[
    {
        "uniprot_canonical_ac": "F7ELW7-1",
        "uniprot_id": "F7ELW7_RAT",
        "mass": 74385.0,
        "length": 708,
        "protein_name": "Proline and serine rich 3",
        "gene_name": "Proser3",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Proser3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Proline and serine rich 3",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 2,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 2,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 2,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005813 centrosome",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F7ELW7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7F8A8-1",
        "uniprot_id": "F7F8A8_RAT",
        "mass": 20408.0,
        "length": 185,
        "protein_name": "Translocon-associated protein subunit beta",
        "gene_name": "Ssr2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ssr2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Translocon-associated protein subunit beta; Signal sequence receptor subunit beta; TRAP-beta",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 1,
        "publication_id_list": "24090084",
        "class_list": "",
        "function": "TRAP proteins are part of a complex whose function is to bind calcium to the ER membrane and thereby regulate the retention of ER resident proteins., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0001701 in utero embryonic development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "F7F8A8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7FG21-1",
        "uniprot_id": "F7FG21_RAT",
        "mass": 43552.0,
        "length": 408,
        "protein_name": "Zinc finger, HIT-type containing 2",
        "gene_name": "Znhit2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Znhit2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger, HIT-type containing 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding",
        "go_cellular_component": "",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F7FG21-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7FG85-1",
        "uniprot_id": "F7FG85_RAT",
        "mass": 115610.0,
        "length": 1020,
        "protein_name": "Alpha-mannosidase",
        "gene_name": "Man2b1",
        "organism": "Rat",
        "refseq_name": "lysosomal alpha-mannosidase isoform X2",
        "refseq_ac": "XP_038953745",
        "gene_names_uniprotkb": "Man2b1",
        "gene_names_refseq": "Man2b1; Manb",
        "protein_names_uniprotkb": "Alpha-mannosidase; 3.2.1.-",
        "protein_names_refseq": "lysosomal alpha-mannosidase isoform X2",
        "tax_id": 10116,
        "disease": "autism spectrum disorder (Disease Ontology:DOID:0060041); Down syndrome (Disease Ontology:DOID:14250); alpha-mannosidosis (Disease Ontology:DOID:3413)",
        "pathway": " (R-RNO-6798695);  (R-RNO-8853383)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Can hydrolyze a variety of glycan substrates containing terminal alpha-mannosidic linkages. Cleaves alpha 1,2-, alpha 1,3-, and alpha 1,6-linked mannose residues on oligosaccharides generated by N-glycoprotein degradation pathways., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 3,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "1.11.2.2;3.4.21.4;3.4.16.-;3.2.1.-;5.3.4.1;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;3.6.4.6;3.1.6.12;2.4.1.1;2.7.11.24;3.1.27.-;3.4.14.1;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",
        "go_molecular_function": "GO:0046872 metal ion binding;GO:0005537 D-mannose binding;GO:0004559 alpha-mannosidase activity",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005764 lysosome;GO:0043202 lysosomal lumen",
        "go_biological_process": "GO:0007611 learning or memory;GO:0006013 mannose metabolic process;GO:0006516 glycoprotein catabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F7FG85-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7FIK1-1",
        "uniprot_id": "F7FIK1_RAT",
        "mass": 110488.0,
        "length": 968,
        "protein_name": "NEDD4-like E3 ubiquitin-protein ligase WWP1",
        "gene_name": "Wwp1",
        "organism": "Rat",
        "refseq_name": "NEDD4-like E3 ubiquitin-protein ligase WWP1 isoform X1",
        "refseq_ac": "XP_006237992",
        "gene_names_uniprotkb": "Wwp1",
        "gene_names_refseq": "Wwp1",
        "protein_names_uniprotkb": "NEDD4-like E3 ubiquitin-protein ligase WWP1; 2.3.2.26; HECT-type E3 ubiquitin transferase WWP1; WW domain-containing protein 1",
        "protein_names_refseq": "NEDD4-like E3 ubiquitin-protein ligase WWP1 isoform X1",
        "tax_id": 10116,
        "disease": "Liddle syndrome (Disease Ontology:DOID:0050477)",
        "pathway": " (R-RNO-1253288);  (R-RNO-2672351);  (R-RNO-983168)",
        "pathway_count": 3,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "2.3.2.26;2.3.2.32;2.3.2.31;2.3.2.23;2.3.2.27;2.7.11.1;2.3.2.34;2.3.2.24;2.3.2.-;2.3.2.25",
        "go_molecular_function": "GO:0061630 ubiquitin protein ligase activity;GO:0004842 ubiquitin-protein transferase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0070161 anchoring junction",
        "go_biological_process": "GO:0045892 negative regulation of DNA-templated transcription;GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process;GO:0016567 protein ubiquitination",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F7FIK1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7FIP9-1",
        "uniprot_id": "F7FIP9_RAT",
        "mass": 53198.0,
        "length": 485,
        "protein_name": "Notchless protein homolog 1",
        "gene_name": "Nle1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Nle1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Notchless protein homolog 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Plays a role in regulating Notch activity. Plays a role in regulating the expression of CDKN1A and several members of the Wnt pathway, probably via its effects on Notch activity. Required during embryogenesis for inner mass cell survival., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005730 nucleolus",
        "go_biological_process": "GO:0007219 Notch signaling pathway;GO:0001822 kidney development;GO:0042273 ribosomal large subunit biogenesis;GO:0045930 negative regulation of mitotic cell cycle;GO:0001756 somitogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F7FIP9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7FPZ3-1",
        "uniprot_id": "F7FPZ3_RAT",
        "mass": 57541.0,
        "length": 530,
        "protein_name": "Negative elongation factor complex member A",
        "gene_name": "Nelfa",
        "organism": "Rat",
        "refseq_name": "negative elongation factor A",
        "refseq_ac": "NP_001008340",
        "gene_names_uniprotkb": "Nelfa",
        "gene_names_refseq": "Nelfa; Whsc2",
        "protein_names_uniprotkb": "Negative elongation factor complex member A",
        "protein_names_refseq": "Wolf-Hirschhorn syndrome candidate 2 protein; negative elongation factor A",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:305455);  (R-RNO-112382);  (R-RNO-113418);  (R-RNO-674695);  (R-RNO-6796648);  (R-RNO-75955)",
        "pathway_count": 6,
        "publication_count": 2,
        "publication_id_list": "22673903;24097989",
        "class_list": "",
        "function": "These studies allow us to position the actions of two new modulators of GR-regulated transactivation, NELF-A and NELF-B, relative to other factors in the overall gene induction sequence., [RefSeq, PubMed]",
        "predicted_glycosites": 3,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 3,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 3,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0060090 molecular adaptor activity;GO:0003682 chromatin binding;GO:0140870 RNA polymerase inhibitor activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0016604 nuclear body;GO:0032021 NELF complex",
        "go_biological_process": "GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0031401 positive regulation of protein modification process;GO:0034244 negative regulation of transcription elongation by RNA polymerase II;GO:0160239 transcription pausing by RNA polymerase II",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "F7FPZ3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "M0R8Y4-1",
        "uniprot_id": "M0R8Y4_RAT",
        "mass": 40745.0,
        "length": 355,
        "protein_name": "Carbohydrate sulfotransferase",
        "gene_name": "Chst14",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Chst14",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Carbohydrate sulfotransferase; 2.8.2.-",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "Ehlers-Danlos syndrome musculocontractural type 1 (Disease Ontology:DOID:0080736)",
        "pathway": " (R-RNO-2022923)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
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        "glyco_site_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "2.8.2.-",
        "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:0050655 dermatan sulfate proteoglycan metabolic process;GO:0050651 dermatan sulfate proteoglycan biosynthetic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "M0R8Y4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0KVV2-1",
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        "length": 183,
        "protein_name": "Suppressor APC domain containing 1",
        "gene_name": "Sapcd1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Sapcd1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Suppressor APC domain containing 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:406170)",
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        "record_id": "A0ABK0KVV2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A6JJF2-1",
        "uniprot_id": "A6JJF2_RAT",
        "mass": 28283.0,
        "length": 250,
        "protein_name": "RT1 class II, locus DOa",
        "gene_name": "RT1-DOa",
        "organism": "Rat",
        "refseq_name": "RT1 class II, locus DOa precursor",
        "refseq_ac": "NP_898874",
        "gene_names_uniprotkb": "RT1-DOa",
        "gene_names_refseq": "H2-Oa; RT1-DOa",
        "protein_names_uniprotkb": "RT1 class II, locus DOa",
        "protein_names_refseq": "RT1 class II, locus DOa precursor; histocompatibility 2, O region alpha locus",
        "tax_id": 10116,
        "disease": "occupational asthma (Disease Ontology:DOID:0080820)",
        "pathway": " (rno:24984)",
        "pathway_count": 1,
        "publication_count": 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": "Q6MGB0",
        "ec_number_list": "",
        "go_molecular_function": "GO:0023026 MHC class II protein complex binding",
        "go_cellular_component": "GO:0042613 MHC class II protein complex",
        "go_biological_process": "GO:0019886 antigen processing and presentation of exogenous peptide antigen via MHC class II;GO:0002250 adaptive immune response;GO:0045580 regulation of T cell differentiation;GO:0002587 negative regulation of antigen processing and presentation of peptide antigen via MHC class II;GO:0019882 antigen processing and presentation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A6JJF2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A6K136-1",
        "uniprot_id": "PPM1K_RAT",
        "mass": 41014.0,
        "length": 372,
        "protein_name": "Protein phosphatase Mn(2+)-dependent 1K",
        "gene_name": "Ppm1k",
        "organism": "Rat",
        "refseq_name": "protein phosphatase Mn(2+)-dependent 1K",
        "refseq_ac": "NP_001101333",
        "gene_names_uniprotkb": "Ppm1k",
        "gene_names_refseq": "BCKDH; BDP; Ppm1k; RGD1308501",
        "protein_names_uniprotkb": "Protein phosphatase Mn(2+)-dependent 1K; 3.1.3.16; 3.1.3.52; BCKDH; BDP; Branched-chain alpha-ketoacid dehydrogenase phosphatase; Protein phosphatase 2C family member; [3-methyl-2-oxobutanoate dehydrogenase (2-methylpropanoyl-transferring)]-phosphatase",
        "protein_names_refseq": "[3-methyl-2-oxobutanoate dehydrogenase (2-methylpropanoyl-transferring)]-phosphatase; branched-chain alpha-ketoacid dehydrogenase phosphatase; protein phosphatase 1K (PP2C domain containing); protein phosphatase 1K, mitochondrial; protein phosphatase 2C family member; protein phosphatase Mn(2+)-dependent 1K",
        "tax_id": 10116,
        "disease": "mild variant of maple syrup urine disease (Disease Ontology:DOID:0061205); maple syrup urine disease (Disease Ontology:DOID:9269)",
        "pathway": " (rno:312381)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "29779826",
        "class_list": "",
        "function": "Serine/threonine-protein phosphatase component of macronutrients metabolism. Together with BCKDK serves as a metabolic regulatory node that coordinates branched-chain amino acids (BCAAs) and protein synthesis with glucose and lipid metabolism via two distinct phosphoprotein targets: BCKDHA/E1a subunit of the branched-chain alpha-ketoacid dehydrogenase (BCKDH) complex and ACLY, a lipogenic enzyme of Krebs cycle (By similarity) (PubMed:29779826). At high levels of branched-chain ketoacids (BCKAs), dephosphorylates and activates mitochondrial BCKDH complex, a multisubunit complex consisting of three components, heterotetrameric E1 composed of BCKDHA and BCKDHB chains, 24-meric E2 core composed of DBT and homodimeric E3 composed of DLD, each involved in different steps of BCAA catabolism. Tightly associates with the E2 subunit of BCKDH complex and dephosphorylates Ser-333 of BCKDHA chain of the E1 subunit likely through on-off binding to individual E2 subunits of the 24-meric E2 core to increase the efficiency of the dephosphorylation reaction (By similarity). Appears to dephosphorylate and inactivate cytosolic ACLY in response to changes of cellular carbohydrate abundance. Overnutrition and in particular high-fructose diet, activates MLXIPL/ChREBP leading to increased BCKDK to PPM1K ratio, phosphorylation of ACLY on Ser-454 and activation of its enzymatic activity that ultimately results in the generation of acetyl-CoA and malonyl-CoA immediate substrates of de novo lipogenesis (By similarity) (PubMed:29779826). Recognizes phosphosites having SxS or RxxS motifs and strictly depends on Mn(2+) ions for the phosphatase activity (By similarity). Regulates Ca(2+)-induced opening of mitochondrial transition pore and apoptotic cell death (By similarity)., [UniProtKB, UniProtKB, PubMed]",
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        "disease_count": 2,
        "glyco_site_count": 0,
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        "secondary_ac_list": "D4A7X5",
        "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:0030145 manganese ion binding;GO:0004722 protein serine/threonine phosphatase activity;GO:0047385 [3-methyl-2-oxobutanoate dehydrogenase (lipoamide)]-phosphatase activity",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005759 mitochondrial matrix",
        "go_biological_process": "GO:0009083 branched-chain amino acid catabolic process;GO:1902108 regulation of mitochondrial membrane permeability involved in apoptotic process",
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        "hit_score": 0.2,
        "record_id": "A6K136-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0AA76ENW5-1",
        "uniprot_id": "A0AA76ENW5_RAT",
        "mass": 82121.0,
        "length": 735,
        "protein_name": "procollagen-proline 3-dioxygenase",
        "gene_name": "P3h3",
        "organism": "Rat",
        "refseq_name": "prolyl 3-hydroxylase 3 precursor",
        "refseq_ac": "NP_001100090",
        "gene_names_uniprotkb": "P3h3",
        "gene_names_refseq": "Leprel2; P3h3",
        "protein_names_uniprotkb": "procollagen-proline 3-dioxygenase; 1.14.11.7",
        "protein_names_refseq": "leprecan-like 2; prolyl 3-hydroxylase 3 precursor",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:297595)",
        "pathway_count": 1,
        "publication_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "1.14.11.7",
        "go_molecular_function": "GO:0005506 iron ion binding;GO:0031418 L-ascorbic acid binding;GO:0019797 procollagen-proline 3-dioxygenase activity;GO:0051213 dioxygenase activity;GO:0016705 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen",
        "go_cellular_component": "GO:1902494 catalytic complex",
        "go_biological_process": "GO:0008285 negative regulation of cell population proliferation;GO:0032964 collagen biosynthetic process;GO:0017185 peptidyl-lysine hydroxylation;GO:0032963 collagen metabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0AA76ENW5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A6N3IN21-1",
        "uniprot_id": "SDSL_RAT",
        "mass": 34953.0,
        "length": 329,
        "protein_name": "Serine dehydratase-like",
        "gene_name": "Sdsl",
        "organism": "Rat",
        "refseq_name": "serine dehydratase-like",
        "refseq_ac": "NP_001101806",
        "gene_names_uniprotkb": "Sdsl; Sdhl; Stdhgr",
        "gene_names_refseq": "Sdhl; Sdsl; TDH",
        "protein_names_uniprotkb": "Serine dehydratase-like; 4.3.1.17; 4.3.1.19; 5.1.1.3; Glutamate racemase; L-serine deaminase; L-serine dehydratase/L-threonine deaminase; L-threonine dehydratase; TDH",
        "protein_names_refseq": "L-serine deaminase; L-serine dehydratase-like; L-serine dehydratase/L-threonine deaminase; L-threonine dehydratase; glutamate racemase; serine dehydratase-like",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:360816)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "33079132",
        "class_list": "",
        "function": "Catalyzes the pyridoxal-phosphate-dependent dehydrative deamination of L-threonine and L-serine to ammonia and alpha-ketobutyrate and pyruvate, respectively (PubMed:33079132). Also exhibits racemase activity towards L-glutamate and D-glutamate (PubMed:33079132)., [UniProtKB, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "D3ZHV7",
        "ec_number_list": "4.3.1.17;4.3.1.19;5.1.1.3;4.3.1.18;5.1.1.18",
        "go_molecular_function": "GO:0030170 pyridoxal phosphate binding;GO:0042802 identical protein binding;GO:0003941 L-serine ammonia-lyase activity;GO:0004794 threonine deaminase activity;GO:0008881 glutamate racemase activity",
        "go_cellular_component": "",
        "go_biological_process": "GO:0006629 lipid metabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A6N3IN21-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7FPS2-1",
        "uniprot_id": "F7FPS2_RAT",
        "mass": 23467.0,
        "length": 218,
        "protein_name": "Adiponectin, C1Q and collagen domain containing",
        "gene_name": "Adipoq",
        "organism": "Rat",
        "refseq_name": "adiponectin isoform X1",
        "refseq_ac": "XP_038943914",
        "gene_names_uniprotkb": "Adipoq",
        "gene_names_refseq": "Acdc; Acrp30; Adid; Adipoq",
        "protein_names_uniprotkb": "Adiponectin, C1Q and collagen domain containing",
        "protein_names_refseq": "adiponectin isoform X1",
        "tax_id": 10116,
        "disease": "inflammatory bowel disease (Disease Ontology:DOID:0050589); cardiomyopathy (Disease Ontology:DOID:0050700); peripheral artery disease (Disease Ontology:DOID:0050830); sleep apnea (Disease Ontology:DOID:0050847); tongue squamous cell carcinoma (Disease Ontology:DOID:0050865); stroke (Disease Ontology:DOID:0051061); colitis (Disease Ontology:DOID:0060180); metabolic dysfunction and alcohol associated liver disease (Disease Ontology:DOID:0070508); metabolic dysfunction-associated steatotic liver disease (Disease Ontology:DOID:0080208); graft-versus-host disease (Disease Ontology:DOID:0081267); Alzheimer's disease (Disease Ontology:DOID:10652); primary open angle glaucoma (Disease Ontology:DOID:1070); polycystic ovary syndrome (Disease Ontology:DOID:11612); familial hyperlipidemia (Disease Ontology:DOID:1168); gestational diabetes (Disease Ontology:DOID:11714); Rett syndrome (Disease Ontology:DOID:1206); Graves' disease (Disease Ontology:DOID:12361); cardiovascular system disease (Disease Ontology:DOID:1287); dementia (Disease Ontology:DOID:1307); proliferative diabetic retinopathy (Disease Ontology:DOID:13207); Behcet's disease (Disease Ontology:DOID:13241); Kawasaki disease (Disease Ontology:DOID:13378); biliary atresia (Disease Ontology:DOID:13608); diffuse scleroderma (Disease Ontology:DOID:1580); breast cancer (Disease Ontology:DOID:1612); vascular disease (Disease Ontology:DOID:178); atherosclerosis (Disease Ontology:DOID:1936); hyperinsulinism (Disease Ontology:DOID:2018); autoimmune hepatitis (Disease Ontology:DOID:2048); multiple sclerosis (Disease Ontology:DOID:2377); prostate adenocarcinoma (Disease Ontology:DOID:2526); Mycobacterium avium complex disease (Disease Ontology:DOID:2755); pulmonary tuberculosis (Disease Ontology:DOID:2957); familial Mediterranean fever (Disease Ontology:DOID:2987); chronic obstructive pulmonary disease (Disease Ontology:DOID:3083); bipolar disorder (Disease Ontology:DOID:3312); coronary aneurysm (Disease Ontology:DOID:3362); coronary artery disease (Disease Ontology:DOID:3393); brain infarction (Disease Ontology:DOID:3454); liver cirrhosis (Disease Ontology:DOID:5082); myocardial infarction (Disease Ontology:DOID:5844); congestive heart failure (Disease Ontology:DOID:6000); hepatocellular carcinoma (Disease Ontology:DOID:684); ankylosing spondylitis (Disease Ontology:DOID:7147); rheumatoid arthritis (Disease Ontology:DOID:7148); end stage renal disease (Disease Ontology:DOID:783); hyperthyroidism (Disease Ontology:DOID:7998); ulcerative colitis (Disease Ontology:DOID:8577); Crohn's disease (Disease Ontology:DOID:8778); diabetic retinopathy (Disease Ontology:DOID:8947); amyloidosis (Disease Ontology:DOID:9120); type 2 diabetes mellitus (Disease Ontology:DOID:9352); steatotic liver disease (Disease Ontology:DOID:9452); type 1 diabetes mellitus (Disease Ontology:DOID:9744); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (rno:246253)",
        "pathway_count": 1,
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        "predicted_glycosites": 1,
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        "reported_n_glycosites": 0,
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        "go_molecular_function": "GO:0005102 signaling receptor binding;GO:0042802 identical protein binding;GO:0042803 protein homodimerization activity;GO:0005179 hormone activity;GO:0043539 protein serine/threonine kinase activator activity",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0005615 extracellular space;GO:0005783 endoplasmic reticulum;GO:0009986 cell surface;GO:0032991 protein-containing complex",
        "go_biological_process": "GO:0006635 fatty acid beta-oxidation;GO:0007584 response to nutrient;GO:0010875 positive regulation of cholesterol efflux;GO:0032869 cellular response to insulin stimulus;GO:0034612 response to tumor necrosis factor",
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        "hit_score": 0.1,
        "record_id": "F7FPS2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABZ3NNA5-1",
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        "length": 430,
        "protein_name": "GATA binding protein 5",
        "gene_name": "Gata5",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Gata5",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "GATA binding protein 5",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "familial atrial fibrillation (Disease Ontology:DOID:0050650); atrial fibrillation (Disease Ontology:DOID:0060224); bicuspid aortic valve disease (Disease Ontology:DOID:0080332); hypertension (Disease Ontology:DOID:10763); essential hypertension (Disease Ontology:DOID:10825); dilated cardiomyopathy (Disease Ontology:DOID:12930); ventricular septal defect (Disease Ontology:DOID:1657); tetralogy of Fallot (Disease Ontology:DOID:6419); acute myocardial infarction (Disease Ontology:DOID:9408)",
        "pathway": " (rno:499951)",
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        "class_list": "",
        "function": "",
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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: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:0000785 chromatin",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0007507 heart development;GO:0010628 positive regulation of gene expression;GO:0010629 negative regulation of gene expression;GO:0045944 positive regulation of transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABZ3NNP3-1",
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        "length": 334,
        "protein_name": "Polycomb complex protein BMI-1",
        "gene_name": "Bmi1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Bmi1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Polycomb complex protein BMI-1; Polycomb group RING finger protein 4",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "chronic pancreatitis (Disease Ontology:DOID:0051065); colorectal carcinoma (Disease Ontology:DOID:0080199); pancreatic ductal carcinoma (Disease Ontology:DOID:3587); esophagus squamous cell carcinoma (Disease Ontology:DOID:3748); renal Wilms' tumor (Disease Ontology:DOID:5176); hepatocellular carcinoma (Disease Ontology:DOID:684); acute myeloid leukemia (Disease Ontology:DOID:9119)",
        "pathway": " (rno:307151)",
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        "function": "Component of a Polycomb group (PcG) multiprotein PRC1-like complex, a complex class required to maintain the transcriptionally repressive state of many genes, including Hox genes, throughout development. PcG PRC1 complex acts via chromatin remodeling and modification of histones; it mediates monoubiquitination of histone H2A 'Lys-119', rendering chromatin heritably changed in its expressibility. The complex composed of RNF2, UB2D3 and BMI1 binds nucleosomes, and has activity only with nucleosomal histone H2A. In the PRC1-like complex, regulates the E3 ubiquitin-protein ligase activity of RNF2/RING2., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003682 chromatin binding;GO:0008270 zinc ion binding;GO:0097027 ubiquitin-protein transferase activator activity;GO:0071535 RING-like zinc finger domain binding;GO:1990841 promoter-specific chromatin binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0016604 nuclear body;GO:0000151 ubiquitin ligase complex;GO:0000792 heterochromatin;GO:0031519 PcG protein complex",
        "go_biological_process": "GO:0033092 positive regulation of immature T cell proliferation in thymus;GO:0021903 rostrocaudal neural tube patterning;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0001701 in utero embryonic development;GO:0006338 chromatin remodeling",
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        "record_type": "protein"
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Thoc3",
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        "protein_names_uniprotkb": "THO complex subunit 3",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:290519)",
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        "function": "Component of the THO subcomplex of the TREX complex which is thought to couple mRNA transcription, processing and nuclear export, and which specifically associates with spliced mRNA and not with unspliced pre-mRNA. Required for efficient export of polyadenylated RNA and spliced mRNA. The THOC1-THOC2-THOC3 core complex alone is sufficient to bind export factor NXF1-NXT1 and promote ATPase activity of DDX39B. TREX is recruited to spliced mRNAs by a transcription-independent mechanism, binds to mRNA upstream of the exon-junction complex (EJC) and is recruited in a splicing- and cap-dependent manner to a region near the 5' end of the mRNA where it functions in mRNA export to the cytoplasm via the TAP/NXF1 pathway., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0000445 THO complex part of transcription export complex;GO:0000346 transcription export complex;GO:0000781 chromosome, telomeric region",
        "go_biological_process": "GO:0006406 mRNA export from nucleus",
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        "hit_score": 0.1,
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        "length": 615,
        "protein_name": "PBX homeobox 2",
        "gene_name": "Pbx2",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Pbx2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "PBX homeobox 2",
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        "go_molecular_function": "GO:0003682 chromatin binding;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0001228 DNA-binding transcription activator activity, RNA polymerase II-specific;GO:0140297 DNA-binding transcription factor binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005667 transcription regulator complex",
        "go_biological_process": "GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0030326 embryonic limb morphogenesis;GO:0009954 proximal/distal pattern formation",
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        "hit_score": 0.2,
        "record_id": "A0ABZ3NN70-1",
        "record_type": "protein"
    },
    {
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        "protein_name": "Nuclear inhibitor of protein phosphatase 1",
        "gene_name": "Ppp1r8",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ppp1r8",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Nuclear inhibitor of protein phosphatase 1; Protein phosphatase 1 regulatory inhibitor subunit 8",
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        "tax_id": 10116,
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        "go_molecular_function": "GO:0019888 protein phosphatase regulator activity;GO:0004521 RNA endonuclease activity;GO:0140678 molecular function inhibitor activity",
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        "length": 133,
        "protein_name": "Lymphocyte antigen 6 family member G6E",
        "gene_name": "Ly6g6e",
        "organism": "Rat",
        "refseq_name": "lymphocyte antigen 6 complex G6E precursor",
        "refseq_ac": "NP_001001972",
        "gene_names_uniprotkb": "Ly6g6e",
        "gene_names_refseq": "Ly6g6e",
        "protein_names_uniprotkb": "Lymphocyte antigen 6 family member G6E",
        "protein_names_refseq": "lymphocyte antigen 6 complex G6E precursor; lymphocyte antigen 6 complex G6E; lymphocyte antigen 6 complex, locus G6E",
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        "protein_name": "TDPOZ2",
        "gene_name": "Spopfm2l1",
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        "gene_names_uniprotkb": "Spopfm2l1; RGD1559714",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "TDPOZ2",
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        "protein_names_uniprotkb": "E3 ubiquitin-protein ligase RNF115; 2.3.2.27; RING finger protein 115; RING-type E3 ubiquitin transferase RNF115; Rab7-interacting RING finger protein; Zinc finger protein 364",
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        "gene_name": "",
        "organism": "Rat",
        "refseq_name": "",
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        "gene_names_uniprotkb": "",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "40S ribosomal protein S24",
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        "length": 476,
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        "gene_names_uniprotkb": "Metap2-ps1; METAP2",
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        "protein_names_uniprotkb": "Methionine aminopeptidase 2; 3.4.11.18; Initiation factor 2-associated 67 kDa glycoprotein; MAP 2; MetAP 2; Peptidase M; p67eIF2; p67",
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        "tax_id": 10116,
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        "function": "Cotranslationally removes the N-terminal methionine from nascent proteins. The N-terminal methionine is often cleaved when the second residue in the primary sequence is small and uncharged (Met-Ala-, Cys, Gly, Pro, Ser, Thr, or Val)., [UniProtKB, HAMAP, UniProtKB]; Protects eukaryotic initiation factor EIF2S1 from translation-inhibiting phosphorylation by inhibitory kinases such as EIF2AK2/PKR and EIF2AK1/HCR. Plays a critical role in the regulation of protein synthesis., [UniProtKB, HAMAP, UniProtKB]",
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        "go_molecular_function": "GO:0046872 metal ion binding;GO:0070006 metalloaminopeptidase activity;GO:0004239 initiator methionyl aminopeptidase activity",
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        "length": 312,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or6b2",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr1343",
        "refseq_ac": "NP_001001088",
        "gene_names_uniprotkb": "Or6b2",
        "gene_names_refseq": "Olr1343; Or6b2",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 1343; olfactory receptor Olr1343; olfactory receptor gene Olr1343",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
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        "length": 329,
        "protein_name": "C5a anaphylatoxin chemotactic receptor 1",
        "gene_name": "C5ar1",
        "organism": "Rat",
        "refseq_name": "C5a anaphylatoxin chemotactic receptor 1 isoform X1",
        "refseq_ac": "XP_038961791",
        "gene_names_uniprotkb": "C5ar1",
        "gene_names_refseq": "C5a-R; C5aR; C5ar1; C5r1",
        "protein_names_uniprotkb": "C5a anaphylatoxin chemotactic receptor 1; C5a anaphylatoxin chemotactic receptor",
        "protein_names_refseq": "C5a anaphylatoxin chemotactic receptor 1 isoform X1",
        "tax_id": 10116,
        "disease": "thrombosis (Disease Ontology:DOID:0060903); Alzheimer's disease (Disease Ontology:DOID:10652); adult respiratory distress syndrome (Disease Ontology:DOID:11394); neutropenia (Disease Ontology:DOID:1227); asthma (Disease Ontology:DOID:2841); severe acute respiratory syndrome (Disease Ontology:DOID:2945); chronic obstructive pulmonary disease (Disease Ontology:DOID:3083); amyotrophic lateral sclerosis (Disease Ontology:DOID:332); rhinitis (Disease Ontology:DOID:4483); lung disease (Disease Ontology:DOID:850); obesity (Disease Ontology:DOID:9970)",
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        "function": "Receptor for the chemotactic and inflammatory peptide anaphylatoxin C5a, stimulating chemotaxis, granule enzyme release, intracellular calcium release and superoxide anion production. Ligand binding causes a conformation change that triggers signaling via guanine nucleotide-binding proteins (G proteins) and modulates the activity of downstream effectors, such as adenylate cyclase. C5AR1 is coupled to G(i)/G(o) (GNAI1 or GNAO1) G alpha proteins and mediates inhibition of adenylate cyclase. The ligand interacts with at least two sites on the receptor: a high-affinity site on the extracellular N-terminus, and a second site in the transmembrane region which activates downstream signaling events., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004878 complement component C5a receptor activity;GO:0001856 complement component C5a binding",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0009986 cell surface;GO:0016323 basolateral plasma membrane;GO:0045177 apical part of cell;GO:0031410 cytoplasmic vesicle",
        "go_biological_process": "GO:0002430 complement receptor mediated signaling pathway;GO:0038178 complement component C5a signaling pathway;GO:0001774 microglial cell activation;GO:0007186 G protein-coupled receptor signaling pathway;GO:0007193 adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway",
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        "record_id": "A0ABK0KWS8-1",
        "record_type": "protein"
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        "length": 165,
        "protein_name": "Peptidyl-prolyl cis-trans isomerase",
        "gene_name": "Pin1",
        "organism": "Rat",
        "refseq_name": "peptidyl-prolyl cis-trans isomerase NIMA-interacting 1",
        "refseq_ac": "NP_001100171",
        "gene_names_uniprotkb": "Pin1",
        "gene_names_refseq": "Pin1",
        "protein_names_uniprotkb": "Peptidyl-prolyl cis-trans isomerase; 5.2.1.8",
        "protein_names_refseq": "peptidyl-prolyl cis-trans isomerase NIMA-interacting 1; protein (peptidyl-prolyl cis/trans isomerase) NIMA-interacting 1",
        "tax_id": 10116,
        "disease": "Alzheimer's disease (Disease Ontology:DOID:10652); secondary hyperparathyroidism (Disease Ontology:DOID:12466); asthma (Disease Ontology:DOID:2841)",
        "pathway": " (rno:298696)",
        "pathway_count": 1,
        "publication_count": 5,
        "publication_id_list": "35058248;35227974;35416857;37567011;38795154",
        "class_list": "",
        "function": "Expression and significance of pin1 in the wound healing. Publication Status: Online-Only, [RefSeq, PubMed]; Pin1 aggravates renal injury induced by ischemia and reperfusion in rats via Nrf2/HO-1 mediated endoplasmic reticulum stress. Publication Status: Online-Only, [RefSeq, PubMed]; Pin1-mediated regulation of articular cartilage stem/progenitor cell aging., [RefSeq, PubMed]; Restoration of miR-328a-5p function curtails hypoxic pulmonary hypertension through a mechanism involving PIN1/GSK3beta/beta-catenin axis., [RefSeq, PubMed]; Targeting peptidyl-prolyl isomerase 1 in experimental pulmonary arterial hypertension. Publication Status: Online-Only, [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "ec_number_list": "5.2.1.8",
        "go_molecular_function": "GO:0031434 mitogen-activated protein kinase kinase binding;GO:0050815 phosphoserine residue binding;GO:0051219 phosphoprotein binding;GO:0008013 beta-catenin binding;GO:0032794 GTPase activating protein binding",
        "go_cellular_component": "GO:0098978 glutamatergic synapse;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0001934 positive regulation of protein phosphorylation;GO:0042127 regulation of cell population proliferation;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0050808 synapse organization;GO:0001666 response to hypoxia",
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        "record_id": "A0ABK0KWT6-1",
        "record_type": "protein"
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        "protein_name": "Ig-like domain-containing protein",
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        "organism": "Rat",
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        "protein_names_uniprotkb": "Ig-like domain-containing protein",
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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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        "record_id": "A0ABK0KWU1-1",
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        "gene_names_uniprotkb": "Igkvl-ps2",
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        "ec_number_list": "4.2.1.1;2.3.2.27;2.7.10.1;3.4.23.-",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0004089 carbonate dehydratase activity;GO:0019899 enzyme binding;GO:0030674 protein-macromolecule adaptor activity;GO:0061133 endopeptidase activator activity",
        "go_cellular_component": "GO:0016323 basolateral plasma membrane;GO:0016324 apical plasma membrane;GO:0005886 plasma membrane;GO:0005769 early endosome;GO:0005783 endoplasmic reticulum",
        "go_biological_process": "GO:0006509 membrane protein ectodomain proteolysis;GO:0007219 Notch signaling pathway;GO:0007220 Notch receptor processing;GO:0016485 protein processing;GO:0042982 amyloid precursor protein metabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0KYA7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L304-1",
        "uniprot_id": "A0ABK0L304_RAT",
        "mass": 67487.0,
        "length": 588,
        "protein_name": "Lipase maturation factor",
        "gene_name": "Lmf1",
        "organism": "Rat",
        "refseq_name": "",
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        "gene_names_uniprotkb": "Lmf1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Lipase maturation factor",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "familial lipase maturation factor 1 deficiency (Disease Ontology:DOID:0111422)",
        "pathway": " (R-RNO-8963889)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Involved in the maturation of specific proteins in the endoplasmic reticulum., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_cellular_component": "GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0051604 protein maturation;GO:0006641 triglyceride metabolic process;GO:0051006 positive regulation of lipoprotein lipase activity;GO:0090181 regulation of cholesterol metabolic process;GO:0009101 glycoprotein biosynthetic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0L304-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L0X6-1",
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        "length": 558,
        "protein_name": "Solute carrier family 19 member 3",
        "gene_name": "Slc19a3",
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        "refseq_name": "",
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        "gene_names_uniprotkb": "Slc19a3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Solute carrier family 19 member 3",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "biotin-responsive basal ganglia disease (Disease Ontology:DOID:0050659); chronic kidney disease (Disease Ontology:DOID:784)",
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        "go_molecular_function": "GO:0015234 thiamine transmembrane transporter activity",
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        "go_biological_process": "GO:0009229 thiamine diphosphate biosynthetic process;GO:0015888 thiamine transport;GO:0071934 thiamine transmembrane transport;GO:0031923 pyridoxine transport",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0L0X6-1",
        "record_type": "protein"
    },
    {
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        "length": 336,
        "protein_name": "Thymidylate kinase",
        "gene_name": "Dtymk",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Dtymk",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Thymidylate kinase; 2.7.4.9; dTMP kinase",
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        "tax_id": 10116,
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        "pathway": " (R-RNO-499943)",
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        "function": "Catalyzes the phosphorylation of thymidine monophosphate (dTMP) to thymidine diphosphate (dTDP), the immediate precursor for the DNA building block dTTP, with ATP as the preferred phosphoryl donor in the presence of Mg(2+)., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005739 mitochondrion;GO:0005759 mitochondrial matrix",
        "go_biological_process": "GO:0006233 dTDP biosynthetic process;GO:0006227 dUDP biosynthetic process;GO:0006235 dTTP biosynthetic process;GO:0046105 thymidine biosynthetic process;GO:0046686 response to cadmium ion",
        "synthesized_glycan_count": 0,
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L1R9-1",
        "uniprot_id": "A0ABK0L1R9_RAT",
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        "length": 798,
        "protein_name": "Mitogen-activated protein kinase kinase kinase kinase",
        "gene_name": "Map4k2",
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        "gene_names_uniprotkb": "Map4k2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Mitogen-activated protein kinase kinase kinase kinase; 2.7.11.1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "ciliopathy (Disease Ontology:DOID:0060340); alcohol use disorder (Disease Ontology:DOID:1574)",
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        "function": "Serine/threonine kinase that plays a role in the response to environmental stress. Appears to act upstream of the JUN N-terminal pathway., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "2.7.11.1;2.7.12.1;2.7.1.153;2.7.1.137;2.7.11.24;2.7.11.25;2.7.11.22;2.7.11.23;2.7.4.6;2.7.1.154;2.7.11.38;2.7.11.17;2.7.11.21;2.7.12.2;2.7.1.40;2.7.11.12;2.7.11.26;2.7.11.34;2.7.10.2;2.7.1.150;2.7.11.13;4.1.1.32;2.7.11.19;2.7.2.3;2.7.11.11;2.7.11.31;3.1.3.16;2.7.11.4;2.3.1.48;3.1.11.-;2.7.13.3;2.7.4.18;3.1.24.-;3.4.19.12;2.7.11.39;2.4.99.18;2.7.11.10",
        "go_molecular_function": "GO:0005524 ATP binding;GO:0008349 MAP kinase kinase kinase kinase activity;GO:0004674 protein serine/threonine kinase activity;GO:0031435 mitogen-activated protein kinase kinase kinase binding",
        "go_cellular_component": "GO:0005737 cytoplasm",
        "go_biological_process": "GO:0035556 intracellular signal transduction;GO:0006468 protein phosphorylation;GO:0046330 positive regulation of JNK cascade;GO:0006903 vesicle targeting;GO:0043507 positive regulation of JUN kinase activity",
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        "record_id": "A0ABK0L1R9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L107-1",
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        "length": 978,
        "protein_name": "Exportin-2",
        "gene_name": "Cse1l",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Cse1l",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Exportin-2; Chromosome segregation 1-like protein; Importin-alpha re-exporter",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:362273)",
