[
    {
        "uniprot_canonical_ac": "A0A8I6GID3-1",
        "uniprot_id": "A0A8I6GID3_RAT",
        "mass": 42353.0,
        "length": 393,
        "protein_name": "methenyltetrahydrofolate cyclohydrolase",
        "gene_name": "Mthfd2",
        "organism": "Rat",
        "refseq_name": "bifunctional methylenetetrahydrofolate dehydrogenase/cyclohydrolase, mitochondrial isoform X1",
        "refseq_ac": "XP_038964266",
        "gene_names_uniprotkb": "Mthfd2; LOC134479019",
        "gene_names_refseq": "Mthfd2",
        "protein_names_uniprotkb": "methenyltetrahydrofolate cyclohydrolase; 3.5.4.9",
        "protein_names_refseq": "bifunctional methylenetetrahydrofolate dehydrogenase/cyclohydrolase, mitochondrial isoform X1",
        "tax_id": 10116,
        "disease": "hepatocellular carcinoma (Disease Ontology:DOID:684)",
        "pathway": " (rno:680308);  (R-RNO-196757)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "28100784",
        "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": 1,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 1,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 1,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 1,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 0,
        "biomarker_type": "",
        "glycan_count": 1,
        "disease_count": 1,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "3.5.4.9;6.3.4.3;1.5.1.5;1.5.1.15",
        "go_molecular_function": "GO:0042301 phosphate ion binding;GO:0000287 magnesium ion binding;GO:0004477 methenyltetrahydrofolate cyclohydrolase activity;GO:0004488 methylenetetrahydrofolate dehydrogenase (NADP+) activity;GO:0004487 methylenetetrahydrofolate dehydrogenase (NAD+) activity",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005759 mitochondrial matrix",
        "go_biological_process": "GO:0035999 tetrahydrofolate interconversion;GO:0046653 tetrahydrofolate metabolic process;GO:0015943 formate biosynthetic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "A0A8I6GID3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZWB2-1",
        "uniprot_id": "A0A8I5ZWB2_RAT",
        "mass": 82796.0,
        "length": 732,
        "protein_name": "Integrator complex subunit 13",
        "gene_name": "Ints13",
        "organism": "Rat",
        "refseq_name": "integrator complex subunit 13 isoform X1",
        "refseq_ac": "XP_038964316",
        "gene_names_uniprotkb": "Ints13; Asun",
        "gene_names_refseq": "Asun; Ints13",
        "protein_names_uniprotkb": "Integrator complex subunit 13",
        "protein_names_refseq": "integrator complex subunit 13 isoform X1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-6807505)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0140297 DNA-binding transcription factor binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0016604 nuclear body;GO:0032039 integrator complex",
        "go_biological_process": "GO:0090435 protein localization to nuclear envelope;GO:0034243 regulation of transcription elongation by RNA polymerase II;GO:0051301 cell division;GO:0007346 regulation of mitotic cell cycle;GO:0016180 snRNA processing",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I5ZWB2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6B5E1-1",
        "uniprot_id": "A0A8I6B5E1_RAT",
        "mass": 34741.0,
        "length": 309,
        "protein_name": "THAP domain containing 7",
        "gene_name": "Thap7",
        "organism": "Rat",
        "refseq_name": "THAP domain-containing protein 7",
        "refseq_ac": "NP_001099333",
        "gene_names_uniprotkb": "Thap7",
        "gene_names_refseq": "Thap7",
        "protein_names_uniprotkb": "THAP domain containing 7",
        "protein_names_refseq": "THAP domain-containing protein 7",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:287944)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0008270 zinc ion binding;GO:0042802 identical protein binding;GO:0042826 histone deacetylase binding;GO:0140296 general transcription initiation factor binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0016607 nuclear speck;GO:0000785 chromatin",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006355 regulation of DNA-templated transcription;GO:0045892 negative regulation of DNA-templated transcription;GO:0006325 chromatin organization",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6B5E1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZZZ0-1",
        "uniprot_id": "A0A8I5ZZZ0_RAT",
        "mass": 76393.0,
        "length": 682,
        "protein_name": "ATP-dependent RNA helicase",
