA with low affinity. The SRP complex possibly participates in the elongation arrest function., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0008312 7S RNA binding",
        "go_cellular_component": "GO:0005786 signal recognition particle, endoplasmic reticulum targeting;GO:0005783 endoplasmic reticulum",
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    {
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        "length": 309,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or2a52",
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        "refseq_name": "olfactory receptor family 2 subfamily A member 52",
        "refseq_ac": "NP_001102817",
        "gene_names_uniprotkb": "Or2a52",
        "gene_names_refseq": "Olr437; Or2a52",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 437; olfactory receptor family 2 subfamily A member 52",
        "tax_id": 10116,
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        "go_cellular_component": "GO:0005743 mitochondrial inner membrane",
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    },
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        "protein_name": "Olfactory receptor",
        "gene_name": "Or1f33",
        "organism": "Rat",
        "refseq_name": "olfactory receptor 1378",
        "refseq_ac": "NP_999993",
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        "gene_names_refseq": "Olr1378; Or1f33",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 1378; olfactory receptor gene Olr1378",
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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_name": "splicing factor YJU2-like",
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        "gene_names_uniprotkb": "LOC134479427; YJU2",
        "gene_names_refseq": "LOC134479427",
        "protein_names_uniprotkb": "Splicing factor YJU2",
        "protein_names_refseq": "splicing factor YJU2-like",
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        "function": "Part of the spliceosome which catalyzes two sequential transesterification reactions, first the excision of the non-coding intron from pre-mRNA and then the ligation of the coding exons to form the mature mRNA. Plays a role in stabilizing the structure of the spliceosome catalytic core and docking of the branch helix into the active site, producing 5'-exon and lariat intron-3'-intermediates. May protect cells from TP53-dependent apoptosis upon dsDNA break damage through association with PRP19-CD5L complex., [UniProtKB, HAMAP]",
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        "length": 274,
        "protein_name": "Vomeronasal type-1 receptor",
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        "organism": "Rat",
        "refseq_name": "vomeronasal 1 receptor 99",
        "refseq_ac": "NP_001160232",
        "gene_names_uniprotkb": "Vom1r99",
        "gene_names_refseq": "Vom1r-ps113; Vom1r99",
        "protein_names_uniprotkb": "Vomeronasal type-1 receptor",
        "protein_names_refseq": "vomeronasal 1 receptor 99; vomeronasal 1 receptor Vom1r99; vomeronasal 1 receptor pseudogene 113",
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        "length": 509,
        "protein_name": "non-specific serine/threonine protein kinase",
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        "gene_names_uniprotkb": "LOC134485071",
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        "protein_names_uniprotkb": "non-specific serine/threonine protein kinase; 2.7.11.1",
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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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    {
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        "protein_name": "Ig-like domain-containing protein",
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        "go_cellular_component": "GO:0005576 extracellular region;GO:0019814 immunoglobulin complex",
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        "record_id": "A0ABK0M649-1",
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        "protein_name": "Golgi apparatus membrane protein TVP23 homolog",
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        "organism": "Rat",
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        "gene_names_uniprotkb": "Tvp23a",
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        "protein_names_uniprotkb": "Golgi apparatus membrane protein TVP23 homolog",
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    },
    {
        "uniprot_canonical_ac": "A0ABK0M8V0-1",
        "uniprot_id": "A0ABK0M8V0_RAT",
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        "length": 356,
        "protein_name": "protein-serine/threonine phosphatase",
        "gene_name": "Ctdsp2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ctdsp2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "protein-serine/threonine phosphatase; 3.1.3.16",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway_count": 0,
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        "function": "Preferentially catalyzes the dephosphorylation of 'Ser-5' within the tandem 7 residue repeats in the C-terminal domain (CTD) of the largest RNA polymerase II subunit POLR2A. Negatively regulates RNA polymerase II transcription, possibly by controlling the transition from initiation/capping to processive transcript elongation. Recruited by REST to neuronal genes that contain RE-1 elements, leading to neuronal gene silencing in non-neuronal cells., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "ec_number_list": "3.1.3.16;3.1.3.48;3.1.3.53;3.1.3.52;3.1.3.67;3.1.3.-;3.1.3.27;2.7.11.22;3.1.3.74",