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        "function": "Export receptor for importin-alpha. Mediates importin-alpha re-export from the nucleus to the cytoplasm after import substrates (cargos) have been released into the nucleoplasm. In the nucleus binds cooperatively to importin-alpha and to the GTPase Ran in its active GTP-bound form. Docking of this trimeric complex to the nuclear pore complex (NPC) is mediated through binding to nucleoporins. Upon transit of a nuclear export complex into the cytoplasm, disassembling of the complex and hydrolysis of Ran-GTP to Ran-GDP (induced by RANBP1 and RANGAP1, respectively) cause release of the importin-alpha from the export receptor. CSE1L/XPO2 then return to the nuclear compartment and mediate another round of transport. The directionality of nuclear export is thought to be conferred by an asymmetric distribution of the GTP- and GDP-bound forms of Ran between the cytoplasm and nucleus., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0031267 small GTPase binding;GO:0005049 nuclear export signal receptor activity",
        "go_cellular_component": "GO:0005635 nuclear envelope;GO:0005829 cytosol;GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0006611 protein export from nucleus;GO:0006886 intracellular protein transport",
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    {
        "uniprot_canonical_ac": "A0ABK0KZE7-1",
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        "protein_name": "Testis expressed 21",
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        "gene_names_uniprotkb": "Tex21",
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        "protein_names_uniprotkb": "Testis expressed 21",
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    },
    {
        "uniprot_canonical_ac": "A0ABK0L139-1",
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        "length": 1622,
        "protein_name": "ATP binding cassette subfamily A member 8",
        "gene_name": "Abca8",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Abca8",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "ATP binding cassette subfamily A member 8",
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        "go_molecular_function": "GO:0005524 ATP binding;GO:0016887 ATP hydrolysis activity;GO:0140359 ABC-type transporter activity;GO:0005319 lipid transporter activity;GO:0042626 ATPase-coupled transmembrane transporter activity",
        "go_cellular_component": "GO:0016020 membrane;GO:0005783 endoplasmic reticulum;GO:0005886 plasma membrane;GO:0016323 basolateral plasma membrane",
        "go_biological_process": "GO:0006686 sphingomyelin biosynthetic process;GO:0006869 lipid transport;GO:0010875 positive regulation of cholesterol efflux;GO:0033344 cholesterol efflux;GO:0006855 xenobiotic transmembrane transport",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0L139-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L284-1",
        "uniprot_id": "A0ABK0L284_RAT",
        "mass": 36667.0,
        "length": 322,
        "protein_name": "PIH1 domain containing 2",
        "gene_name": "Pih1d2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Pih1d2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "PIH1 domain containing 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:315645)",
        "pathway_count": 1,
        "publication_count": 0,
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        "class_list": "",
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0031267 small GTPase binding",
        "go_cellular_component": "GO:0097255 R2TP complex;GO:0005737 cytoplasm;GO:1990904 ribonucleoprotein complex;GO:0101031 protein folding chaperone complex",
        "go_biological_process": "GO:0006364 rRNA processing;GO:0000492 box C/D snoRNP assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0L284-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L269-1",
        "uniprot_id": "A0ABK0L269_RAT",
        "mass": 48660.0,
        "length": 435,
        "protein_name": "Dual specificity mitogen-activated protein kinase kinase 4",
        "gene_name": "Map2k4",
        "organism": "Rat",
        "refseq_name": "dual specificity mitogen-activated protein kinase kinase 4 isoform X2",
        "refseq_ac": "XP_063124697",
        "gene_names_uniprotkb": "Map2k4",
        "gene_names_refseq": "MKK4; Map2k4; Sek1",
        "protein_names_uniprotkb": "Dual specificity mitogen-activated protein kinase kinase 4; 2.7.12.2; JNK-activating kinase 1; MAPK/ERK kinase 4; SAPK/ERK kinase 1",
        "protein_names_refseq": "dual specificity mitogen-activated protein kinase kinase 4 isoform X2",
        "tax_id": 10116,
        "disease": "tongue squamous cell carcinoma (Disease Ontology:DOID:0050865); ovarian serous carcinoma (Disease Ontology:DOID:0050933); urinary bladder cancer (Disease Ontology:DOID:11054); lung cancer (Disease Ontology:DOID:1324); pancreatic cancer (Disease Ontology:DOID:1793); transient cerebral ischemia (Disease Ontology:DOID:224); laryngeal squamous cell carcinoma (Disease Ontology:DOID:2876); invasive ductal carcinoma (Disease Ontology:DOID:3008); chronic obstructive pulmonary disease (Disease Ontology:DOID:3083); gastric adenocarcinoma (Disease Ontology:DOID:3717); lung non-small cell carcinoma (Disease Ontology:DOID:3908); hepatocellular carcinoma (Disease Ontology:DOID:684); prostate carcinoma in situ (Disease Ontology:DOID:8634); colorectal cancer (Disease Ontology:DOID:9256); nasopharynx carcinoma (Disease Ontology:DOID:9261)",
        "pathway": " (rno:287398)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 2,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 15,
        "glyco_site_count": 2,
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        "secondary_ac_list": "",
        "ec_number_list": "2.7.11.1;2.7.12.1;2.7.10.1;2.7.1.153;2.7.1.137;2.7.10.2;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;2.7.1.150;2.7.11.13;4.1.1.32;2.7.11.19;2.7.2.3;2.7.11.11;2.7.10.4;2.7.11.31;3.1.3.16;2.7.11.4;2.3.1.48;2.7.1.32;2.7.1.82;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:0004708 MAP kinase kinase activity;GO:0060090 molecular adaptor activity",
        "go_cellular_component": "GO:0005829 cytosol;GO:0030424 axon;GO:0043204 perikaryon;GO:0032839 dendrite cytoplasm",
        "go_biological_process": "GO:0033554 cellular response to stress;GO:0038127 ERBB signaling pathway;GO:0072709 cellular response to sorbitol;GO:0001934 positive regulation of protein phosphorylation;GO:0006468 protein phosphorylation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0L269-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0KXB0-1",
        "uniprot_id": "A0ABK0KXB0_RAT",
        "mass": 51157.0,
        "length": 452,
        "protein_name": "Mannosidase, endo-alpha-like",
        "gene_name": "Maneal",
        "organism": "Rat",
        "refseq_name": "mannosidase, endo-alpha-like",
        "refseq_ac": "NP_001418135",
        "gene_names_uniprotkb": "Maneal",
        "gene_names_refseq": "Maneal; RGD1563973",
        "protein_names_uniprotkb": "Mannosidase, endo-alpha-like",
        "protein_names_refseq": "mannosidase, endo-alpha-like",
        "tax_id": 10116,
        "disease": "",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0004559 alpha-mannosidase activity;GO:0016798 hydrolase activity, acting on glycosyl bonds",
        "go_cellular_component": "GO:0000139 Golgi membrane",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0KXB0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0KYT3-1",
        "uniprot_id": "A0ABK0KYT3_RAT",
        "mass": 16369.0,
        "length": 141,
        "protein_name": "Vesicle-associated membrane protein 4",
        "gene_name": "Vamp4",
        "organism": "Rat",
        "refseq_name": "vesicle-associated membrane protein 4 isoform 2",
        "refseq_ac": "NP_001416818",
        "gene_names_uniprotkb": "Vamp4",
        "gene_names_refseq": "Vamp4",
        "protein_names_uniprotkb": "Vesicle-associated membrane protein 4",
        "protein_names_refseq": "vesicle-associated membrane protein 4 isoform 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:364033);  (R-RNO-6811440);  (R-RNO-8856825);  (R-RNO-8856828)",
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        "publication_count": 5,
        "publication_id_list": "18713833;22673903;26607000;32532887;34496238",
        "class_list": "",
        "function": "Data show that VAMP4, an R-SNARE that has never been shown to participate in regulated exocytoses, appears to be harboured in the membrane of enlargeosomes and to be a member of the machinery mediating their regulated exocytosis., [RefSeq, PubMed]; Involved in the pathway that functions to remove an inhibitor (probably synaptotagmin-4) of calcium-triggered exocytosis during the maturation of secretory granules. May be a marker for this sorting pathway that is critical for remodeling the secretory response of granule., [UniProtKB, UniProtKB, UniProtKB]; The results of this study suggested that the VAMP4 is the first identified Activity-dependent bulk endocytosis cargo and is essential for this endocytosis mode to proceed., [RefSeq, PubMed]; The vSNAREs VAMP2 and VAMP4 control recycling and intracellular sorting of post-synaptic receptors in neuronal dendrites., [RefSeq, PubMed]; VAMP4 Maintains a Ca(2+)-Sensitive Pool of Spontaneously Recycling Synaptic Vesicles., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
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        "total_reported_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005802 trans-Golgi network;GO:0031201 SNARE complex;GO:0098954 presynaptic endosome membrane;GO:0098978 glutamatergic synapse;GO:0005794 Golgi apparatus",
        "go_biological_process": "GO:0042996 regulation of Golgi to plasma membrane protein transport;GO:0015031 protein transport;GO:0090161 Golgi ribbon formation;GO:0032456 endocytic recycling;GO:0098887 neurotransmitter receptor transport, endosome to postsynaptic membrane",
        "synthesized_glycan_count": 0,
        "hit_score": 0.6,
        "record_id": "A0ABK0KYT3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L120-1",
        "uniprot_id": "A0ABK0L120_RAT",
        "mass": 52394.0,
        "length": 497,
        "protein_name": "Flt3-interacting zinc finger protein 1",
        "gene_name": "Fiz1",
        "organism": "Rat",
        "refseq_name": "flt3-interacting zinc finger protein 1",
        "refseq_ac": "NP_001425199",
        "gene_names_uniprotkb": "Fiz1",
        "gene_names_refseq": "Fiz1; RGD1306359",
        "protein_names_uniprotkb": "Flt3-interacting zinc finger protein 1",
        "protein_names_refseq": "Flt3 interacting zinc finger protein 1; flt3-interacting zinc finger protein 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:292584)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "May be a transcriptional repressor of NRL function in photoreceptors. Does not repress CRX-mediated transactivation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0030971 receptor tyrosine kinase binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0000785 chromatin",
        "go_biological_process": "GO:0001934 positive regulation of protein phosphorylation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0L120-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L225-1",
        "uniprot_id": "A0ABK0L225_RAT",
        "mass": 47154.0,
        "length": 410,
        "protein_name": "DNA/RNA-binding protein KIN17",
        "gene_name": "Kin",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Kin",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "DNA/RNA-binding protein KIN17; Binding to curved DNA",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:689197);  (R-RNO-8876725)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Involved in DNA replication and the cellular response to DNA damage. May participate in DNA replication factories and create a bridge between DNA replication and repair mediated by high molecular weight complexes. May play a role in illegitimate recombination and regulation of gene expression. May participate in mRNA processing. Binds, in vitro, to double-stranded DNA. Also shown to bind preferentially to curved DNA in vitro and in vivo. Binds via its C-terminal domain to RNA in vitro., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003723 RNA binding;GO:0008270 zinc ion binding;GO:0003690 double-stranded DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005654 nucleoplasm;GO:0005829 cytosol;GO:0005681 spliceosomal complex",
        "go_biological_process": "GO:0006281 DNA repair;GO:0006310 DNA recombination;GO:0006397 mRNA processing;GO:0006260 DNA replication;GO:0006974 DNA damage response",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0L225-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L2E2-1",
        "uniprot_id": "A0ABK0L2E2_RAT",
        "mass": 43326.0,
        "length": 382,
        "protein_name": "Ssu-2 homolog",
        "gene_name": "Ssuh2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ssuh2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ssu-2 homolog",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "dentin dysplasia (Disease Ontology:DOID:701)",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
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        "predicted_glycosites": 0,
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    },
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        "protein_name": "Leishmanolysin-like peptidase",
        "gene_name": "Lmln",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Lmln",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Leishmanolysin-like peptidase; 3.4.24.-",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "function": "Metalloprotease., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0004222 metalloendopeptidase activity;GO:0046872 metal ion binding;GO:0008233 peptidase activity",
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    },
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        "protein_name": "Small nuclear ribonucleoprotein Sm D3",
        "gene_name": "Snrpd3",
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        "gene_names_uniprotkb": "Snrpd3; LOC687711; SNRPD3",
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        "protein_names_uniprotkb": "Small nuclear ribonucleoprotein Sm D3; Sm-D3; snRNP core protein D3",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "systemic lupus erythematosus (Disease Ontology:DOID:9074)",
        "pathway": " (rno:687711);  (R-RNO-111367);  (R-RNO-191859);  (R-RNO-72163);  (R-RNO-72165);  (R-RNO-73856);  (R-RNO-77588);  (R-RNO-9770562);  (R-RNO-9943411)",
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        "protein_names_uniprotkb": "Lymphocyte antigen 6 family member G6C",
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        "protein_names_uniprotkb": "[histone H3]-lysine(9) N-methyltransferase; 2.1.1.367",
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        "length": 837,
        "protein_name": "Oxysterol-binding protein",
        "gene_name": "Osbpl7",
        "organism": "Rat",
        "refseq_name": "oxysterol-binding protein-related protein 7 isoform 1",
        "refseq_ac": "NP_001427081",
        "gene_names_uniprotkb": "Osbpl7",
        "gene_names_refseq": "Osbpl7",
        "protein_names_uniprotkb": "Oxysterol-binding protein",
        "protein_names_refseq": "oxysterol-binding protein-related protein 7 isoform 1; oxysterol-binding protein-related protein 7",
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        "disease": "cholangiocarcinoma (Disease Ontology:DOID:4947)",
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        "go_molecular_function": "GO:0015485 cholesterol binding",
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        "go_biological_process": "GO:0120009 intermembrane lipid transfer;GO:0006869 lipid transport;GO:0071397 cellular response to cholesterol;GO:1901800 positive regulation of proteasomal protein catabolic process",
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        "uniprot_canonical_ac": "A0ABK0L3E5-1",
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        "length": 761,
        "protein_name": "Pleckstrin homology domain-containing family M member 3",
        "gene_name": "Plekhm3",
        "organism": "Rat",
        "refseq_name": "pleckstrin homology domain containing M3",
        "refseq_ac": "NP_001418184",
        "gene_names_uniprotkb": "Plekhm3",
        "gene_names_refseq": "Dapr; Plekhm1l; Plekhm3; RGD1307151",
        "protein_names_uniprotkb": "Pleckstrin homology domain-containing family M member 3",
        "protein_names_refseq": "differentiation associated protein; pleckstrin homology domain containing M3; pleckstrin homology domain containing, family M, member 1-like; pleckstrin homology domain containing, family M, member 3",
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        "disease": "",
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        "function": "Involved in skeletal muscle differentiation. May act as a scaffold protein for AKT1 during muscle differentiation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0008270 zinc ion binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005794 Golgi apparatus;GO:0005886 plasma membrane",
        "go_biological_process": "GO:0045445 myoblast differentiation",
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        "record_id": "A0ABK0KYD7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L397-1",
        "uniprot_id": "A0ABK0L397_RAT",
        "mass": 132370.0,
        "length": 1164,
        "protein_name": "RAN binding protein 17",
        "gene_name": "Ranbp17",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ranbp17",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "RAN binding protein 17",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:303029)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0031267 small GTPase binding;GO:0005049 nuclear export signal receptor activity",
        "go_cellular_component": "GO:0005643 nuclear pore;GO:0005737 cytoplasm;GO:0005634 nucleus",
        "go_biological_process": "GO:0006611 protein export from nucleus;GO:0006886 intracellular protein transport",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0L397-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0KXK2-1",
        "uniprot_id": "A0ABK0KXK2_RAT",
        "mass": 62107.0,
        "length": 572,
        "protein_name": "Solute carrier family 41 member",
        "gene_name": "Slc41a2",
        "organism": "Rat",
        "refseq_name": "solute carrier family 41 member 2 isoform 1",
        "refseq_ac": "NP_001388010",
        "gene_names_uniprotkb": "Slc41a2",
        "gene_names_refseq": "Slc41a2",
        "protein_names_uniprotkb": "Solute carrier family 41 member",
        "protein_names_refseq": "solute carrier family 41 (magnesium transporter), member 2; solute carrier family 41 member 2 isoform 1",
        "tax_id": 10116,
        "disease": "Parkinson's disease (Disease Ontology:DOID:14330)",
        "pathway": " (rno:362861);  (R-RNO-425410)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Acts as a magnesium transporter., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Acts as a plasma-membrane magnesium transporter. Can also mediate the transport of other divalent metal cations in an order of Ba(2+) > Ni(2+) > Co(2+) > Fe(2+) > Mn(2+)., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
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        "mined_o_glycosites": 0,
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        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
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        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 1,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "2.7.11.1",
        "go_molecular_function": "GO:0008324 monoatomic cation transmembrane transporter activity;GO:0022857 transmembrane transporter activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0015693 magnesium ion transport;GO:0030001 metal ion transport;GO:0006826 iron ion transport;GO:0006828 manganese ion transport;GO:0015675 nickel cation transport",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0KXK2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0KXQ6-1",
        "uniprot_id": "A0ABK0KXQ6_RAT",
        "mass": 27726.0,
        "length": 237,
        "protein_name": "Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase",
        "gene_name": "Hacd4",
        "organism": "Rat",
        "refseq_name": "very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 4 isoform X1",
        "refseq_ac": "XP_006238438",
        "gene_names_uniprotkb": "Hacd4; Ptplad2",
        "gene_names_refseq": "Hacd4; Ptplad2; RGD1310339",
        "protein_names_uniprotkb": "Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase; 4.2.1.134",
        "protein_names_refseq": "very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 4 isoform X1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-75876)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Catalyzes the third of the four reactions of the long-chain fatty acids elongation cycle. This endoplasmic reticulum-bound enzymatic process, allows the addition of two carbons to the chain of long- and very long-chain fatty acids/VLCFAs per cycle. This enzyme catalyzes the dehydration of the 3-hydroxyacyl-CoA intermediate into trans-2,3-enoyl-CoA, within each cycle of fatty acid elongation. Thereby, it participates to the production of VLCFAs of different chain lengths that are involved in multiple biological processes as precursors of membrane lipids and lipid mediators., [UniProtKB, UniProtKB, 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_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "4.2.1.134;1.1.1.n12;4.2.1.107;4.2.1.119",
        "go_molecular_function": "GO:0102158 very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase activity;GO:0019899 enzyme binding;GO:0018812 3-hydroxyacyl-CoA dehydratase activity",
        "go_cellular_component": "GO:0005789 endoplasmic reticulum membrane;GO:0005783 endoplasmic reticulum",
        "go_biological_process": "GO:0006633 fatty acid biosynthetic process;GO:0030148 sphingolipid biosynthetic process;GO:0030497 fatty acid elongation;GO:0042761 very long-chain fatty acid biosynthetic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0KXQ6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L0N8-1",
        "uniprot_id": "A0ABK0L0N8_RAT",
        "mass": 75375.0,
        "length": 716,
        "protein_name": "Regulatory factor X5",
        "gene_name": "Rfx5",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Rfx5",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Regulatory factor X5",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "severe combined immunodeficiency (Disease Ontology:DOID:627)",
        "pathway": " (rno:310659)",
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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:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0043565 sequence-specific DNA binding;GO:0001228 DNA-binding transcription activator activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0090575 RNA polymerase II transcription regulator complex",
        "go_biological_process": "GO:0006357 regulation of transcription by RNA polymerase II;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0045348 positive regulation of MHC class II biosynthetic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0L0N8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L368-1",
        "uniprot_id": "A0ABK0L368_RAT",
        "mass": 93676.0,
        "length": 823,
        "protein_name": "F-box and leucine-rich repeat protein 13",
        "gene_name": "Fbxl13",
        "organism": "Rat",
        "refseq_name": "F-box and leucine-rich repeat protein 13 isoform X1",
        "refseq_ac": "XP_038962809",
        "gene_names_uniprotkb": "Fbxl13",
        "gene_names_refseq": "Fbxl13",
        "protein_names_uniprotkb": "F-box and leucine-rich repeat protein 13; Dynein regulatory complex subunit 6; F-box/LRR-repeat protein 13",
        "protein_names_refseq": "F-box and leucine-rich repeat protein 13 isoform X1",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Substrate-recognition component of the SCF (SKP1-CUL1-F-box protein)-type E3 ubiquitin ligase complex. Component of the nexin-dynein regulatory complex (N-DRC), a key regulator of ciliary/flagellar motility which maintains the alignment and integrity of the distal axoneme and regulates microtubule sliding in motile axonemes. Specifically targets CEP192 isoform 3 for ubiquitin-mediated proteolysis and thereby acts as a regulator of microtubule nucleation activity., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "reported_phosphosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005737 cytoplasm",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0L368-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L1R3-1",
        "uniprot_id": "A0ABK0L1R3_RAT",
        "mass": 59850.0,
        "length": 552,
        "protein_name": "Adenylyltransferase and sulfurtransferase MOCS3",
        "gene_name": "Mocs3",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Mocs3; MOCS3; UBA4",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Adenylyltransferase and sulfurtransferase MOCS3; Adenylyltransferase MOCS3; Molybdenum cofactor synthesis protein 3; Sulfur carrier protein MOCS2A adenylyltransferase; Sulfur carrier protein MOCS2A sulfurtransferase; Sulfurtransferase MOCS3",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-947581)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Plays a central role in 2-thiolation of mcm(5)S(2)U at tRNA wobble positions of cytosolic tRNA(Lys), tRNA(Glu) and tRNA(Gln). Also essential during biosynthesis of the molybdenum cofactor. Acts by mediating the C-terminal thiocarboxylation of sulfur carriers URM1 and MOCS2A. Its N-terminus first activates URM1 and MOCS2A as acyl-adenylates (-COAMP), then the persulfide sulfur on the catalytic cysteine is transferred to URM1 and MOCS2A to form thiocarboxylation (-COSH) of their C-terminus. The reaction probably involves hydrogen sulfide that is generated from the persulfide intermediate and that acts as nucleophile towards URM1 and MOCS2A. Subsequently, a transient disulfide bond is formed. Does not use thiosulfate as sulfur donor; NFS1 probably acting as a sulfur donor for thiocarboxylation reactions., [UniProtKB, HAMAP, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "reported_s_glycosites_with_glycan": 0,
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        "reported_mutagensis": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "2.7.7.80;2.8.1.11",
        "go_molecular_function": "GO:0005524 ATP binding;GO:0046872 metal ion binding;GO:0016779 nucleotidyltransferase activity;GO:0004792 thiosulfate-cyanide sulfurtransferase activity;GO:0042292 URM1 activating enzyme activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0002143 tRNA wobble position uridine thiolation;GO:0006777 Mo-molybdopterin cofactor biosynthetic process;GO:0032447 protein urmylation;GO:0034227 tRNA thio-modification;GO:0002098 tRNA wobble uridine modification",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0L1R3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0KZC1-1",
        "uniprot_id": "A0ABK0KZC1_RAT",
        "mass": 34635.0,
        "length": 307,
        "protein_name": "Transmembrane inner ear",
        "gene_name": "Tmie",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Tmie",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Transmembrane inner ear",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "autosomal recessive nonsyndromic deafness 6 (Disease Ontology:DOID:0110512); sensorineural hearing loss (Disease Ontology:DOID:10003)",
        "pathway": " (rno:501061)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "",
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005886 plasma membrane",
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        "length": 515,
        "protein_name": "Fatty acyl-CoA reductase",
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        "refseq_name": "fatty acyl-CoA reductase 2",
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        "gene_names_refseq": "Far2; Mlstd1; RGD1565966",
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        "protein_names_refseq": "fatty acyl-CoA reductase 2; male sterility domain containing 1",
        "tax_id": 10116,
        "disease": "dry eye syndrome (Disease Ontology:DOID:10140); alopecia (Disease Ontology:DOID:987)",
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        "function": "Catalyzes the reduction of fatty acyl-CoA to fatty alcohols., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_biological_process": "GO:0035336 long-chain fatty-acyl-CoA metabolic process;GO:1901568 fatty acid derivative metabolic process",
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        "length": 168,
        "protein_name": "Calcium binding protein 2",
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        "protein_names_uniprotkb": "Calcium binding protein 2",
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        "disease": "autosomal recessive nonsyndromic deafness 93 (Disease Ontology:DOID:0110537)",
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        "gene_names_uniprotkb": "Samd13; LOC56764",
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        "protein_names_uniprotkb": "Sterile alpha motif domain containing 13",
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    {
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        "length": 531,
        "protein_name": "Heat shock transcription factor 2",
        "gene_name": "Hsf2",
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        "refseq_name": "heat shock factor protein 2 isoform 2",
        "refseq_ac": "NP_001421483",
        "gene_names_uniprotkb": "Hsf2",
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        "protein_names_uniprotkb": "Heat shock transcription factor 2",
        "protein_names_refseq": "heat shock factor 2; heat shock factor protein 2 isoform 2; heat shock factor protein 2; heat shock transcription factor hsf2",
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        "publication_id_list": "16889897;21480429;28295305;28796250;35182974",
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        "function": "Both heat shock transcription 2 is linked to the heat shock response in retinal ganglion cells., [RefSeq, PubMed]; DOX induced mitochondrial ROS release to activate ERK1/2-mediated HSF2 nuclear translocation and AT1 R upregulation causing DOX-damaged heart failure in vitro and in vivo., [RefSeq, PubMed]; Heat shock transcription factor HSF2 modulates the autophagy response through the BTG2-SOD2 axis., [RefSeq, PubMed]; P53-mediated miR-18 repression activates HSF2 for IGF-IIR-dependent myocyte hypertrophy in hypertension-induced heart failure Publication Status: Online-Only, [RefSeq, PubMed]; The Hsf2 is mainly expressed in round spermatids in control testis. Hsf2 expression is significantly increased in both nuclei and cytoplasm of spermatocytes in 7-day cryptorchid testis., [RefSeq, PubMed]",
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        "refseq_ac": "XP_063137275",
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        "protein_names_uniprotkb": "Similar to human chromosome 1 open reading frame 54",
        "protein_names_refseq": "uncharacterized protein C1orf54 homolog isoform X4",
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        "protein_names_uniprotkb": "Regulator of nonsense transcripts 2; Up-frameshift suppressor 2 homolog",
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        "go_biological_process": "GO:0000184 nuclear-transcribed mRNA catabolic process, nonsense-mediated decay;GO:0001889 liver development;GO:0031100 animal organ regeneration",
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        "record_type": "protein"
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    {
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        "length": 676,
        "protein_name": "Protein NEDD1",
        "gene_name": "Nedd1",
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        "gene_names_uniprotkb": "Nedd1",
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        "protein_names_uniprotkb": "Protein NEDD1; Neural precursor cell expressed developmentally down-regulated protein 1",
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        "tax_id": 10116,
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        "pathway": " (rno:299730);  (R-RNO-2565942);  (R-RNO-380259);  (R-RNO-380270);  (R-RNO-380284);  (R-RNO-380320);  (R-RNO-5620912);  (R-RNO-8854518)",
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        "go_molecular_function": "GO:0043015 gamma-tubulin binding",
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        "go_biological_process": "GO:0000278 mitotic cell cycle;GO:0007020 microtubule nucleation;GO:0051301 cell division",
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        "length": 1108,
        "protein_name": "WW and C2 domain containing 1",
        "gene_name": "Wwc1",
        "organism": "Rat",
        "refseq_name": "protein KIBRA",
        "refseq_ac": "NP_001414291",
        "gene_names_uniprotkb": "Wwc1",
        "gene_names_refseq": "RGD1308329; Wwc1",
        "protein_names_uniprotkb": "WW and C2 domain containing 1",
        "protein_names_refseq": "WW, C2 and coiled-coil domain containing 1; protein KIBRA",
        "tax_id": 10116,
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        "pathway": " (rno:303039);  (R-RNO-2028269)",
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        "publication_id_list": "24117625;24141945;38906255",
        "class_list": "",
        "function": "KIBRA levels in the rodent hippocampus correlate closely both to spatial memory performance in rodents and to PKMzeta, [RefSeq, PubMed]; Results provide the first evidence that KIBRA as well as PKMzeta is closely related to reference memory but not working memory in rats, [RefSeq, PubMed]; WWC1 upregulation accelerates hyperuricemia by reduction in renal uric acid excretion through Hippo signaling pathway., [RefSeq, PubMed]",
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        "go_biological_process": "GO:0046621 negative regulation of organ growth;GO:0035330 regulation of hippo signaling;GO:0006351 DNA-templated transcription;GO:0016477 cell migration;GO:0006355 regulation of DNA-templated transcription",
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        "protein_name": "Teashirt zinc finger homeobox 2",
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        "gene_names_uniprotkb": "Tshz2",
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        "protein_names_uniprotkb": "Teashirt zinc finger homeobox 2",
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    {
        "uniprot_canonical_ac": "A0ABK0KXT4-1",
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        "length": 490,
        "protein_name": "Zinc finger protein 3",
        "gene_name": "Zfp113",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Zfp113",
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        "protein_names_uniprotkb": "Zinc finger protein 3",
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        "gene_names_refseq": "Sec22c",
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        "protein_names_refseq": "chondroitin beta1,4 N-acetylgalactosaminyltransferase; chondroitin sulfate N-acetylgalactosaminyltransferase 1",
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    },
    {
        "uniprot_canonical_ac": "A0ABK0L3M9-1",
        "uniprot_id": "A0ABK0L3M9_RAT",
        "mass": 46778.0,
        "length": 422,
        "protein_name": "RT1 class I, locus1",
        "gene_name": "RT1-CE1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "RT1-CE1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "RT1 class I, locus1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "Stevens-Johnson syndrome (Disease Ontology:DOID:0050426); colitis (Disease Ontology:DOID:0060180); Cytomegalovirus retinitis (Disease Ontology:DOID:0080160); COVID-19 (Disease Ontology:DOID:0080600); ankylosing spondylitis 1 (Disease Ontology:DOID:0080603); erythema nodosum (Disease Ontology:DOID:0080750); occupational asthma (Disease Ontology:DOID:0080820); birdshot chorioretinopathy (Disease Ontology:DOID:0111079); psoriasis 1 (Disease Ontology:DOID:0111286); sensorineural hearing loss (Disease Ontology:DOID:10003); spondyloarthropathy (Disease Ontology:DOID:1123); trachoma (Disease Ontology:DOID:11265); sarcoidosis (Disease Ontology:DOID:11335); retinal vasculitis (Disease Ontology:DOID:11563); otosclerosis (Disease Ontology:DOID:12185); Graves' disease (Disease Ontology:DOID:12361); respiratory syncytial virus infectious disease (Disease Ontology:DOID:1273); retinopathy of prematurity (Disease Ontology:DOID:13025); uveitis (Disease Ontology:DOID:13141); Behcet's disease (Disease Ontology:DOID:13241); anterior uveitis (Disease Ontology:DOID:1407); cystic fibrosis (Disease Ontology:DOID:1485); hepatitis C (Disease Ontology:DOID:1883); Takayasu's arteritis (Disease Ontology:DOID:2508); synovitis (Disease Ontology:DOID:2703); dermatitis (Disease Ontology:DOID:2723); asthma (Disease Ontology:DOID:2841); severe acute respiratory syndrome (Disease Ontology:DOID:2945); cerebral infarction (Disease Ontology:DOID:3526); acute retinal necrosis syndrome (Disease Ontology:DOID:3611); thrombophlebitis (Disease Ontology:DOID:3875); tuberculosis (Disease Ontology:DOID:399); cervical cancer (Disease Ontology:DOID:4362); allergic rhinitis (Disease Ontology:DOID:4481); human immunodeficiency virus infectious disease (Disease Ontology:DOID:526); uveal melanoma (Disease Ontology:DOID:6039); reactive arthritis (Disease Ontology:DOID:6196); myositis (Disease Ontology:DOID:633); ankylosing spondylitis (Disease Ontology:DOID:7147); diabetic retinopathy (Disease Ontology:DOID:8947); allergic asthma (Disease Ontology:DOID:9415); Meniere's disease (Disease Ontology:DOID:9849); alopecia (Disease Ontology:DOID:987); mitral valve prolapse (Disease Ontology:DOID:988)",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Involved in the presentation of foreign antigens to the immune system., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "biomarker_type": "",
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        "glyco_site_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0030670 phagocytic vesicle membrane;GO:0042612 MHC class I protein complex;GO:0098553 lumenal side of endoplasmic reticulum membrane",
        "go_biological_process": "GO:0002474 antigen processing and presentation of peptide antigen via MHC class I",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0L3M9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L3Q2-1",
        "uniprot_id": "A0ABK0L3Q2_RAT",
        "mass": 37887.0,
        "length": 334,
        "protein_name": "Ig-like domain-containing protein",
        "gene_name": "RT1-M10-ps4",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "RT1-M10-ps4; H2-M10.3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ig-like domain-containing protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "Stevens-Johnson syndrome (Disease Ontology:DOID:0050426); colitis (Disease Ontology:DOID:0060180); Cytomegalovirus retinitis (Disease Ontology:DOID:0080160); COVID-19 (Disease Ontology:DOID:0080600); ankylosing spondylitis 1 (Disease Ontology:DOID:0080603); erythema nodosum (Disease Ontology:DOID:0080750); occupational asthma (Disease Ontology:DOID:0080820); birdshot chorioretinopathy (Disease Ontology:DOID:0111079); psoriasis 1 (Disease Ontology:DOID:0111286); sensorineural hearing loss (Disease Ontology:DOID:10003); spondyloarthropathy (Disease Ontology:DOID:1123); trachoma (Disease Ontology:DOID:11265); sarcoidosis (Disease Ontology:DOID:11335); retinal vasculitis (Disease Ontology:DOID:11563); otosclerosis (Disease Ontology:DOID:12185); Graves' disease (Disease Ontology:DOID:12361); retinopathy of prematurity (Disease Ontology:DOID:13025); uveitis (Disease Ontology:DOID:13141); Behcet's disease (Disease Ontology:DOID:13241); anterior uveitis (Disease Ontology:DOID:1407); Takayasu's arteritis (Disease Ontology:DOID:2508); synovitis (Disease Ontology:DOID:2703); dermatitis (Disease Ontology:DOID:2723); asthma (Disease Ontology:DOID:2841); severe acute respiratory syndrome (Disease Ontology:DOID:2945); cerebral infarction (Disease Ontology:DOID:3526); acute retinal necrosis syndrome (Disease Ontology:DOID:3611); thrombophlebitis (Disease Ontology:DOID:3875); tuberculosis (Disease Ontology:DOID:399); cervical cancer (Disease Ontology:DOID:4362); human immunodeficiency virus infectious disease (Disease Ontology:DOID:526); uveal melanoma (Disease Ontology:DOID:6039); reactive arthritis (Disease Ontology:DOID:6196); ankylosing spondylitis (Disease Ontology:DOID:7147); diabetic retinopathy (Disease Ontology:DOID:8947); allergic asthma (Disease Ontology:DOID:9415); Meniere's disease (Disease Ontology:DOID:9849); alopecia (Disease Ontology:DOID:987); mitral valve prolapse (Disease Ontology:DOID:988)",
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        "pathway_count": 0,
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        "function": "Involved in the presentation of foreign antigens to the immune system., [UniProtKB, UniProtKB]",
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0016020 membrane",
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        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0L3Q2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L539-1",
        "uniprot_id": "A0ABK0L539_RAT",
        "mass": 40722.0,
        "length": 369,
        "protein_name": "G patch domain and ankyrin repeats 1",
        "gene_name": "Gpank1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Gpank1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "G patch domain and ankyrin repeats 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway_count": 0,
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        "reported_c_glycosites_with_glycan": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003676 nucleic acid binding",
        "go_cellular_component": "",
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        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0L539-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L608-1",
        "uniprot_id": "A0ABK0L608_RAT",
        "mass": 47314.0,
        "length": 423,
        "protein_name": "Peptidyl-prolyl cis-trans isomerase E",
        "gene_name": "Ppie",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ppie",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Peptidyl-prolyl cis-trans isomerase E; 5.2.1.8; Cyclophilin E; Rotamase E",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-6781823);  (R-RNO-6782135);  (R-RNO-6782210);  (R-RNO-6798695);  (R-RNO-72163)",
        "pathway_count": 5,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Catalyzes the cis-trans isomerization of proline imidic peptide bonds in proteins., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Involved in pre-mRNA splicing as component of the spliceosome. Combines RNA-binding and PPIase activities. Binds mRNA and has a preference for single-stranded RNA molecules with poly-A and poly-U stretches, suggesting it binds to the poly(A)-region in the 3'-UTR of mRNA molecules. Catalyzes the cis-trans isomerization of proline imidic peptide bonds in proteins. Inhibits KMT2A activity; this requires proline isomerase activity., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "6.5.1.1;3.6.4.13;2.3.2.32;2.7.7.7;5.2.1.8;5.6.2.3;1.1.1.205;3.2.1.23;2.7.7.6;3.5.4.5;2.3.2.5;2.4.1.25;3.2.1.33;4.2.99.18;5.6.2.4;4.1.2.4;2.4.1.186;3.5.4.6;3.1.1.47;2.7.1.35;3.1.11.-;3.4.22.1;1.11.1.6;2.5.1.18;4.1.2.13;3.6.5.-;4.2.1.24;3.2.1.31;2.4.1.1;2.7.10.2;2.7.11.1;2.7.1.40;1.13.11.-;1.13.11.34;3.4.19.1;2.3.3.8;1.16.3.1;2.7.4.6;2.7.13.3;3.4.23.5;5.4.2.11;5.4.2.4;2.7.1.1;3.3.2.6;3.4.11.4;2.7.1.11;5.3.2.1;5.3.3.12;3.4.21.46;3.1.6.4;2.4.2.7;5.4.2.2;1.1.1.42;3.6.4.6;3.4.24.35;3.1.6.12;2.3.2.26;2.7.11.22;2.7.11.23;2.7.11.24;3.6.4.10;2.4.2.1;3.4.22.52;3.4.22.27;3.4.19.12;2.7.11.39;5.3.1.9;5.1.3.-;3.5.1.23;3.5.1.-;3.6.1.6;3.4.25.1;2.3.2.27;3.4.18.1;1.11.1.24",
        "go_molecular_function": "GO:0003723 RNA binding;GO:0003755 peptidyl-prolyl cis-trans isomerase activity;GO:0016018 cyclosporin A binding;GO:0003729 mRNA binding;GO:0008143 poly(A) binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0071013 catalytic step 2 spliceosome;GO:0005634 nucleus;GO:0016607 nuclear speck;GO:0005681 spliceosomal complex",
        "go_biological_process": "GO:0006457 protein folding;GO:0000398 mRNA splicing, via spliceosome;GO:0006355 regulation of DNA-templated transcription;GO:0045070 positive regulation of viral genome replication",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0L608-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L6V7-1",
        "uniprot_id": "A0ABK0L6V7_RAT",
        "mass": 181736.0,
        "length": 1598,
        "protein_name": "Phosphatidylinositol 3,4,5-trisphosphate-dependent Rac exchanger 2 protein",
        "gene_name": "Prex2",
        "organism": "Rat",
        "refseq_name": "phosphatidylinositol 3,4,5-trisphosphate-dependent Rac exchanger 2 protein",
        "refseq_ac": "NP_001380724",
        "gene_names_uniprotkb": "Prex2",
        "gene_names_refseq": "Depdc2; Prex2",
        "protein_names_uniprotkb": "Phosphatidylinositol 3,4,5-trisphosphate-dependent Rac exchanger 2 protein; DEP domain-containing protein 2",
        "protein_names_refseq": "DEP domain containing 2; phosphatidylinositol 3,4,5-trisphosphate-dependent Rac exchanger 2 protein",
        "tax_id": 10116,
        "disease": "hepatitis B (Disease Ontology:DOID:2043); lung squamous cell carcinoma (Disease Ontology:DOID:3907); lung non-small cell carcinoma (Disease Ontology:DOID:3908); Klatskin's tumor (Disease Ontology:DOID:4927); cholangiocarcinoma (Disease Ontology:DOID:4947); hepatocellular carcinoma (Disease Ontology:DOID:684)",