        "gene_name": "Ddx31",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ddx31",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "ATP-dependent RNA helicase; 3.6.4.13",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "May have DNA helicase activity and RNA helicase activity. Probably have ssDNA and RNA dependent ATPase activity. Plays a role in ribosome biogenesis and TP53/p53 regulation through its interaction with NPM1., [UniProtKB, UniProtKB, UniProtKB]; RNA helicase., [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": "5.6.2.3;3.6.4.13;3.6.4.12;2.7.11.1;3.6.1.5;3.6.4.10;3.6.4.-;2.3.2.27;5.6.2.4;3.6.5.-;5.6.2.-;3.1.-.-;2.7.7.7;2.7.7.49;3.1.13.1;4.2.99.18;7.6.2.2;7.6.2.3;7.6.2.-;5.6.1.6;7.2.2.-;3.6.1.15;3.6.4.6;3.1.3.1;3.9.1.1;6.1.1.12;3.6.1.-;2.7.4.3;3.1.4.-;3.4.24.-;3.6.-.-;3.4.21.53;5.6.2.5",
        "go_molecular_function": "GO:0003723 RNA binding;GO:0005524 ATP binding;GO:0016787 hydrolase activity;GO:0003724 RNA helicase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005730 nucleolus",
        "go_biological_process": "GO:0042254 ribosome biogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I5ZZZ0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7EUL0-1",
        "uniprot_id": "F7EUL0_RAT",
        "mass": 28309.0,
        "length": 247,
        "protein_name": "V-type proton ATPase subunit D",
        "gene_name": "Atp6v1d",
        "organism": "Rat",
        "refseq_name": "V-type proton ATPase subunit D",
        "refseq_ac": "NP_955418",
        "gene_names_uniprotkb": "Atp6v1d",
        "gene_names_refseq": "Atp6v1d",
        "protein_names_uniprotkb": "V-type proton ATPase subunit D; V-ATPase 28 kDa accessory protein; V-type proton ATPase subunit d; Vacuolar proton pump subunit D",
        "protein_names_refseq": "ATPase, H+ transporting, lysosomal 34kDa, V1 subunit D; ATPase, H+ transporting, lysosomal V1 subunit D; V-type proton ATPase subunit D",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:299159);  (R-RNO-1222556);  (R-RNO-6798695);  (R-RNO-77387);  (R-RNO-917977);  (R-RNO-9639288);  (R-RNO-983712)",
        "pathway_count": 7,
        "publication_count": 2,
        "publication_id_list": "32165585;38900912",
        "class_list": "",
        "function": "Subunit of the V1 complex of vacuolar(H+)-ATPase (V-ATPase), a multisubunit enzyme composed of a peripheral complex (V1) that hydrolyzes ATP and a membrane integral complex (V0) that translocates protons. V-ATPase is responsible for acidifying and maintaining the pH of intracellular compartments and in some cell types, is targeted to the plasma membrane, where it is responsible for acidifying the extracellular environment. May play a role in cilium biogenesis through regulation of the transport and the localization of proteins to the cilium., [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,
        "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:0046961 proton-transporting ATPase activity, rotational mechanism",
        "go_cellular_component": "GO:0033176 proton-transporting V-type ATPase complex;GO:0030665 clathrin-coated vesicle membrane;GO:0098850 extrinsic component of synaptic vesicle membrane;GO:0005813 centrosome;GO:0005886 plasma membrane",
        "go_biological_process": "GO:0007035 vacuolar acidification;GO:0060271 cilium assembly;GO:0061512 protein localization to cilium;GO:0097401 synaptic vesicle lumen acidification",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "F7EUL0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6ASP1-1",
        "uniprot_id": "A0A8I6ASP1_RAT",
        "mass": 203570.0,
        "length": 1856,
        "protein_name": "Inactive histone-lysine N-methyltransferase 2E",
        "gene_name": "Kmt2e",
        "organism": "Rat",
        "refseq_name": "inactive histone-lysine N-methyltransferase 2E",
        "refseq_ac": "NP_001094321",
        "gene_names_uniprotkb": "Kmt2e",
        "gene_names_refseq": "Kmt2e; Mll5",
        "protein_names_uniprotkb": "Inactive histone-lysine N-methyltransferase 2E",
        "protein_names_refseq": "histone-lysine N-methyltransferase 2E; histone-lysine N-methyltransferase MLL5; inactive histone-lysine N-methyltransferase 2E; lysine (K)-specific methyltransferase 2E; myeloid/lymphoid or mixed-lineage leukemia 5 (trithorax homolog, Drosophila)",
        "tax_id": 10116,
        "disease": "acute promyelocytic leukemia (Disease Ontology:DOID:0060318); prostate cancer (Disease Ontology:DOID:10283); autistic disorder (Disease Ontology:DOID:12849); breast cancer (Disease Ontology:DOID:1612); cervical cancer (Disease Ontology:DOID:4362); human immunodeficiency virus infectious disease (Disease Ontology:DOID:526)",