        "go_molecular_function": "GO:0008420 RNA polymerase II CTD heptapeptide repeat phosphatase activity",
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        "go_biological_process": "GO:0001933 negative regulation of protein phosphorylation;GO:0006470 protein dephosphorylation;GO:2000134 negative regulation of G1/S transition of mitotic cell cycle",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABZ3NNQ8-1",
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        "length": 318,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or13c7c",
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        "refseq_name": "olfactory receptor Olr839",
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        "gene_names_uniprotkb": "Or13c7c; Or13c7b",
        "gene_names_refseq": "Olr839; Or13c7c",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 839; olfactory receptor Olr839; olfactory receptor gene Olr839",
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        "disease": "",
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        "function": "Odorant receptor., [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_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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        "record_id": "A0ABZ3NNQ8-1",
        "record_type": "protein"
    },
    {
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        "protein_name": "Inhibitor of nuclear factor kappa-B kinase subunit epsilon",
        "gene_name": "Ikbke",
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        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ikbke",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Inhibitor of nuclear factor kappa-B kinase subunit epsilon; 2.7.11.10; Inducible I kappa-B kinase",
        "protein_names_refseq": "",
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        "pathway": " (rno:363984);  (R-RNO-4755510);  (R-RNO-5357786);  (R-RNO-5357905);  (R-RNO-936440);  (R-RNO-936964);  (R-RNO-9824878);  (R-RNO-9860927)",
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        "ec_number_list": "2.3.2.27;2.7.11.10;2.7.11.1;2.3.2.31;3.1.3.48;2.3.2.-;3.4.19.12",
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        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005634 nucleus;GO:0005829 cytosol;GO:0031966 mitochondrial membrane;GO:0016605 PML body",
        "go_biological_process": "GO:0002218 activation of innate immune response;GO:0032481 positive regulation of type I interferon production;GO:0010628 positive regulation of gene expression;GO:0006955 immune response;GO:0048255 mRNA stabilization",
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    },
    {
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        "protein_name": "Zinc finger protein 248",
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        "gene_names_uniprotkb": "Zfp248; Zfp9; Znf248",
        "gene_names_refseq": "RGD1561270; Zfp248; Znf248",
        "protein_names_uniprotkb": "Zinc finger protein 248",
        "protein_names_refseq": "zinc finger protein 248",
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        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB, UniProtKB]",
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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:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0006357 regulation of transcription by RNA polymerase II;GO:0006355 regulation of DNA-templated transcription",
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        "record_id": "A0ABZ3NNW1-1",
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    },
    {
        "uniprot_canonical_ac": "A0ABK0M9W7-1",
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        "length": 799,
        "protein_name": "Zinc finger protein X-linked",
        "gene_name": "Zfx",
        "organism": "Rat",
        "refseq_name": "zinc finger X-chromosomal protein",
        "refseq_ac": "NP_001102487",
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        "gene_names_refseq": "RGD1562664; Zfx",
        "protein_names_uniprotkb": "Zinc finger protein X-linked",
        "protein_names_refseq": "zinc finger X-chromosomal protein",
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        "disease": "syndromic X-linked intellectual disability (Disease Ontology:DOID:0060309)",
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        "go_molecular_function": "GO:0003677 DNA binding;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",
        "go_cellular_component": "GO:0005634 nucleus;GO:0000785 chromatin",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006355 regulation of DNA-templated transcription;GO:0007281 germ cell development;GO:0060746 parental behavior;GO:0006357 regulation of transcription by RNA polymerase II",
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        "hit_score": 0.2,
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0M9P9-1",
        "uniprot_id": "A0ABK0M9P9_RAT",
        "mass": 125517.0,
        "length": 1130,
        "protein_name": "AP-4 complex subunit epsilon",