        "pathway": " (R-RNO-8948751);  (R-RNO-8980692);  (R-RNO-9013148);  (R-RNO-9013149)",
        "pathway_count": 4,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Functions as a RAC1 guanine nucleotide exchange factor (GEF), activating Rac proteins by exchanging bound GDP for free GTP. Its activity is synergistically activated by phosphatidylinositol 3,4,5-trisphosphate and the beta gamma subunits of heterotrimeric G protein. Mediates the activation of RAC1 in a PI3K-dependent manner. May be an important mediator of Rac signaling, acting directly downstream of both G protein-coupled receptors and phosphoinositide 3-kinase., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "reported_phosphosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 6,
        "glyco_site_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005085 guanyl-nucleotide exchange factor activity;GO:0005096 GTPase activator activity;GO:0030291 protein serine/threonine kinase inhibitor activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0035556 intracellular signal transduction;GO:0007186 G protein-coupled receptor signaling pathway;GO:0032007 negative regulation of TOR signaling;GO:0008344 adult locomotory behavior;GO:0048813 dendrite morphogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0L6V7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L514-1",
        "uniprot_id": "A0ABK0L514_RAT",
        "mass": 103771.0,
        "length": 918,
        "protein_name": "BBSome complex member BBS5",
        "gene_name": "Bbs5",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Bbs5",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "BBSome complex member BBS5; Kelch repeat and BTB domain-containing protein 10; Kelch-like protein 41",
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        "tax_id": 10116,
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        "protein_names_refseq": "discoidin, CUB and LCCL domain-containing protein 1 isoform 2 precursor; discoidin, CUB and LCCL domain-containing protein 1",
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        "protein_name": "Calcineurin-like EF-hand protein 1 like 1",
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        "ec_number_list": "2.3.2.32;2.7.7.7;5.6.2.3;2.4.2.-;2.3.2.27;3.1.-.-;2.7.7.49;3.6.4.12;3.1.11.-;2.3.2.-;4.2.99.18;4.2.99.-;2.4.2.30;3.1.11.2;3.1.21.-;2.7.11.22;2.7.11.23;2.7.11.24;5.6.2.4;1.14.11.-;2.3.2.23;3.6.-.-;3.2.1.143",
        "go_molecular_function": "GO:0016779 nucleotidyltransferase activity;GO:0003950 NAD+ poly-ADP-ribosyltransferase activity;GO:0140806 NAD+-protein-aspartate ADP-ribosyltransferase activity;GO:0140807 NAD+-protein-glutamate ADP-ribosyltransferase activity;GO:1990404 NAD+-protein mono-ADP-ribosyltransferase activity",
        "go_cellular_component": "GO:0005730 nucleolus;GO:0005694 chromosome;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0090734 site of DNA damage",
        "go_biological_process": "GO:0006302 double-strand break repair;GO:0070213 protein auto-ADP-ribosylation;GO:0006281 DNA repair;GO:0006284 base-excision repair;GO:0006974 DNA damage response",
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        "protein_name": "Ras GTPase-activating protein-binding protein 2",
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        "gene_names_uniprotkb": "G3bp2",
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        "protein_names_uniprotkb": "Ras GTPase-activating protein-binding protein 2; GAP SH3 domain-binding protein 2",
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        "tax_id": 10116,
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        "publication_id_list": "38843836",
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        "function": "Scaffold protein that plays an essential role in cytoplasmic stress granule formation which acts as a platform for antiviral signaling. Plays an essential role in stress granule formation. Stress granules are membraneless compartments that store mRNAs and proteins, such as stalled translation pre-initiation complexes, in response to stress. Promotes formation of stress granules phase-separated membraneless compartment by undergoing liquid-liquid phase separation (LLPS) upon unfolded RNA-binding: functions as a molecular switch that triggers RNA-dependent LLPS in response to a rise in intracellular free RNA concentrations., [UniProtKB, UniProtKB, UniProtKB]",
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    },
    {
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        "refseq_name": "",
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        "gene_names_uniprotkb": "Zfp14; LOC102546354",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "ZFP14 zinc finger protein",
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        "class_list": "",
        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "protein_names_uniprotkb": "Transmembrane protein 190",
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        "protein_name": "HYLS1, centriolar and ciliogenesis associated",
        "gene_name": "Hyls1",
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        "refseq_name": "centriolar and ciliogenesis-associated protein HYLS1",
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        "protein_names_uniprotkb": "HYLS1, centriolar and ciliogenesis associated",
        "protein_names_refseq": "centriolar and ciliogenesis-associated protein HYLS1; hydrolethalus syndrome 1; hydrolethalus syndrome protein 1",
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        "disease": "hydrolethalus syndrome (Disease Ontology:DOID:0050779); hydrolethalus syndrome 1 (Disease Ontology:DOID:0111355)",
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        "go_cellular_component": "GO:0005814 centriole;GO:0097730 non-motile cilium;GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005813 centrosome",
        "go_biological_process": "GO:0060271 cilium assembly;GO:0030030 cell projection organization",
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    {
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        "protein_name": "Single-pass membrane protein with coiled-coil domains 3 like 1",
        "gene_name": "Smco3l1; Smco3",
        "organism": "Rat",
        "refseq_name": "single-pass membrane and coiled-coil domain-containing protein 3",
        "refseq_ac": "XP_038964799",
        "gene_names_uniprotkb": "Smco3l1; Smco3; LOC100912259; RGD1560652; Smco3",
        "gene_names_refseq": "Smco3l1",
        "protein_names_uniprotkb": "Single-pass membrane protein with coiled-coil domains 3 like 1",
        "protein_names_refseq": "single-pass membrane and coiled-coil domain-containing protein 3",
        "tax_id": 10116,
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        "pathway": " (rno:100912259);  (rno:108348150)",
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    {
        "uniprot_canonical_ac": "A0ABK0L5Q0-1",
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        "length": 268,
        "protein_name": "JNK pathway associated phosphatase",
        "gene_name": "Dusp22",
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        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Dusp22",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "JNK pathway associated phosphatase; 3.1.3.16; 3.1.3.48; Low molecular weight dual specificity phosphatase 2",
        "protein_names_refseq": "",
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        "function": "Dual specificity phosphatase; can dephosphorylate both phosphotyrosine and phosphoserine or phosphothreonine residues. Activates the JNK signaling pathway. Inhibits T-cell receptor signaling and T-cell mediated immune responses, acting, at least in part, by inducing degradation of E3 ubiquitin ligase UBR2. Dephosphorylates and thereby induces 'Lys-48'-linked ubiquitination of UBR2, leading to proteasomal degradation of UBR2. Dephosphorylates and thereby inactivates tyrosine kinase LCK. Inhibits UBR2-mediated 'Lys-63'-linked ubiquitination of LCK. May play a role in B-cell receptor (BCR) signaling and B-cell function., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "3.1.3.48;3.1.3.16;2.7.10.1;3.1.3.53;3.1.3.2;3.1.3.52;3.1.3.21;3.1.3.18;3.1.3.67;3.1.3.-;3.1.3.27;3.1.3.5;2.7.11.22;3.1.3.74",
        "go_molecular_function": "GO:0004722 protein serine/threonine phosphatase activity;GO:0004725 protein tyrosine phosphatase activity;GO:1990782 protein tyrosine kinase binding;GO:0008138 protein tyrosine/serine/threonine phosphatase activity;GO:0030292 protein tyrosine kinase inhibitor activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0061851 leading edge of lamellipodium;GO:0031941 filamentous actin",
        "go_biological_process": "GO:0007162 negative regulation of cell adhesion;GO:0046330 positive regulation of JNK cascade;GO:0007179 transforming growth factor beta receptor signaling pathway;GO:0050860 negative regulation of T cell receptor signaling pathway;GO:0002710 negative regulation of T cell mediated immunity",
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    {
        "uniprot_canonical_ac": "A0ABK0L579-1",
        "uniprot_id": "A0ABK0L579_RAT",
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        "length": 395,
        "protein_name": "Small ribosomal subunit protein uS2m",
        "gene_name": "Mrps2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Mrps2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Small ribosomal subunit protein uS2m; 28S ribosomal protein S2, mitochondrial",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "intrinsic cardiomyopathy (Disease Ontology:DOID:0060036); combined oxidative phosphorylation deficiency 36 (Disease Ontology:DOID:0111482)",
        "pathway": " (rno:362094);  (R-RNO-5389840);  (R-RNO-5419276);  (R-RNO-9837999);  (R-RNO-9937383)",
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        "class_list": "",
        "function": "Required for mitoribosome formation and stability, and mitochondrial translation., [UniProtKB, UniProtKB, UniProtKB]",
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        "length": 234,
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        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Rnd1",
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        "protein_names_uniprotkb": "Rho family GTPase 1",
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        "pathway": " (rno:362993);  (R-RNO-416550);  (R-RNO-416572);  (R-RNO-9696273)",
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        "function": "Lacks intrinsic GTPase activity. Has a low affinity for GDP, and constitutively binds GTP. Controls rearrangements of the actin cytoskeleton. Induces the Rac-dependent neuritic process formation in part by disruption of the cortical actin filaments. Causes the formation of many neuritic processes from the cell body with disruption of the cortical actin filaments., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003924 GTPase activity;GO:0005525 GTP binding;GO:0019901 protein kinase binding;GO:0005102 signaling receptor binding",
        "go_cellular_component": "GO:0005829 cytosol;GO:0005856 cytoskeleton;GO:0005886 plasma membrane;GO:0005912 adherens junction;GO:0015629 actin cytoskeleton",
        "go_biological_process": "GO:0007015 actin filament organization;GO:0007165 signal transduction;GO:0032956 regulation of actin cytoskeleton organization;GO:0007264 small GTPase-mediated signal transduction;GO:0007162 negative regulation of cell adhesion",
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    },
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        "protein_name": "NCK associated protein 1 like",
        "gene_name": "Nckap1l",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Nckap1l",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "NCK associated protein 1 like",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "developmental disorder of mental health (Disease Ontology:DOID:0060037); immunodeficiency 72 (Disease Ontology:DOID:0112015)",
        "pathway": " (rno:315348);  (R-RNO-2029482);  (R-RNO-4420097);  (R-RNO-5663213);  (R-RNO-6798695);  (R-RNO-9013149);  (R-RNO-9013404);  (R-RNO-9013423)",
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        "protein_name": "Kinesin family member 16B",
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        "refseq_ac": "",
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        "protein_names_uniprotkb": "Kinesin family member 16B",
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        "pathway": " (R-RNO-6811434);  (R-RNO-983189)",
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        "function": "Plus end-directed microtubule-dependent motor protein involved in endosome transport and receptor recycling and degradation. Regulates the plus end motility of early endosomes and the balance between recycling and degradation of receptors such as EGF receptor (EGFR) and FGF receptor (FGFR). Regulates the Golgi to endosome transport of FGFR-containing vesicles during early development, a key process for developing basement membrane and epiblast and primitive endoderm lineages during early postimplantation development., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005524 ATP binding;GO:0008017 microtubule binding;GO:0003777 microtubule motor activity;GO:0035091 phosphatidylinositol binding;GO:0016887 ATP hydrolysis activity",
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        "go_biological_process": "GO:0007018 microtubule-based movement;GO:0007169 cell surface receptor protein tyrosine kinase signaling pathway;GO:0016192 vesicle-mediated transport;GO:0047496 vesicle transport along microtubule;GO:0001919 regulation of receptor recycling",
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        "protein_name": "Conserved oligomeric Golgi complex subunit 5",
        "gene_name": "Cog5",
        "organism": "Rat",
        "refseq_name": "conserved oligomeric Golgi complex subunit 5",
        "refseq_ac": "NP_001385716",
        "gene_names_uniprotkb": "Cog5",
        "gene_names_refseq": "Cog5; RGD1563296",
        "protein_names_uniprotkb": "Conserved oligomeric Golgi complex subunit 5",
        "protein_names_refseq": "conserved oligomeric Golgi complex subunit 5",
        "tax_id": 10116,
        "disease": "congenital disorder of glycosylation type IIi (Disease Ontology:DOID:0070261)",
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        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0017119 Golgi transport complex;GO:0005794 Golgi apparatus",
        "go_biological_process": "GO:0006891 intra-Golgi vesicle-mediated transport;GO:0007030 Golgi organization;GO:0000301 retrograde transport, vesicle recycling within Golgi;GO:0048219 inter-Golgi cisterna vesicle-mediated transport",
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        "uniprot_id": "A0ABK0L4S1_RAT",
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        "length": 315,
        "protein_name": "NADH-cytochrome b5 reductase-like",
        "gene_name": "Cyb5rl",
        "organism": "Rat",
        "refseq_name": "cytochrome b5 reductase-like",
        "refseq_ac": "NP_001398802",
        "gene_names_uniprotkb": "Cyb5rl",
        "gene_names_refseq": "Cyb5rl",
        "protein_names_uniprotkb": "NADH-cytochrome b5 reductase-like; 1.6.2.2",
        "protein_names_refseq": "NADH-cytochrome b5 reductase-like; cytochrome b5 reductase-like",
        "tax_id": 10116,
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        "pathway": " (R-RNO-1237044)",
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        "publication_id_list": "",
        "class_list": "",
        "function": "NADH-cytochrome b5 reductases are involved in desaturation and elongation of fatty acids, cholesterol biosynthesis, drug metabolism, and, in erythrocyte, methemoglobin reduction., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "ec_number_list": "1.6.2.2",
        "go_molecular_function": "GO:0016491 oxidoreductase activity;GO:0090524 cytochrome-b5 reductase activity, acting on NADH;GO:0004128 cytochrome-b5 reductase activity, acting on NAD(P)H",
        "go_cellular_component": "GO:0005789 endoplasmic reticulum membrane",
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    {
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        "protein_name": "Serine/threonine-protein kinase Nek10",
        "gene_name": "Nek10",
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        "gene_names_uniprotkb": "Nek10; RGD1564342",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Serine/threonine-protein kinase Nek10; 2.7.11.1; Never in mitosis A-related kinase 10",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "primary ciliary dyskinesia 44 (Disease Ontology:DOID:0111851)",
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        "ec_number_list": "2.7.11.1;2.7.12.1;2.7.1.153;2.7.1.137;2.7.11.24;2.7.11.25;2.7.11.22;2.7.11.23;2.7.4.6;2.7.1.154;2.7.11.38;2.7.11.17;2.7.11.21;2.7.12.2;2.7.1.40;2.7.11.12;2.7.11.26;2.7.11.34;2.7.10.2;2.7.1.150;2.7.11.13;4.1.1.32;2.7.11.19;2.7.2.3;2.7.11.11;2.7.11.31;3.1.3.16;2.7.11.4;2.3.1.48;3.1.11.-;2.7.13.3;2.7.4.18;3.1.24.-;3.4.19.12;2.7.11.39;2.4.99.18;2.7.11.10",
        "go_molecular_function": "GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding;GO:0004672 protein kinase activity",
        "go_cellular_component": "GO:1902911 protein kinase complex;GO:0005576 extracellular region",
        "go_biological_process": "GO:1902749 regulation of cell cycle G2/M phase transition;GO:0006468 protein phosphorylation;GO:0043406 positive regulation of MAP kinase activity;GO:0070372 regulation of ERK1 and ERK2 cascade;GO:0031954 positive regulation of protein autophosphorylation",
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        "gene_name": "Lrrc74b",
        "organism": "Rat",
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        "gene_names_uniprotkb": "Lrrc74b; LOC100361946",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Leucine rich repeat containing 74B",
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        "tax_id": 10116,
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        "gene_names_uniprotkb": "Mmab",
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        "protein_names_uniprotkb": "Corrinoid adenosyltransferase MMAB; ATP:co(I)rrinoid adenosyltransferase MMAB",
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        "function": "Converts cob(I)alamin to adenosylcobalamin (adenosylcob(III)alamin), a coenzyme for methylmalonyl-CoA mutase, therefore participates in the final step of the vitamin B12 conversion. Generates adenosylcobalamin (AdoCbl) and directly delivers the cofactor to MUT in a transfer that is stimulated by ATP-binding to MMAB and gated by MMAA., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "protein_names_uniprotkb": "Olfactory receptor family 12 subfamily D member 2",
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        "protein_name": "Interleukin-17B",
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        "protein_names_uniprotkb": "Interleukin-17B; Neuronal interleukin-17-related factor",
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        "protein_name": "Solute carrier family 36 member 4",
        "gene_name": "Slc36a4",
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        "protein_names_uniprotkb": "Solute carrier family 36 member 4",
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        "go_cellular_component": "GO:0005774 vacuolar membrane;GO:0005765 lysosomal membrane",
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        "protein_names_uniprotkb": "Guanine nucleotide exchange factor subunit RIC1; Protein RIC1 homolog; RAB6A-GEF complex partner protein 1",
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        "pathway": " (R-RNO-6811438);  (R-RNO-6811440);  (R-RNO-8876198)",
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        "function": "The RIC1-RGP1 complex acts as a guanine nucleotide exchange factor (GEF), which activates RAB6A by exchanging bound GDP for free GTP, and may thereby be required for efficient fusion of endosome-derived vesicles with the Golgi compartment. The RIC1-RGP1 complex participates in the recycling of mannose-6-phosphate receptors. Required for phosphorylation and localization of GJA1. Is a regulator of procollagen transport and secretion, and is required for correct cartilage morphogenesis and development of the craniofacial skeleton., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "protein_names_refseq": "biogenesis of lysosome-related organelles complex 1 subunit 3; biogenesis of lysosome-related organelles complex-1, subunit 3",
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        "disease": "Hermansky-Pudlak syndrome 8 (Disease Ontology:DOID:0060546)",
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        "function": "Component of the BLOC-1 complex, a complex that is required for normal biogenesis of lysosome-related organelles (LRO)., [UniProtKB, UniProtKB]",
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        "protein_names_uniprotkb": "Beta-sarcoglycan",
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        "disease": "autosomal recessive limb-girdle muscular dystrophy type 2E (Disease Ontology:DOID:0110279); muscular dystrophy (Disease Ontology:DOID:9884)",
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        "function": "Component of the sarcoglycan complex, a subcomplex of the dystrophin-glycoprotein complex which forms a link between the F-actin cytoskeleton and the extracellular matrix., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "protein_name": "Cytosolic carboxypeptidase 1",
        "gene_name": "Agtpbp1",
        "organism": "Rat",
        "refseq_name": "cytosolic carboxypeptidase 1 isoform 1",
        "refseq_ac": "NP_001099570",
        "gene_names_uniprotkb": "Agtpbp1",
        "gene_names_refseq": "Agtpbp1",
        "protein_names_uniprotkb": "Cytosolic carboxypeptidase 1; 3.4.17.24; ATP/GTP-binding protein 1; Protein deglutamylase CCP1",
        "protein_names_refseq": "ATP/GTP binding protein 1; cytosolic carboxypeptidase 1 isoform 1; cytosolic carboxypeptidase 1",
        "tax_id": 10116,
        "disease": "retinitis pigmentosa (Disease Ontology:DOID:10584)",
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        "protein_names_refseq": "hydroxyacylglutathione hydrolase-like protein isoform X1",
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        "protein_names_uniprotkb": "Ras-related protein Rab-36; 3.6.5.2",
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        "function": "The small GTPases Rab are key regulators of intracellular membrane trafficking, from the formation of transport vesicles to their fusion with membranes. Rabs cycle between an inactive GDP-bound form and an active GTP-bound form that is able to recruit to membranes different sets of downstream effectors directly responsible for vesicle formation, movement, tethering and fusion., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "function": "Coreceptor for SEMA3A, SEMA3C, SEMA3F and SEMA6D. Necessary for signaling by class 3 semaphorins and subsequent remodeling of the cytoskeleton. Plays a role in axon guidance, invasive growth and cell migration. Class 3 semaphorins bind to a complex composed of a neuropilin and a plexin. The plexin modulates the affinity of the complex for specific semaphorins, and its cytoplasmic domain is required for the activation of down-stream signaling events in the cytoplasm. Acts as coreceptor of TREM2 for SEMA6D in dendritic cells and is involved in the generation of immune responses and skeletal homeostasis., [UniProtKB, UniProtKB, UniProtKB]",
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        "protein_name": "COP9 signalosome complex subunit 9",
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        "protein_names_refseq": "COP9 signalosome complex subunit 9; myeloma overexpressed 2",
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        "length": 392,
        "protein_name": "SRY-box transcription factor 1",
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        "refseq_name": "transcription factor SOX-1",
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        "protein_names_uniprotkb": "SRY-box transcription factor 1",
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        "disease": "X-linked panhypopituitarism (Disease Ontology:DOID:0111779)",
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        "function": "Results show that Sox-1 expression decreases as the number of seizures increases, and this is probably due to an altered glutamate regulation by a dysfunctional Bergmann s glia, and suggest this mechanism as a one possible explanation of how the cerebellum participates in the pathophysiology of epilepsy., [RefSeq, PubMed]",
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    {
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        "length": 286,
        "protein_name": "Spermidine synthase",
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        "organism": "Rat",
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        "gene_names_uniprotkb": "LOC120101528",
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        "protein_names_uniprotkb": "Spermidine synthase; 2.5.1.16; Putrescine aminopropyltransferase",
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        "function": "Catalyzes the production of spermidine from putrescine and decarboxylated S-adenosylmethionine (dcSAM). Has a strong preference for putrescine as substrate, and has very low activity towards 1,3-diaminopropane. Has extremely low activity towards spermidine., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "protein_name": "Olfactory receptor",
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        "protein_names_refseq": "COX17 cytochrome c oxidase assembly homolog; COX17 cytochrome c oxidase copper chaperone; COX17 homolog, cytochrome c oxidase assembly protein; cytochrome c oxidase assembly homolog 17; cytochrome c oxidase, subunit XVII assembly protein homolog",
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        "protein_names_refseq": "charged multivesicular body protein 1b; chromatin modifying protein 1B",
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        "protein_names_refseq": "solute carrier family 25 (pyrimidine nucleotide carrier), member 33; solute carrier family 25 member 33",
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        "gene_names_refseq": "LOC134479709",
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        "protein_name": "G protein-coupled receptor 21",
        "gene_name": "Gpr21",
        "organism": "Rat",
        "refseq_name": "probable G-protein coupled receptor 21",
        "refseq_ac": "NP_001383750",
        "gene_names_uniprotkb": "Gpr21",
        "gene_names_refseq": "Gpr21",
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        "protein_names_refseq": "probable G-protein coupled receptor 21",
        "tax_id": 10116,
        "disease": "renal fibrosis (Disease Ontology:DOID:0050855); alcohol use disorder (Disease Ontology:DOID:1574)",
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        "function": "Modifications in GPR21 and GPR82 genes expression as a consequence of metabolic syndrome etiology., [RefSeq, PubMed]",
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        "protein_name": "non-specific serine/threonine protein kinase",
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        "protein_name": "Multifunctional fusion protein",
        "gene_name": "Fgf1",
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        "refseq_name": "fibroblast growth factor 1 isoform X2",
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        "gene_names_uniprotkb": "Fgf1",
        "gene_names_refseq": "FGF-1; Fgf1; Fgf2b; HBGF-1; HBGF1",
        "protein_names_uniprotkb": "Multifunctional fusion protein; Acidic fibroblast growth factor; Heparin-binding growth factor 1",
        "protein_names_refseq": "fibroblast growth factor 1 isoform X2",
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        "disease": "metabolic dysfunction-associated steatohepatitis (Disease Ontology:DOID:0080547); Alzheimer's disease (Disease Ontology:DOID:10652); urinary bladder cancer (Disease Ontology:DOID:11054); leiomyoma (Disease Ontology:DOID:127); extrahepatic cholestasis (Disease Ontology:DOID:13619); endometrial cancer (Disease Ontology:DOID:1380); brain ischemia (Disease Ontology:DOID:2316); ovarian cancer (Disease Ontology:DOID:2394); transitional cell carcinoma (Disease Ontology:DOID:2671); cerebrotendinous xanthomatosis (Disease Ontology:DOID:4810); schizophrenia (Disease Ontology:DOID:5419); myocardial infarction (Disease Ontology:DOID:5844); cleft lip (Disease Ontology:DOID:9296)",
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        "function": "Plays an important role in the regulation of cell survival, cell division, angiogenesis, cell differentiation and cell migration. Functions as potent mitogen in vitro. Acts as a ligand for FGFR1 and integrins. Binds to FGFR1 in the presence of heparin leading to FGFR1 dimerization and activation via sequential autophosphorylation on tyrosine residues which act as docking sites for interacting proteins, leading to the activation of several signaling cascades. Binds to integrins. Its binding to integrins and subsequent ternary complex formation with integrins and FGFR1 are essential for FGF1 signaling., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005178 integrin binding;GO:0008201 heparin binding;GO:0044548 S100 protein binding;GO:0008083 growth factor activity;GO:0030544 Hsp70 protein binding",
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        "protein_name": "Non-histone chromosomal protein HMG-17",
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        "protein_names_uniprotkb": "Non-histone chromosomal protein HMG-17; High mobility group nucleosome-binding domain-containing protein 2",
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        "protein_name": "Olfactory receptor",
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        "protein_names_refseq": "olfactory receptor 1138; olfactory receptor 7G1-like; olfactory receptor Olr1138; olfactory receptor gene Olr1138",
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        "gene_names_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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        "uniprot_canonical_ac": "A0ABK0L773-1",
        "uniprot_id": "A0ABK0L773_RAT",
        "mass": 82108.0,
        "length": 743,
        "protein_name": "Exocyst complex component 3-like protein",
        "gene_name": "Exoc3l1",
        "organism": "Rat",
        "refseq_name": "exocyst complex component 3-like protein",
        "refseq_ac": "NP_001099648",
        "gene_names_uniprotkb": "Exoc3l1",
        "gene_names_refseq": "Exoc3l1; Exoc3l; RGD1311132",
        "protein_names_uniprotkb": "Exocyst complex component 3-like protein",
        "protein_names_refseq": "exocyst complex component 3-like protein",
        "tax_id": 10116,
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        "pathway": " (rno:291961)",
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        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "As part of the exocyst, may play a role in regulated exocytosis of insulin granules., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0030141 secretory granule;GO:0000145 exocyst",
        "go_biological_process": "GO:0006887 exocytosis;GO:0030072 peptide hormone secretion",
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        "record_id": "A0ABK0L773-1",
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    },
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        "length": 319,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or8g20b",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr1280",
        "refseq_ac": "NP_001000517",
        "gene_names_uniprotkb": "Or8g20b",
        "gene_names_refseq": "Olr1280; Or8g20b",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 1280; olfactory receptor 144-like; olfactory receptor 1537-like; olfactory receptor Olr1280; olfactory receptor gene Olr1280",
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        "pathway": " (rno:315571)",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "protein_name": "Carboxylic ester hydrolase",
        "gene_name": "Ces1e",
        "organism": "Rat",
        "refseq_name": "carboxylesterase 1E precursor",
        "refseq_ac": "NP_113753",
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        "protein_names_uniprotkb": "Carboxylic ester hydrolase; 3.1.1.-",
        "protein_names_refseq": "ES-HTEL; carboxyesterase ES-3; carboxylesterase 1E precursor; carboxylesterase 1; egasyn; esterase 22; liver carboxylesterase 3; pI 5.5 esterase",
        "tax_id": 10116,
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        "function": "Comparative analysis of CES1 and CES2 in liver and small intestine of humans, monkeys, dogs, rabbits and rats, [RefSeq, PubMed]; Results demonstrate elevation of FC and depletion of cholesteryl esters by over-expression of hncCEH, which were resistant to compensatory responses by other enzymes of cholesterol homeostasis, [RefSeq, PubMed]",
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        "record_id": "A0ABK0L778-1",
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    },
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        "length": 1670,
        "protein_name": "NAC alpha domain containing",
        "gene_name": "Nacad",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Nacad",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "NAC alpha domain containing",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0051082 unfolded protein binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005854 nascent polypeptide-associated complex",
        "go_biological_process": "GO:0006612 protein targeting to membrane",
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        "hit_score": 0.2,
        "record_id": "A0ABK0L8A8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L7E8-1",
        "uniprot_id": "A0ABK0L7E8_RAT",
        "mass": 15546.0,
        "length": 151,
        "protein_name": "Transmembrane protein 242",
        "gene_name": "Tmem242",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Tmem242; RGD1307262",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Transmembrane protein 242",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:292228)",
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        "publication_id_list": "",
        "class_list": "",
        "function": "Scaffold protein that participates in the c-ring assembly of mitochondrial ATP synthase (F(1)F(0) ATP synthase or complex V) by facilitating the membrane insertion and oligomer formation of the subunit c/ATP5MC3. Participates in the incorporation of the c-ring into vestigial complexes. Additionally influences the incorporation of subunits MT-ATP6, MT-ATP8, ATP5MJ, and ATP5MK in the ATP synthase., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005743 mitochondrial inner membrane",
        "go_biological_process": "GO:0033615 mitochondrial proton-transporting ATP synthase complex assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0L7E8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L8K7-1",
        "uniprot_id": "A0ABK0L8K7_RAT",
        "mass": 36801.0,
        "length": 342,
        "protein_name": "AKT1 substrate 1",
        "gene_name": "Akt1s1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Akt1s1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "AKT1 substrate 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-165159);  (R-RNO-166208);  (R-RNO-198323);  (R-RNO-3371571)",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004860 protein kinase inhibitor activity;GO:0030291 protein serine/threonine kinase inhibitor activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0032991 protein-containing complex;GO:0031931 TORC1 complex",
        "go_biological_process": "GO:0048011 neurotrophin TRK receptor signaling pathway;GO:1904262 negative regulation of TORC1 signaling;GO:0032007 negative regulation of TOR signaling;GO:0006469 negative regulation of protein kinase activity;GO:0042981 regulation of apoptotic process",
        "synthesized_glycan_count": 0,
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        "record_id": "A0ABK0L8K7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LAB0-1",
        "uniprot_id": "A0ABK0LAB0_RAT",
        "mass": 128184.0,
        "length": 1182,
        "protein_name": "Tyrosine-protein kinase",
        "gene_name": "Abl2",
        "organism": "Rat",
        "refseq_name": "tyrosine-protein kinase ABL2",
        "refseq_ac": "NP_001382059",
        "gene_names_uniprotkb": "Abl2",
        "gene_names_refseq": "Abl2; Abll; Arg",
        "protein_names_uniprotkb": "Tyrosine-protein kinase; 2.7.10.2",
        "protein_names_refseq": "Abelson murine leukemia viral (v-abl) oncogene homolog 2; Abelson tyrosine-protein kinase 2; Abl1-related gene product; arg tyrosine kinase; c-abl oncogene 2, non-receptor tyrosine kinase; tyrosine-protein kinase ABL2; v-abl Abelson murine leukemia viral oncogene 2; v-abl Abelson murine leukemia viral oncogene homolog 2 (arg, Abelson-related gene)",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-9013149);  (R-RNO-9013423)",
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        "publication_count": 2,
        "publication_id_list": "22673903;32399753",
        "class_list": "",
        "function": "Abelson Kinases Mediate the Depression of Spontaneous Synaptic Activity Induced by Amyloid Beta 1-42 Peptides., [RefSeq, PubMed]",
        "predicted_glycosites": 1,
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        "ec_number_list": "2.7.12.1;2.7.10.1;2.7.11.1;2.7.1.153;2.7.1.137;2.7.10.2;2.7.12.2;2.7.1.40;2.7.11.13;3.6.5.2;2.7.10.4;3.1.4.4;2.7.1.32;2.7.1.82;2.7.11.23;1.6.3.-",
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        "refseq_ac": "NP_001178807",
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        "gene_names_refseq": "Polr3b; RGD1565311",
        "protein_names_uniprotkb": "DNA-directed RNA polymerase subunit beta; 2.7.7.6",
        "protein_names_refseq": "DNA-directed RNA polymerase III subunit RPC2; polymerase (RNA) III (DNA directed) polypeptide B; polymerase (RNA) III subunit B",
        "tax_id": 10116,
        "disease": "hypomyelinating leukodystrophy (Disease Ontology:DOID:0060786); hypomyelinating leukodystrophy 8 (Disease Ontology:DOID:0060797); Charcot-Marie-Tooth disease (Disease Ontology:DOID:10595)",
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        "go_biological_process": "GO:0006354 DNA-templated transcription elongation;GO:0042796 snRNA transcription by RNA polymerase III;GO:0006383 transcription by RNA polymerase III;GO:0006386 termination of RNA polymerase III transcription;GO:0045089 positive regulation of innate immune response",
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        "protein_names_uniprotkb": "Synphilin-1; Alpha-synuclein-interacting protein",
        "protein_names_refseq": "synphilin-1 isoform 2; synphilin-1; synuclein, alpha interacting protein (synphilin)",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:307309)",
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        "publication_id_list": "11956199;19224863",
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        "function": "Our data indicated that synphilin-1 is a synaptic partner of alpha-synuclein, and it may mediate synaptic roles attributed to alpha-synuclein. Erratum:[J Biol Chem 2002 Sep 13;277(37):34651-4], [RefSeq, PubMed]; Synphilin-1A has a novel role as a regulator of SIAH activity, modulating alpha-synuclein, and formation of Lewy body-like inclusions, [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0031625 ubiquitin protein ligase binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0036464 cytoplasmic ribonucleoprotein granule",
        "go_biological_process": "GO:0046928 regulation of neurotransmitter secretion;GO:0042417 dopamine metabolic process;GO:0090083 regulation of inclusion body assembly",
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    },
    {
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        "length": 286,
        "protein_name": "Leucine rich repeat containing 72",
        "gene_name": "Lrrc72",
        "organism": "Rat",
        "refseq_name": "leucine-rich repeat-containing protein 72",
        "refseq_ac": "NP_001418815",
        "gene_names_uniprotkb": "Lrrc72",
        "gene_names_refseq": "Lrrc72; RGD1560395",
        "protein_names_uniprotkb": "Leucine rich repeat containing 72",
        "protein_names_refseq": "leucine-rich repeat-containing protein 72",
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        "record_id": "A0ABK0L945-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L9M4-1",
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        "mass": 65219.0,
        "length": 572,
        "protein_name": "Spermatogenesis-associated protein 16",
        "gene_name": "Spata16",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Spata16",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Spermatogenesis-associated protein 16",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "spermatogenic failure 6 (Disease Ontology:DOID:0070167); male infertility (Disease Ontology:DOID:12336)",
        "pathway": " (rno:294932)",
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        "function": "",
        "predicted_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005794 Golgi apparatus",
        "go_biological_process": "GO:0007283 spermatogenesis;GO:0007286 spermatid development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0L9M4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LA32-1",
        "uniprot_id": "A0ABK0LA32_RAT",
        "mass": 122847.0,
        "length": 1106,
        "protein_name": "OTU domain-containing protein 4",
        "gene_name": "Otud4",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Otud4",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "OTU domain-containing protein 4; 3.4.19.12",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
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        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Deubiquitinase which hydrolyzes the isopeptide bond between the ubiquitin C-terminus and the lysine epsilon-amino group of the target protein. May negatively regulate inflammatory and pathogen recognition signaling in innate immune response. Upon phosphorylation at Ser-202 and Ser-204 residues, via IL-1 receptor and Toll-like receptor signaling pathway, specifically deubiquitinates 'Lys-63'-polyubiquitinated MYD88 adapter protein triggering down-regulation of NF-kappa-B-dependent transcription of inflammatory mediators. Independently of the catalytic activity, acts as a scaffold for alternative deubiquitinases to assemble specific deubiquitinase-substrate complexes. Associates with USP7 and USP9X deubiquitinases to stabilize alkylation repair enzyme ALKBH3, thereby promoting the repair of alkylated DNA lesions., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004843 cysteine-type deubiquitinase activity;GO:0061578 K63-linked deubiquitinase activity;GO:0060090 molecular adaptor activity",
        "go_cellular_component": "GO:0005829 cytosol",
        "go_biological_process": "GO:2000660 negative regulation of interleukin-1-mediated signaling pathway;GO:0006508 proteolysis;GO:0034122 negative regulation of toll-like receptor signaling pathway;GO:0070536 protein K63-linked deubiquitination;GO:0006307 DNA alkylation repair",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0LA32-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L7N2-1",
        "uniprot_id": "A0ABK0L7N2_RAT",
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        "length": 1028,
        "protein_name": "Caprin-2",
        "gene_name": "Caprin2",
        "organism": "Rat",
        "refseq_name": "caprin-2 isoform X1",
        "refseq_ac": "XP_038964833",
        "gene_names_uniprotkb": "Caprin2",
        "gene_names_refseq": "Adir; Caprin2; Rng140",
        "protein_names_uniprotkb": "Caprin-2; C1q domain-containing protein 1; Cytoplasmic activation/proliferation-associated protein 2; RNA granule protein 140",
        "protein_names_refseq": "caprin-2 isoform X1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:686779)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Promotes phosphorylation of the Wnt coreceptor LRP6, leading to increased activity of the canonical Wnt signaling pathway. Facilitates constitutive LRP6 phosphorylation by CDK14/CCNY during G2/M stage of the cell cycle, which may potentiate cells for Wnt signaling. May regulate the transport and translation of mRNAs, modulating for instance the expression of proteins involved in synaptic plasticity in neurons. Involved in regulation of growth as erythroblasts shift from a highly proliferative state towards their terminal phase of differentiation. May be involved in apoptosis., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "missing_score": 10000,
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        "ec_number_list": "",
        "go_molecular_function": "GO:0003723 RNA binding;GO:0046872 metal ion binding;GO:0005102 signaling receptor binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005886 plasma membrane;GO:0005739 mitochondrion;GO:0005829 cytosol;GO:0043235 receptor complex",