        "pathway": " (rno:311968)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Associates with chromatin regions downstream of transcriptional start sites of active genes and thus regulates gene transcription. Chromatin interaction is mediated via the binding to tri-methylated histone H3 at 'Lys-4' (H3K4me3). Key regulator of hematopoiesis involved in terminal myeloid differentiation and in the regulation of hematopoietic stem cell (HSCs) self-renewal by a mechanism that involves DNA methylation. Also acts as an important cell cycle regulator, participating in cell cycle regulatory network machinery at multiple cell cycle stages including G1/S transition, S phase progression and mitotic entry. Recruited to E2F1 responsive promoters by HCFC1 where it stimulates tri-methylation of histone H3 at 'Lys-4' and transcriptional activation and thereby facilitates G1 to S phase transition. During myoblast differentiation, required to suppress inappropriate expression of S-phase-promoting genes and maintain expression of determination genes in quiescent cells., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 11,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 11,
        "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": 6,
        "glyco_site_count": 11,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0003713 transcription coactivator activity;GO:0019899 enzyme binding;GO:0140002 histone H3K4me3 reader activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005813 centrosome;GO:0005829 cytosol;GO:0016607 nuclear speck",
        "go_biological_process": "GO:0006338 chromatin remodeling;GO:0006351 DNA-templated transcription;GO:0002446 neutrophil mediated immunity;GO:0006355 regulation of DNA-templated transcription;GO:0030218 erythrocyte differentiation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6ASP1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6B2J6-1",
        "uniprot_id": "A0A8I6B2J6_RAT",
        "mass": 85428.0,
        "length": 762,
        "protein_name": "Zinc finger protein 280C",
        "gene_name": "Zfp280c",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Zfp280c; Suhw3; Zfp981",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger protein 280C",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:302812)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "May function as a transcription factor., [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,
        "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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    {
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        "protein_names_refseq": "periostin isoform 2 precursor; periostin, osteoblast specific factor; periostin-like factor",
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        "disease": "bone structure disease (Disease Ontology:DOID:0080010); hypertension (Disease Ontology:DOID:10763); aggressive periodontitis (Disease Ontology:DOID:1474); myocardial infarction (Disease Ontology:DOID:5844); congestive heart failure (Disease Ontology:DOID:6000); abdominal aortic aneurysm (Disease Ontology:DOID:7693); end stage renal disease (Disease Ontology:DOID:783); chronic kidney disease (Disease Ontology:DOID:784); periodontitis (Disease Ontology:DOID:824); degenerative disc disease (Disease Ontology:DOID:90); tendinitis (Disease Ontology:DOID:971)",
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        "function": "Induces cell attachment and spreading and plays a role in cell adhesion. Enhances incorporation of BMP1 in the fibronectin matrix of connective tissues, and subsequent proteolytic activation of lysyl oxidase LOX., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Overexpression of the periostin gene led to cardiac dysfunction. Periostin contributes to cardiac dilation., [RefSeq, PubMed]; POSTN promotes diabetic vascular calcification by interfering with autophagic flux., [RefSeq, PubMed]; POSTN promotes nucleus pulposus cell senescence and extracellular matrix metabolism via activing Wnt/beta-catenin and NF-kappaB signal pathway in intervertebral disc degeneration., [RefSeq, PubMed]; Periostin aggravates the early phase of traumatic brain injury via the MAPK/ERK pathway., [RefSeq, PubMed]; Periostin promotes arterial calcification through PPARgamma-related glucose metabolism reprogramming., [RefSeq, PubMed]; Self-amplifying loop of NF-kappaB and periostin initiated by PIEZO1 accelerates mechano-induced senescence of nucleus pulposus cells and intervertebral disc degeneration., [RefSeq, PubMed]; This study demonstrates that growth factor-induced expression of PN in PASMCs is mediated through PI3K/p70S6K, Ras/MEK1/2, and Ras/p38MAPK signaling pathways, whereas the expression of OPN is mediated through Ras/MEK1/2 and Ras/JNK signaling pathways., [RefSeq, PubMed]",
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        "ec_number_list": "2.7.11.1;2.7.12.1;2.7.1.153;2.7.1.137;2.7.11.24;2.7.11.25;2.7.11.22;2.7.11.23;2.7.4.6;2.7.1.154;2.7.11.38;2.7.11.17;2.7.12.2;3.1.3.16;3.1.3.48;2.7.11.12;2.7.11.26;2.7.11.21;2.7.11.34;2.7.1.150;2.7.10.2;2.7.11.13;2.7.11.19;2.7.2.3;2.7.11.11;2.7.11.31;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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        "gene_names_refseq": "Fbxl12",
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        "protein_names_refseq": "F-box/LRR-repeat protein 12 isoform 1; F-box/LRR-repeat protein 12",