        "gene_name": "Ap4e1",
        "organism": "Rat",
        "refseq_name": "AP-4 complex subunit epsilon-1",
        "refseq_ac": "NP_001178671",
        "gene_names_uniprotkb": "Ap4e1",
        "gene_names_refseq": "Ap4e1; RGD1562199",
        "protein_names_uniprotkb": "AP-4 complex subunit epsilon",
        "protein_names_refseq": "AP-4 complex subunit epsilon-1; adaptor-related protein complex 4, epsilon 1 subunit; adaptor-related protein complex AP-4, epsilon 1",
        "tax_id": 10116,
        "disease": "stuttering (Disease Ontology:DOID:0060243); hereditary spastic paraplegia 51 (Disease Ontology:DOID:0110803)",
        "pathway": " (rno:311404);  (R-RNO-432720);  (R-RNO-432722)",
        "pathway_count": 3,
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        "class_list": "",
        "function": "Component of the adaptor protein complex 4 (AP-4). Adaptor protein complexes are vesicle coat components involved both in vesicle formation and cargo selection. They control the vesicular transport of proteins in different trafficking pathways. AP-4 forms a non clathrin-associated coat on vesicles departing the trans-Golgi network (TGN) and may be involved in the targeting of proteins from the trans-Golgi network (TGN) to the endosomal-lysosomal system. It is also involved in protein sorting to the basolateral membrane in epithelial cells and the proper asymmetric localization of somatodendritic proteins in neurons. AP-4 is involved in the recognition and binding of tyrosine-based sorting signals found in the cytoplasmic part of cargos, but may also recognize other types of sorting signal., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0140312 cargo adaptor activity",
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        "hit_score": 0.2,
        "record_id": "A0ABK0M9P9-1",
        "record_type": "protein"
    },
    {
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        "length": 355,
        "protein_name": "Vasohibin 2",
        "gene_name": "Vash2",
        "organism": "Rat",
        "refseq_name": "tubulinyl-Tyr carboxypeptidase 2 isoform 2",
        "refseq_ac": "NP_001381302",
        "gene_names_uniprotkb": "Vash2",
        "gene_names_refseq": "RGD1564105; Vash2",
        "protein_names_uniprotkb": "Vasohibin 2",
        "protein_names_refseq": "tubulinyl-Tyr carboxypeptidase 2 isoform 2; tubulinyl-Tyr carboxypeptidase 2",
        "tax_id": 10116,
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        "go_molecular_function": "GO:0003779 actin binding;GO:0008017 microtubule binding;GO:0004181 metallocarboxypeptidase activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0000768 syncytium formation by plasma membrane fusion;GO:0006508 proteolysis;GO:0045766 positive regulation of angiogenesis;GO:0001938 positive regulation of endothelial cell proliferation;GO:0045765 regulation of angiogenesis",
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    {
        "uniprot_canonical_ac": "A0ABK0M9B1-1",
        "uniprot_id": "A0ABK0M9B1_RAT",
        "mass": 176206.0,
        "length": 1561,
        "protein_name": "DNA excision repair protein ERCC-6-like 2",
        "gene_name": "Ercc6l2",
        "organism": "Rat",
        "refseq_name": "DNA excision repair protein ERCC-6-like 2 isoform X1",
        "refseq_ac": "XP_038952187",
        "gene_names_uniprotkb": "Ercc6l2",
        "gene_names_refseq": "Ercc6l2; RGD1561537",
        "protein_names_uniprotkb": "DNA excision repair protein ERCC-6-like 2; DNA repair and recombination protein RAD26-like",
        "protein_names_refseq": "DNA excision repair protein ERCC-6-like 2 isoform X1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:361197)",
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        "publication_id_list": "",
        "class_list": "",
        "function": "Promotes double-strand break (DSB) end-joining and facilitates programmed recombination by controlling how DNA ends are joined in a spatially oriented manner during repair. Also plays a role in DNA repair by restricting DNA end resection in double strand break (DSB) repair. Facilitates replication of complex DNA regions and regulates the maintenance of chromatin structure., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "ec_number_list": "",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0005524 ATP binding;GO:0016787 hydrolase activity;GO:0004386 helicase activity;GO:0019901 protein kinase binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005739 mitochondrion;GO:0005813 centrosome;GO:0000775 chromosome, centromeric region;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0097680 double-strand break repair via classical nonhomologous end joining;GO:0036297 interstrand cross-link repair;GO:0006974 DNA damage response;GO:0034614 cellular response to reactive oxygen species",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0M9B1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0M9W1-1",
        "uniprot_id": "A0ABK0M9W1_RAT",
        "mass": 15022.0,
        "length": 127,
        "protein_name": "Ribosomal protein L32 like 3",
        "gene_name": "Rpl32l3",
        "organism": "Rat",
        "refseq_name": "large ribosomal subunit protein eL32-like",
        "refseq_ac": "XP_038967055",
        "gene_names_uniprotkb": "Rpl32l3; LOC688684",
        "gene_names_refseq": "Rpl32l3",
        "protein_names_uniprotkb": "Ribosomal protein L32 like 3",