        "go_biological_process": "GO:0030154 cell differentiation;GO:0017148 negative regulation of translation;GO:0090263 positive regulation of canonical Wnt signaling pathway;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0030308 negative regulation of cell growth",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0L7N2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L9X6-1",
        "uniprot_id": "A0ABK0L9X6_RAT",
        "mass": 59880.0,
        "length": 569,
        "protein_name": "Small ArfGAP 1",
        "gene_name": "Smap1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Smap1; LOC684800",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Small ArfGAP 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "candidiasis (Disease Ontology:DOID:1508)",
        "pathway": " (rno:684800)",
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        "predicted_glycosites": 1,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005096 GTPase activator activity;GO:0008270 zinc ion binding;GO:0030276 clathrin binding",
        "go_cellular_component": "GO:0005737 cytoplasm",
        "go_biological_process": "GO:2000369 regulation of clathrin-dependent endocytosis;GO:0045648 positive regulation of erythrocyte differentiation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0L9X6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LAD0-1",
        "uniprot_id": "A0ABK0LAD0_RAT",
        "mass": 255796.0,
        "length": 2388,
        "protein_name": "Adenomatous polyposis coli protein 2",
        "gene_name": "Apc2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Apc2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Adenomatous polyposis coli protein 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "nicotine dependence (Disease Ontology:DOID:0050742); complex cortical dysplasia with other brain malformations 10 (Disease Ontology:DOID:0061143); familial adenomatous polyposis 1 (Disease Ontology:DOID:0080409); autosomal recessive intellectual developmental disorder 74 (Disease Ontology:DOID:0081218); Sotos syndrome 3 (Disease Ontology:DOID:0112104); intestinal cancer (Disease Ontology:DOID:10155); alcohol use disorder (Disease Ontology:DOID:1574); colorectal cancer (Disease Ontology:DOID:9256)",
        "pathway": " (rno:299611)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Stabilizes microtubules and may regulate actin fiber dynamics through the activation of Rho family GTPases. May also function in Wnt signaling by promoting the rapid degradation of CTNNB1., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 4,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 8,
        "glyco_site_count": 4,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008017 microtubule binding;GO:0008013 beta-catenin binding;GO:0045295 gamma-catenin binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0016342 catenin complex;GO:0030877 beta-catenin destruction complex;GO:0005794 Golgi apparatus;GO:0005874 microtubule",
        "go_biological_process": "GO:0001708 cell fate specification;GO:0007399 nervous system development;GO:0016477 cell migration;GO:0090090 negative regulation of canonical Wnt signaling pathway;GO:0016055 Wnt signaling pathway",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LAD0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L9L9-1",
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        "length": 745,
        "protein_name": "Microtubule-associated protein 7",
        "gene_name": "Map7",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Map7",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Microtubule-associated protein 7",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "publication_count": 1,
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        "biomarker_type": "",
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        "go_molecular_function": "GO:0005102 signaling receptor binding",
        "go_cellular_component": "GO:0015630 microtubule cytoskeleton;GO:0030424 axon;GO:0005829 cytosol;GO:0005886 plasma membrane",
        "go_biological_process": "GO:0000226 microtubule cytoskeleton organization;GO:0006970 response to osmotic stress;GO:0007283 spermatogenesis;GO:0008283 cell population proliferation;GO:0009566 fertilization",
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    },
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        "protein_name": "AMMECR1 like",
        "gene_name": "Ammecr1l",
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        "gene_names_uniprotkb": "Ammecr1l",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "AMMECR1 like",
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        "tax_id": 10116,
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        "pathway": " (rno:307526)",
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        "go_cellular_component": "GO:0005634 nucleus",
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        "record_id": "A0ABK0L963-1",
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    },
    {
        "uniprot_canonical_ac": "A0ABK0L995-1",
        "uniprot_id": "A0ABK0L995_RAT",
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        "length": 328,
        "protein_name": "Serine protease 55",
        "gene_name": "Prss55",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Prss55; LOC683415",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Serine protease 55",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (rno:683415)",
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        "go_molecular_function": "GO:0004252 serine-type endopeptidase activity;GO:0008236 serine-type peptidase activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0005829 cytosol;GO:0001669 acrosomal vesicle",
        "go_biological_process": "GO:0016485 protein processing;GO:0006508 proteolysis;GO:0007339 binding of sperm to zona pellucida;GO:0030317 flagellated sperm motility",
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        "hit_score": 0.1,
        "record_id": "A0ABK0L995-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LA20-1",
        "uniprot_id": "A0ABK0LA20_RAT",
        "mass": 51210.0,
        "length": 455,
        "protein_name": "E3 ubiquitin-protein ligase RNF25",
        "gene_name": "Rnf25",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Rnf25",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "E3 ubiquitin-protein ligase RNF25; 2.3.2.27; RING finger protein 25; RING finger protein AO7",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:301515);  (R-RNO-983168)",
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        "function": "E3 ubiquitin-protein ligase that plays a key role in the RNF14-RNF25 translation quality control pathway, a pathway that takes place when a ribosome has stalled during translation, and which promotes ubiquitination and degradation of translation factors on stalled ribosomes. Catalyzes ubiquitination of RPS27A in response to ribosome collisions, promoting activation of RNF14. RNF25 catalyzes ubiquitination of other ribosomal proteins on stalled ribosomes, such as RPL0, RPL1, RPL12, RPS13 and RPS17. Also involved in ubiquitination and degradation of stalled ETF1/eRF1. Independently of its function in the response to stalled ribosomes, mediates ubiquitination and subsequent proteasomal degradation of NKD2. May also stimulate transcription mediated by NF-kappa-B via its interaction with RELA/p65., [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",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0061630 ubiquitin protein ligase activity;GO:0051059 NF-kappaB binding;GO:0004842 ubiquitin-protein transferase activity",
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        "go_biological_process": "GO:0072344 rescue of stalled ribosome;GO:0006511 ubiquitin-dependent protein catabolic process;GO:0016567 protein ubiquitination;GO:0085020 protein K6-linked ubiquitination;GO:0160127 protein-RNA covalent cross-linking repair",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LA20-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L833-1",
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        "length": 478,
        "protein_name": "Metallophosphoesterase domain containing 1",
        "gene_name": "Mpped1",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Mpped1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Metallophosphoesterase domain containing 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (rno:362971)",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0004112 cyclic-nucleotide phosphodiesterase activity;GO:0016787 hydrolase activity",
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        "go_biological_process": "",
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        "hit_score": 0.1,
        "record_id": "A0ABK0L833-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L935-1",
        "uniprot_id": "A0ABK0L935_RAT",
        "mass": 91950.0,
        "length": 779,
        "protein_name": "Zinc finger protein 51",
        "gene_name": "Zfp51",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Zfp51; LOC103691005",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger protein 51",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:103691005)",
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        "class_list": "",
        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000976 transcription cis-regulatory region binding",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0006355 regulation of DNA-templated transcription",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0L935-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L8M4-1",
        "uniprot_id": "A0ABK0L8M4_RAT",
        "mass": 41057.0,
        "length": 364,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or5h18",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Or5h18",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (rno:404981)",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "",
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        "hit_score": 0.1,
        "record_id": "A0ABK0L8M4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L854-1",
        "uniprot_id": "A0ABK0L854_RAT",
        "mass": 52187.0,
        "length": 460,
        "protein_name": "Protein maelstrom homolog",
        "gene_name": "Mael",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Mael",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Protein maelstrom homolog",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:364039)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Plays a central role during spermatogenesis by repressing transposable elements and preventing their mobilization, which is essential for the germline integrity. Acts via the piRNA metabolic process, which mediates the repression of transposable elements during meiosis by forming complexes composed of piRNAs and Piwi proteins and governs the methylation and subsequent repression of transposons. Its association with piP-bodies suggests a participation in the secondary piRNAs metabolic process. Required for the localization of germ-cell factors to the meiotic nuage., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0043565 sequence-specific DNA binding;GO:0003677 DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0043186 P granule;GO:0005737 cytoplasm;GO:0048471 perinuclear region of cytoplasm;GO:0000785 chromatin",
        "go_biological_process": "GO:0007283 spermatogenesis;GO:0030154 cell differentiation;GO:0060964 regulation of miRNA-mediated gene silencing;GO:0045892 negative regulation of DNA-templated transcription;GO:0007140 male meiotic nuclear division",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0L854-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L940-1",
        "uniprot_id": "A0ABK0L940_RAT",
        "mass": 95706.0,
        "length": 887,
        "protein_name": "PAN2-PAN3 deadenylation complex subunit PAN3",
        "gene_name": "Pan3",
        "organism": "Rat",
        "refseq_name": "PAN2-PAN3 deadenylation complex subunit PAN3 isoform X1",
        "refseq_ac": "XP_006248904",
        "gene_names_uniprotkb": "Pan3; PAN3",
        "gene_names_refseq": "Pan3",
        "protein_names_uniprotkb": "PAN2-PAN3 deadenylation complex subunit PAN3; PAB1P-dependent poly(A)-specific ribonuclease; PAN deadenylation complex subunit 3; Poly(A)-nuclease deadenylation complex subunit 3",
        "protein_names_refseq": "PAN2-PAN3 deadenylation complex subunit PAN3 isoform X1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-429947)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Decreases PAN2-mediated deadenylation, possibly by preventing progression into the second CCR4-NOT mediated stage of biphasic deadenylation. Has a significant effect on mRNA stability, generally stabilizing a subset of the transcriptome. Stabilizes mRNAs degraded by the AU-rich element (ARE)-mediated mRNA decay pathway but promotes degradation of mRNAs by the microRNA-mediated pathway. Its activity influences mRNP remodeling, specifically reducing formation of a subset of P-bodies containing GW220, an isoform of TNRC6A., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Enhances PAN2 deadenylase activity and has an extensive effect on mRNA stability, generally enhancing mRNA decay across the transcriptome by multiple pathways, including the AU-rich element (ARE)-mediated pathway, microRNA-mediated pathway and the nonsense-mediated pathway (NMD). Its activity is required for efficient P-body formation. May be involved in regulating mRNAs of genes involved in cell cycle progression and cell proliferation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Regulatory subunit of the poly(A)-nuclease (PAN) deadenylation complex, one of two cytoplasmic mRNA deadenylases involved in general and miRNA-mediated mRNA turnover. PAN specifically shortens poly(A) tails of RNA and the activity is stimulated by poly(A)-binding protein (PABP). PAN deadenylation is followed by rapid degradation of the shortened mRNA tails by the CCR4-NOT complex. Deadenylated mRNAs are then degraded by two alternative mechanisms, namely exosome-mediated 3'-5' exonucleolytic degradation, or deadenlyation-dependent mRNA decaping and subsequent 5'-3' exonucleolytic degradation by XRN1. PAN3 acts as a positive regulator for PAN activity, recruiting the catalytic subunit PAN2 to mRNA via its interaction with RNA and PABP, and to miRNA targets via its interaction with GW182 family proteins., [UniProtKB, HAMAP, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004672 protein kinase activity;GO:0005524 ATP binding;GO:0008270 zinc ion binding;GO:0008143 poly(A) binding;GO:0003723 RNA binding",
        "go_cellular_component": "GO:0000932 P-body;GO:0031251 PAN complex",
        "go_biological_process": "GO:0006397 mRNA processing;GO:0010606 positive regulation of cytoplasmic mRNA processing body assembly;GO:0000289 nuclear-transcribed mRNA poly(A) tail shortening;GO:0000290 deadenylation-dependent decapping of nuclear-transcribed mRNA;GO:0006605 protein targeting",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0L940-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L9D5-1",
        "uniprot_id": "A0ABK0L9D5_RAT",
        "mass": 60202.0,
        "length": 542,
        "protein_name": "Carboxypeptidase N subunit 2",
        "gene_name": "Cpn2",
        "organism": "Rat",
        "refseq_name": "carboxypeptidase N subunit 2 isoform X1",
        "refseq_ac": "XP_063126561",
        "gene_names_uniprotkb": "Cpn2",
        "gene_names_refseq": "Cpn2; RGD1305170",
        "protein_names_uniprotkb": "Carboxypeptidase N subunit 2; Carboxypeptidase N 83 kDa chain; Carboxypeptidase N large subunit; Carboxypeptidase N polypeptide 2; Carboxypeptidase N regulatory subunit",
        "protein_names_refseq": "carboxypeptidase N subunit 2 isoform X1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:303861);  (R-RNO-977606)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "The 83 kDa subunit binds and stabilizes the catalytic subunit at 37 degrees Celsius and keeps it in circulation. Under some circumstances it may be an allosteric modifier of the catalytic subunit., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "mined_s_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0038023 signaling receptor activity",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0005886 plasma membrane",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0L9D5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L7J5-1",
        "uniprot_id": "A0ABK0L7J5_RAT",
        "mass": 72787.0,
        "length": 645,
        "protein_name": "Establishment of sister chromatid cohesion N-acetyltransferase 2",
        "gene_name": "Esco2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Esco2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Establishment of sister chromatid cohesion N-acetyltransferase 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "lung cancer (Disease Ontology:DOID:1324); lung adenocarcinoma (Disease Ontology:DOID:3910); Roberts syndrome (Disease Ontology:DOID:5325); rheumatoid arthritis (Disease Ontology:DOID:7148)",
        "pathway": " (rno:691979);  (R-RNO-2468052)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "reported_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 4,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "2.3.1.48;2.3.1.-;2.7.11.1;2.7.11.4;2.3.1.259;2.3.1.80",
        "go_molecular_function": "GO:0061733 protein-lysine-acetyltransferase activity;GO:0008270 zinc ion binding;GO:0016407 acetyltransferase activity;GO:0004468 L-lysine N-acetyltransferase activity, acting on acetyl phosphate as donor",
        "go_cellular_component": "GO:0005634 nucleus;GO:0000785 chromatin;GO:0005654 nucleoplasm;GO:0035861 site of double-strand break;GO:0005694 chromosome",
        "go_biological_process": "GO:0007064 mitotic sister chromatid cohesion;GO:0007059 chromosome segregation;GO:0006302 double-strand break repair;GO:0006275 regulation of DNA replication;GO:0002244 hematopoietic progenitor cell differentiation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0L7J5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L829-1",
        "uniprot_id": "A0ABK0L829_RAT",
        "mass": 24068.0,
        "length": 211,
        "protein_name": "Dickkopf like acrosomal protein 1",
        "gene_name": "Dkkl1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Dkkl1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Dickkopf like acrosomal protein 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:499150)",
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        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
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        "reported_o_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0048019 receptor antagonist activity;GO:0039706 co-receptor binding",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0001669 acrosomal vesicle",
        "go_biological_process": "GO:0090090 negative regulation of canonical Wnt signaling pathway;GO:0043065 positive regulation of apoptotic process;GO:0045600 positive regulation of fat cell differentiation;GO:0060070 canonical Wnt signaling pathway;GO:0007341 penetration of zona pellucida",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0L829-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L7Q4-1",
        "uniprot_id": "A0ABK0L7Q4_RAT",
        "mass": 66195.0,
        "length": 583,
        "protein_name": "Atlastin GTPase 2",
        "gene_name": "Atl2",
        "organism": "Rat",
        "refseq_name": "atlastin-2",
        "refseq_ac": "NP_001094141",
        "gene_names_uniprotkb": "Atl2",
        "gene_names_refseq": "Arl6ip2; Atl2",
        "protein_names_uniprotkb": "Atlastin GTPase 2",
        "protein_names_refseq": "ADP-ribosylation factor-like 6 interacting protein 2; atlastin-2",
        "tax_id": 10116,
        "disease": "hereditary spastic paraplegia 3A (Disease Ontology:DOID:0110791); hereditary spastic paraplegia (Disease Ontology:DOID:2476)",
        "pathway": " (rno:298757)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "",
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "3.6.5.2;3.6.1.1;3.6.5.-;3.6.5.3;2.3.2.27;2.7.11.1;3.6.5.5;3.6.1.5;3.6.1.-;3.6.5.4",
        "go_molecular_function": "GO:0003924 GTPase activity;GO:0005525 GTP binding;GO:0140523 GTPase-dependent fusogenic activity",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005789 endoplasmic reticulum membrane;GO:0098826 endoplasmic reticulum tubular network membrane",
        "go_biological_process": "GO:0051260 protein homooligomerization;GO:0007029 endoplasmic reticulum organization;GO:1990809 endoplasmic reticulum tubular network membrane organization;GO:0016320 endoplasmic reticulum membrane fusion",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0L7Q4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L9U0-1",
        "uniprot_id": "A0ABK0L9U0_RAT",
        "mass": 136736.0,
        "length": 1294,
        "protein_name": "Protein crumbs homolog 2",
        "gene_name": "Crb2",
        "organism": "Rat",
        "refseq_name": "protein crumbs homolog 2 isoform X1",
        "refseq_ac": "XP_063140332",
        "gene_names_uniprotkb": "Crb2",
        "gene_names_refseq": "Crb2; RGD1309368",
        "protein_names_uniprotkb": "Protein crumbs homolog 2; Crumbs-like protein 2",
        "protein_names_refseq": "protein crumbs homolog 2 isoform X1",
        "tax_id": 10116,
        "disease": "Leber congenital amaurosis 8 (Disease Ontology:DOID:0110079); retinitis pigmentosa 12 (Disease Ontology:DOID:0110358); focal segmental glomerulosclerosis 9 (Disease Ontology:DOID:0111134); ventriculomegaly - cystic kidney disease (Disease Ontology:DOID:0111625); retinitis pigmentosa (Disease Ontology:DOID:10584); Leber congenital amaurosis (Disease Ontology:DOID:14791); retinal disease (Disease Ontology:DOID:5679)",
        "pathway": " (rno:366031)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0005509 calcium ion binding;GO:0044877 protein-containing complex binding;GO:0019828 aspartic-type endopeptidase inhibitor activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0016324 apical plasma membrane;GO:0032991 protein-containing complex;GO:0035003 subapical complex;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0072359 circulatory system development;GO:0060042 retina morphogenesis in camera-type eye;GO:0003407 neural retina development;GO:0045494 photoreceptor cell maintenance;GO:0001756 somitogenesis",
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        "hit_score": 0.1,
        "record_id": "A0ABK0L9U0-1",
        "record_type": "protein"
    },
    {
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        "uniprot_id": "A0ABK0L8H6_RAT",
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        "length": 649,
        "protein_name": "Zinc finger CW-type and PWWP domain containing 1",
        "gene_name": "Zcwpw1",
        "organism": "Rat",
        "refseq_name": "zinc finger CW-type PWWP domain protein 1 isoform 3",
        "refseq_ac": "NP_001419010",
        "gene_names_uniprotkb": "Zcwpw1",
        "gene_names_refseq": "RGD1566138; Zcwpw1",
        "protein_names_uniprotkb": "Zinc finger CW-type and PWWP domain containing 1",
        "protein_names_refseq": "zinc finger CW-type PWWP domain protein 1 isoform 3; zinc finger CW-type PWWP domain protein 1; zinc finger, CW-type with PWWP domain 1",
        "tax_id": 10116,
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        "publication_id_list": "22673903",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0140566 histone reader activity;GO:0140002 histone H3K4me3 reader activity;GO:0140003 histone H3K36me3 reader activity",
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        "function": "As part of the central apparatus of the cilium axoneme may play a role in cilium movement. May play an important role in sperm architecture and function., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "protein_names_uniprotkb": "DNA 3'-5' helicase; 5.6.2.4",
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    {
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        "protein_name": "Integrin alpha-11",
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        "gene_names_uniprotkb": "Itga11",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Integrin alpha-11",
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        "tax_id": 10116,
        "disease": "pancreatic cancer (Disease Ontology:DOID:1793)",
        "pathway": " (rno:315744)",
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        "function": "Integrin alpha-11/beta-1 is a receptor for collagen., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0046872 metal ion binding;GO:0038023 signaling receptor activity;GO:0005518 collagen binding;GO:0038064 collagen receptor activity;GO:0098639 collagen binding involved in cell-matrix adhesion",
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        "go_biological_process": "GO:0007229 integrin-mediated signaling pathway;GO:0098609 cell-cell adhesion;GO:0007160 cell-matrix adhesion;GO:0033627 cell adhesion mediated by integrin;GO:0006929 substrate-dependent cell migration",
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        "gene_names_uniprotkb": "Iglon5",
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        "protein_names_uniprotkb": "IgLON family member 5",
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    {
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        "gene_names_uniprotkb": "Rgs20",
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        "protein_names_uniprotkb": "Regulator of G-protein signaling 20",
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        "function": "Inhibits signal transduction by increasing the GTPase activity of G protein alpha subunits thereby driving them into their inactive GDP-bound form. Binds selectively to G(z)-alpha and G(alpha)-i2 subunits, accelerates their GTPase activity and regulates their signaling activities. The G(z)-alpha activity is inhibited by the phosphorylation and palmitoylation of the G-protein. Negatively regulates mu-opioid receptor-mediated activation of the G-proteins., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005096 GTPase activator activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0009898 cytoplasmic side of plasma membrane;GO:0005802 trans-Golgi network",
        "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0001975 response to amphetamine;GO:0045744 negative regulation of G protein-coupled receptor signaling pathway;GO:0009968 negative regulation of signal transduction",
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    },
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        "uniprot_canonical_ac": "A0ABK0L8F8-1",
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        "length": 511,
        "protein_name": "Tripartite motif-containing 5",
        "gene_name": "Trim30d; Trim5",
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        "refseq_name": "",
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        "gene_names_uniprotkb": "Trim30d; Trim5; Trim30d; Trim5",
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        "protein_names_uniprotkb": "Tripartite motif-containing 5",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0003713 transcription coactivator activity;GO:0019901 protein kinase binding;GO:0030674 protein-macromolecule adaptor activity;GO:0042802 identical protein binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0000932 P-body;GO:1990462 omegasome",
        "go_biological_process": "GO:0044790 suppression of viral release by host;GO:0043410 positive regulation of MAPK cascade;GO:0045087 innate immune response;GO:0032880 regulation of protein localization;GO:0043123 positive regulation of canonical NF-kappaB signal transduction",
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    {
        "uniprot_canonical_ac": "A0ABK0L925-1",
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        "length": 910,
        "protein_name": "E3 ubiquitin-protein ligase RNF216",
        "gene_name": "Rnf216",
        "organism": "Rat",
        "refseq_name": "E3 ubiquitin-protein ligase RNF216 isoform 1",
        "refseq_ac": "NP_001100592",
        "gene_names_uniprotkb": "Rnf216",
        "gene_names_refseq": "RGD1565135; Rnf216",
        "protein_names_uniprotkb": "E3 ubiquitin-protein ligase RNF216; 2.3.2.27; RING finger protein 216; RING-type E3 ubiquitin transferase RNF216; Triad domain-containing protein 3; Ubiquitin-conjugating enzyme 7-interacting protein 1",
        "protein_names_refseq": "E3 ubiquitin-protein ligase RNF216 isoform 1; E3 ubiquitin-protein ligase RNF216",
        "tax_id": 10116,
        "disease": "Gordon Holmes syndrome (Disease Ontology:DOID:0111587)",
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        "function": "RNF216 mediates neuronal injury following experimental subarachnoid hemorrhage through the Arc/Arg3.1-AMPAR pathway. Erratum:[FASEB J. 2024 May 15;38(9):e23652. doi: 10.1096/fj.202400924. PMID: 38708783], [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0016740 transferase activity;GO:0061630 ubiquitin protein ligase activity",
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        "go_biological_process": "GO:0050691 regulation of defense response to virus by host;GO:0032648 regulation of interferon-beta production;GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process;GO:0070936 protein K48-linked ubiquitination;GO:0099546 protein catabolic process, modulating synaptic transmission",
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        "protein_name": "Alkaline phosphatase",
        "gene_name": "Akp3",
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        "gene_names_uniprotkb": "Akp3",
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        "protein_names_uniprotkb": "Alkaline phosphatase; 3.1.3.1",
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        "tax_id": 10116,
        "disease": "inflammatory bowel disease (Disease Ontology:DOID:0050589); ulcerative colitis (Disease Ontology:DOID:8577); Crohn's disease (Disease Ontology:DOID:8778)",
        "pathway": " (rno:64621);  (R-RNO-163125);  (R-RNO-6811438)",
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        "ec_number_list": "2.4.2.31;3.1.3.2;3.1.3.1;3.1.3.48;3.9.1.1;3.1.3.5;3.6.5.2;3.5.1.92;3.2.2.6;3.1.4.50;3.4.11.9",
        "go_molecular_function": "GO:0004035 alkaline phosphatase activity;GO:0046872 metal ion binding;GO:0000287 magnesium ion binding;GO:0008270 zinc ion binding",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0098552 side of membrane;GO:0009897 external side of plasma membrane",
        "go_biological_process": "GO:0031667 response to nutrient levels",
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        "record_id": "A0ABK0L8R7-1",
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    {
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        "length": 569,
        "protein_name": "Far upstream element binding protein 3",
        "gene_name": "Fubp3",
        "organism": "Rat",
        "refseq_name": "far upstream element-binding protein 3 isoform b",
        "refseq_ac": "NP_001034426",
        "gene_names_uniprotkb": "Fubp3",
        "gene_names_refseq": "Fubp3; Marta2",
        "protein_names_uniprotkb": "Far upstream element binding protein 3",
        "protein_names_refseq": "MAP2 RNA trans-acting protein 2; far upstream element (FUSE) binding protein 3; far upstream element-binding protein 3 isoform b",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:362106)",
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        "publication_id_list": "23121659",
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        "function": "In neurons MARTA2 appears to represent a key trans-acting factor involved in dendritic targeting of MAP2 mRNAs., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0003676 nucleic acid binding;GO:0003730 mRNA 3'-UTR binding;GO:0003697 single-stranded DNA binding;GO:0003723 RNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0043025 neuronal cell body;GO:0043198 dendritic shaft",
        "go_biological_process": "GO:0006355 regulation of DNA-templated transcription;GO:0006351 DNA-templated transcription;GO:0010628 positive regulation of gene expression;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0045893 positive regulation of DNA-templated transcription",
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    {
        "uniprot_canonical_ac": "A0ABK0L9C0-1",
        "uniprot_id": "A0ABK0L9C0_RAT",
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        "length": 951,
        "protein_name": "Carnosine synthase 1",
        "gene_name": "Carns1",
        "organism": "Rat",
        "refseq_name": "carnosine synthase 1",
        "refseq_ac": "NP_001414721",
        "gene_names_uniprotkb": "Carns1; RGD1308234",
        "gene_names_refseq": "Carns1; RGD1308234",
        "protein_names_uniprotkb": "Carnosine synthase 1; 6.3.2.11; ATP-grasp domain-containing protein 1",
        "protein_names_refseq": "carnosine synthase 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:309150);  (R-RNO-70921)",
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        "publication_id_list": "34038814",
        "class_list": "",
        "function": "Catalyzes the synthesis of carnosine and homocarnosine. Carnosine is synthesized more efficiently than homocarnosine., [UniProtKB, UniProtKB, UniProtKB]; Histidine dipeptides are key regulators of excitation-contraction coupling in cardiac muscle: Evidence from a novel CARNS1 knockout rat model., [RefSeq, PubMed]",
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        "ec_number_list": "6.3.2.11",
        "go_molecular_function": "GO:0005524 ATP binding;GO:0046872 metal ion binding;GO:0016887 ATP hydrolysis activity;GO:0047730 carnosine synthase activity;GO:0102102 homocarnosine synthase activity",
        "go_cellular_component": "",
        "go_biological_process": "GO:0035499 carnosine biosynthetic process;GO:1901652 response to peptide",
        "synthesized_glycan_count": 0,
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        "record_id": "A0ABK0L9C0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L7N0-1",
        "uniprot_id": "A0ABK0L7N0_RAT",
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        "length": 322,
        "protein_name": "FUN14 domain-containing protein 2",
        "gene_name": "Fundc2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Fundc2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "FUN14 domain-containing protein 2; Hepatitis C virus core-binding protein 6",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
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        "pathway_count": 0,
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        "function": "Binds directly and specifically 1,2-Diacyl-sn-glycero-3-phospho-(1'-myo-inositol-3',4',5'-bisphosphate) (PIP3) leading to the recruitment of PIP3 to mitochondria and may play a role in the regulation of the platelet activation via AKT/GSK3B/cGMP signaling pathways. May act as transcription factor that regulates SREBP1 (isoform SREBP-1C) expression in order to modulate triglyceride (TG) homeostasis in hepatocytes., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005547 phosphatidylinositol-3,4,5-trisphosphate binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005741 mitochondrial outer membrane;GO:0005739 mitochondrion",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0000422 autophagy of mitochondrion;GO:0010543 regulation of platelet activation;GO:0035356 intracellular triglyceride homeostasis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0L7N0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L8S1-1",
        "uniprot_id": "A0ABK0L8S1_RAT",
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        "length": 216,
        "protein_name": "MOB kinase activator 3B",
        "gene_name": "Mob3b",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Mob3b",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "MOB kinase activator 3B",
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        "go_molecular_function": "GO:0046872 metal ion binding;GO:0030295 protein kinase activator activity",
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        "length": 747,
        "protein_name": "Kinesin-like protein",
        "gene_name": "Kif3b",
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        "refseq_name": "kinesin-like protein KIF3B",
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        "protein_names_refseq": "kinesin-like protein KIF3B",
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        "pathway": " (rno:296284);  (R-RNO-2132295);  (R-RNO-5620924);  (R-RNO-6811434);  (R-RNO-983189)",
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        "publication_id_list": "22962609;23093447",
        "class_list": "",
        "function": "A novel role for miR-127 has been shown in cell adhesion and its regulation by HIF-1alpha. KIF3B is identified for the first time as a miR-127 target., [RefSeq, PubMed]; KIF3B gene expression in neurons and microglia is upregulated after spinal cord injury., [RefSeq, PubMed]; Microtubule-based molecular motor that transport intracellular cargos, such as vesicles, organelles and protein complexes. Uses ATP hydrolysis to generate force to bind and move along the microtubule. Plays a role in cilia formation. Involved in photoreceptor integrity and opsin trafficking in rod photoreceptors. Transports vesicles containing N-methyl-D-aspartate (NMDA) receptor subunit GRIN2A into neuronal dendrites., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005524 ATP binding;GO:0008017 microtubule binding;GO:0016887 ATP hydrolysis activity;GO:0003777 microtubule motor activity;GO:0031267 small GTPase binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005874 microtubule;GO:0005871 kinesin complex;GO:0098978 glutamatergic synapse;GO:0005813 centrosome",
        "go_biological_process": "GO:0007018 microtubule-based movement;GO:0090307 mitotic spindle assembly;GO:0060271 cilium assembly;GO:0016192 vesicle-mediated transport;GO:0042073 intraciliary transport",
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        "protein_name": "Ubiquitin-associated and SH3 domain-containing protein A",
        "gene_name": "Ubash3a",
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        "gene_names_uniprotkb": "Ubash3a",
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        "protein_names_uniprotkb": "Ubiquitin-associated and SH3 domain-containing protein A; Suppressor of T-cell receptor signaling 2; T-cell ubiquitin ligand 1",
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        "protein_name": "MTCL family member 3",
        "gene_name": "Mtcl3",
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        "refseq_name": "microtubule cross-linking factor 3 isoform X1",
        "refseq_ac": "XP_063132644",
        "gene_names_uniprotkb": "Mtcl3; NEWGENE_1307525; Soga3",
        "gene_names_refseq": "Mtcl3",
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        "protein_names_refseq": "microtubule cross-linking factor 3 isoform X1",
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    {
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        "protein_name": "tRNA-splicing endonuclease subunit Sen34",
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        "gene_names_uniprotkb": "Tsen34",
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        "protein_names_uniprotkb": "tRNA-splicing endonuclease subunit Sen34; 4.6.1.16",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "pontocerebellar hypoplasia type 2C (Disease Ontology:DOID:0060269)",
        "pathway": " (rno:292534)",
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        "function": "Constitutes one of the two catalytic subunit of the tRNA-splicing endonuclease complex, a complex responsible for identification and cleavage of the splice sites in pre-tRNA. It cleaves pre-tRNA at the 5'- and 3'-splice sites to release the intron. The products are an intron and two tRNA half-molecules bearing 2',3'-cyclic phosphate and 5'-OH termini. There are no conserved sequences at the splice sites, but the intron is invariably located at the same site in the gene, placing the splice sites an invariant distance from the constant structural features of the tRNA body., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_biological_process": "GO:0006397 mRNA processing;GO:0000379 tRNA-type intron splice site recognition and cleavage",
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    {
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        "length": 273,
        "protein_name": "Chondrolectin",
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        "refseq_name": "chondrolectin precursor",
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        "gene_names_refseq": "Chodl",
        "protein_names_uniprotkb": "Chondrolectin",
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        "protein_name": "Serine and arginine rich splicing factor 11",
        "gene_name": "Srsf11",
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        "protein_names_uniprotkb": "Serine and arginine rich splicing factor 11",
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        "tax_id": 10116,
        "disease": "myelodysplastic syndrome (Disease Ontology:DOID:0050908); autism spectrum disorder (Disease Ontology:DOID:0060041)",
        "pathway": " (R-RNO-159236);  (R-RNO-72163);  (R-RNO-72203);  (R-RNO-9770562)",
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        "go_molecular_function": "GO:0003723 RNA binding;GO:0042802 identical protein binding",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0016607 nuclear speck",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L8D4-1",
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        "length": 119,
        "protein_name": "DNA polymerase epsilon subunit 4",
        "gene_name": "Pole4",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Pole4",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "DNA polymerase epsilon subunit 4; DNA polymerase II subunit 4; DNA polymerase epsilon subunit p12",
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        "pathway": " (rno:362385);  (R-RNO-110314);  (R-RNO-5651801);  (R-RNO-5656169);  (R-RNO-5685942);  (R-RNO-5693537);  (R-RNO-5696397);  (R-RNO-5696400);  (R-RNO-6782135);  (R-RNO-6782210);  (R-RNO-68952);  (R-RNO-68962)",
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        "function": "Accessory component of the DNA polymerase epsilon complex. Participates in DNA repair and in chromosomal DNA replication., [UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "",
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        "go_cellular_component": "GO:0008622 epsilon DNA polymerase complex;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0140672 ATAC complex",
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    },
    {
        "uniprot_canonical_ac": "A0ABK0L8U6-1",
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        "length": 879,
        "protein_name": "Molybdenum cofactor sulfurase",
        "gene_name": "Mocos",
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        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Mocos; MOCOS",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Molybdenum cofactor sulfurase; 2.8.1.9; MCS; MOS; MoCo sulfurase; Molybdenum cofactor sulfurtransferase",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "autism spectrum disorder (Disease Ontology:DOID:0060041); obstructive nephropathy (Disease Ontology:DOID:0070314); xanthinuria type II (Disease Ontology:DOID:0070453)",
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        "function": "Sulfurates the molybdenum cofactor. Sulfation of molybdenum is essential for xanthine dehydrogenase (XDH) and aldehyde oxidase (ADO) enzymes in which molybdenum cofactor is liganded by 1 oxygen and 1 sulfur atom in active form., [UniProtKB, HAMAP, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_cellular_component": "",
        "go_biological_process": "GO:0006777 Mo-molybdopterin cofactor biosynthetic process;GO:0043545 molybdopterin cofactor metabolic process;GO:0032324 molybdopterin cofactor biosynthetic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L8L8-1",
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        "mass": 28063.0,
        "length": 258,
        "protein_name": "Coordinator of PRMT5 and differentiation stimulator",
        "gene_name": "Coprs",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Coprs; RGD1565675",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Coordinator of PRMT5 and differentiation stimulator",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (R-RNO-3214858)",
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        "go_molecular_function": "GO:0042393 histone binding",
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        "record_type": "protein"
    },
    {
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        "protein_name": "Zinc finger protein 661",
        "gene_name": "LOC100909998",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "LOC100909998",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger protein 661",
        "protein_names_refseq": "",
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        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0008270 zinc ion binding",
        "go_cellular_component": "GO:0005634 nucleus",
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    {
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        "protein_name": "Solute carrier family 25, member 35",
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        "gene_names_uniprotkb": "Slc25a35",
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        "protein_names_uniprotkb": "Solute carrier family 25, member 35",
        "protein_names_refseq": "",
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        "class_list": "",
        "function": "Putative antiporter that exchanges dicarboxylates and sulfur oxoanions across the inner membrane of mitochondria., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005743 mitochondrial inner membrane",
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        "hit_score": 0.1,
        "record_id": "A0ABK0L7L9-1",
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    },
    {
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        "length": 425,
        "protein_name": "NOP2/Sun RNA methyltransferase 3",
        "gene_name": "Nsun3",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Nsun3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "NOP2/Sun RNA methyltransferase 3",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "combined oxidative phosphorylation deficiency 48 (Disease Ontology:DOID:0112112)",
        "pathway": " (rno:100360437)",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0003723 RNA binding;GO:0008168 methyltransferase activity;GO:0008173 RNA methyltransferase activity;GO:0016428 tRNA (cytidine-5-)-methyltransferase activity",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005759 mitochondrial matrix",
        "go_biological_process": "GO:0031167 rRNA methylation;GO:0006396 RNA processing;GO:0001510 RNA methylation;GO:0070129 regulation of mitochondrial translation;GO:0002127 tRNA wobble base cytosine methylation",
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        "hit_score": 0.1,
        "record_id": "A0ABK0L7V7-1",
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    },
    {
        "uniprot_canonical_ac": "A0ABK0L9Z6-1",
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        "length": 536,
        "protein_name": "RING-type E3 ubiquitin-protein ligase PPIL2",
        "gene_name": "Ppil2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ppil2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "RING-type E3 ubiquitin-protein ligase PPIL2; 2.3.2.27; CYC4; Probable inactive peptidyl-prolyl cis-trans isomerase-like 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
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        "function": "Has a ubiquitin-protein ligase activity acting as an E3 ubiquitin protein ligase or as an ubiquitin-ubiquitin ligase promoting elongation of ubiquitin chains on substrates. By mediating 'Lys-48'-linked polyubiquitination of proteins could target them for proteasomal degradation. May also function as a chaperone, playing a role in transport to the cell membrane of BSG/Basigin for instance. Probable inactive PPIase with no peptidyl-prolyl cis-trans isomerase activity. As a component of the minor spliceosome, involved in the splicing of U12-type introns in pre-mRNAs., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0061630 ubiquitin protein ligase activity;GO:0003755 peptidyl-prolyl cis-trans isomerase activity;GO:0004842 ubiquitin-protein transferase activity;GO:0034450 ubiquitin-ubiquitin ligase activity",
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        "go_biological_process": "GO:0006457 protein folding;GO:0016567 protein ubiquitination;GO:0072659 protein localization to plasma membrane;GO:0000209 protein polyubiquitination",
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        "hit_score": 0.1,
        "record_id": "A0ABK0L9Z6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L9R6-1",
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        "length": 402,
        "protein_name": "F-box and leucine-rich repeat protein 14",
        "gene_name": "Fbxl14",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Fbxl14",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "F-box and leucine-rich repeat protein 14",
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        "go_molecular_function": "GO:0004842 ubiquitin-protein transferase activity",
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    {
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        "refseq_name": "elongin-C-like",
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        "gene_names_uniprotkb": "LOC134482335; LOC134482328; LOC134482347",
        "gene_names_refseq": "LOC134482335",
        "protein_names_uniprotkb": "Elongin-C; Elongin 15 kDa subunit; RNA polymerase II transcription factor SIII subunit C; SIII p15; Stromal membrane-associated protein SMAP1B homolog; Transcription elongation factor B polypeptide 1",
        "protein_names_refseq": "elongin-C-like",
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        "function": "SIII, also known as elongin, is a general transcription elongation factor that increases the RNA polymerase II transcription elongation past template-encoded arresting sites. Subunit A is transcriptionally active and its transcription activity is strongly enhanced by binding to the dimeric complex of the SIII regulatory subunits B and C (elongin BC complex). In embryonic stem cells, the elongin BC complex is recruited by EPOP to Polycomb group (PcG) target genes in order generate genomic region that display both active and repressive chromatin properties, an important feature of pluripotent stem cells., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005634 nucleus",
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    },
    {
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        "protein_name": "Cytochrome c oxidase subunit 7A1, mitochondrial",
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        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Cox7a1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Cytochrome c oxidase subunit 7A1, mitochondrial; Cytochrome c oxidase subunit VIIa-heart",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "dilated cardiomyopathy (Disease Ontology:DOID:12930); epilepsy (Disease Ontology:DOID:1826); cytochrome-c oxidase deficiency disease (Disease Ontology:DOID:3762)",
        "pathway": "",
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        "function": "Component of the mitochondrial respiratory complex IV (CIV, also named cytochrome c oxidase complex), the last enzyme in the mitochondrial electron transport chain which drives oxidative phosphorylation. The CIV complex is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Acts as an assembly factor that specifically drives the homodimerization of CIV complexes, mediating the formation of mitochondrial respiratory supercomplexes (respirasomes) containing two CIV: supercomplxes with two molecules of CIV show improved activity. Despite being highly expressed in brown adipose tissue, not required for thermogenesis., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0016491 oxidoreductase activity",
        "go_cellular_component": "GO:0005743 mitochondrial inner membrane;GO:0045277 respiratory chain complex IV",
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        "length": 304,
        "protein_name": "Vomeronasal type-1 receptor",
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        "organism": "Rat",
        "refseq_name": "vomeronasal type-1 receptor 1-like isoform X2",
        "refseq_ac": "XP_038951937",
        "gene_names_uniprotkb": "LOC120093107; Vom1r35",
        "gene_names_refseq": "LOC120093107",
        "protein_names_uniprotkb": "Vomeronasal type-1 receptor",
        "protein_names_refseq": "vomeronasal type-1 receptor 1-like isoform X2",
        "tax_id": 10116,
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        "pathway": " (rno:494268)",
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        "class_list": "",
        "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",
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        "protein_name": "Ataxin 7-like 3B",
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        "protein_names_uniprotkb": "Ataxin 7-like 3B",
        "protein_names_refseq": "ataxin-7-like protein 3B; putative ataxin-7-like protein 3B",
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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": "LINE-1 retrotransposable element ORF1 protein",
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        "gene_names_refseq": "",
        "protein_names_uniprotkb": "LINE-1 retrotransposable element ORF1 protein; LINE retrotransposable element 1; LINE1 retrotransposable element 1",
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        "protein_name": "Transmembrane 74B, opposite strand",
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        "organism": "Rat",
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        "gene_names_refseq": "Tmem74bos",
        "protein_names_uniprotkb": "Transmembrane 74B, opposite strand",
        "protein_names_refseq": "mCG140681-like; transmembrane 74B, opposite strand; uncharacterized protein C20orf202 homolog",
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        "gene_names_uniprotkb": "St13-ps2",
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        "protein_names_uniprotkb": "ST13, Hsp70 interacting protein, pseudogene 2",
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        "go_cellular_component": "GO:0042101 T cell receptor complex",
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        "record_id": "A0ABK0L876-1",
        "record_type": "protein"
    },
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        "length": 276,
        "protein_name": "Signal peptidase complex subunit 3",
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        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Signal peptidase complex subunit 3",
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        "go_cellular_component": "GO:0005787 signal peptidase complex",
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        "record_id": "A0ABK0L878-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L886-1",
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        "protein_name": "Dolichyl-diphosphooligosaccharide-protein glycosyltransferase subunit TMEM258",
        "gene_name": "Tmem258",
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        "refseq_name": "transmembrane protein 258",
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        "gene_names_refseq": "RGD1560328; Tmem258",
        "protein_names_uniprotkb": "Dolichyl-diphosphooligosaccharide-protein glycosyltransferase subunit TMEM258; Transmembrane protein 258",
        "protein_names_refseq": "transmembrane protein 258",
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        "function": "Subunit of the oligosaccharyl transferase (OST) complex that catalyzes the initial transfer of a defined glycan (Glc(3)Man(9)GlcNAc(2) in eukaryotes) from the lipid carrier dolichol-pyrophosphate to an asparagine residue within an Asn-X-Ser/Thr consensus motif in nascent polypeptide chains, the first step in protein N-glycosylation. N-glycosylation occurs cotranslationally and the complex associates with the Sec61 complex at the channel-forming translocon complex that mediates protein translocation across the endoplasmic reticulum (ER). All subunits are required for a maximal enzyme activity., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0062062 oligosaccharyltransferase complex binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005783 endoplasmic reticulum;GO:0016020 membrane;GO:0008250 oligosaccharyltransferase complex;GO:0160226 oligosaccharyltransferase complex A",
        "go_biological_process": "GO:0006954 inflammatory response;GO:0006487 protein N-linked glycosylation;GO:0009306 protein secretion;GO:0034976 response to endoplasmic reticulum stress;GO:1904019 epithelial cell apoptotic process",
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        "hit_score": 0.1,
        "record_id": "A0ABK0L886-1",
        "record_type": "protein"
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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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    },
    {
        "uniprot_canonical_ac": "A0ABK0L896-1",
        "uniprot_id": "A0ABK0L896_RAT",
        "mass": 20465.0,
        "length": 169,
        "protein_name": "Sex-determining region Y protein",
        "gene_name": "LOC134484451",
        "organism": "Rat",
        "refseq_name": "sex-determining region Y protein-like",
        "refseq_ac": "XP_063136741",
        "gene_names_uniprotkb": "LOC134484451",
        "gene_names_refseq": "LOC134484451",
        "protein_names_uniprotkb": "Sex-determining region Y protein; Testis-determining factor",
        "protein_names_refseq": "sex-determining region Y protein-like",
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        "function": "Transcriptional regulator that controls a genetic switch in male development. It is necessary and sufficient for initiating male sex determination by directing the development of supporting cell precursors (pre-Sertoli cells) as Sertoli rather than granulosa cells. Involved in different aspects of gene regulation including promoter activation or repression. Binds to the DNA consensus sequence 5'-[AT]AACAA[AT]-3'. SRY HMG box recognizes DNA by partial intercalation in the minor groove and promotes DNA bending. Also involved in pre-mRNA splicing. In male adult brain involved in the maintenance of motor functions of dopaminergic neurons., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0005516 calmodulin binding",
        "go_cellular_component": "GO:0016607 nuclear speck",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0030154 cell differentiation;GO:0007548 sex differentiation",
        "synthesized_glycan_count": 0,
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        "record_id": "A0ABK0L896-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L8A2-1",
        "uniprot_id": "A0ABK0L8A2_RAT",
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        "length": 518,
        "protein_name": "Importin subunit alpha",
        "gene_name": "Kpna2l1",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Kpna2l1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Importin subunit alpha",
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        "function": "Functions in nuclear protein import as an adapter protein for nuclear receptor KPNB1. Binds specifically and directly to substrates containing either a simple or bipartite NLS motif. Docking of the importin/substrate complex to the nuclear pore complex (NPC) is mediated by KPNB1 through binding to nucleoporin FxFG repeats and the complex is subsequently translocated through the pore by an energy requiring, Ran-dependent mechanism. At the nucleoplasmic side of the NPC, Ran binds to importin-beta and the three components separate and importin-alpha and -beta are re-exported from the nucleus to the cytoplasm where GTP hydrolysis releases Ran from importin. The directionality of nuclear import is thought to be conferred by an asymmetric distribution of the GTP- and GDP-bound forms of Ran between the cytoplasm and nucleus. Mediator of PR-DUB complex component BAP1 nuclear import; acts redundantly with KPNA1 and Transportin-1/TNPO1., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0061608 nuclear import signal receptor activity",
        "go_cellular_component": "GO:0005737 cytoplasm",
        "go_biological_process": "GO:0006606 protein import into nucleus",
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        "record_id": "A0ABK0L8A2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0L8A4-1",
        "uniprot_id": "A0ABK0L8A4_RAT",
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        "length": 307,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or5h24",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr1548",
        "refseq_ac": "NP_001001108",
        "gene_names_uniprotkb": "Or5h24",
        "gene_names_refseq": "Olr1548; Or5h24",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 1548; olfactory receptor 183-like; olfactory receptor Olr1548; olfactory receptor gene Olr1548",
        "tax_id": 10116,
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        "pathway": " (rno:406004)",
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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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    },
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        "length": 98,
        "protein_name": "Protein S100-A13",
        "gene_name": "S100a13",
        "organism": "Rat",
        "refseq_name": "protein S100-A13",
        "refseq_ac": "NP_001178536",
        "gene_names_uniprotkb": "S100a13",
        "gene_names_refseq": "S100A1; S100a13",
        "protein_names_uniprotkb": "Protein S100-A13; S100 calcium-binding protein A13",
        "protein_names_refseq": "protein S100-A13",
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        "function": "Plays a role in the export of proteins that lack a signal peptide and are secreted by an alternative pathway. Binds two calcium ions per subunit. Binds one copper ion. Binding of one copper ion does not interfere with calcium binding. Required for the copper-dependent stress-induced export of IL1A and FGF1. The calcium-free protein binds to lipid vesicles containing phosphatidylserine, but not to vesicles containing phosphatidylcholine., [UniProtKB, UniProtKB]; Results suggest necrosis-inducing stress induces an extacellular release of prothymosin-alpha in a non-vesicular manner; apoptosis-inducing stress does not, owing to loss of its interaction with S100A13, a cargo molecule for extracellular release, [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0050786 RAGE receptor binding;GO:0008270 zinc ion binding;GO:0042803 protein homodimerization activity;GO:0005509 calcium ion binding;GO:0005507 copper ion binding",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0048471 perinuclear region of cytoplasm",
        "go_biological_process": "GO:0032730 positive regulation of interleukin-1 alpha production;GO:0008284 positive regulation of cell population proliferation;GO:0001819 positive regulation of cytokine production;GO:0043123 positive regulation of canonical NF-kappaB signal transduction;GO:0008360 regulation of cell shape",
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        "protein_name": "Olfactory receptor",
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        "refseq_name": "olfactory receptor Olr758",
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        "gene_names_refseq": "Olr758; Or4g7; ratchr3-96934523-96935461_ORF",
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        "protein_names_refseq": "olfactory receptor 758; olfactory receptor Olr758; olfactory receptor gene Olr758",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "protein_names_refseq": "Y-linked testis-specific protein 1-like",
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        "protein_name": "Olfactory receptor",
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        "length": 366,
        "protein_name": "RT1 class Ib, locus M4",
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        "organism": "Rat",
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        "gene_names_uniprotkb": "RT1-M4",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "RT1 class Ib, locus M4",
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        "function": "Involved in the presentation of foreign antigens to the immune system., [UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0042612 MHC class I protein complex",
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        "length": 166,
        "protein_name": "Protein FAM162A",
        "gene_name": "LOC120095320",
        "organism": "Rat",
        "refseq_name": "protein FAM162A-like",
        "refseq_ac": "XP_063126168",
        "gene_names_uniprotkb": "LOC120095320",
        "gene_names_refseq": "LOC120095320",
        "protein_names_uniprotkb": "Protein FAM162A",
        "protein_names_refseq": "protein FAM162A-like",
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        "function": "Proposed to be involved in regulation of apoptosis; the exact mechanism may differ between cell types/tissues. May be involved in hypoxia-induced cell death of transformed cells implicating cytochrome C release and caspase activation (such as CASP9) and inducing mitochondrial permeability transition. May be involved in hypoxia-induced cell death of neuronal cells probably by promoting release of AIFM1 from mitochondria to cytoplasm and its translocation to the nucleus; however, the involvement of caspases has been reported conflictingly., [UniProtKB, UniProtKB]",
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    {
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        "length": 547,
        "protein_name": "Solute carrier family 9 member B2",
        "gene_name": "Slc9b2",
        "organism": "Rat",
        "refseq_name": "sodium/hydrogen exchanger 9B2",
        "refseq_ac": "NP_001102855",
        "gene_names_uniprotkb": "Slc9b2",
        "gene_names_refseq": "Nhedc2; Slc9b2",
        "protein_names_uniprotkb": "Solute carrier family 9 member B2",
        "protein_names_refseq": "Na+/H+ exchanger domain containing 2; mitochondrial sodium/hydrogen exchanger 9B2; mitochondrial sodium/hydrogen exchanger NHA2; sodium/hydrogen exchanger 9B2; solute carrier family 9, subfamily B (NHA2, cation proton antiporter 2), member 2; solute carrier family 9, subfamily B (cation proton antiporter 2), member 2",
        "tax_id": 10116,
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        "go_molecular_function": "GO:0015385 sodium:proton antiporter activity;GO:0042802 identical protein binding;GO:0010348 lithium:proton antiporter activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0016323 basolateral plasma membrane;GO:0031966 mitochondrial membrane;GO:0055037 recycling endosome;GO:0016324 apical plasma membrane",
        "go_biological_process": "GO:2001206 positive regulation of osteoclast development;GO:0030317 flagellated sperm motility;GO:0072583 clathrin-dependent endocytosis;GO:0061178 regulation of insulin secretion involved in cellular response to glucose stimulus;GO:0006814 sodium ion transport",
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        "length": 78,
        "protein_name": "Small integral membrane protein 1 (Vel blood group)",
        "gene_name": "Smim1",
        "organism": "Rat",
        "refseq_name": "small integral membrane protein 1",
        "refseq_ac": "NP_001157195",
        "gene_names_uniprotkb": "Smim1",
        "gene_names_refseq": "RGD1564257; Smim1",
        "protein_names_uniprotkb": "Small integral membrane protein 1 (Vel blood group)",
        "protein_names_refseq": "small integral membrane protein 1",
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        "gene_name": "Vom2r61",
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        "refseq_name": "vomeronasal 2 receptor 61",
        "refseq_ac": "NP_001092978",
        "gene_names_uniprotkb": "Vom2r61",
        "gene_names_refseq": "RGD1562930; Vom2r61",
        "protein_names_uniprotkb": "Vomeronasal 2 receptor, 61",
        "protein_names_refseq": "vomeronasal 2 receptor 61; vomeronasal type-2 receptor 116-like",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity",
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        "protein_name": "Ig-like domain-containing protein",
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        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ig-like domain-containing protein",
        "protein_names_refseq": "",
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        "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": "A0ABK0LAD3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LAD9-1",
        "uniprot_id": "A0ABK0LAD9_RAT",
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        "length": 501,
        "protein_name": "non-specific serine/threonine protein kinase",
        "gene_name": "LOC134485004",
        "organism": "Rat",
        "refseq_name": "sperm motility kinase 2B-like",
        "refseq_ac": "XP_063136898",
        "gene_names_uniprotkb": "LOC134485004",
        "gene_names_refseq": "LOC134485004",
        "protein_names_uniprotkb": "non-specific serine/threonine protein kinase; 2.7.11.1",
        "protein_names_refseq": "sperm motility kinase 2B-like",
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        "function": "May play a role in sperm motility, especially in the regulation of flagellar function., [UniProtKB, UniProtKB]",
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        "ec_number_list": "2.7.11.1;2.7.12.1;2.7.1.153;2.7.1.137;2.7.11.24;2.7.11.25;2.7.11.22;2.7.11.23;2.7.4.6;2.7.1.154;2.7.11.38;2.7.11.17;2.7.11.21;2.7.12.2;2.7.1.40;2.7.11.12;2.7.11.26;2.7.11.34;2.7.10.2;2.7.1.150;2.7.11.13;4.1.1.32;2.7.11.19;2.7.2.3;2.7.11.11;2.7.11.31;3.1.3.16;2.7.11.4;2.3.1.48;3.1.11.-;2.7.13.3;2.7.4.18;3.1.24.-;3.4.19.12;2.7.11.39;2.4.99.18;2.7.11.10",
        "go_molecular_function": "GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding",
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        "length": 311,
        "protein_name": "Olfactory receptor family 10 subfamily D member 1",
        "gene_name": "Or10d1",
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        "refseq_name": "olfactory receptor Olr1307",
        "refseq_ac": "NP_001000519",
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        "gene_names_refseq": "Olr1307; Or10d1; tpcr18",
        "protein_names_uniprotkb": "Olfactory receptor family 10 subfamily D member 1",
        "protein_names_refseq": "olfactory receptor 1307; olfactory receptor Olr1307; olfactory receptor gene Olr1307",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
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    },
    {
        "uniprot_canonical_ac": "A0ABK0LBB8-1",
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        "length": 234,
        "protein_name": "Phosphatidylinositol glycan anchor biosynthesis, class P",
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        "gene_names_uniprotkb": "Pigp",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Phosphatidylinositol glycan anchor biosynthesis, class P",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "developmental and epileptic encephalopathy 55 (Disease Ontology:DOID:0080283)",
        "pathway": " (R-RNO-162710)",
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        "publication_id_list": "",
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        "function": "Part of the complex catalyzing the transfer of N-acetylglucosamine from UDP-N-acetylglucosamine to phosphatidylinositol, the first step of GPI biosynthesis., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0017176 phosphatidylinositol N-acetylglucosaminyltransferase activity",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0016020 membrane;GO:0000506 glycosylphosphatidylinositol-N-acetylglucosaminyltransferase (GPI-GnT) complex;GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0006506 GPI anchor biosynthetic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LBB8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LBP7-1",
        "uniprot_id": "A0ABK0LBP7_RAT",
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        "length": 346,
        "protein_name": "Tumor protein D52",
        "gene_name": "Tpd52",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Tpd52",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Tumor protein D52",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-432722)",
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        "publication_id_list": "22673903",
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        "biomarker_type": "",
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        "secondary_ac_list": "",
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        "go_molecular_function": "GO:0042802 identical protein binding;GO:0042803 protein homodimerization activity;GO:0005509 calcium ion binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0098978 glutamatergic synapse;GO:0005783 endoplasmic reticulum;GO:0045202 synapse;GO:0048471 perinuclear region of cytoplasm",
        "go_biological_process": "GO:0008284 positive regulation of cell population proliferation;GO:0030183 B cell differentiation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0LBP7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LAK9-1",
        "uniprot_id": "A0ABK0LAK9_RAT",
        "mass": 77433.0,
        "length": 706,
        "protein_name": "Zinc transporter ZIP12",
        "gene_name": "Slc39a12",
        "organism": "Rat",
        "refseq_name": "zinc transporter ZIP12 isoform X1",
        "refseq_ac": "XP_038951487",
        "gene_names_uniprotkb": "Slc39a12",
        "gene_names_refseq": "Slc39a12",
        "protein_names_uniprotkb": "Zinc transporter ZIP12; Solute carrier family 39 member 12; Zrt- and Irt-like protein 12",
        "protein_names_refseq": "zinc transporter ZIP12 isoform X1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:291328)",
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        "secondary_ac_list": "",
        "ec_number_list": "2.7.11.1",
        "go_molecular_function": "GO:0005385 zinc ion transmembrane transporter activity;GO:0140410 monoatomic cation:bicarbonate symporter activity;GO:0046873 metal ion transmembrane transporter activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0048471 perinuclear region of cytoplasm;GO:0016020 membrane",
        "go_biological_process": "GO:1903672 positive regulation of sprouting angiogenesis;GO:0007165 signal transduction;GO:0031113 regulation of microtubule polymerization;GO:0010975 regulation of neuron projection development;GO:0071578 zinc ion import across plasma membrane",
        "synthesized_glycan_count": 0,
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        "record_id": "A0ABK0LAK9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LBV7-1",
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        "mass": 45492.0,
        "length": 427,
        "protein_name": "Poly(rC) binding protein 3",
        "gene_name": "Pcbp3",
        "organism": "Rat",
        "refseq_name": "",
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        "gene_names_uniprotkb": "Pcbp3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Poly(rC) binding protein 3",
        "protein_names_refseq": "",
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    },
    {
        "uniprot_canonical_ac": "A0ABK0LD14-1",
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        "length": 1929,
        "protein_name": "Receptor-type tyrosine-protein phosphatase delta",
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        "organism": "Rat",
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        "gene_names_uniprotkb": "Ptprd",
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        "protein_names_uniprotkb": "Receptor-type tyrosine-protein phosphatase delta; 3.1.3.48",
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        "disease": "restless legs syndrome (Disease Ontology:DOID:0050425); hypertension (Disease Ontology:DOID:10763); azoospermia (Disease Ontology:DOID:14227); coronary artery disease (Disease Ontology:DOID:3393); diabetes mellitus (Disease Ontology:DOID:9351); type 2 diabetes mellitus (Disease Ontology:DOID:9352)",
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        "function": "Can bidirectionally induce pre- and post-synaptic differentiation of neurons by mediating interaction with IL1RAP and IL1RAPL1 trans-synaptically. Involved in pre-synaptic differentiation through interaction with SLITRK2., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0004725 protein tyrosine phosphatase activity;GO:0005102 signaling receptor binding;GO:0050839 cell adhesion molecule binding",
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        "go_biological_process": "GO:0099054 presynapse assembly;GO:0050776 regulation of immune response;GO:0071456 cellular response to hypoxia;GO:0030182 neuron differentiation;GO:0051965 positive regulation of synapse assembly",
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    },
    {
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        "protein_name": "Cyclin-dependent kinase-like 5",
        "gene_name": "Cdkl5",
        "organism": "Rat",
        "refseq_name": "cyclin-dependent kinase-like 5",
        "refseq_ac": "NP_001408462",
        "gene_names_uniprotkb": "Cdkl5",
        "gene_names_refseq": "Cdkl5",
        "protein_names_uniprotkb": "Cyclin-dependent kinase-like 5; 2.7.11.22",
        "protein_names_refseq": "cyclin-dependent kinase-like 5",
        "tax_id": 10116,
        "disease": "developmental and epileptic encephalopathy 2 (Disease Ontology:DOID:0080467); developmental and epileptic encephalopathy (Disease Ontology:DOID:0112202); intellectual disability (Disease Ontology:DOID:1059); Rett syndrome (Disease Ontology:DOID:1206)",
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        "publication_id_list": "20211261;20861382;22673903;27940108;30288694;36759195;38877552",
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        "function": "Cdkl5 is a MeCP2-repressed target gene providing a link between genes the mutation of which generates overlapping symptoms: DNA methylation changes are a potential mechanism participating in the long-term plasticity triggered by pharmacological agents, [RefSeq, PubMed]; Characterization of Cdkl5 transcript isoforms in the rat has been described., [RefSeq, PubMed]; Enhanced hippocampal LTP but normal NMDA receptor and AMPA receptor function in a rat model of CDKL5 deficiency disorder. Publication Status: Online-Only, [RefSeq, PubMed]; Epilepsy-Related CDKL5 Deficiency Slows Synaptic Vesicle Endocytosis in Central Nerve Terminals., [RefSeq, PubMed]; Mediates phosphorylation of MECP2. May regulate ciliogenesis., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; The molecular pathology in CDKL5 disorder may have distinct neuron-type specific origins and effects., [RefSeq, PubMed]; These results demonstrate a critical role of CDKL5 in neuronal morphogenesis and identify a Rho GTPase signaling pathway which may contribute to CDKL5-related disorders., [RefSeq, PubMed]",
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        "gene_names_refseq": "Fnip2; RGD1562174",
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        "protein_names_refseq": "folliculin-interacting protein 2 isoform X1",
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    {
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        "length": 1554,
        "protein_name": "Roundabout guidance receptor 2",
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        "gene_names_uniprotkb": "Robo2",
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        "protein_names_uniprotkb": "Roundabout guidance receptor 2",
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        "disease": "myoclonic-atonic epilepsy (Disease Ontology:DOID:0060475); transient cerebral ischemia (Disease Ontology:DOID:224); vesicoureteral reflux (Disease Ontology:DOID:9620)",
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    {
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        "length": 378,
        "protein_name": "WD repeat domain 73",
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        "gene_names_uniprotkb": "Wdr73",
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        "protein_names_uniprotkb": "WD repeat domain 73",
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        "go_molecular_function": "GO:0030674 protein-macromolecule adaptor activity",
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    {
        "uniprot_canonical_ac": "A0ABK0LBR7-1",
        "uniprot_id": "A0ABK0LBR7_RAT",
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        "length": 313,
        "protein_name": "Endoplasmic reticulum-Golgi intermediate compartment protein",
        "gene_name": "Ergic1",
        "organism": "Rat",
        "refseq_name": "endoplasmic reticulum-Golgi intermediate compartment protein 1 isoform X1",
        "refseq_ac": "XP_063124642",
        "gene_names_uniprotkb": "Ergic1",
        "gene_names_refseq": "Ergic1",
        "protein_names_uniprotkb": "Endoplasmic reticulum-Golgi intermediate compartment protein",
        "protein_names_refseq": "endoplasmic reticulum-Golgi intermediate compartment protein 1 isoform X1",
        "tax_id": 10116,
        "disease": "neurogenic-type arthrogryposis multiplex congenita-2 (Disease Ontology:DOID:0090124)",
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        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005789 endoplasmic reticulum membrane;GO:0033116 endoplasmic reticulum-Golgi intermediate compartment membrane;GO:0005654 nucleoplasm;GO:0005783 endoplasmic reticulum",
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        "length": 384,
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        "organism": "Rat",
        "refseq_name": "tetratricopeptide repeat protein 4 isoform X1",
        "refseq_ac": "XP_038966222",
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        "function": "Co-chaperone that recruits molecular chaperones Hsp90 (HSC82 and HSP82) and Hsp70 (SSA1) to nascent polypeptides, facilitating their proper folding into functional proteins. Client proteins include eukaryotic elongation factor eEF2, a key player in cellular translation. Stimulates SSA1 ATPase activity, but not Hsp90 ATPase activity., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0051879 Hsp90 protein binding;GO:0030544 Hsp70 protein binding",
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        "record_type": "protein"
    },
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        "length": 233,
        "protein_name": "Cilia- and flagella-associated protein 299",
        "gene_name": "Cfap299",
        "organism": "Rat",
        "refseq_name": "cilia and flagella associated protein 299",
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        "gene_names_uniprotkb": "Cfap299",
        "gene_names_refseq": "Cfap299",
        "protein_names_uniprotkb": "Cilia- and flagella-associated protein 299",
        "protein_names_refseq": "cilia and flagella associated protein 299; uncharacterized protein C4orf22 homolog",
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        "pathway_count": 0,
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        "class_list": "",
        "function": "May be involved in spermatogenesis., [UniProtKB, UniProtKB, UniProtKB]",
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        "length": 2324,
        "protein_name": "C2 domain-containing protein 3",
        "gene_name": "C2cd3",
        "organism": "Rat",
        "refseq_name": "C2 domain-containing protein 3 isoform X1",
        "refseq_ac": "XP_017444439",
        "gene_names_uniprotkb": "C2cd3",
        "gene_names_refseq": "C2cd3; RGD1307366",
        "protein_names_uniprotkb": "C2 domain-containing protein 3",
        "protein_names_refseq": "C2 domain-containing protein 3 isoform X1",
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        "disease": "orofaciodigital syndrome XIV (Disease Ontology:DOID:0060958)",
        "pathway": " (rno:293148);  (R-RNO-5620912)",
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        "function": "Component of the centrioles that acts as a positive regulator of centriole elongation. Promotes assembly of centriolar distal appendage, a structure at the distal end of the mother centriole that acts as an anchor of the cilium, and is required for recruitment of centriolar distal appendages proteins CEP83, SCLT1, CEP89, FBF1 and CEP164. Not required for centriolar satellite integrity or RAB8 activation. Required for primary cilium formation. Required for sonic hedgehog/SHH signaling and for proteolytic processing of GLI3., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_biological_process": "GO:0060271 cilium assembly;GO:0071539 protein localization to centrosome;GO:0061511 centriole elongation;GO:0001701 in utero embryonic development;GO:0016485 protein processing",
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    {
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        "protein_name": "MCF.2 cell line derived transforming sequence",
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        "refseq_name": "proto-oncogene DBL isoform X1",
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        "gene_names_refseq": "Mcf2; RGD1566098",
        "protein_names_uniprotkb": "MCF.2 cell line derived transforming sequence",
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        "pathway": " (R-RNO-193634);  (R-RNO-193648);  (R-RNO-416482);  (R-RNO-8980692);  (R-RNO-9013026);  (R-RNO-9013106);  (R-RNO-9013148);  (R-RNO-9013149);  (R-RNO-9013404);  (R-RNO-9013408);  (R-RNO-9013423)",
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        "record_type": "protein"
    },
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        "uniprot_canonical_ac": "A0ABK0LCV2-1",
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        "length": 1811,
        "protein_name": "Kinesin family member 13A",
        "gene_name": "Kif13a",
        "organism": "Rat",
        "refseq_name": "kinesin-like protein KIF13A isoform X6",
        "refseq_ac": "XP_063132602",
        "gene_names_uniprotkb": "Kif13a",
        "gene_names_refseq": "Kif13a",
        "protein_names_uniprotkb": "Kinesin family member 13A",
        "protein_names_refseq": "kinesin-like protein KIF13A isoform X6",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:308173)",
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        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005874 microtubule;GO:0005871 kinesin complex;GO:0005813 centrosome;GO:0032588 trans-Golgi network membrane",
        "go_biological_process": "GO:0006886 intracellular protein transport;GO:0007018 microtubule-based movement;GO:0047496 vesicle transport along microtubule;GO:0008333 endosome to lysosome transport;GO:0032438 melanosome organization",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0LCV2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LBZ4-1",
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        "length": 85,
        "protein_name": "Coiled-coil-helix-coiled-coil-helix domain-containing protein 7",
        "gene_name": "Chchd7",
        "organism": "Rat",
        "refseq_name": "coiled-coil-helix-coiled-coil-helix domain-containing protein 7",
        "refseq_ac": "NP_001386566",
        "gene_names_uniprotkb": "Chchd7; LOC684258",
        "gene_names_refseq": "Chchd7",
        "protein_names_uniprotkb": "Coiled-coil-helix-coiled-coil-helix domain-containing protein 7",
        "protein_names_refseq": "coiled-coil-helix-coiled-coil-helix domain-containing protein 7",
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        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005758 mitochondrial intermembrane space",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LBX1-1",
        "uniprot_id": "A0ABK0LBX1_RAT",
        "mass": 212953.0,
        "length": 1920,
        "protein_name": "Bromodomain adjacent to zinc finger domain protein 2B",
        "gene_name": "Baz2a",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Baz2a",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Bromodomain adjacent to zinc finger domain protein 2B",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006338 chromatin remodeling;GO:0000183 rDNA heterochromatin formation;GO:0016479 negative regulation of transcription by RNA polymerase I;GO:0006346 DNA methylation-dependent constitutive heterochromatin formation",
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0036126 sperm flagellum;GO:0005879 axonemal microtubule;GO:0160111 axonemal A tubule inner sheath",
        "go_biological_process": "GO:0030317 flagellated sperm motility;GO:0007368 determination of left/right symmetry;GO:0003341 cilium movement;GO:0035082 axoneme assembly",
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        "hit_score": 0.1,
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        "record_type": "protein"
    },
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        "length": 370,
        "protein_name": "Hes family bHLH transcription factor 7",
        "gene_name": "Hes7",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Hes7",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Hes family bHLH transcription factor 7",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "spondylocostal dysostosis (Disease Ontology:DOID:0050568); spondylocostal dysostosis 4 (Disease Ontology:DOID:0112364)",
        "pathway": " (rno:287423)",
        "pathway_count": 1,
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        "publication_id_list": "",
        "class_list": "",
        "function": "Transcriptional repressor. Represses transcription from both N box- and E box-containing promoters. May with HES1, cooperatively regulate somite formation in the presomitic mesoderm (PSM). May function as a segmentation clock, which is essential for coordinated somite segmentation., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0046983 protein dimerization activity;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0003677 DNA binding;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0009952 anterior/posterior pattern specification;GO:0050767 regulation of neurogenesis;GO:0006355 regulation of DNA-templated transcription",
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        "length": 275,
        "protein_name": "Programmed cell death 1 ligand 2",