        "protein_names_refseq": "large ribosomal subunit protein eL32-like",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:688684)",
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        "biomarker_type": "",
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        "go_molecular_function": "GO:0003735 structural constituent of ribosome",
        "go_cellular_component": "GO:0022625 cytosolic large ribosomal subunit;GO:0005737 cytoplasm;GO:0005840 ribosome;GO:1990904 ribonucleoprotein complex",
        "go_biological_process": "GO:0006412 translation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0M9W1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A6JNN4-1",
        "uniprot_id": "ICAM5_RAT",
        "mass": 96905.0,
        "length": 917,
        "protein_name": "Intercellular adhesion molecule 5",
        "gene_name": "Icam5",
        "organism": "Rat",
        "refseq_name": "intercellular adhesion molecule 5 precursor",
        "refseq_ac": "NP_001165550",
        "gene_names_uniprotkb": "Icam5; Tlcn",
        "gene_names_refseq": "ICAM-5; Icam5",
        "protein_names_uniprotkb": "Intercellular adhesion molecule 5; ICAM-5; Telencephalin",
        "protein_names_refseq": "intercellular adhesion molecule 5 precursor; intercellular adhesion molecule 5, telencephalin",
        "tax_id": 10116,
        "disease": "dilated cardiomyopathy (Disease Ontology:DOID:12930)",
        "pathway": " (rno:313785);  (R-RNO-198933);  (R-RNO-216083)",
        "pathway_count": 3,
        "publication_count": 7,
        "publication_id_list": "10741396;10893271;18223167;19733219;22187327;24090084;38843836",
        "class_list": "",
        "function": "Cell adhesion molecule that functions as a receptor ligand of the signaling receptor ITGAL:ITGB2/LFA-1 (lymphocyte-function associated (LFA) molecule 1) ensuring neuron cell-leukocyte adhesion. Creates homophilic cell adhesion promoting dendritogenesis and arborization of hippocampal neurons., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, PubMed, PubMed]; Elucidation of the roles of the N-glycans expressed in neural cells, including those present on ICAM-5., [RefSeq, PubMed]; ICAM-5 is involved in immune privilege of the brain and acts as an anti-inflammatory agent., [RefSeq, PubMed]; The Asn54-linked glycan is necessary for normal trafficking and function of ICAM-5, but is unassociated with ER-associated degradation of it., [RefSeq, PubMed]",
        "predicted_glycosites": 15,
        "predicted_n_glycosites": 15,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005178 integrin binding;GO:0048018 receptor ligand activity",
        "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0031259 uropod membrane;GO:0032591 dendritic spine membrane;GO:0005886 plasma membrane;GO:0098794 postsynapse",
        "go_biological_process": "GO:0051289 protein homotetramerization;GO:0033631 cell-cell adhesion mediated by integrin;GO:0051963 regulation of synapse assembly;GO:0007156 homophilic cell adhesion via plasma membrane adhesion molecules;GO:0007158 neuron cell-cell adhesion",
        "synthesized_glycan_count": 0,
        "hit_score": 1.0,
        "record_id": "A6JNN4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABZ3NNQ7-1",
        "uniprot_id": "A0ABZ3NNQ7_RAT",
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        "length": 309,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or2t45",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr1451",
        "refseq_ac": "NP_001000957",
        "gene_names_uniprotkb": "Or2t45; Olr1451",
        "gene_names_refseq": "Olr1451",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor Olr1451; olfactory receptor gene Olr1451",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:405046);  (rno:405306)",
        "pathway_count": 2,
        "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]",
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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",
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        "record_id": "A0ABZ3NNQ7-1",
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    {
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        "length": 527,
        "protein_name": "Zinc finger protein 397",
        "gene_name": "Zfp397",
        "organism": "Rat",
        "refseq_name": "zinc finger protein 397",
        "refseq_ac": "NP_001258404",
        "gene_names_uniprotkb": "Zfp397",
        "gene_names_refseq": "Zfp397; Znf397",
        "protein_names_uniprotkb": "Zinc finger protein 397",
        "protein_names_refseq": "zinc finger protein 397",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:100909408)",
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        "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:0042803 protein homodimerization activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0006357 regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0045892 negative regulation of DNA-templated transcription",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0M9Y3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6AJ35-1",
        "uniprot_id": "A0A8I6AJ35_RAT",
        "mass": 49714.0,
        "length": 454,
        "protein_name": "Perilipin",
        "gene_name": "Plin2",
        "organism": "Rat",
        "refseq_name": "perilipin-2 isoform X2",
        "refseq_ac": "XP_038965447",