        "gene_name": "Pdcd1lg2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Pdcd1lg2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Programmed cell death 1 ligand 2; Butyrophilin B7-DC",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "pulmonary tuberculosis (Disease Ontology:DOID:2957)",
        "pathway": " (rno:309304);  (R-RNO-389948);  (R-RNO-9931295)",
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        "class_list": "",
        "function": "Plays a critical role in induction and maintenance of immune tolerance to self. Acts as a ligand for the inhibitory receptor PDCD1/PD-1, inhibiting T-cell proliferation by blocking cell cycle progression and cytokine production., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0048018 receptor ligand activity",
        "go_cellular_component": "GO:0009897 external side of plasma membrane;GO:0005886 plasma membrane",
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        "record_type": "protein"
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        "length": 1119,
        "protein_name": "Adenylate cyclase type 1",
        "gene_name": "Adcy1",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Adcy1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Adenylate cyclase type 1; 4.6.1.1",
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        "tax_id": 10116,
        "disease": "autosomal recessive nonsyndromic deafness 44 (Disease Ontology:DOID:0110501); alcohol use disorder (Disease Ontology:DOID:1574)",
        "pathway": " (R-RNO-163615);  (R-RNO-170660);  (R-RNO-170670);  (R-RNO-418597);  (R-RNO-5610787)",
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        "function": "Catalyzes the formation of the signaling molecule cAMP in response to G-protein signaling., [UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "4.6.1.1;3.6.5.-",
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        "go_cellular_component": "GO:0005886 plasma membrane;GO:0098978 glutamatergic synapse;GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0014069 postsynaptic density",
        "go_biological_process": "GO:0006171 cAMP biosynthetic process;GO:0007189 adenylate cyclase-activating G protein-coupled receptor signaling pathway;GO:0035556 intracellular signal transduction;GO:0007409 axonogenesis;GO:1900273 positive regulation of long-term synaptic potentiation",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Nfatc1; RGD1560225",
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        "protein_names_uniprotkb": "Nuclear factor of activated T-cells 1",
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        "disease": "ventricular septal defect (Disease Ontology:DOID:1657); congenital heart disease (Disease Ontology:DOID:1682); aortic valve stenosis (Disease Ontology:DOID:1712); kidney disease (Disease Ontology:DOID:557); osteoarthritis (Disease Ontology:DOID:8398)",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005667 transcription regulator complex;GO:0005654 nucleoplasm;GO:0048471 perinuclear region of cytoplasm",
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        "length": 2015,
        "protein_name": "TRIO and F-actin binding protein",
        "gene_name": "Triobp",
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        "gene_names_uniprotkb": "Triobp",
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        "protein_names_uniprotkb": "TRIO and F-actin binding protein",
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        "tax_id": 10116,
        "disease": "autosomal recessive nonsyndromic deafness 28 (Disease Ontology:DOID:0110486)",
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        "go_molecular_function": "GO:0051015 actin filament binding;GO:0003779 actin binding;GO:0031625 ubiquitin protein ligase binding",
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        "go_biological_process": "GO:1900026 positive regulation of substrate adhesion-dependent cell spreading;GO:0051017 actin filament bundle assembly;GO:0007605 sensory perception of sound;GO:0060088 auditory receptor cell stereocilium organization",
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        "hit_score": 0.2,
        "record_id": "A0ABK0LC42-1",
        "record_type": "protein"
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        "protein_name": "Adaptor related protein complex 5 subunit sigma 1",
        "gene_name": "Ap5s1",
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        "refseq_name": "AP-5 complex subunit sigma-1",
        "refseq_ac": "NP_001385841",
        "gene_names_uniprotkb": "Ap5s1",
        "gene_names_refseq": "Ap5s1; RGD1561852",
        "protein_names_uniprotkb": "Adaptor related protein complex 5 subunit sigma 1",
        "protein_names_refseq": "AP-5 complex subunit sigma-1; adaptor-related protein complex 5, sigma 1 subunit",
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        "pathway": " (rno:499893)",
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        "record_id": "A0ABK0LBV3-1",
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    },
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        "length": 615,
        "protein_name": "Nuclear RNA export factor 5",
        "gene_name": "Nxf5",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Nxf5",
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        "protein_names_uniprotkb": "Nuclear RNA export factor 5",
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        "function": "May play a role in vesicular transport during the biogenesis of melanosomes., [UniProtKB, UniProtKB, UniProtKB]",
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        "protein_name": "Sodium/potassium-transporting ATPase subunit beta-1-interacting protein",
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        "protein_names_refseq": "sodium/potassium-transporting ATPase subunit beta-1-interacting protein 3 isoform X1",
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        "refseq_name": "zinc finger protein 92 homolog isoform X1",
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        "protein_name": "C-C motif chemokine receptor 4",
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        "protein_names_uniprotkb": "C-C motif chemokine receptor 4",
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        "disease": "pancreatic cancer (Disease Ontology:DOID:1793); asthma (Disease Ontology:DOID:2841); cervical squamous cell carcinoma (Disease Ontology:DOID:3744); pulmonary fibrosis (Disease Ontology:DOID:3770); rheumatoid arthritis (Disease Ontology:DOID:7148); osteoarthritis (Disease Ontology:DOID:8398)",
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        "protein_names_refseq": "formin-like protein 2 isoform X1",
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        "go_biological_process": "GO:0006355 regulation of DNA-templated transcription;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006357 regulation of transcription by RNA polymerase II",
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        "hit_score": 0.1,
        "record_id": "A0ABK0LCD7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LB68-1",
        "uniprot_id": "A0ABK0LB68_RAT",
        "mass": 15293.0,
        "length": 135,
        "protein_name": "CDGSH iron-sulfur domain-containing protein 2",
        "gene_name": "Cisd2",
        "organism": "Rat",
        "refseq_name": "CDGSH iron-sulfur domain-containing protein 2",
        "refseq_ac": "NP_001178537",
        "gene_names_uniprotkb": "Cisd2",
        "gene_names_refseq": "Cisd2; RGD1566242",
        "protein_names_uniprotkb": "CDGSH iron-sulfur domain-containing protein 2",
        "protein_names_refseq": "CDGSH iron-sulfur domain-containing protein 2",
        "tax_id": 10116,
        "disease": "Wolfram syndrome 2 (Disease Ontology:DOID:0110630)",
        "pathway": " (rno:295457)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "34740104",
        "class_list": "",
        "function": "Cisd2 plays an essential role in corneal epithelial regeneration., [RefSeq, PubMed]; Regulator of autophagy that contributes to antagonize BECN1-mediated cellular autophagy at the endoplasmic reticulum. Participates in the interaction of BCL2 with BECN1 and is required for BCL2-mediated depression of endoplasmic reticulum Ca(2+) stores during autophagy., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0046872 metal ion binding;GO:0051537 2 iron, 2 sulfur cluster binding;GO:0042803 protein homodimerization activity",
        "go_cellular_component": "GO:0005741 mitochondrial outer membrane;GO:0005789 endoplasmic reticulum membrane;GO:0005783 endoplasmic reticulum;GO:0097038 perinuclear endoplasmic reticulum;GO:0032991 protein-containing complex",
        "go_biological_process": "GO:0010506 regulation of autophagy;GO:0000422 autophagy of mitochondrion;GO:0006914 autophagy",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0LB68-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LAI2-1",
        "uniprot_id": "A0ABK0LAI2_RAT",
        "mass": 53915.0,
        "length": 489,
        "protein_name": "SPRY domain-containing SOCS box protein 3",
        "gene_name": "Mrps34; Spsb3",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Mrps34; Spsb3; Mrps34; Spsb3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "SPRY domain-containing SOCS box protein 3",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "combined oxidative phosphorylation deficiency 32 (Disease Ontology:DOID:0111492)",
        "pathway": " (rno:287126);  (R-RNO-5389840);  (R-RNO-5419276);  (R-RNO-8951664);  (R-RNO-9937383)",
        "pathway_count": 5,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Substrate-recognition component of a cullin-5-RING E3 ubiquitin-protein ligase complex (ECS complex, also named CRL5 complex), which mediates the ubiquitination and subsequent proteasomal degradation of target proteins, such as CGAS and SNAI1. The ECS(SPSB3) complex catalyzes 'Lys-48'-linked ubiquitination of nuclear CGAS in cycling cells, leading to its degradation. Recognizes and binds nucleosome-bound CGAS: ubiquitination and degradation of nuclear CGAS during G1 and G2 phases is required to promote low intranuclear CGAS abundance before the next mitotic cycle. The ECS(SPSB3) complex also mediates ubiquitination and degradation of phosphorylated SNAI1., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003735 structural constituent of ribosome;GO:1990756 ubiquitin-like ligase-substrate adaptor activity",
        "go_cellular_component": "GO:0005763 mitochondrial small ribosomal subunit;GO:0005634 nucleus;GO:0019005 SCF ubiquitin ligase complex;GO:0005739 mitochondrion;GO:0031466 Cul5-RING ubiquitin ligase complex",
        "go_biological_process": "GO:0032543 mitochondrial translation;GO:0016567 protein ubiquitination;GO:0006511 ubiquitin-dependent protein catabolic process;GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process;GO:0070936 protein K48-linked ubiquitination",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LAI2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LCK5-1",
        "uniprot_id": "A0ABK0LCK5_RAT",
        "mass": 16242.0,
        "length": 143,
        "protein_name": "A-kinase anchoring protein 19",
        "gene_name": "Akap19",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Akap19; C9h2orf88; LOC685203",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "A-kinase anchoring protein 19; Small membrane A-kinase anchor protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:685203)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
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        "function": "",
        "predicted_glycosites": 0,
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        "biomarker_type": "",
        "glycan_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0034237 protein kinase A regulatory subunit binding",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0LCK5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LBT8-1",
        "uniprot_id": "A0ABK0LBT8_RAT",
        "mass": 78583.0,
        "length": 700,
        "protein_name": "Hedgehog-interacting protein",
        "gene_name": "Hhip",
        "organism": "Rat",
        "refseq_name": "hedgehog-interacting protein precursor",
        "refseq_ac": "NP_001178746",
        "gene_names_uniprotkb": "Hhip",
        "gene_names_refseq": "Hhip; RGD1564108",
        "protein_names_uniprotkb": "Hedgehog-interacting protein",
        "protein_names_refseq": "hedgehog-interacting protein precursor",
        "tax_id": 10116,
        "disease": "primary biliary cholangitis (Disease Ontology:DOID:12236); chronic obstructive pulmonary disease (Disease Ontology:DOID:3083); diabetic neuropathy (Disease Ontology:DOID:9743)",
        "pathway": " (rno:291936);  (R-RNO-5632681)",
        "pathway_count": 2,
        "publication_count": 0,
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        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "total_reported_n_glycosites": 0,
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        "total_n_glycosites": 0,
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        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 3,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0097108 hedgehog family protein binding;GO:0008270 zinc ion binding",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0005886 plasma membrane;GO:0009986 cell surface",
        "go_biological_process": "GO:0040036 regulation of fibroblast growth factor receptor signaling pathway;GO:0007165 signal transduction;GO:0043066 negative regulation of apoptotic process;GO:0009887 animal organ morphogenesis;GO:0048705 skeletal system morphogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LBT8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LCF1-1",
        "uniprot_id": "A0ABK0LCF1_RAT",
        "mass": 74793.0,
        "length": 681,
        "protein_name": "non-specific serine/threonine protein kinase",
        "gene_name": "Pak6",
        "organism": "Rat",
        "refseq_name": "serine/threonine-protein kinase PAK 6",
        "refseq_ac": "NP_001099968",
        "gene_names_uniprotkb": "Pak6",
        "gene_names_refseq": "Pak6",
        "protein_names_uniprotkb": "non-specific serine/threonine protein kinase; 2.7.11.1",
        "protein_names_refseq": "p21 (CDKN1A)-activated kinase 6; p21 protein (Cdc42/Rac)-activated kinase 6; p21-activated kinase 6; serine/threonine-protein kinase PAK 6",
        "tax_id": 10116,
        "disease": "Parkinson's disease (Disease Ontology:DOID:14330); clear cell renal cell carcinoma (Disease Ontology:DOID:4467)",
        "pathway": " (rno:296078);  (R-RNO-9013149);  (R-RNO-9013407);  (R-RNO-9013424)",
        "pathway_count": 4,
        "publication_count": 2,
        "publication_id_list": "21541790;32679145",
        "class_list": "",
        "function": "After injury, the expression of PAK6 was increased significantly in the astrocytes and neurons, [RefSeq, PubMed]; MiR-27a promotion resulting from silencing of HDAC3 facilitates the recovery of spinal cord injury by inhibiting PAK6 expression in rats., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 2,
        "glyco_site_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "2.7.11.1;2.7.12.1;3.4.19.12;2.7.1.153;2.7.1.137;2.7.11.24;2.7.10.2;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;2.3.1.-;2.7.11.34;2.7.10.1;2.7.1.150;2.7.11.13;4.1.1.32;3.6.5.2;2.7.11.19;2.7.2.3;2.7.11.11;2.7.10.4;3.6.4.6;2.7.11.31;3.1.3.16;3.1.4.4;2.7.11.4;2.3.1.48;3.1.11.-;2.7.13.3;2.7.4.18;3.1.24.-;2.7.11.39;1.6.3.-;3.6.5.-;2.3.2.27;2.4.99.18;2.7.11.10;2.1.1.13",
        "go_molecular_function": "GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005654 nucleoplasm;GO:0014069 postsynaptic density;GO:0001650 fibrillar center",
        "go_biological_process": "GO:0035556 intracellular signal transduction;GO:0009267 cellular response to starvation;GO:0043408 regulation of MAPK cascade;GO:0007612 learning;GO:0007613 memory",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "A0ABK0LCF1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LCE3-1",
        "uniprot_id": "A0ABK0LCE3_RAT",
        "mass": 33238.0,
        "length": 289,
        "protein_name": "Proteasome assembly chaperone 1",
        "gene_name": "Psmg1",
        "organism": "Rat",
        "refseq_name": "proteasome assembly chaperone 1",
        "refseq_ac": "NP_001386166",
        "gene_names_uniprotkb": "Psmg1",
        "gene_names_refseq": "Dscr2; Psmg1",
        "protein_names_uniprotkb": "Proteasome assembly chaperone 1",
        "protein_names_refseq": "Down syndrome critical region gene 2; Down syndrome critical region homolog 2; proteasome (prosome, macropain) assembly chaperone 1; proteasome assembly chaperone 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-9907900)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Chaperone protein which promotes assembly of the 20S proteasome as part of a heterodimer with PSMG2. The PSMG1-PSMG2 heterodimer binds to the PSMA5 and PSMA7 proteasome subunits, promotes assembly of the proteasome alpha subunits into the heteroheptameric alpha ring and prevents alpha ring dimerization., [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": "",
        "go_molecular_function": "GO:0060090 molecular adaptor activity;GO:0070628 proteasome binding",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005794 Golgi apparatus;GO:0005829 cytosol",
        "go_biological_process": "GO:0043248 proteasome assembly;GO:0021930 cerebellar granule cell precursor proliferation;GO:0080129 proteasome core complex assembly;GO:0051131 chaperone-mediated protein complex assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LCE3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LAT9-1",
        "uniprot_id": "A0ABK0LAT9_RAT",
        "mass": 27512.0,
        "length": 245,
        "protein_name": "Intraflagellar transport associated protein",
        "gene_name": "Iftap",
        "organism": "Rat",
        "refseq_name": "intraflagellar transport-associated protein isoform 1",
        "refseq_ac": "NP_001099961",
        "gene_names_uniprotkb": "Iftap; RGD1309730",
        "gene_names_refseq": "Iftap; RGD1309730",
        "protein_names_uniprotkb": "Intraflagellar transport associated protein",
        "protein_names_refseq": "intraflagellar transport-associated protein isoform 1; uncharacterized protein C11orf74 homolog",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 1,
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        "protein_names_refseq": "fatty acid hydroxylase domain-containing protein 2 isoform X1",
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        "uniprot_canonical_ac": "A0ABK0LAZ2-1",
        "uniprot_id": "A0ABK0LAZ2_RAT",
        "mass": 29896.0,
        "length": 264,
        "protein_name": "Telethonin",
        "gene_name": "Tcap",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Tcap",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Telethonin; Titin cap protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "autosomal recessive limb-girdle muscular dystrophy type 2G (Disease Ontology:DOID:0110281); hypertrophic cardiomyopathy 25 (Disease Ontology:DOID:0110328)",
        "pathway": " (rno:688173);  (R-RNO-390522)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Muscle assembly regulating factor. Mediates the antiparallel assembly of titin (TTN) molecules at the sarcomeric Z-disk., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "reported_s_glycosites": 0,
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        "reported_o_glycosites_with_glycan": 0,
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        "biomarker_type": "",
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        "disease_count": 2,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0030674 protein-macromolecule adaptor activity;GO:0008307 structural constituent of muscle;GO:0031432 titin binding;GO:0060090 molecular adaptor activity;GO:0044325 transmembrane transporter binding",
        "go_cellular_component": "GO:0030018 Z disc;GO:0031674 I band;GO:1990733 titin-telethonin complex",
        "go_biological_process": "GO:0035995 detection of muscle stretch;GO:0003009 skeletal muscle contraction;GO:0030240 skeletal muscle thin filament assembly;GO:0055003 cardiac myofibril assembly;GO:0055008 cardiac muscle tissue morphogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LAZ2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LBE2-1",
        "uniprot_id": "A0ABK0LBE2_RAT",
        "mass": 19289.0,
        "length": 170,
        "protein_name": "Spermidine/spermine N1-acetyltransferase family member 2",
        "gene_name": "Sat2",
        "organism": "Rat",
        "refseq_name": "thialysine N-epsilon-acetyltransferase",
        "refseq_ac": "NP_001101748",
        "gene_names_uniprotkb": "Sat2",
        "gene_names_refseq": "Sat2",
        "protein_names_uniprotkb": "Spermidine/spermine N1-acetyltransferase family member 2",
        "protein_names_refseq": "diamine N-acetyltransferase 2; diamine acetyltransferase 2; spermidine/spermine N1-acetyl transferase 2; thialysine N-epsilon-acetyltransferase",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:360547)",
        "pathway_count": 1,
        "publication_count": 4,
        "publication_id_list": "18832333;19233140;19751803;26617791",
        "class_list": "",
        "function": "Our results indicate that both isoforms are expressed in MNTB principal neurons, and demonstrate that functional system A transporters are present in the plasma membrane of neurons., [RefSeq, PubMed]; Pronounced expression of SN1 and SAT2 in B-cells and A-cells, respectively, was shown suggesting pronounced expression of SN1 and SAT2 in B-cells and A-cells, respectively., [RefSeq, PubMed]; SAT2 maintains a key metabolic glutamine/glutamate balance underpinning retrograde signaling by dendritic release of the neurotransmitter glutamate, [RefSeq, PubMed]; Ulinastatin can effectively reduce the cardiac function damage caused by cardiopulmonary resuscitation, which could be related with the increased SSAT2 and decreased AQP4. Publication Status: Online-Only, [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0042802 identical protein binding;GO:0004145 diamine N-acetyltransferase activity;GO:0008080 N-acetyltransferase activity;GO:0016747 acyltransferase activity, transferring groups other than amino-acyl groups",
        "go_cellular_component": "",
        "go_biological_process": "GO:0032918 spermidine acetylation;GO:0032919 spermine acetylation;GO:0032920 putrescine acetylation;GO:0046204 nor-spermidine metabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.5,
        "record_id": "A0ABK0LBE2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LD49-1",
        "uniprot_id": "A0ABK0LD49_RAT",
        "mass": 64446.0,
        "length": 568,
        "protein_name": "MARVEL domain containing 2",
        "gene_name": "Marveld2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Marveld2; Ocln",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "MARVEL domain containing 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "pseudo-TORCH syndrome 1 (Disease Ontology:DOID:0050656); metabolic dysfunction and alcohol associated liver disease (Disease Ontology:DOID:0070508); autosomal recessive nonsyndromic deafness 49 (Disease Ontology:DOID:0110506); transient cerebral ischemia (Disease Ontology:DOID:224); Crohn's disease (Disease Ontology:DOID:8778); diabetic retinopathy (Disease Ontology:DOID:8947)",
        "pathway": " (rno:365657)",
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        "class_list": "",
        "function": "",
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        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 6,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005923 bicellular tight junction;GO:0016323 basolateral plasma membrane;GO:0030054 cell junction;GO:0016324 apical plasma membrane",
        "go_biological_process": "GO:0061028 establishment of endothelial barrier;GO:0007605 sensory perception of sound;GO:0070830 bicellular tight junction assembly;GO:0045216 cell-cell junction organization",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LD49-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LBN1-1",
        "uniprot_id": "A0ABK0LBN1_RAT",
        "mass": 192592.0,
        "length": 1757,
        "protein_name": "BCL6 co-repressor",
        "gene_name": "Bcor",
        "organism": "Rat",
        "refseq_name": "BCL-6 corepressor isoform 1",
        "refseq_ac": "NP_001178515",
        "gene_names_uniprotkb": "Bcor",
        "gene_names_refseq": "Bcor; RGD1562735",
        "protein_names_uniprotkb": "BCL6 co-repressor",
        "protein_names_refseq": "BCL-6 corepressor isoform 1; BCL-6 corepressor; Bcl6 interacting corepressor",
        "tax_id": 10116,
        "disease": "syndromic microphthalmia 1 (Disease Ontology:DOID:0111799); syndromic microphthalmia 2 (Disease Ontology:DOID:0111809); stomach cancer (Disease Ontology:DOID:10534); proliferative diabetic retinopathy (Disease Ontology:DOID:13207); dental caries (Disease Ontology:DOID:216); stomach carcinoma (Disease Ontology:DOID:5517); cataract (Disease Ontology:DOID:83); colorectal cancer (Disease Ontology:DOID:9256)",
        "pathway": " (rno:317346)",
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        "class_list": "",
        "function": "",
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003714 transcription corepressor activity;GO:0031072 heat shock protein binding;GO:0042826 histone deacetylase binding;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0000976 transcription cis-regulatory region binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0140261 BCOR complex",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006338 chromatin remodeling;GO:0007507 heart development;GO:0045892 negative regulation of DNA-templated transcription;GO:0042476 odontogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LBN1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LBE8-1",
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        "length": 672,
        "protein_name": "Polycomb protein SCMH1",
        "gene_name": "Scmh1",
        "organism": "Rat",
        "refseq_name": "polycomb protein SCMH1 isoform X3",
        "refseq_ac": "XP_038966231",
        "gene_names_uniprotkb": "Scmh1",
        "gene_names_refseq": "Scmh1",
        "protein_names_uniprotkb": "Polycomb protein SCMH1; Sex comb on midleg homolog 1",
        "protein_names_refseq": "polycomb protein SCMH1 isoform X3",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:362581)",
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        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Associates with Polycomb group (PcG) multiprotein complexes; the complex class is required to maintain the transcriptionally repressive state of some genes., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "missing_score": 10000,
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0010369 chromocenter",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006355 regulation of DNA-templated transcription;GO:0006338 chromatin remodeling;GO:0007283 spermatogenesis;GO:0009952 anterior/posterior pattern specification",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LBE8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LAZ7-1",
        "uniprot_id": "A0ABK0LAZ7_RAT",
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        "length": 247,
        "protein_name": "Uncharacterized protein",
        "gene_name": "Pym1-ps4",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Pym1-ps4",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Uncharacterized protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
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        "biomarker_type": "",
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        "record_id": "A0ABK0LAZ7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LBQ0-1",
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        "length": 363,
        "protein_name": "RNA binding motif protein 43",
        "gene_name": "Rbm43",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Rbm43",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "RNA binding motif protein 43",
        "protein_names_refseq": "",
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        "secondary_ac_list": "",
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        "go_molecular_function": "GO:0003723 RNA binding;GO:0003676 nucleic acid binding",
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        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LBQ0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LAJ4-1",
        "uniprot_id": "A0ABK0LAJ4_RAT",
        "mass": 76402.0,
        "length": 659,
        "protein_name": "Zinc finger protein 54",
        "gene_name": "Zfp54",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Zfp54",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger protein 54",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:308232)",
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        "class_list": "",
        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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    },
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        "function": "Key assembly factor specifically required for the stability of axonemal dynein heavy chains in cytoplasm., [UniProtKB, UniProtKB, UniProtKB]",
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    },
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        "gene_names_refseq": "LOC134482775",
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        "protein_names_refseq": "prolactin-3D1-like isoform 2 precursor",
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        "go_molecular_function": "GO:0005179 hormone activity",
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        "protein_name": "Prostamide/prostaglandin F synthase",
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        "gene_names_uniprotkb": "Prxl2b",
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        "protein_names_uniprotkb": "Prostamide/prostaglandin F synthase; 1.11.1.20; Peroxiredoxin-like 2B",
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        "function": "Catalyzes the reduction of prostaglandin-ethanolamide H(2) (prostamide H(2)) to prostamide F(2alpha) with NADPH as proton donor. Also able to reduce prostaglandin H(2) to prostaglandin F(2alpha)., [UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "1.11.1.20",
        "go_molecular_function": "GO:0016616 oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor;GO:0036130 prostaglandin H2 endoperoxidase reductase activity;GO:0047017 prostaglandin F synthase activity;GO:0008379 thioredoxin peroxidase activity;GO:0016491 oxidoreductase activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005783 endoplasmic reticulum;GO:0005829 cytosol;GO:0043209 myelin sheath",
        "go_biological_process": "GO:0019371 cyclooxygenase pathway;GO:0001516 prostaglandin biosynthetic process",
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        "record_id": "A0ABK0LB38-1",
        "record_type": "protein"
    },
    {
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        "protein_name": "D-dopachrome decarboxylase",
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        "protein_names_uniprotkb": "D-dopachrome decarboxylase; 4.1.1.84",
        "protein_names_refseq": "D-dopachrome decarboxylase isoform X1",
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        "function": "Tautomerization of D-dopachrome with decarboxylation to give 5,6-dihydroxyindole (DHI)., [UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005615 extracellular space;GO:0005737 cytoplasm",
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        "protein_names_uniprotkb": "RanBP2-type domain-containing protein",
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        "disease": "amyotrophic lateral sclerosis type 6 (Disease Ontology:DOID:0060198); essential tremor 4 (Disease Ontology:DOID:0111431); sarcoma (Disease Ontology:DOID:1115); neurodegenerative disease (Disease Ontology:DOID:1289); amyotrophic lateral sclerosis (Disease Ontology:DOID:332); liposarcoma (Disease Ontology:DOID:3382); frontotemporal dementia (Disease Ontology:DOID:9255)",
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        "protein_name": "Y-linked testis-specific protein 1-like",
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        "refseq_name": "Y-linked testis-specific protein 1-like",
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        "gene_names_refseq": "LOC134484306",
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        "protein_names_refseq": "Y-linked testis-specific protein 1-like",
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        "protein_name": "Ig-like domain-containing protein",
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        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ig-like domain-containing protein",
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        "go_cellular_component": "GO:0042101 T cell receptor complex",
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        "length": 323,
        "protein_name": "Olfactory receptor",
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        "refseq_name": "olfactory receptor Olr1346",
        "refseq_ac": "NP_001000520",
        "gene_names_uniprotkb": "Or9s23b",
        "gene_names_refseq": "Olr1346; Or9s23b; ratchr9-91970057-91971028_ORF",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 1346; olfactory receptor Olr1346; olfactory receptor gene Olr1346",
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        "go_molecular_function": "GO:0003735 structural constituent of ribosome",
        "go_cellular_component": "GO:0022625 cytosolic large ribosomal subunit",
        "go_biological_process": "GO:0006412 translation;GO:0000463 maturation of LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA)",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LC39-1",
        "uniprot_id": "A0ABK0LC39_RAT",
        "mass": 42781.0,
        "length": 421,
        "protein_name": "POU domain protein",
        "gene_name": "Pou4f1",
        "organism": "Rat",
        "refseq_name": "POU domain, class 4, transcription factor 1",
        "refseq_ac": "NP_001406467",
        "gene_names_uniprotkb": "Pou4f1",
        "gene_names_refseq": "Brn3a; Pou4f1; brn-3A",
        "protein_names_uniprotkb": "POU domain protein",
        "protein_names_refseq": "POU domain, class 4, transcription factor 1; brain-3A; brain-specific homeobox/POU domain protein 3A",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 2,
        "publication_id_list": "21315070;26200499",
        "class_list": "",
        "function": "Brn3a is a reliable retinal ganglion cell marker that can be used to accurately measure the potential effect of a given neuroprotective therapy., [RefSeq, PubMed]; Phenotypic and molecular changes that may represent an effort to resist degeneration and/or preferential survival of m+RGCs capable of synthesizing Brn3a., [RefSeq, PubMed]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0003682 chromatin binding;GO:0003700 DNA-binding transcription factor activity;GO:0051020 GTPase binding;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0043005 neuron projection;GO:0000785 chromatin;GO:0090575 RNA polymerase II transcription regulator complex",
        "go_biological_process": "GO:0060384 innervation;GO:0048880 sensory system development;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0001967 suckling behavior;GO:0007283 spermatogenesis",
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        "hit_score": 0.3,
        "record_id": "A0ABK0LC39-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LC45-1",
        "uniprot_id": "A0ABK0LC45_RAT",
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        "length": 120,
        "protein_name": "Ig-like domain-containing protein",
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        "organism": "Rat",
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        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ig-like domain-containing protein",
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        "biomarker_type": "",
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        "record_id": "A0ABK0LC45-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LC50-1",
        "uniprot_id": "A0ABK0LC50_RAT",
        "mass": 34874.0,
        "length": 310,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or7a38d",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr1079",
        "refseq_ac": "NP_001000711",
        "gene_names_uniprotkb": "Or7a38d",
        "gene_names_refseq": "Olr1079; Or7a38d",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory protein; olfactory receptor 1079; olfactory receptor Olr1079; olfactory receptor gene Olr1079",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:404960)",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
        "predicted_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
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        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LC50-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LC55-1",
        "uniprot_id": "A0ABK0LC55_RAT",
        "mass": 55387.0,
        "length": 492,
        "protein_name": "non-specific serine/threonine protein kinase",
        "gene_name": "Smokl7",
        "organism": "Rat",
        "refseq_name": "putative sperm motility kinase W",
        "refseq_ac": "XP_038936413",
        "gene_names_uniprotkb": "Smokl7",
        "gene_names_refseq": "Smokl7",
        "protein_names_uniprotkb": "non-specific serine/threonine protein kinase; 2.7.11.1",
        "protein_names_refseq": "putative sperm motility kinase W",
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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": 0,
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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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        "hit_score": 0.1,
        "record_id": "A0ABK0LC55-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LC58-1",
        "uniprot_id": "A0ABK0LC58_RAT",
        "mass": 37365.0,
        "length": 339,
        "protein_name": "Peptidoglycan recognition protein 3",
        "gene_name": "LOC134485743",
        "organism": "Rat",
        "refseq_name": "peptidoglycan recognition protein 3-like",
        "refseq_ac": "XP_063138839",
        "gene_names_uniprotkb": "LOC134485743",
        "gene_names_refseq": "LOC134485743",
        "protein_names_uniprotkb": "Peptidoglycan recognition protein 3",
        "protein_names_refseq": "peptidoglycan recognition protein 3-like",
        "tax_id": 10116,
        "disease": "",
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        "pathway_count": 0,
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        "publication_id_list": "",
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        "function": "Pattern receptor that binds to murein peptidoglycans (PGN) of Gram-positive bacteria. Has bactericidal activity towards Gram-positive bacteria. May kill Gram-positive bacteria by interfering with peptidoglycan biosynthesis. Also binds to Gram-negative bacteria, and has bacteriostatic activity towards Gram-negative bacteria. Plays a role in innate immunity., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "ec_number_list": "",
        "go_molecular_function": "GO:0008745 N-acetylmuramoyl-L-alanine amidase activity;GO:0008270 zinc ion binding",
        "go_cellular_component": "",
        "go_biological_process": "GO:0009253 peptidoglycan catabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LC58-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LC59-1",
        "uniprot_id": "A0ABK0LC59_RAT",
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        "length": 326,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or4f4b",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Or4f4b; Olfr1289",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "",
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LC59-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LC63-1",
        "uniprot_id": "A0ABK0LC63_RAT",
        "mass": 40342.0,
        "length": 352,
        "protein_name": "Ig-like domain-containing protein",
        "gene_name": "RT1-T24-4",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "RT1-T24-4",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ig-like domain-containing protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
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        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Involved in the presentation of foreign antigens to the immune system., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0016020 membrane",
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        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LC63-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LC67-1",
        "uniprot_id": "A0ABK0LC67_RAT",
        "mass": 20381.0,
        "length": 168,
        "protein_name": "High mobility group protein B4",
        "gene_name": "LOC108352140",
        "organism": "Rat",
        "refseq_name": "high mobility group protein B4-like",
        "refseq_ac": "XP_017453216",
        "gene_names_uniprotkb": "LOC108352140",
        "gene_names_refseq": "LOC108352140",
        "protein_names_uniprotkb": "High mobility group protein B4",
        "protein_names_refseq": "high mobility group protein B4-like",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:103694587);  (rno:108352140)",
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        "predicted_glycosites": 0,
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        "length": 163,
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        "refseq_name": "dual specificity phosphatase 28",
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        "protein_names_uniprotkb": "Disks large homolog 5 N-terminal domain-containing protein",
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        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 2,
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        "secondary_ac_list": "",
        "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:0004722 protein serine/threonine phosphatase activity;GO:0017017 MAP kinase tyrosine/serine/threonine phosphatase activity",
        "go_cellular_component": "",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LD64-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LEP2-1",
        "uniprot_id": "A0ABK0LEP2_RAT",
        "mass": 1011355.0,
        "length": 8820,
        "protein_name": "Nesprin-1",
        "gene_name": "Syne1",
        "organism": "Rat",
        "refseq_name": "nesprin-1",
        "refseq_ac": "NP_001406778",
        "gene_names_uniprotkb": "Syne1",
        "gene_names_refseq": "CPG2; Myne-1; Syne1",
        "protein_names_uniprotkb": "Nesprin-1; Enaptin; KASH domain-containing protein 1; Myocyte nuclear envelope protein 1; Nuclear envelope spectrin repeat protein 1; Synaptic nuclear envelope protein 1",
        "protein_names_refseq": "nesprin-1-like; nesprin-1; spectrin repeat containing, nuclear envelope 1",
        "tax_id": 10116,
        "disease": "cerebellar ataxia (Disease Ontology:DOID:0050753); autosomal dominant Emery-Dreifuss muscular dystrophy 4 (Disease Ontology:DOID:0070249); arthrogryposis multiplex congenita (Disease Ontology:DOID:0080954); arthrogryposis multiplex congenita-3 (Disease Ontology:DOID:0080979); autosomal recessive spinocerebellar ataxia 8 (Disease Ontology:DOID:0111618); Emery-Dreifuss muscular dystrophy (Disease Ontology:DOID:11726); bipolar disorder (Disease Ontology:DOID:3312); muscular dystrophy (Disease Ontology:DOID:9884)",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 2,
        "publication_id_list": "26776730;31428857",
        "class_list": "",
        "function": "Elevated expression of cellular SYNE1, MMP10, and GTPase1 and their regulatory role in hepatocellular carcinoma progression., [RefSeq, PubMed]; Through direct interactions with F-actin and EndoB2, CPG2 physically bridges the spine cytoskeleton and the endocytic machinery, and this tripartite association is critical specifically for activity-dependent clathrin-mediated endocytosis of synaptic glutamate receptors., [RefSeq, PubMed]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
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        "disease_count": 8,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003779 actin binding;GO:0005102 signaling receptor binding;GO:0019899 enzyme binding;GO:0042802 identical protein binding;GO:0042803 protein homodimerization activity",
        "go_cellular_component": "GO:0005856 cytoskeleton;GO:0005640 nuclear outer membrane;GO:0031965 nuclear membrane;GO:0098978 glutamatergic synapse;GO:0098871 postsynaptic actin cytoskeleton",
        "go_biological_process": "GO:2001054 negative regulation of mesenchymal cell apoptotic process;GO:0090292 nuclear matrix anchoring at nuclear membrane;GO:0048814 regulation of dendrite morphogenesis;GO:0048260 positive regulation of receptor-mediated endocytosis;GO:0055007 cardiac muscle cell differentiation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "A0ABK0LEP2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LDR0-1",
        "uniprot_id": "A0ABK0LDR0_RAT",
        "mass": 51015.0,
        "length": 461,
        "protein_name": "Protein phosphatase, Mg2+/Mn2+ dependent, 1M",
        "gene_name": "Ppm1m",
        "organism": "Rat",
        "refseq_name": "protein phosphatase, Mg2+/Mn2+ dependent, 1M",
        "refseq_ac": "NP_001417327",