        "gene_names_uniprotkb": "Plin2",
        "gene_names_refseq": "Adfp; Adrp; Plin2",
        "protein_names_uniprotkb": "Perilipin",
        "protein_names_refseq": "perilipin-2 isoform X2",
        "tax_id": 10116,
        "disease": "metabolic dysfunction-associated steatotic liver disease (Disease Ontology:DOID:0080208); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (rno:298199)",
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        "publication_count": 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:0005811 lipid droplet;GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005886 plasma membrane",
        "go_biological_process": "GO:0042149 cellular response to glucose starvation;GO:0019915 lipid storage;GO:0009410 response to xenobiotic stimulus;GO:0015909 long-chain fatty acid transport;GO:1905691 lipid droplet disassembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6AJ35-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0M8U6-1",
        "uniprot_id": "A0ABK0M8U6_RAT",
        "mass": 60110.0,
        "length": 555,
        "protein_name": "Cochlin",
        "gene_name": "Coch",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Coch",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Cochlin; COCH-5B2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "autosomal dominant nonsyndromic deafness 9 (Disease Ontology:DOID:0110593); autosomal recessive nonsyndromic deafness 110 (Disease Ontology:DOID:0111644)",
        "pathway": " (rno:362735)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Plays a role in the control of cell shape and motility in the trabecular meshwork., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "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:0005518 collagen binding",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0031012 extracellular matrix",
        "go_biological_process": "GO:0007605 sensory perception of sound;GO:0008360 regulation of cell shape",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0M8U6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0M8H5-1",
        "uniprot_id": "A0ABK0M8H5_RAT",
        "mass": 142195.0,
        "length": 1281,
        "protein_name": "Protein Jumonji",
        "gene_name": "Jarid2",
        "organism": "Rat",
        "refseq_name": "protein Jumonji isoform X1",
        "refseq_ac": "XP_017456196",
        "gene_names_uniprotkb": "Jarid2; LOC681740",
        "gene_names_refseq": "Jarid2",
        "protein_names_uniprotkb": "Protein Jumonji; Jumonji/ARID domain-containing protein 2",
        "protein_names_refseq": "protein Jumonji isoform X1",
        "tax_id": 10116,
        "disease": "autistic disorder (Disease Ontology:DOID:12849); aortic valve stenosis (Disease Ontology:DOID:1712)",
        "pathway": " (rno:681740);  (R-RNO-212300)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Regulator of histone methyltransferase complexes that plays an essential role in embryonic development, including heart and liver development, neural tube fusion process and hematopoiesis. Acts as an accessory subunit for the core PRC2 (Polycomb repressive complex 2) complex, which mediates histone H3K27 (H3K27me3) trimethylation on chromatin. Binds DNA and mediates the recruitment of the PRC2 complex to target genes in embryonic stem cells, thereby playing a key role in stem cell differentiation and normal embryonic development. In cardiac cells, it is required to repress expression of cyclin-D1 (CCND1) by activating methylation of 'Lys-9' of histone H3 (H3K9me) by the GLP1/EHMT1 and G9a/EHMT2 histone methyltransferases. Also acts as a transcriptional repressor of ANF via its interaction with GATA4 and NKX2-5. Participates in the negative regulation of cell proliferation signaling. Does not have histone demethylase activity., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0061649 ubiquitin-modified histone reader activity;GO:0003682 chromatin binding;GO:0043130 ubiquitin binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0000785 chromatin;GO:0035098 ESC/E(Z) complex;GO:0035097 histone methyltransferase complex",
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        "protein_name": "FAM3 metabolism regulating signaling molecule D",
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        "gene_names_uniprotkb": "Fam3d",
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        "protein_names_uniprotkb": "FAM3 metabolism regulating signaling molecule D",
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        "go_molecular_function": "GO:0005125 cytokine activity;GO:0030246 carbohydrate binding",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005576 extracellular region",
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        "length": 429,
        "protein_name": "Mitochondrial calcium uniporter regulator 1",
        "gene_name": "Mcur1",
        "organism": "Rat",
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        "gene_names_uniprotkb": "Mcur1",
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        "protein_names_uniprotkb": "Mitochondrial calcium uniporter regulator 1",
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        "go_molecular_function": "GO:0030674 protein-macromolecule adaptor activity;GO:0044877 protein-containing complex binding",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005743 mitochondrial inner membrane",