        "gene_names_uniprotkb": "Ppm1m",
        "gene_names_refseq": "Ppm1m",
        "protein_names_uniprotkb": "Protein phosphatase, Mg2+/Mn2+ dependent, 1M",
        "protein_names_refseq": "protein phosphatase 1M; protein phosphatase, Mg2+/Mn2+ dependent, 1M",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "go_molecular_function": "GO:0004741 [pyruvate dehydrogenase (acetyl-transferring)]-phosphatase activity;GO:0030145 manganese ion binding;GO:0004721 phosphoprotein phosphatase activity;GO:0004722 protein serine/threonine phosphatase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005739 mitochondrion",
        "go_biological_process": "GO:0006470 protein dephosphorylation",
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        "hit_score": 0.1,
        "record_id": "A0ABK0LDR0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LEC1-1",
        "uniprot_id": "A0ABK0LEC1_RAT",
        "mass": 62557.0,
        "length": 545,
        "protein_name": "Prolyl 3-hydroxylase OGFOD1",
        "gene_name": "Ogfod1",
        "organism": "Rat",
        "refseq_name": "prolyl 3-hydroxylase OGFOD1",
        "refseq_ac": "NP_001100881",
        "gene_names_uniprotkb": "Ogfod1",
        "gene_names_refseq": "Ogfod1; RGD1308848",
        "protein_names_uniprotkb": "Prolyl 3-hydroxylase OGFOD1; 2-oxoglutarate and iron-dependent oxygenase domain-containing protein 1; uS12 prolyl 3-hydroxylase",
        "protein_names_refseq": "2-oxoglutarate and iron-dependent oxygenase domain-containing protein 1; prolyl 3-hydroxylase OGFOD1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:307657);  (R-RNO-9629569)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Prolyl 3-hydroxylase that catalyzes 3-hydroxylation of 'Pro-62' of small ribosomal subunit uS12 (RPS23), thereby regulating protein translation termination efficiency. Involved in stress granule formation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "reported_c_glycosites_with_glycan": 0,
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        "ec_number_list": "",
        "go_molecular_function": "GO:0005506 iron ion binding;GO:0031418 L-ascorbic acid binding;GO:0016706 2-oxoglutarate-dependent dioxygenase activity;GO:0031543 peptidyl-proline dioxygenase activity;GO:0031544 peptidyl-proline 3-dioxygenase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005654 nucleoplasm;GO:0005829 cytosol;GO:0010494 cytoplasmic stress granule",
        "go_biological_process": "GO:0006449 regulation of translational termination;GO:0008283 cell population proliferation;GO:0034063 stress granule assembly;GO:0019511 peptidyl-proline hydroxylation;GO:0018126 protein hydroxylation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LEC1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LF12-1",
        "uniprot_id": "A0ABK0LF12_RAT",
        "mass": 19617.0,
        "length": 175,
        "protein_name": "Mitochondrial inner membrane protease subunit",
        "gene_name": "Immp2l",
        "organism": "Rat",
        "refseq_name": "mitochondrial inner membrane protease subunit 2",
        "refseq_ac": "NP_001385633",
        "gene_names_uniprotkb": "Immp2l",
        "gene_names_refseq": "Immp2l",
        "protein_names_uniprotkb": "Mitochondrial inner membrane protease subunit; 3.4.21.-",
        "protein_names_refseq": "IMP2 inner mitochondrial membrane peptidase-like; mitochondrial inner membrane protease subunit 2; rCG61688-like",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:100359529)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Catalyzes the removal of transit peptides required for the targeting of proteins from the mitochondrial matrix, across the inner membrane, into the inter-membrane space. Known to process the nuclear encoded protein DIABLO., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "predicted_o_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0004175 endopeptidase activity;GO:0004252 serine-type endopeptidase activity;GO:0008233 peptidase activity;GO:0009003 signal peptidase activity",
        "go_cellular_component": "GO:0042720 mitochondrial inner membrane peptidase complex",
        "go_biological_process": "GO:0006627 protein processing involved in protein targeting to mitochondrion;GO:0006465 signal peptide processing;GO:0033108 mitochondrial respiratory chain complex assembly;GO:0061300 cerebellum vasculature development;GO:0007283 spermatogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LF12-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LFN1-1",
        "uniprot_id": "A0ABK0LFN1_RAT",
        "mass": 138955.0,
        "length": 1234,
        "protein_name": "Tight junction protein 2",
        "gene_name": "Tjp2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Tjp2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Tight junction protein 2; Tight junction protein ZO-2; Zona occludens protein 2; Zonula occludens protein 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "disease of metabolism (Disease Ontology:DOID:0014667); familial hypercholanemia 1 (Disease Ontology:DOID:0061181); progressive familial intrahepatic cholestasis 4 (Disease Ontology:DOID:0070224); hypertension (Disease Ontology:DOID:10763)",
        "pathway": " (rno:115769);  (R-RNO-2028269);  (R-RNO-351906);  (R-RNO-8980692);  (R-RNO-9013026);  (R-RNO-9013106)",
        "pathway_count": 6,
        "publication_count": 3,
        "publication_id_list": "16396499;16641100;22673903",
        "class_list": "",
        "function": "Plays a role in tight junctions and adherens junctions. Acts as a positive regulator of RANKL-induced osteoclast differentiation, potentially via mediating downstream transcriptional activity., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, 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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        "disease_count": 4,
        "glyco_site_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0050839 cell adhesion molecule binding;GO:0019904 protein domain specific binding;GO:0030674 protein-macromolecule adaptor activity;GO:0044325 transmembrane transporter binding;GO:1990782 protein tyrosine kinase binding",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0005923 bicellular tight junction;GO:0005634 nucleus;GO:0005911 cell-cell junction;GO:0009986 cell surface",
        "go_biological_process": "GO:0150105 protein localization to cell-cell junction;GO:0098609 cell-cell adhesion;GO:0090557 establishment of endothelial intestinal barrier;GO:0045216 cell-cell junction organization;GO:1905605 positive regulation of blood-brain barrier permeability",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "A0ABK0LFN1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LDP4-1",
        "uniprot_id": "A0ABK0LDP4_RAT",
        "mass": 37982.0,
        "length": 347,
        "protein_name": "E3 ubiquitin-protein ligase",
        "gene_name": "Dtx3",
        "organism": "Rat",
        "refseq_name": "probable E3 ubiquitin-protein ligase DTX3",
        "refseq_ac": "NP_001178918",
        "gene_names_uniprotkb": "Dtx3",
        "gene_names_refseq": "Dtx3; RGD1566181",
        "protein_names_uniprotkb": "E3 ubiquitin-protein ligase; 2.3.2.27",
        "protein_names_refseq": "deltex 3 homolog; deltex 3, E3 ubiquitin ligase; deltex homolog 3; probable E3 ubiquitin-protein ligase DTX3; protein deltex-3",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:500847)",
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        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
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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:0061630 ubiquitin protein ligase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0007219 Notch signaling pathway;GO:0016567 protein ubiquitination;GO:0008593 regulation of Notch signaling pathway",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LDP4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LE77-1",
        "uniprot_id": "A0ABK0LE77_RAT",
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        "length": 916,
        "protein_name": "Epithelial cell transforming 2 like",
        "gene_name": "Ect2l",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ect2l",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Epithelial cell transforming 2 like",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "gene_name": "Mrps18c",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Mrps18c; Gpat3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Glycerol-3-phosphate acyltransferase 3",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (rno:289469);  (R-RNO-5389840);  (R-RNO-5419276);  (R-RNO-9937383)",
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        "go_cellular_component": "GO:0005763 mitochondrial small ribosomal subunit;GO:0005789 endoplasmic reticulum membrane",
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        "hit_score": 0.1,
        "record_id": "A0ABK0LDD4-1",
        "record_type": "protein"
    },
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        "length": 844,
        "protein_name": "Anoctamin",
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        "refseq_name": "",
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        "gene_names_uniprotkb": "Ano10",
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        "protein_names_uniprotkb": "Anoctamin",
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        "tax_id": 10116,
        "disease": "autosomal recessive spinocerebellar ataxia 10 (Disease Ontology:DOID:0050999)",
        "pathway": " (rno:301111);  (R-RNO-2672351)",
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        "go_molecular_function": "GO:0005227 calcium-activated cation channel activity;GO:0005229 intracellularly calcium-gated chloride channel activity",
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        "record_id": "A0ABK0LE79-1",
        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "A0ABK0LEZ3-1",
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        "length": 923,
        "protein_name": "ATP-dependent DNA helicase DDX11",
        "gene_name": "Ddx11; ENSRNOG00000068893",
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        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ddx11; ENSRNOG00000068893",
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        "protein_names_uniprotkb": "ATP-dependent DNA helicase DDX11; 5.6.2.3; DEAD/H-box protein 11; DNA 5'-3' helicase DDX11",
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        "tax_id": 10116,
        "disease": "Warsaw breakage syndrome (Disease Ontology:DOID:0060535)",
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        "ec_number_list": "5.6.2.3;3.6.4.13;3.6.4.12;2.7.11.1;3.6.1.5;3.6.4.10;3.6.4.-;2.3.2.27;5.6.2.4;3.6.5.-;5.6.2.-;3.1.-.-;2.7.7.7;2.7.7.49;3.1.13.1;4.2.99.18;7.6.2.2;7.6.2.3;7.6.2.-;5.6.1.6;7.2.2.-;3.6.1.15;3.6.4.6;3.1.3.1;3.9.1.1;6.1.1.12;3.6.1.-;2.7.4.3;3.1.4.-;3.4.24.-;3.6.-.-;3.4.21.53;5.6.2.5",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0005524 ATP binding;GO:0046872 metal ion binding;GO:0003678 DNA helicase activity;GO:0016818 hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides",
        "go_cellular_component": "GO:0005634 nucleus;GO:0000922 spindle pole;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005813 centrosome",
        "go_biological_process": "GO:0006139 nucleobase-containing compound metabolic process;GO:0034085 establishment of sister chromatid cohesion;GO:0006974 DNA damage response;GO:0072719 cellular response to cisplatin;GO:0072711 cellular response to hydroxyurea",
        "synthesized_glycan_count": 0,
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        "record_id": "A0ABK0LEZ3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LDS2-1",
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        "protein_name": "Dual specificity protein phosphatase",
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        "refseq_name": "dual specificity protein phosphatase 3 isoform X1",
        "refseq_ac": "XP_006247464",
        "gene_names_uniprotkb": "Dusp3",
        "gene_names_refseq": "Dusp3; RGD1560049",
        "protein_names_uniprotkb": "Dual specificity protein phosphatase; 3.1.3.16; 3.1.3.48",
        "protein_names_refseq": "dual specificity protein phosphatase 3 isoform X1",
        "tax_id": 10116,
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        "pathway": " (R-RNO-202670)",
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        "function": "Dual specificity phosphatase able to dephosphorylate phosphotyrosine, phosphoserine and phosphothreonine residues, with a preference for phosphotyrosine as a substrate., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Shows activity both for tyrosine-protein phosphate and serine-protein phosphate, but displays a strong preference toward phosphotyrosines. Specifically dephosphorylates and inactivates ERK1 and ERK2., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "ec_number_list": "3.1.3.48;3.1.3.16;2.7.10.1;3.1.3.53;3.1.3.2;3.1.3.52;3.1.3.21;3.1.3.18;2.7.11.22;3.1.3.67;3.1.3.-;3.1.3.27;2.7.11.24;3.1.3.5;3.1.3.74",
        "go_molecular_function": "GO:0004722 protein serine/threonine phosphatase activity;GO:0008138 protein tyrosine/serine/threonine phosphatase activity;GO:0033549 MAP kinase phosphatase activity;GO:0004725 protein tyrosine phosphatase activity;GO:0019901 protein kinase binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0036126 sperm flagellum",
        "go_biological_process": "GO:0045931 positive regulation of mitotic cell cycle;GO:0070373 negative regulation of ERK1 and ERK2 cascade;GO:0046329 negative regulation of JNK cascade;GO:0050860 negative regulation of T cell receptor signaling pathway;GO:0050868 negative regulation of T cell activation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LDS2-1",
        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "A0ABK0LFC3-1",
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        "length": 454,
        "protein_name": "GA-binding protein alpha chain",
        "gene_name": "Gabpa",
        "organism": "Rat",
        "refseq_name": "GA-binding protein alpha chain",
        "refseq_ac": "NP_001102311",
        "gene_names_uniprotkb": "Gabpa",
        "gene_names_refseq": "Gabpa; Nrf-2alpha; Nrf2a",
        "protein_names_uniprotkb": "GA-binding protein alpha chain",
        "protein_names_refseq": "GA binding protein transcription factor, alpha subunit 60kDa; GA repeat binding protein, alpha; GA-binding protein alpha chain; nuclear respiratory factor 2 alpha",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:363735);  (R-RNO-2151201)",
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        "publication_count": 5,
        "publication_id_list": "12618435;15016074;25783764;26095579;27683241",
        "class_list": "",
        "function": "GA-binding protein (GABPalpha/GABPbeta)is critical and functionally relevant Ets factor that regulates prolactin promoter activity via the basal transcription element site., [RefSeq, PubMed]; Increase in the mitochondrial biogenesis-associated transcription factor NRF-2/GABPalpha following cerebral hypoxic-ischemia in females, in contrast to the decrease observed with males, [RefSeq, PubMed]; Its activation enhanced by enteral glutamine mediates induction of glutathione in intestines., [RefSeq, PubMed]; NRF-2alpha and NRF-2beta respond to increased neuronal activity by translocating from the cytoplasm to the nucleus, where they engage in transcriptional activation of target genes., [RefSeq, PubMed]; Nrf2a gene mutation represents an early progression of carcinogenesis in rats., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
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        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003682 chromatin binding;GO:0000976 transcription cis-regulatory region binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0001228 DNA-binding transcription activator activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0000785 chromatin",
        "go_biological_process": "GO:0038127 ERBB signaling pathway;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0001701 in utero embryonic development;GO:0006357 regulation of transcription by RNA polymerase II;GO:0007528 neuromuscular junction development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.6,
        "record_id": "A0ABK0LFC3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LDA6-1",
        "uniprot_id": "A0ABK0LDA6_RAT",
        "mass": 93754.0,
        "length": 851,
        "protein_name": "Dynein axonemal assembly factor 5",
        "gene_name": "Dnaaf5",
        "organism": "Rat",
        "refseq_name": "dynein axonemal assembly factor 5",
        "refseq_ac": "NP_001128329",
        "gene_names_uniprotkb": "Dnaaf5; Heatr2",
        "gene_names_refseq": "Dnaaf5; Heatr2",
        "protein_names_uniprotkb": "Dynein axonemal assembly factor 5; HEAT repeat-containing protein 2",
        "protein_names_refseq": "HEAT repeat containing 2; HEAT repeat-containing protein 2; dynein assembly factor 5, axonemal; dynein axonemal assembly factor 5",
        "tax_id": 10116,
        "disease": "primary ciliary dyskinesia 18 (Disease Ontology:DOID:0110604); male infertility (Disease Ontology:DOID:12336); primary ciliary dyskinesia (Disease Ontology:DOID:9562)",
        "pathway": " (rno:304332)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Cytoplasmic protein involved in the delivery of the dynein machinery to the motile cilium. It is required for the assembly of the axonemal dynein inner and outer arms, two structures attached to the peripheral outer doublet A microtubule of the axoneme, that play a crucial role in cilium motility., [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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        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0045505 dynein intermediate chain binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0003341 cilium movement;GO:0036158 outer dynein arm assembly;GO:0036159 inner dynein arm assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LDA6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LE87-1",
        "uniprot_id": "A0ABK0LE87_RAT",
        "mass": 55002.0,
        "length": 496,
        "protein_name": "WD repeat-containing protein 37",
        "gene_name": "Wdr37",
        "organism": "Rat",
        "refseq_name": "WD repeat-containing protein 37 isoform 1",
        "refseq_ac": "NP_001386226",
        "gene_names_uniprotkb": "Wdr37",
        "gene_names_refseq": "Wdr37",
        "protein_names_uniprotkb": "WD repeat-containing protein 37",
        "protein_names_refseq": "WD repeat-containing protein 37 isoform 1; WD repeat-containing protein 37",
        "tax_id": 10116,
        "disease": "neurooculocardiogenitourinary syndrome (Disease Ontology:DOID:0111675)",
        "pathway": " (rno:307075)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Required for normal ER Ca2+ handling in lymphocytes. Together with PACS1, it plays an essential role in stabilizing peripheral lymphocyte populations., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0002260 lymphocyte homeostasis;GO:0022038 corpus callosum development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LE87-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LE75-1",
        "uniprot_id": "A0ABK0LE75_RAT",
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        "length": 552,
        "protein_name": "Succinyl-CoA:3-ketoacid-coenzyme A transferase",
        "gene_name": "Bmp8a; Oxct2a",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Bmp8a; Oxct2a; Bmp8a; Oxct2a",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Succinyl-CoA:3-ketoacid-coenzyme A transferase; 2.8.3.5",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "diabetes mellitus (Disease Ontology:DOID:9351); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (rno:100361036);  (rno:680931);  (R-RNO-77108)",
        "pathway_count": 3,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Key enzyme for ketone body catabolism. Transfers the CoA moiety from succinate to acetoacetate. Formation of the enzyme-CoA intermediate proceeds via an unstable anhydride species formed between the carboxylate groups of the enzyme and substrate., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
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        "reported_c_glycosites_with_glycan": 0,
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        "total_n_glycosites": 0,
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        "reported_phosphosites": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "2.8.3.5",
        "go_molecular_function": "GO:0005125 cytokine activity;GO:0008083 growth factor activity;GO:0008260 succinyl-CoA:3-oxo-acid CoA-transferase activity",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005739 mitochondrion",
        "go_biological_process": "GO:0007179 transforming growth factor beta receptor signaling pathway;GO:0030509 BMP signaling pathway;GO:0007281 germ cell development;GO:0001503 ossification;GO:0051216 cartilage development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LE75-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LFP4-1",
        "uniprot_id": "A0ABK0LFP4_RAT",
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        "length": 831,
        "protein_name": "Solute carrier family 37 member 2",
        "gene_name": "Ccdc15; Slc37a2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ccdc15; Slc37a2; Ccdc15; Slc37a2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Solute carrier family 37 member 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:367056);  (rno:500973);  (R-RNO-70263)",
        "pathway_count": 3,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Inorganic phosphate and glucose-6-phosphate antiporter. May transport cytoplasmic glucose-6-phosphate into the lumen of the endoplasmic reticulum and translocate inorganic phosphate into the opposite direction. Independent of a lumenal glucose-6-phosphatase. May not play a role in homeostatic regulation of blood glucose levels., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0061513 glucose 6-phosphate:phosphate antiporter activity",
        "go_cellular_component": "GO:0005789 endoplasmic reticulum membrane;GO:0005813 centrosome;GO:0012505 endomembrane system;GO:0005814 centriole",
        "go_biological_process": "GO:0015760 glucose-6-phosphate transport;GO:0035435 phosphate ion transmembrane transport;GO:0060271 cilium assembly;GO:1903724 positive regulation of centriole elongation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0LFP4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LFP9-1",
        "uniprot_id": "A0ABK0LFP9_RAT",
        "mass": 606108.0,
        "length": 5678,
        "protein_name": "AHNAK nucleoprotein",
        "gene_name": "Ahnak",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ahnak",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "AHNAK nucleoprotein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "autoimmune disease (Disease Ontology:DOID:417)",
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        "publication_id_list": "16641100;22673903;38843836",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0097493 structural molecule activity conferring elasticity;GO:0042802 identical protein binding;GO:0044548 S100 protein binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0015629 actin cytoskeleton",
        "go_biological_process": "GO:0043484 regulation of RNA splicing",
        "synthesized_glycan_count": 0,
        "hit_score": 0.6,
        "record_id": "A0ABK0LFP9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LDR4-1",
        "uniprot_id": "A0ABK0LDR4_RAT",
        "mass": 163971.0,
        "length": 1496,
        "protein_name": "Pogo transposable element with ZNF domain",
        "gene_name": "Pogz",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Pogz",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Pogo transposable element with ZNF domain",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "autism spectrum disorder (Disease Ontology:DOID:0060041); White-Sutton syndrome (Disease Ontology:DOID:0070067); intellectual disability (Disease Ontology:DOID:1059)",
        "pathway": " (rno:310658)",
        "pathway_count": 1,
        "publication_count": 3,
        "publication_id_list": "16641100;21606357;22673903",
        "class_list": "",
        "function": "Plays a role in mitotic cell cycle progression and is involved in kinetochore assembly and mitotic sister chromatid cohesion. Probably through its association with CBX5 plays a role in mitotic chromosome segregation by regulating aurora kinase B/AURKB activation and AURKB and CBX5 dissociation from chromosome arms. Promotes the repair of DNA double-strand breaks through the homologous recombination pathway., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 3,
        "predicted_n_glycosites": 0,
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        "missing_score": 0,
        "biomarker_type": "",
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        "glyco_site_count": 4,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003700 DNA-binding transcription factor activity;GO:0008270 zinc ion binding;GO:0000976 transcription cis-regulatory region binding;GO:0003677 DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005694 chromosome;GO:0005654 nucleoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0006355 regulation of DNA-templated transcription;GO:0006281 DNA repair;GO:0006310 DNA recombination;GO:0051301 cell division;GO:0051382 kinetochore assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.6,
        "record_id": "A0ABK0LDR4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LEM6-1",
        "uniprot_id": "A0ABK0LEM6_RAT",
        "mass": 93280.0,
        "length": 837,
        "protein_name": "Neural cell adhesion molecule 2",
        "gene_name": "Ncam2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ncam2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Neural cell adhesion molecule 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:288280)",
        "pathway_count": 1,
        "publication_count": 3,
        "publication_id_list": "22673903;24090084;38843836",
        "class_list": "",
        "function": "May play important roles in selective fasciculation and zone-to-zone projection of the primary olfactory axons., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0042802 identical protein binding",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0030424 axon;GO:0043005 neuron projection;GO:0097060 synaptic membrane",
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    },
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        "length": 525,
        "protein_name": "BCL3, transcription coactivator",
        "gene_name": "Bcl3",
        "organism": "Rat",
        "refseq_name": "",
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        "gene_names_uniprotkb": "Bcl3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "BCL3, transcription coactivator",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0003714 transcription corepressor activity;GO:0003713 transcription coactivator activity;GO:0030674 protein-macromolecule adaptor activity;GO:0042826 histone deacetylase binding;GO:0140297 DNA-binding transcription factor binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005829 cytosol;GO:0032996 Bcl3-Bcl10 complex;GO:0033257 Bcl3/NF-kappaB2 complex;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:1901222 regulation of non-canonical NF-kappaB signal transduction;GO:0030198 extracellular matrix organization;GO:0043066 negative regulation of apoptotic process;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0002455 humoral immune response mediated by circulating immunoglobulin",
        "synthesized_glycan_count": 0,
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        "record_type": "protein"
    },
    {
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        "uniprot_id": "A0ABK0LEZ9_RAT",
        "mass": 106609.0,
        "length": 948,
        "protein_name": "MAP7 domain containing 3",
        "gene_name": "Map7d3",
        "organism": "Rat",
        "refseq_name": "MAP7 domain-containing protein 3 isoform X2",
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        "gene_names_uniprotkb": "Map7d3; RGD1565514",
        "gene_names_refseq": "Map7d3; RGD1565514",
        "protein_names_uniprotkb": "MAP7 domain containing 3",
        "protein_names_refseq": "MAP7 domain-containing protein 3 isoform X2",
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        "disease": "",
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        "record_type": "protein"
    },
    {
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        "mass": 64836.0,
        "length": 569,
        "protein_name": "Protein NDNF",
        "gene_name": "Ndnf",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ndnf",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Protein NDNF",
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        "tax_id": 10116,
        "disease": "hypogonadotropic hypogonadism (Disease Ontology:DOID:0090070)",
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        "function": "Secretory protein that plays a role in various cellular processes. Acts as a chemorepellent acting on gonadotropin-releasing hormone (GnRH) expressing neurons regulating their migration to the hypothalamus. Also promotes neuron migration, growth and survival as well as neurite outgrowth and is involved in the development of the olfactory system. May also act through the regulation of growth factors activity and downstream signaling. Also regulates extracellular matrix assembly and cell adhesiveness. Promotes endothelial cell survival, vessel formation and plays an important role in the process of revascularization through NOS3-dependent mechanisms., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0008201 heparin binding;GO:0005539 glycosaminoglycan binding",
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        "go_biological_process": "GO:0007399 nervous system development;GO:0030198 extracellular matrix organization;GO:0001525 angiogenesis;GO:0002931 response to ischemia;GO:0010976 positive regulation of neuron projection development",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LDY4-1",
        "uniprot_id": "A0ABK0LDY4_RAT",
        "mass": 91947.0,
        "length": 837,
        "protein_name": "non-specific serine/threonine protein kinase",
        "gene_name": "Braf",
        "organism": "Rat",
        "refseq_name": "serine/threonine-protein kinase B-raf isoform X1",
        "refseq_ac": "XP_063141466",
        "gene_names_uniprotkb": "Braf",
        "gene_names_refseq": "Braf",
        "protein_names_uniprotkb": "non-specific serine/threonine protein kinase; 2.7.11.1",
        "protein_names_refseq": "serine/threonine-protein kinase B-raf isoform X1",
        "tax_id": 10116,
        "disease": "cardiomyopathy (Disease Ontology:DOID:0050700); colorectal adenocarcinoma (Disease Ontology:DOID:0050861); cardiofaciocutaneous syndrome (Disease Ontology:DOID:0060233); Noonan syndrome 7 (Disease Ontology:DOID:0060585); Noonan syndrome with multiple lentigines 3 (Disease Ontology:DOID:0080550); cardiofaciocutaneous syndrome 1 (Disease Ontology:DOID:0111460); lung cancer (Disease Ontology:DOID:1324); colon carcinoma (Disease Ontology:DOID:1520); cancer (Disease Ontology:DOID:162); pancreatic cancer (Disease Ontology:DOID:1793); melanoma (Disease Ontology:DOID:1909); prostate adenocarcinoma (Disease Ontology:DOID:2526); Langerhans-cell histiocytosis (Disease Ontology:DOID:2571); dysembryoplastic neuroepithelial tumor (Disease Ontology:DOID:2679); endometrial carcinoma (Disease Ontology:DOID:2871); malignant astrocytoma (Disease Ontology:DOID:3069); high grade glioma (Disease Ontology:DOID:3070); germinoma (Disease Ontology:DOID:3304); papillary thyroid carcinoma (Disease Ontology:DOID:3969); pleomorphic xanthoastrocytoma (Disease Ontology:DOID:4852); intrahepatic cholangiocarcinoma (Disease Ontology:DOID:4928); cholangiocarcinoma (Disease Ontology:DOID:4947); bile duct adenoma (Disease Ontology:DOID:5381); pancreatic acinar cell adenocarcinoma (Disease Ontology:DOID:5742); familial melanoma (Disease Ontology:DOID:6846); colorectal cancer (Disease Ontology:DOID:9256)",
        "pathway": " (rno:114486);  (R-RNO-1295596);  (R-RNO-170968);  (R-RNO-5673000);  (R-RNO-5674135);  (R-RNO-5674499);  (R-RNO-5675221)",
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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;2.3.2.27;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;3.6.5.2;2.7.11.19;2.7.2.3;2.7.11.11;2.7.10.4;3.1.3.16;2.7.11.31;3.6.4.-;3.1.3.53;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:0046872 metal ion binding;GO:0004709 MAP kinase kinase kinase activity;GO:0004672 protein kinase activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005739 mitochondrion;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0098978 glutamatergic synapse",
        "go_biological_process": "GO:0007165 signal transduction;GO:0000165 MAPK cascade;GO:0002318 myeloid progenitor cell differentiation;GO:0010764 negative regulation of fibroblast migration;GO:0030878 thyroid gland development",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LDI1-1",
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        "length": 632,
        "protein_name": "GATA zinc finger domain containing 2A",
        "gene_name": "Gatad2a",
        "organism": "Rat",
        "refseq_name": "transcriptional repressor p66-alpha isoform 2",
        "refseq_ac": "NP_001423706",
        "gene_names_uniprotkb": "Gatad2a",
        "gene_names_refseq": "Gatad2a; RGD1310596",
        "protein_names_uniprotkb": "GATA zinc finger domain containing 2A",
        "protein_names_refseq": "p66 alpha; transcriptional repressor p66-alpha isoform 2; transcriptional repressor p66-alpha",
        "tax_id": 10116,
        "disease": "intellectual disability (Disease Ontology:DOID:1059)",
        "pathway": " (rno:290669);  (R-RNO-3214815);  (R-RNO-6804758);  (R-RNO-73762);  (R-RNO-8943724);  (R-RNO-9937850);  (R-RNO-9940951)",
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        "go_molecular_function": "GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0030674 protein-macromolecule adaptor activity",
        "go_cellular_component": "GO:0016581 NuRD complex;GO:0005634 nucleus;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006338 chromatin remodeling;GO:0006351 DNA-templated transcription;GO:0001842 neural fold formation;GO:0010172 embryonic body morphogenesis",
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        "hit_score": 0.2,
        "record_id": "A0ABK0LDI1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LFR7-1",
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        "mass": 81318.0,
        "length": 698,
        "protein_name": "Zinc finger protein 748, pseudogene 1",
        "gene_name": "Zfp748-ps1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Zfp748-ps1; LOC682206",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger protein 748, pseudogene 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway_count": 0,
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        "class_list": "",
        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000976 transcription cis-regulatory region binding;GO:0003677 DNA binding",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0006357 regulation of transcription by RNA polymerase II;GO:0006355 regulation of DNA-templated transcription;GO:0006351 DNA-templated transcription",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LFR7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LE63-1",
        "uniprot_id": "A0ABK0LE63_RAT",
        "mass": 114770.0,
        "length": 1027,
        "protein_name": "E3 ubiquitin-protein ligase TRIM37",
        "gene_name": "Trim37",
        "organism": "Rat",
        "refseq_name": "E3 ubiquitin-protein ligase TRIM37 isoform X1",
        "refseq_ac": "XP_006247161",
        "gene_names_uniprotkb": "Trim37",
        "gene_names_refseq": "Trim37",
        "protein_names_uniprotkb": "E3 ubiquitin-protein ligase TRIM37; 2.3.2.27; RING-type E3 ubiquitin transferase TRIM37; Tripartite motif-containing protein 37",
        "protein_names_refseq": "E3 ubiquitin-protein ligase TRIM37 isoform X1",
        "tax_id": 10116,
        "disease": "mulibrey nanism (Disease Ontology:DOID:0050436)",
        "pathway": " (rno:360592);  (R-RNO-983168)",
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        "biomarker_type": "",
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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",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0061630 ubiquitin protein ligase activity;GO:0003682 chromatin binding;GO:0003713 transcription coactivator activity;GO:0042803 protein homodimerization activity",
        "go_cellular_component": "GO:0005778 peroxisomal membrane;GO:0048471 perinuclear region of cytoplasm;GO:0005694 chromosome;GO:0005737 cytoplasm;GO:0005777 peroxisome",
        "go_biological_process": "GO:0016567 protein ubiquitination;GO:0045814 negative regulation of gene expression, epigenetic;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0050821 protein stabilization;GO:0051865 protein autoubiquitination",
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        "hit_score": 0.1,
        "record_id": "A0ABK0LE63-1",
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    },
    {
        "uniprot_canonical_ac": "A0ABK0LDL2-1",
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        "length": 108,
        "protein_name": "TAL bHLH transcription factor 2",
        "gene_name": "Tal2",
        "organism": "Rat",
        "refseq_name": "T-cell acute lymphocytic leukemia protein 2",
        "refseq_ac": "NP_001102932",
        "gene_names_uniprotkb": "Tal2",
        "gene_names_refseq": "Tail2; Tal2",
        "protein_names_uniprotkb": "TAL bHLH transcription factor 2",
        "protein_names_refseq": "T-cell acute lymphocytic leukemia 2; T-cell acute lymphocytic leukemia protein 2; tail anomaly lethal 2",
        "tax_id": 10116,
        "disease": "adult T-cell leukemia/lymphoma (Disease Ontology:DOID:0050523); acute lymphoblastic leukemia (Disease Ontology:DOID:9952)",
        "pathway": " (rno:685229)",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0046983 protein dimerization activity;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0003677 DNA binding",
        "go_cellular_component": "",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0035264 multicellular organism growth;GO:0009791 post-embryonic development;GO:0030901 midbrain development",
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        "hit_score": 0.1,
        "record_id": "A0ABK0LDL2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LFA2-1",
        "uniprot_id": "A0ABK0LFA2_RAT",
        "mass": 57053.0,
        "length": 507,
        "protein_name": "Cholesterol 24-hydroxylase",
        "gene_name": "Cyp46a1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Cyp46a1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Cholesterol 24-hydroxylase; 1.14.14.25; Cholesterol 24-monooxygenase; Cholesterol 24S-hydroxylase; Cytochrome P450 46A1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "Alzheimer's disease (Disease Ontology:DOID:10652); alcohol use disorder (Disease Ontology:DOID:1574)",
        "pathway": " (rno:362782);  (R-RNO-193775);  (R-RNO-211976)",
        "pathway_count": 3,
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        "class_list": "",
        "function": "P450 monooxygenase that plays a major role in cholesterol homeostasis in the brain. Primarily catalyzes the hydroxylation (with S stereochemistry) at C-24 of cholesterol side chain, triggering cholesterol diffusion out of neurons and its further degradation. By promoting constant cholesterol elimination in neurons, may activate the mevalonate pathway and coordinate the synthesis of new cholesterol and nonsterol isoprenoids involved in synaptic activity and learning. Further hydroxylates cholesterol derivatives and hormone steroids on both the ring and side chain of these molecules, converting them into active oxysterols involved in lipid signaling and biosynthesis. Acts as an epoxidase converting cholesta-5,24-dien-3beta-ol/desmosterol into (24S),25-epoxycholesterol, an abundant lipid ligand of nuclear NR1H2 and NR1H3 receptors shown to promote neurogenesis in developing brain. May also catalyze the oxidative metabolism of xenobiotics, such as clotrimazole., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "1.14.14.25;1.14.14.1;1.14.14.19;1.14.14.32;4.2.1.152",
        "go_molecular_function": "GO:0005506 iron ion binding;GO:0020037 heme binding;GO:0033781 cholesterol 24-hydroxylase activity;GO:0008395 steroid hydroxylase activity",
        "go_cellular_component": "GO:0030425 dendrite;GO:0005789 endoplasmic reticulum membrane;GO:0098794 postsynapse;GO:0098793 presynapse",
        "go_biological_process": "GO:0006707 cholesterol catabolic process;GO:0006805 xenobiotic metabolic process;GO:1900271 regulation of long-term synaptic potentiation;GO:0042448 progesterone metabolic process;GO:1903044 protein localization to membrane raft",
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        "record_id": "A0ABK0LFA2-1",
        "record_type": "protein"
    },
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        "length": 237,
        "protein_name": "Claudin",
        "gene_name": "Cldn2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Cldn2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Claudin",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:300920)",
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        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Claudins function as major constituents of the tight junction complexes that regulate the permeability of epithelia., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005198 structural molecule activity;GO:0042802 identical protein binding;GO:0160187 paracellular tight junction channel activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0005923 bicellular tight junction;GO:0005911 cell-cell junction;GO:0030054 cell junction;GO:0016328 lateral plasma membrane",
        "go_biological_process": "GO:1904729 regulation of intestinal lipid absorption;GO:0045471 response to ethanol;GO:0098609 cell-cell adhesion;GO:0002227 innate immune response in mucosa;GO:0016338 calcium-independent cell-cell adhesion via plasma membrane cell-adhesion molecules",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LD71-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LDI8-1",
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        "length": 405,
        "protein_name": "Double PHD fingers 2",
        "gene_name": "Dpf2",
        "organism": "Rat",
        "refseq_name": "zinc finger protein ubi-d4 isoform X1",
        "refseq_ac": "XP_006230912",
        "gene_names_uniprotkb": "Dpf2",
        "gene_names_refseq": "Dpf2",
        "protein_names_uniprotkb": "Double PHD fingers 2",
        "protein_names_refseq": "zinc finger protein ubi-d4 isoform X1",
        "tax_id": 10116,
        "disease": "Coffin-Siris syndrome 7 (Disease Ontology:DOID:0112369); alcohol use disorder (Disease Ontology:DOID:1574)",
        "pathway": " (rno:361711);  (R-RNO-9933937);  (R-RNO-9933946);  (R-RNO-9934037)",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0003712 transcription coregulator activity;GO:0140015 histone H3K14ac reader activity;GO:0140046 histone H4K16ac reader activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005654 nucleoplasm;GO:0000785 chromatin",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006915 apoptotic process;GO:0006355 regulation of DNA-templated transcription;GO:1905454 negative regulation of myeloid progenitor cell differentiation",
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        "hit_score": 0.2,
        "record_id": "A0ABK0LDI8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LEJ5-1",
        "uniprot_id": "A0ABK0LEJ5_RAT",
        "mass": 34942.0,
        "length": 316,
        "protein_name": "Transmembrane protein 71",
        "gene_name": "Tmem71",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Tmem71",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Transmembrane protein 71",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (rno:690657)",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005739 mitochondrion",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LEJ5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LFS0-1",
        "uniprot_id": "A0ABK0LFS0_RAT",
        "mass": 75434.0,
        "length": 665,
        "protein_name": "Metal-response element-binding transcription factor 2",
        "gene_name": "Mtf2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Mtf2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Metal-response element-binding transcription factor 2; Metal regulatory transcription factor 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:360905);  (R-RNO-212300)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Polycomb group (PcG) protein that specifically binds histone H3 trimethylated at 'Lys-36' (H3K36me3) and recruits the PRC2 complex, thus enhancing PRC2 H3K27me3 methylation activity. Regulates the transcriptional networks during embryonic stem cell self-renewal and differentiation. Promotes recruitment of the PRC2 complex to the inactive X chromosome in differentiating XX ES cells and PRC2 recruitment to target genes in undifferentiated ES cells. Required to repress Hox genes by enhancing H3K27me3 methylation of the PRC2 complex. In some conditions may act as an inhibitor of PRC2 activity: able to activate the CDKN2A gene and promote cellular senescence by suppressing the catalytic activity of the PRC2 complex locally. Binds to the metal-regulating-element (MRE) of MT1A gene promoter., [UniProtKB, UniProtKB, 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:0003677 DNA binding;GO:0003682 chromatin binding;GO:0008270 zinc ion binding;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0001222 transcription corepressor binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0035098 ESC/E(Z) complex",
        "go_biological_process": "GO:0048863 stem cell differentiation;GO:1990830 cellular response to leukemia inhibitory factor;GO:0019827 stem cell population maintenance;GO:0007379 segment specification;GO:0045814 negative regulation of gene expression, epigenetic",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LFS0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LFM1-1",
        "uniprot_id": "A0ABK0LFM1_RAT",
        "mass": 97376.0,
        "length": 860,
        "protein_name": "Ribosomal protein S6 kinase",
        "gene_name": "Rps6ka6",
        "organism": "Rat",
        "refseq_name": "ribosomal protein S6 kinase alpha-6",
        "refseq_ac": "NP_001178650",
        "gene_names_uniprotkb": "Rps6ka6",
        "gene_names_refseq": "RGD1560817; Rps6ka6",
        "protein_names_uniprotkb": "Ribosomal protein S6 kinase; 2.7.11.1",
        "protein_names_refseq": "ribosomal protein S6 kinase alpha-6; ribosomal protein S6 kinase polypeptide 6",
        "tax_id": 10116,
        "disease": "Coffin-Lowry syndrome (Disease Ontology:DOID:3783)",
        "pathway": " (rno:317203);  (R-RNO-442742);  (R-RNO-444257)",
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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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        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0045202 synapse",
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        "length": 279,
        "protein_name": "Uroplakin-1a",
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        "refseq_name": "uroplakin-1a isoform X2",
        "refseq_ac": "XP_063125188",
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        "gene_names_refseq": "Upk1a",
        "protein_names_uniprotkb": "Uroplakin-1a; Uroplakin Ia",
        "protein_names_refseq": "uroplakin-1a isoform X2",
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        "function": "Component of the asymmetric unit membrane (AUM); a highly specialized biomembrane elaborated by terminally differentiated urothelial cells. May play an important role in normal bladder epithelial physiology, possibly in regulating membrane permeability of superficial umbrella cells or in stabilizing the apical membrane through AUM/cytoskeletal interactions., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0016020 membrane;GO:0120001 apical plasma membrane urothelial plaque;GO:0009986 cell surface;GO:0016324 apical plasma membrane",
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        "record_id": "A0ABK0LE96-1",
        "record_type": "protein"
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        "length": 339,
        "protein_name": "X-C motif chemokine receptor 1",
        "gene_name": "Xcr1",
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        "refseq_name": "chemokine XC receptor 1 isoform X1",
        "refseq_ac": "XP_063121383",
        "gene_names_uniprotkb": "Xcr1",
        "gene_names_refseq": "Xcr1",
        "protein_names_uniprotkb": "X-C motif chemokine receptor 1",
        "protein_names_refseq": "chemokine XC receptor 1 isoform X1",
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        "pathway": " (rno:301086);  (R-RNO-380108);  (R-RNO-416476)",
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        "go_biological_process": "GO:0006955 immune response;GO:0007204 positive regulation of cytosolic calcium ion concentration;GO:0019722 calcium-mediated signaling;GO:0060326 cell chemotaxis;GO:0006935 chemotaxis",
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        "refseq_ac": "NP_001430622",
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        "protein_names_refseq": "TNFAIP3-interacting protein 1 isoform 2",
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        "length": 520,
        "protein_name": "Cell division cycle 14B",
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        "refseq_name": "dual specificity protein phosphatase CDC14B isoform 1",
        "refseq_ac": "NP_001101874",
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        "gene_names_refseq": "Cdc14b",
        "protein_names_uniprotkb": "Cell division cycle 14B",
        "protein_names_refseq": "CDC14 cell division cycle 14 homolog B; dual specificity protein phosphatase CDC14B isoform 1; dual specificity protein phosphatase CDC14B",
        "tax_id": 10116,
        "disease": "renal cell carcinoma (Disease Ontology:DOID:4450)",
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        "protein_name": "Ubiquitin specific peptidase like 1",
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        "protein_names_uniprotkb": "Ubiquitin specific peptidase like 1",
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        "length": 2306,
        "protein_name": "DOP1 leucine zipper like protein B",
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        "refseq_name": "protein dopey-2 isoform X1",
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        "protein_names_refseq": "protein dopey-2 isoform X1",
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        "predicted_glycosites": 2,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 2,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
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        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
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        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 2,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005768 endosome;GO:0005829 cytosol;GO:0005802 trans-Golgi network;GO:0031901 early endosome membrane",
        "go_biological_process": "GO:0015031 protein transport;GO:0006895 Golgi to endosome transport;GO:0050890 cognition;GO:0009880 embryonic pattern specification",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "A0ABK0LFK5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LED6-1",
        "uniprot_id": "A0ABK0LED6_RAT",
        "mass": 28394.0,
        "length": 256,
        "protein_name": "palmitoyl-protein hydrolase",
        "gene_name": "Lyplal1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Lyplal1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "palmitoyl-protein hydrolase; 3.1.2.22",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:289357)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Palmitoyl thioesterase that catalyzes depalmitoylation of CGAS and KCNMA1. Acts as a regulator of innate immunity by mediating depalmitoylation of CGAS, thereby preventing CGAS homodimerization and cyclic GMP-AMP synthase activity. Does not exhibit phospholipase nor triacylglycerol lipase activity, able to hydrolyze only short chain substrates due to its shallow active site., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "3.1.2.22;2.3.1.21;3.1.2.2;3.1.2.-;3.4.-.-;3.1.1.93;3.4.19.12",
        "go_molecular_function": "GO:0008474 palmitoyl-(protein) hydrolase activity;GO:0016788 hydrolase activity, acting on ester bonds",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0042997 negative regulation of Golgi to plasma membrane protein transport;GO:0002084 protein depalmitoylation;GO:0160049 negative regulation of cGAS/STING signaling pathway",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LED6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LF07-1",
        "uniprot_id": "A0ABK0LF07_RAT",
        "mass": 80581.0,
        "length": 704,
        "protein_name": "mRNA (2'-O-methyladenosine-N(6)-)-methyltransferase",
        "gene_name": "Pcif1",
        "organism": "Rat",
        "refseq_name": "mRNA (2'-O-methyladenosine-N(6)-)-methyltransferase",
        "refseq_ac": "NP_001102075",
        "gene_names_uniprotkb": "Pcif1; Pcif1l1",
        "gene_names_refseq": "Pcif1; RGD1310800",
        "protein_names_uniprotkb": "mRNA (2'-O-methyladenosine-N(6)-)-methyltransferase; 2.1.1.62; Cap-specific adenosine methyltransferase; Phosphorylated CTD-interacting factor 1",
        "protein_names_refseq": "PDX1 C-terminal inhibiting factor 1; mRNA (2'-O-methyladenosine-N(6)-)-methyltransferase",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:103691999);  (rno:362269)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Cap-specific adenosine methyltransferase that catalyzes formation of N(6),2'-O-dimethyladenosine cap (m6A(m)) by methylating the adenosine at the second transcribed position of capped mRNAs. Recruited to the early elongation complex of RNA polymerase II (RNAPII) via interaction with POLR2A and mediates formation of m6A(m) co-transcriptionally., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
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        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0016422 mRNA (2'-O-methyladenosine-N6-)-methyltransferase activity;GO:0099122 RNA polymerase II C-terminal domain binding;GO:1904047 S-adenosyl-L-methionine binding;GO:1990269 RNA polymerase II C-terminal domain phosphoserine binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0015630 microtubule cytoskeleton;GO:0045171 intercellular bridge",
        "go_biological_process": "GO:0032259 methylation;GO:0006397 mRNA processing;GO:0017148 negative regulation of translation;GO:0045727 positive regulation of translation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0LF07-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LFM8-1",
        "uniprot_id": "A0ABK0LFM8_RAT",
        "mass": 40006.0,
        "length": 365,
        "protein_name": "Cellular communication network factor 6",
        "gene_name": "Ccn6",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ccn6; Wisp3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Cellular communication network factor 6; CCN family member 6; WNT1-inducible-signaling pathway protein 3",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "progressive pseudorheumatoid arthropathy of childhood (Disease Ontology:DOID:0090004); arthropathy (Disease Ontology:DOID:381); breast metaplastic carcinoma (Disease Ontology:DOID:4680)",
        "pathway": " (rno:499461)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 3,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005178 integrin binding;GO:0008201 heparin binding;GO:0008083 growth factor activity",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005739 mitochondrion;GO:0031012 extracellular matrix;GO:0005576 extracellular region",
        "go_biological_process": "GO:0007155 cell adhesion;GO:0007165 signal transduction;GO:0045597 positive regulation of cell differentiation;GO:0051239 regulation of multicellular organismal process;GO:0008285 negative regulation of cell population proliferation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LFM8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LER7-1",
        "uniprot_id": "A0ABK0LER7_RAT",
        "mass": 142858.0,
        "length": 1276,
        "protein_name": "Exportin-4",
        "gene_name": "Xpo4",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Xpo4",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Exportin-4",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005049 nuclear export signal receptor activity;GO:0031267 small GTPase binding",
        "go_cellular_component": "GO:0005643 nuclear pore;GO:0005737 cytoplasm;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0006611 protein export from nucleus;GO:0046827 positive regulation of protein export from nucleus",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0ABK0LER7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LFG1-1",
        "uniprot_id": "A0ABK0LFG1_RAT",
        "mass": 37984.0,
        "length": 336,
        "protein_name": "Transmembrane protein 241",
        "gene_name": "Slc35d4",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Slc35d4; LOC684948; Tmem241",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Transmembrane protein 241",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:680558)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
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        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0015297 antiporter activity;GO:0005458 GDP-mannose transmembrane transporter activity;GO:0005462 UDP-N-acetylglucosamine transmembrane transporter activity",
        "go_cellular_component": "GO:0016020 membrane;GO:0005794 Golgi apparatus",
        "go_biological_process": "GO:1990570 GDP-mannose transmembrane transport;GO:1990569 UDP-N-acetylglucosamine transmembrane transport",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LFG1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LE13-1",
        "uniprot_id": "A0ABK0LE13_RAT",
        "mass": 15102.0,
        "length": 135,
        "protein_name": "Pro-neuregulin-4, membrane-bound isoform",
        "gene_name": "Nrg4",
        "organism": "Rat",
        "refseq_name": "pro-neuregulin-4, membrane-bound isoform isoform X2",
        "refseq_ac": "XP_063122244",
        "gene_names_uniprotkb": "Nrg4",
        "gene_names_refseq": "Nrg4",
        "protein_names_uniprotkb": "Pro-neuregulin-4, membrane-bound isoform",
        "protein_names_refseq": "pro-neuregulin-4, membrane-bound isoform isoform X2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:690919)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Low affinity ligand for the ERBB4 tyrosine kinase receptor. Concomitantly recruits ERBB1 and ERBB2 coreceptors, resulting in ligand-stimulated tyrosine phosphorylation and activation of the ERBB receptors. Does not bind to the ERBB1, ERBB2 and ERBB3 receptors., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008083 growth factor activity;GO:0048018 receptor ligand activity",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0005886 plasma membrane;GO:0005615 extracellular space;GO:0016020 membrane",
        "go_biological_process": "GO:0038138 ERBB4-ERBB4 signaling pathway",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LE13-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LFN5-1",
        "uniprot_id": "A0ABK0LFN5_RAT",
        "mass": 77270.0,
        "length": 686,
        "protein_name": "Twinkle mtDNA helicase",
        "gene_name": "Twnk",
        "organism": "Rat",
        "refseq_name": "twinkle mtDNA helicase isoform X1",
        "refseq_ac": "XP_008758651",
        "gene_names_uniprotkb": "Twnk; Peo1",
        "gene_names_refseq": "Peo1; Twnk",
        "protein_names_uniprotkb": "Twinkle mtDNA helicase; 5.6.2.3; T7 gp4-like protein with intramitochondrial nucleoid localization; T7-like mitochondrial DNA helicase; Twinkle protein, mitochondrial",
        "protein_names_refseq": "twinkle mtDNA helicase isoform X1",
        "tax_id": 10116,
        "disease": "Perrault syndrome (Disease Ontology:DOID:0050857); mitochondrial DNA depletion syndrome (Disease Ontology:DOID:0070329); mitochondrial DNA depletion syndrome 7 (Disease Ontology:DOID:0080126); autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5 (Disease Ontology:DOID:0111518); autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 (Disease Ontology:DOID:0111520); chronic progressive external ophthalmoplegia (Disease Ontology:DOID:12558); Parkinson's disease (Disease Ontology:DOID:14330)",
        "pathway": " (rno:309441);  (R-RNO-9837999);  (R-RNO-9913635)",
        "pathway_count": 3,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Mitochondrial helicase involved in mtDNA replication and repair. Might have a role in mtDNA repair. Has DNA strand separation activity needed to form a processive replication fork for leading strand synthesis which is catalyzed by the formation of a replisome complex with POLG and mtSDB. Preferentially unwinds DNA substrates with pre-existing 5'-and 3'- single-stranded tails but is also active on a 5'- flap substrate. Can dissociate the invading strand of immobile or mobile D-loop DNA structures irrespective of the single strand polarity of the third strand. In addition to its DNA strand separation activity, also has DNA strand annealing, DNA strand-exchange and DNA branch migration activities., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_cellular_component": "GO:0005739 mitochondrion;GO:0042645 mitochondrial nucleoid;GO:0000262 mitochondrial chromosome",
        "go_biological_process": "GO:0006264 mitochondrial DNA replication;GO:0071333 cellular response to glucose stimulus;GO:0006260 DNA replication;GO:0006261 DNA-templated DNA replication;GO:0034214 protein hexamerization",
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        "length": 1778,
        "protein_name": "NLR family, pyrin domain containing 5",
        "gene_name": "Nlrp5",
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        "gene_names_uniprotkb": "Nlrp5",
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        "protein_names_uniprotkb": "NLR family, pyrin domain containing 5",
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        "go_cellular_component": "GO:0061702 canonical inflammasome complex;GO:0005634 nucleus;GO:0005739 mitochondrion;GO:0005829 cytosol;GO:0005938 cell cortex",
        "go_biological_process": "GO:0006954 inflammatory response;GO:0045087 innate immune response;GO:0050727 regulation of inflammatory response;GO:0051293 establishment of spindle localization;GO:0043487 regulation of RNA stability",
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        "length": 662,
        "protein_name": "CD180 antigen",
        "gene_name": "Cd180",
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        "refseq_name": "CD180 antigen precursor",
        "refseq_ac": "NP_001099875",
        "gene_names_uniprotkb": "Cd180",
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        "protein_names_uniprotkb": "CD180 antigen; Radioprotective 105 kDa protein",
        "protein_names_refseq": "CD180 antigen precursor; CD180 antigen; lymphocyte antigen 78; radioprotective 105 kDa protein",
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        "pathway": " (rno:294706);  (R-RNO-166016)",
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        "function": "CD180 protected PC12 cells from oxygenglucose deprivation/reoxygenation injury through promotion of the PI3K/AKT pathway., [RefSeq, PubMed]; Data show that overexpression of radioprotective 105 kDa protein (RP105; CD180) led to the repression of toll-like receptor 4 (TLR4) activity and the phosphorylation of NF-Kappa B p65., [RefSeq, PubMed]; Inhibition of miR-141-3p reduced hypoxia-induced apoptosis in H9c2 cardiomyocytes in vitro by activating the RP105-dependent PI3K/AKT signaling pathway. Publication Status: Online-Only, [RefSeq, PubMed]; Pattern recognition receptor predominantly expressed on B-cells, dendritic cells, and certain monocytes/macrophages, structurally resembling Toll-like receptors (TLRs) that plays a role in modulating immune responses. While ressembling a TLR, lacks the intracellular TIR (Toll/IL-1R) signaling domain and thus does not directly transduce signals. Instead, modulates immune responses, often in conjunction with other TLRs. For example, in cooperation with MD-1/LY86, interacts directly with the TLR4 signaling complex, inhibiting its ability to bind microbial ligand., [UniProtKB, UniProtKB, UniProtKB]; RP105 plays a cardioprotective role in myocardial ischemia reperfusion injury by regulating the Tolllike receptor 2/4 signaling pathways., [RefSeq, PubMed]; RP105 was minimally expressed in cardiac microvascular endothelial cells subjected to hypoxiareoxygenation injury., [RefSeq, PubMed]; The anti-inflammatory roles of radioprotective 105 kDa protein (RP105) and its potential in preventing and treating myocardial ischemia-reperfusion (I/R) injury., [RefSeq, PubMed]",
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        "gene_names_uniprotkb": "Gigyf1",
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        "protein_names_uniprotkb": "GRB10 interacting GYF protein 1",
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        "length": 597,
        "protein_name": "Outer dynein arm docking complex subunit 3",
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        "refseq_name": "outer dynein arm-docking complex subunit 3 isoform X2",
        "refseq_ac": "XP_063121409",
        "gene_names_uniprotkb": "Odad3; Ccdc151",
        "gene_names_refseq": "Ccdc151; Odad3; RGD1310048",
        "protein_names_uniprotkb": "Outer dynein arm docking complex subunit 3",
        "protein_names_refseq": "outer dynein arm-docking complex subunit 3 isoform X2",
        "tax_id": 10116,
        "disease": "Kartagener syndrome (Disease Ontology:DOID:0050144); primary ciliary dyskinesia 30 (Disease Ontology:DOID:0110624)",
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        "go_cellular_component": "GO:0035253 ciliary rootlet;GO:0036064 ciliary basal body;GO:0097542 ciliary tip;GO:0005929 cilium;GO:0005814 centriole",
        "go_biological_process": "GO:0003341 cilium movement;GO:0036158 outer dynein arm assembly;GO:0007368 determination of left/right symmetry;GO:1902017 regulation of cilium assembly",
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    {
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        "length": 354,
        "protein_name": "THUMP domain-containing protein 1",
        "gene_name": "AABR07005588.1; Thumpd1",
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        "gene_names_uniprotkb": "AABR07005588.1; Thumpd1; AABR07005588.1; Thumpd1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "THUMP domain-containing protein 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
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    {
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        "length": 796,
        "protein_name": "RALBP1 associated Eps domain containing 1",
        "gene_name": "Reps1",
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        "refseq_name": "ralBP1-associated Eps domain-containing protein 1 isoform 3",
        "refseq_ac": "NP_001402727",
        "gene_names_uniprotkb": "Reps1",
        "gene_names_refseq": "Reps1",
        "protein_names_uniprotkb": "RALBP1 associated Eps domain containing 1",
        "protein_names_refseq": "RalBP1 associated Eps domain containing protein; ralBP1-associated Eps domain-containing protein 1 isoform 3; ralBP1-associated Eps domain-containing protein 1-like; ralBP1-associated Eps domain-containing protein 1",
        "tax_id": 10116,
        "disease": "neurodegeneration with brain iron accumulation (Disease Ontology:DOID:0110734)",
        "pathway": " (R-RNO-8856825);  (R-RNO-8856828)",
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        "protein_names_refseq": "protein ripply2 isoform 1; ripply2 homolog",
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        "protein_names_uniprotkb": "von Willebrand factor A domain-containing protein 2; A domain-containing protein similar to matrilin and collagen",
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        "go_molecular_function": "GO:0042802 identical protein binding;GO:0005509 calcium ion binding",
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    },
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        "protein_name": "Zinc finger protein 865",
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        "gene_names_uniprotkb": "Ccdc106; Znf865; Ccdc106; LOC100911196; Znf865",
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        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0008270 zinc ion binding;GO:0003700 DNA-binding transcription factor activity;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II",
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    },
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        "protein_name": "Death domain-containing protein CRADD",
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        "protein_names_uniprotkb": "Death domain-containing protein CRADD; Caspase and RIP adapter with death domain",
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        "disease": "autosomal recessive intellectual developmental disorder 34 (Disease Ontology:DOID:0081200)",
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        "function": "Adapter protein that associates with PIDD1 and the caspase CASP2 to form the PIDDosome, a complex that activates CASP2 and triggers apoptosis. Also recruits CASP2 to the TNFR-1 signaling complex through its interaction with RIPK1 and TRADD and may play a role in the tumor necrosis factor-mediated signaling pathway., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_biological_process": "GO:2001235 positive regulation of apoptotic signaling pathway;GO:0030330 DNA damage response, signal transduction by p53 class mediator;GO:0042981 regulation of apoptotic process;GO:0043065 positive regulation of apoptotic process;GO:0097190 apoptotic signaling pathway",
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    {
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        "protein_name": "Cytochrome c oxidase assembly factor 6 homolog",
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        "gene_names_uniprotkb": "Coa6",
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        "protein_names_uniprotkb": "Cytochrome c oxidase assembly factor 6 homolog",
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        "disease": "cardiomyopathy (Disease Ontology:DOID:0050700); COX deficiency, infantile mitochondrial myopathy (Disease Ontology:DOID:0050713); mitochondrial complex IV deficiency nuclear type 13 (Disease Ontology:DOID:0080360); cytochrome-c oxidase deficiency disease (Disease Ontology:DOID:3762)",
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        "function": "Involved in the maturation of the mitochondrial respiratory chain complex IV subunit MT-CO2/COX2. Thereby, may regulate early steps of complex IV assembly. Mitochondrial respiratory chain complex IV or cytochrome c oxidase is the component of the respiratory chain that catalyzes the transfer of electrons from intermembrane space cytochrome c to molecular oxygen in the matrix and as a consequence contributes to the proton gradient involved in mitochondrial ATP synthesis. May also be required for efficient formation of respiratory supercomplexes comprised of complexes III and IV., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005507 copper ion binding;GO:0015035 protein-disulfide reductase activity",
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        "length": 1105,
        "protein_name": "DNA mismatch repair protein",
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        "refseq_name": "DNA mismatch repair protein Msh3",
        "refseq_ac": "NP_001178886",
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        "protein_names_refseq": "DNA mismatch repair protein Msh3",
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        "disease": "colorectal carcinoma (Disease Ontology:DOID:0080199); familial adenomatous polyposis 4 (Disease Ontology:DOID:0080412); endometrial cancer (Disease Ontology:DOID:1380); endometrial carcinoma (Disease Ontology:DOID:2871); lung non-small cell carcinoma (Disease Ontology:DOID:3908)",
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        "function": "Component of the post-replicative DNA mismatch repair system (MMR)., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0005524 ATP binding;GO:0019899 enzyme binding;GO:0003684 damaged DNA binding;GO:0019237 centromeric DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0032302 MutSbeta complex",
        "go_biological_process": "GO:0006281 DNA repair;GO:0007283 spermatogenesis;GO:0006298 mismatch repair;GO:0045910 negative regulation of DNA recombination;GO:0043570 maintenance of DNA repeat elements",
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    {
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        "protein_name": "CutA divalent cation tolerance homolog-like",
        "gene_name": "Cutal",
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        "gene_names_uniprotkb": "Cutal; RGD1564854",
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        "protein_names_uniprotkb": "CutA divalent cation tolerance homolog-like",
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        "go_biological_process": "GO:0010038 response to metal ion",
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        "record_type": "protein"
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    {
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        "protein_name": "Adaptor related protein complex 1 subunit sigma 1",
        "gene_name": "Ap1s1",
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        "gene_names_uniprotkb": "Ap1s1",
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        "protein_names_uniprotkb": "Adaptor related protein complex 1 subunit sigma 1",
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        "tax_id": 10116,
        "disease": "MEDNIK syndrome (Disease Ontology:DOID:0060483)",
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        "protein_names_uniprotkb": "Solute carrier family 16, member 4",
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    },
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        "protein_name": "BICD cargo adaptor 2",
        "gene_name": "Bicd2",
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        "gene_names_uniprotkb": "Bicd2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "BICD cargo adaptor 2",
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        "tax_id": 10116,
        "disease": "spinal muscular atrophy with lower extremity predominant 2A (Disease Ontology:DOID:0070349); spinal muscular atrophy with lower extremity predominant 2B (Disease Ontology:DOID:0070350)",
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        "go_molecular_function": "GO:0008093 cytoskeletal anchor activity;GO:0070840 dynein complex binding;GO:0031267 small GTPase binding;GO:0034452 dynactin binding;GO:0051959 dynein light intermediate chain binding",
        "go_cellular_component": "GO:0005635 nuclear envelope;GO:0005643 nuclear pore;GO:0005737 cytoplasm;GO:0005794 Golgi apparatus;GO:0005813 centrosome",
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        "gene_names_refseq": "Cog3",
        "protein_names_uniprotkb": "Conserved oligomeric Golgi complex subunit 3; Component of oligomeric Golgi complex 3",
        "protein_names_refseq": "conserved oligomeric Golgi complex subunit 3 isoform X2",
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        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005801 cis-Golgi network;GO:0005794 Golgi apparatus;GO:0005829 cytosol;GO:0005886 plasma membrane",
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        "protein_name": "Battenin",
        "gene_name": "Cln3",
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        "gene_names_uniprotkb": "Cln3",
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        "protein_names_uniprotkb": "Battenin",
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        "tax_id": 10116,
        "disease": "neuronal ceroid lipofuscinosis 1 (Disease Ontology:DOID:0110721); neuronal ceroid lipofuscinosis 3 (Disease Ontology:DOID:0110731); neuronal ceroid lipofuscinosis (Disease Ontology:DOID:14503)",
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        "go_molecular_function": "GO:0048306 calcium-dependent protein binding;GO:0051861 glycolipid binding;GO:0120146 sulfatide binding",
        "go_cellular_component": "GO:0005769 early endosome;GO:0045121 membrane raft;GO:0005765 lysosomal membrane;GO:0005770 late endosome;GO:0043005 neuron projection",
        "go_biological_process": "GO:0006897 endocytosis;GO:0043066 negative regulation of apoptotic process;GO:0061024 membrane organization;GO:0007040 lysosome organization;GO:0030162 regulation of proteolysis",
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        "record_id": "A0ABK0LEL9-1",
        "record_type": "protein"
    },
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        "uniprot_canonical_ac": "A0ABK0LEN0-1",
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        "length": 313,
        "protein_name": "Pyridoxal kinase",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Pdxkl1; RGD1566085",
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        "protein_names_uniprotkb": "Pyridoxal kinase; 2.7.1.35; Pyridoxine kinase",
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        "tax_id": 10116,
        "disease": "Parkinson's disease (Disease Ontology:DOID:14330)",
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        "publication_id_list": "",
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        "function": "Catalyzes the phosphorylation of the dietary vitamin B6 vitamers pyridoxal (PL), pyridoxine (PN) and pyridoxamine (PM) to form pyridoxal 5'-phosphate (PLP), pyridoxine 5'-phosphate (PNP) and pyridoxamine 5'-phosphate (PMP), respectively. PLP is the active form of vitamin B6, and acts as a cofactor for over 140 different enzymatic reactions., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "2.7.1.35",
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        "hit_score": 0.1,
        "record_id": "A0ABK0LEN0-1",
        "record_type": "protein"
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        "uniprot_canonical_ac": "A0ABK0LF30-1",
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        "length": 620,
        "protein_name": "Short chain dehydrogenase/reductase family 42E, member 2",
        "gene_name": "Sdr42e2",
        "organism": "Rat",
        "refseq_name": "putative short-chain dehydrogenase/reductase family 42E member 2",
        "refseq_ac": "XP_038957121",
        "gene_names_uniprotkb": "Sdr42e2",
        "gene_names_refseq": "Sdr42e2",
        "protein_names_uniprotkb": "Short chain dehydrogenase/reductase family 42E, member 2",
        "protein_names_refseq": "putative short-chain dehydrogenase/reductase family 42E member 2",
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        "go_molecular_function": "GO:0016616 oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor",
        "go_cellular_component": "GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0006694 steroid biosynthetic process",
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        "uniprot_canonical_ac": "A0ABK0LF19-1",
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        "mass": 167923.0,
        "length": 1485,
        "protein_name": "Receptor-type tyrosine-protein phosphatase kappa",
        "gene_name": "Ptprk",
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        "refseq_name": "receptor-type tyrosine-protein phosphatase kappa isoform X1",
        "refseq_ac": "XP_063121937",
        "gene_names_uniprotkb": "Ptprk",
        "gene_names_refseq": "Ptprk; Rptpk",
        "protein_names_uniprotkb": "Receptor-type tyrosine-protein phosphatase kappa; 3.1.3.48",
        "protein_names_refseq": "receptor-type tyrosine-protein phosphatase kappa isoform X1",
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        "function": "Regulation of processes involving cell contact and adhesion such as growth control, tumor invasion, and metastasis. Negative regulator of EGFR signaling pathway. Forms complexes with beta-catenin and gamma-catenin/plakoglobin. Beta-catenin may be a substrate for the catalytic activity of PTPRK/PTP-kappa., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "3.1.3.48;2.7.10.1;3.1.3.16;3.1.3.2;3.1.3.21;3.1.3.18;3.1.3.67;3.1.3.-;3.1.3.27;3.1.3.5",
        "go_molecular_function": "GO:0004725 protein tyrosine phosphatase activity;GO:0019901 protein kinase binding;GO:0008013 beta-catenin binding;GO:0045295 gamma-catenin binding",
        "go_cellular_component": "GO:0016020 membrane;GO:0005886 plasma membrane;GO:0005911 cell-cell junction;GO:0009986 cell surface;GO:0030054 cell junction",
        "go_biological_process": "GO:0007155 cell adhesion;GO:0007165 signal transduction;GO:0008285 negative regulation of cell population proliferation;GO:0016477 cell migration;GO:0031175 neuron projection development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0ABK0LF19-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0ABK0LEW3-1",
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        "mass": 66501.0,
        "length": 591,
        "protein_name": "receptor protein-tyrosine kinase",
        "gene_name": "Ryk",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ryk",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "receptor protein-tyrosine kinase; 2.7.10.1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "intellectual disability (Disease Ontology:DOID:1059)",
        "pathway": " (rno:140585)",
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        "function": "May be a coreceptor along with FZD8 of Wnt proteins, such as WNT1, WNT3, WNT3A and WNT5A. Involved in neuron differentiation, axon guidance, corpus callosum establishment and neurite outgrowth. In response to WNT3 stimulation, receptor C-terminal cleavage occurs in its transmembrane region and allows the C-terminal intracellular product to translocate from the cytoplasm to the nucleus where it plays a crucial role in neuronal development., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0004672 protein kinase activity;GO:0005524 ATP binding;GO:0004888 transmembrane signaling receptor activity;GO:0005109 frizzled binding;GO:0017147 Wnt-protein binding",
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        "go_biological_process": "GO:0007409 axonogenesis;GO:0031175 neuron projection development;GO:0043410 positive regulation of MAPK cascade;GO:0030182 neuron differentiation;GO:0016055 Wnt signaling pathway",
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    },
    {
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        "length": 490,
        "protein_name": "ETS variant transcription factor 1",
        "gene_name": "Etv1",
        "organism": "Rat",
        "refseq_name": "ETS translocation variant 1 isoform X1",
        "refseq_ac": "XP_063118166",
        "gene_names_uniprotkb": "Etv1",
        "gene_names_refseq": "Etv1",
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        "protein_names_refseq": "ETS translocation variant 1 isoform X1",
        "tax_id": 10116,
        "disease": "bipolar disorder (Disease Ontology:DOID:3312); obesity (Disease Ontology:DOID:9970)",
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        "go_molecular_function": "GO:0003700 DNA-binding transcription factor activity;GO:0043565 sequence-specific DNA 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:0006357 regulation of transcription by RNA polymerase II;GO:0045893 positive regulation of DNA-templated transcription;GO:0007638 mechanosensory behavior;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0007517 muscle organ development",
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        "record_type": "protein"
    },
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        "protein_name": "Multifunctional fusion protein",
        "gene_name": "Aldh4a1",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Aldh4a1",
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        "protein_names_uniprotkb": "Multifunctional fusion protein; L-glutamate gamma-semialdehyde dehydrogenase",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "disease of metabolism (Disease Ontology:DOID:0014667); hyperprolinemia type 2 (Disease Ontology:DOID:0080543)",
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        "function": "Irreversible conversion of delta-1-pyrroline-5-carboxylate (P5C), derived either from proline or ornithine, to glutamate. This is a necessary step in the pathway interconnecting the urea and tricarboxylic acid cycles. The preferred substrate is glutamic gamma-semialdehyde, other substrates include succinic, glutaric and adipic semialdehydes., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "protein_name": "Sesquipedalian",
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        "refseq_name": "pleckstrin homology domain-containing family J member 1 isoform X5",
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        "gene_names_uniprotkb": "Plekhj1",
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        "protein_names_uniprotkb": "Sesquipedalian; PH domain-containing endocytic trafficking adaptor; Ses",
        "protein_names_refseq": "pleckstrin homology domain-containing family J member 1 isoform X5",
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        "function": "Plays a role in endocytic trafficking. Required for receptor recycling from endosomes, both to the trans-Golgi network and the plasma membrane., [UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005769 early endosome;GO:0005829 cytosol;GO:0055037 recycling endosome;GO:0030136 clathrin-coated vesicle;GO:0005802 trans-Golgi network",
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    },
    {
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        "length": 210,
        "protein_name": "Sperm microtubule inner protein 1",
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        "protein_names_uniprotkb": "Sperm microtubule inner protein 1",
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    },
    {
        "uniprot_canonical_ac": "A0ABK0LFE4-1",
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        "length": 372,
        "protein_name": "2-oxoglutarate and iron-dependent oxygenase domain containing 2",
        "gene_name": "Ogfod2",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Ogfod2",
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        "protein_names_uniprotkb": "2-oxoglutarate and iron-dependent oxygenase domain containing 2",
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        "go_molecular_function": "GO:0031418 L-ascorbic acid binding;GO:0005506 iron ion binding;GO:0051213 dioxygenase activity;GO:0016705 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0016604 nuclear body",
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    },
    {
        "uniprot_canonical_ac": "A0ABK0LE23-1",
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        "length": 1125,
        "protein_name": "AP-3 complex subunit beta",
        "gene_name": "Ap3b2",
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        "refseq_name": "AP-3 complex subunit beta-2 isoform X1",
        "refseq_ac": "XP_063118782",
        "gene_names_uniprotkb": "Ap3b2",
        "gene_names_refseq": "Ap3b2",
        "protein_names_uniprotkb": "AP-3 complex subunit beta",
        "protein_names_refseq": "AP-3 complex subunit beta-2 isoform X1",
        "tax_id": 10116,
        "disease": "developmental and epileptic encephalopathy 48 (Disease Ontology:DOID:0080448)",
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        "function": "Subunit of non-clathrin- and clathrin-associated adaptor protein complex 3 (AP-3) that plays a role in protein sorting in the late-Golgi/trans-Golgi network (TGN) and/or endosomes. The AP complexes mediate both the recruitment of clathrin to membranes and the recognition of sorting signals within the cytosolic tails of transmembrane cargo molecules. AP-3 appears to be involved in the sorting of a subset of transmembrane proteins targeted to lysosomes and lysosome-related organelles. In concert with the BLOC-1 complex, AP-3 is required to target cargos into vesicles assembled at cell bodies for delivery into neurites and nerve terminals., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005794 Golgi apparatus;GO:0030665 clathrin-coated vesicle membrane;GO:0030123 AP-3 adaptor complex;GO:1904115 axon cytoplasm;GO:0098793 presynapse",
        "go_biological_process": "GO:0006886 intracellular protein transport;GO:0016192 vesicle-mediated transport;GO:0008344 adult locomotory behavior;GO:0008089 anterograde axonal transport;GO:0048490 anterograde synaptic vesicle transport",
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    },
    {
        "uniprot_canonical_ac": "A0ABK0LE20-1",
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        "length": 206,
        "protein_name": "Small ribosomal subunit protein uS15",
        "gene_name": "",
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        "function": "Component of the small ribosomal subunit. The ribosome is a large ribonucleoprotein complex responsible for the synthesis of proteins in the cell. Part of the small subunit (SSU) processome, first precursor of the small eukaryotic ribosomal subunit. During the assembly of the SSU processome in the nucleolus, many ribosome biogenesis factors, an RNA chaperone and ribosomal proteins associate with the nascent pre-rRNA and work in concert to generate RNA folding, modifications, rearrangements and cleavage as well as targeted degradation of pre-ribosomal RNA by the RNA exosome., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "length": 302,
        "protein_name": "Vomeronasal type-1 receptor",
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        "protein_names_refseq": "putative vomeronasal receptor-like protein 4; vomernasal 1 receptor Vom1r85; vomeronasal 1 receptor 85; vomeronasal 1 receptor, C44; vomeronasal V1r-type receptor V1rc44; vomeronasal type-1 receptor 100-like",
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        "protein_name": "Olfactory receptor",
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