        "go_biological_process": "GO:0036444 calcium import into the mitochondrion;GO:0051561 positive regulation of mitochondrial calcium ion concentration;GO:0006091 generation of precursor metabolites and energy;GO:0008283 cell population proliferation;GO:0016477 cell migration",
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        "protein_name": "Toll/interleukin-1 receptor domain-containing adapter protein",
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        "gene_names_uniprotkb": "Tirap",
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        "protein_names_uniprotkb": "Toll/interleukin-1 receptor domain-containing adapter protein; TIR domain-containing adapter protein",
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        "function": "Adapter involved in the TLR2 and TLR4 signaling pathways in the innate immune response., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0042802 identical protein binding;GO:0035662 Toll-like receptor 4 binding;GO:0035663 Toll-like receptor 2 binding;GO:0060090 molecular adaptor activity;GO:0005546 phosphatidylinositol-4,5-bisphosphate binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005886 plasma membrane;GO:0009986 cell surface;GO:0031234 extrinsic component of cytoplasmic side of plasma membrane;GO:0030139 endocytic vesicle",
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        "protein_name": "TRAF family member-associated NFKB activator",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0060090 molecular adaptor activity;GO:0042802 identical protein binding;GO:0031625 ubiquitin protein ligase binding;GO:0035800 deubiquitinase activator activity",
        "go_cellular_component": "GO:0005730 nucleolus;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0032991 protein-containing complex",
        "go_biological_process": "GO:0043124 negative regulation of canonical NF-kappaB signal transduction;GO:0006974 DNA damage response;GO:0010804 negative regulation of tumor necrosis factor-mediated signaling pathway;GO:0071356 cellular response to tumor necrosis factor;GO:0071347 cellular response to interleukin-1",
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        "protein_name": "type I protein arginine methyltransferase",
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        "refseq_name": "protein arginine N-methyltransferase 8",
        "refseq_ac": "NP_001258314",
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        "gene_names_refseq": "Prmt8",
        "protein_names_uniprotkb": "type I protein arginine methyltransferase; 2.1.1.319",
        "protein_names_refseq": "protein arginine N-methyltransferase 8",
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        "function": "Protein arginine methyltransferase 8 regulates ferroptosis and macrophage polarization in spinal cord injury via glial cell-derived neurotrophic factor., [RefSeq, PubMed]",
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        "go_cellular_component": "GO:0005886 plasma membrane;GO:0098978 glutamatergic synapse;GO:0098794 postsynapse;GO:0009898 cytoplasmic side of plasma membrane",
        "go_biological_process": "GO:0006338 chromatin remodeling;GO:0006355 regulation of DNA-templated transcription;GO:0032259 methylation;GO:0051260 protein homooligomerization;GO:0006479 protein methylation",
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        "gene_names_uniprotkb": "Ssbp2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Single-stranded DNA binding protein 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "go_molecular_function": "GO:0003697 single-stranded DNA binding;GO:0003713 transcription coactivator activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm",
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        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "A0ABZ3NNB6-1",
        "uniprot_id": "A0ABZ3NNB6_RAT",
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        "length": 604,
        "protein_name": "Nucleolus and neural progenitor protein",
        "gene_name": "Rmp64",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Rmp64; Nepro; RGD1311458",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Nucleolus and neural progenitor protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "anauxetic dysplasia 3 (Disease Ontology:DOID:0080963)",
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        "total_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": "",
        "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:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0000172 ribonuclease MRP complex",
        "go_biological_process": "GO:0006396 RNA processing;GO:0045665 negative regulation of neuron differentiation;GO:0045747 positive regulation of Notch signaling pathway",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABZ3NNB6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7F8V6-1",
        "uniprot_id": "F7F8V6_RAT",
        "mass": 77530.0,
        "length": 690,
        "protein_name": "Bardet-Biedl syndrome 7",
        "gene_name": "Bbs7",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Bbs7",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Bardet-Biedl syndrome 7",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "Bardet-Biedl syndrome 7 (Disease Ontology:DOID:0110129); Bardet-Biedl syndrome (Disease Ontology:DOID:1935)",
        "pathway": " (rno:361930)",
        "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,
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        "mined_o_glycosites": 0,
        "mined_c_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": 2,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0061629 RNA polymerase II-specific DNA-binding transcription factor binding",
        "go_cellular_component": "GO:0034464 BBSome;GO:0005634 nucleus;GO:0005813 centrosome;GO:0016020 membrane;GO:0005930 axoneme",
        "go_biological_process": "GO:1905515 non-motile cilium assembly;GO:0006357 regulation of transcription by RNA polymerase II;GO:0007507 heart development;GO:0007420 brain development;GO:0045444 fat cell differentiation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F7F8V6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABZ3NNL2-1",
        "uniprot_id": "A0ABZ3NNL2_RAT",
        "mass": 42982.0,
        "length": 375,
        "protein_name": "Post-GPI attachment to proteins factor 3",
        "gene_name": "Pgap3",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Pgap3; Perld1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Post-GPI attachment to proteins factor 3",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "hyperphosphatasia with impaired intellectual development syndrome (Disease Ontology:DOID:0070431); hyperphosphatasia with impaired intellectual development syndrome 4 (Disease Ontology:DOID:0070436); chronic asthma (Disease Ontology:DOID:0080809); allergic asthma (Disease Ontology:DOID:9415)",
        "pathway": " (rno:688174)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Involved in the fatty acid remodeling steps of GPI-anchor maturation where the unsaturated acyl chain at sn-2 of inositol phosphate is replaced by a saturated stearoyl chain. May catalyze the first step of the fatty acid remodeling, by removing the unsaturated acyl chain at sn-2 of inositol phosphate, generating a lyso-GPI intermediate. The fatty acid remodeling steps is critical for the integration of GPI-APs into lipid rafts., [UniProtKB, UniProtKB, UniProtKB]; Involved in the lipid remodeling steps of GPI-anchor maturation., [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,
        "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": "",
        "glycan_count": 0,
        "disease_count": 4,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0016788 hydrolase activity, acting on ester bonds",
        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0031410 cytoplasmic vesicle",
        "go_biological_process": "GO:0006506 GPI anchor biosynthetic process;GO:0006505 GPI anchor metabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABZ3NNL2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABZ3NNM5-1",
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        "mass": 31289.0,
        "length": 278,
        "protein_name": "Family with sequence similarity 151, member B",
        "gene_name": "Fam151b",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Fam151b",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Family with sequence similarity 151, member B",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:499507)",
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        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
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        "predicted_c_glycosites": 0,
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        "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,
        "reported_s_glycosites_with_glycan": 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,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "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_biological_process": "GO:0042461 photoreceptor cell development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABZ3NNM5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7ENB2-1",
        "uniprot_id": "F7ENB2_RAT",
        "mass": 59032.0,
        "length": 523,
        "protein_name": "Sorting nexin-2",
        "gene_name": "Snx2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Snx2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Sorting nexin-2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:291464);  (R-RNO-432722)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Involved in several stages of intracellular trafficking. Interacts with membranes containing phosphatidylinositol 3-phosphate (PtdIns(3P)) or phosphatidylinositol 3,5-bisphosphate (PtdIns(3,5)P2). Acts in part as component of the retromer membrane-deforming SNX-BAR subcomplex. The SNX-BAR retromer mediates retrograde transport of cargo proteins from endosomes to the trans-Golgi network (TGN) and is involved in endosome-to-plasma membrane transport for cargo protein recycling. The SNX-BAR subcomplex functions to deform the donor membrane into a tubular profile called endosome-to-TGN transport carrier (ETC). Can sense membrane curvature and has in vitro vesicle-to-membrane remodeling activity. Required for retrograde endosome-to-TGN transport of TGN38. Promotes KALRN- and RHOG-dependent but retromer-independent membrane remodeling such as lamellipodium formation; the function is dependent on GEF activity of KALRN., [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_with_glycan": 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:0035091 phosphatidylinositol binding;GO:0005158 insulin receptor binding;GO:0042802 identical protein binding;GO:0042803 protein homodimerization activity;GO:0046982 protein heterodimerization activity",
        "go_cellular_component": "GO:0005768 endosome;GO:0005829 cytosol;GO:0030027 lamellipodium;GO:0031901 early endosome membrane;GO:0010008 endosome membrane",
        "go_biological_process": "GO:0006886 intracellular protein transport;GO:0034498 early endosome to Golgi transport;GO:0072673 lamellipodium morphogenesis;GO:0042147 retrograde transport, endosome to Golgi",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "F7ENB2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABZ3NNP0-1",
        "uniprot_id": "A0ABZ3NNP0_RAT",
        "mass": 93762.0,
        "length": 832,
        "protein_name": "S-adenosyl-L-methionine-dependent tRNA 4-demethylwyosine synthase TYW1",
        "gene_name": "Tyw1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Tyw1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "S-adenosyl-L-methionine-dependent tRNA 4-demethylwyosine synthase TYW1; 4.1.3.44; Radical S-adenosyl methionine and flavodoxin domain-containing protein 1; tRNA wybutosine-synthesizing protein 1 homolog; tRNA-yW-synthesizing protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:304423)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Probable component of the wybutosine biosynthesis pathway. Wybutosine is a hyper modified guanosine with a tricyclic base found at the 3'-position adjacent to the anticodon of eukaryotic phenylalanine tRNA. Catalyzes the condensation of N-methylguanine with 2 carbon atoms from pyruvate to form the tricyclic 4-demethylwyosine, an intermediate in wybutosine biosynthesis., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
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        "reported_o_glycosites": 0,
        "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,
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        "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,
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        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "4.1.3.44",
        "go_molecular_function": "GO:0046872 metal ion binding;GO:0051539 4 iron, 4 sulfur cluster binding;GO:0010181 FMN binding;GO:0102521 tRNA-4-demethylwyosine synthase activity",
        "go_cellular_component": "",
        "go_biological_process": "GO:0008033 tRNA processing",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABZ3NNP0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABZ3NNA7-1",
        "uniprot_id": "A0ABZ3NNA7_RAT",
        "mass": 23732.0,
        "length": 211,
        "protein_name": "peptidylprolyl isomerase",
        "gene_name": "Fkbp14",
        "organism": "Rat",
        "refseq_name": "peptidyl-prolyl cis-trans isomerase FKBP14 isoform X1",
        "refseq_ac": "XP_017448176",
        "gene_names_uniprotkb": "Fkbp14",
        "gene_names_refseq": "Fkbp14",
        "protein_names_uniprotkb": "peptidylprolyl isomerase; 5.2.1.8",
        "protein_names_refseq": "peptidyl-prolyl cis-trans isomerase FKBP14 isoform X1",
        "tax_id": 10116,
        "disease": "Ehlers-Danlos syndrome kyphoscoliotic type 2 (Disease Ontology:DOID:0080735)",
        "pathway": " (rno:362366)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_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": "5.2.1.8",
        "go_molecular_function": "GO:0003755 peptidyl-prolyl cis-trans isomerase activity",
        "go_cellular_component": "",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABZ3NNA7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0M8L4-1",
        "uniprot_id": "A0ABK0M8L4_RAT",
        "mass": 76350.0,
        "length": 671,
        "protein_name": "cGMP-dependent protein kinase",
        "gene_name": "AABR07006724.1; Prkg1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "AABR07006724.1; Prkg1; AABR07006724.1; Prkg1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "cGMP-dependent protein kinase; 2.7.11.12",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "ciliopathy (Disease Ontology:DOID:0060340); hypertension (Disease Ontology:DOID:10763); thoracic aortic aneurysm (Disease Ontology:DOID:14004); epilepsy (Disease Ontology:DOID:1826); impotence (Disease Ontology:DOID:1875); hypogonadism (Disease Ontology:DOID:1924); allergic rhinitis (Disease Ontology:DOID:4481); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (rno:54286);  (R-RNO-392517);  (R-RNO-418457)",
        "pathway_count": 3,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
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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": 8,
        "glyco_site_count": 0,
        "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:0004692 cGMP-dependent protein kinase activity;GO:0005524 ATP binding;GO:0005246 calcium channel regulator activity;GO:0030553 cGMP binding;GO:0004672 protein kinase activity",
        "go_cellular_component": "GO:0005794 Golgi apparatus;GO:0005886 plasma membrane;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0001669 acrosomal vesicle",
        "go_biological_process": "GO:0007165 signal transduction;GO:0060087 relaxation of vascular associated smooth muscle;GO:0043114 regulation of vascular permeability;GO:0048668 collateral sprouting;GO:0007168 receptor guanylyl cyclase signaling pathway",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0M8L4-1",
        "record_type": "protein"
    }
]