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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_cellular_component": "GO:0097598 sperm cytoplasmic droplet;GO:0005634 nucleus;GO:0005737 cytoplasm",
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        "protein_names_uniprotkb": "Formyl peptide receptor 2",
        "protein_names_refseq": "formyl peptide receptor, related sequence 2-like; formyl peptide receptor, related sequence 2; formyl peptide receptor-like 1; lipoxin A 4 receptor",
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        "organism": "Rat",
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        "refseq_ac": "",
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        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Butyrophilin-like 12",
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        "gene_names_uniprotkb": "ENSRNOG00000064134",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ig-like domain-containing protein",
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        "refseq_name": "beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 4",
        "refseq_ac": "NP_001386718",
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        "gene_names_refseq": "Gcnt4; RGD1563891",
        "protein_names_uniprotkb": "Glucosaminyl (N-acetyl) transferase 4",
        "protein_names_refseq": "beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 4; glucosaminyl (N-acetyl) transferase 4, core 2",
        "tax_id": 10116,
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        "pathway": " (rno:120100673);  (R-RNO-913709)",
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        "gene_names_uniprotkb": "Slc50a1-ps1",
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        "protein_names_uniprotkb": "Sugar transporter SWEET",
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        "length": 171,
        "protein_name": "protein-tyrosine-phosphatase",
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        "refseq_name": "similar to protein tyrosine phosphatase 4a2",
        "refseq_ac": "NP_001388827",
        "gene_names_uniprotkb": "Ptp4a2l1; RGD1563405",
        "gene_names_refseq": "Ptp4a2l1; RGD1563405",
        "protein_names_uniprotkb": "protein-tyrosine-phosphatase; 3.1.3.48",
        "protein_names_refseq": "similar to protein tyrosine phosphatase 4a2",
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        "length": 336,
        "protein_name": "Homeobox D11",
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        "refseq_name": "homeobox protein Hox-D11",
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        "gene_names_refseq": "Hoxd11",
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        "protein_names_refseq": "homeobox protein Hox-D11",
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        "protein_names_uniprotkb": "Heat shock protein 90 alpha family class B member 1, pseudogene 13",
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        "protein_name": "NLR family, apoptosis inhibitory protein 5",
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        "organism": "Rat",
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        "gene_names_uniprotkb": "Naip5",
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        "protein_names_uniprotkb": "NLR family, apoptosis inhibitory protein 5",
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        "disease": "oral squamous cell carcinoma (Disease Ontology:DOID:0050866)",
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        "gene_name": "Sec61gl4",
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        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Sec61gl4",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Protein transport protein Sec61 subunit gamma",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (R-RNO-9609523)",
        "pathway_count": 1,
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        "function": "Component of SEC61 channel-forming translocon complex that mediates transport of signal peptide-containing precursor polypeptides across the endoplasmic reticulum (ER). Forms a ribosome receptor and a gated pore in the ER membrane, both functions required for cotranslational translocation of nascent polypeptides. The SEC61 channel is also involved in ER membrane insertion of transmembrane proteins: it mediates membrane insertion of the first few transmembrane segments of proteins, while insertion of subsequent transmembrane regions of multi-pass membrane proteins is mediated by the multi-pass translocon (MPT) complex. The SEC61 channel cooperates with the translocating protein TRAM1 to import nascent proteins into the ER., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0008320 protein transmembrane transporter activity",
        "go_cellular_component": "GO:0071261 Ssh1 translocon complex",
        "go_biological_process": "GO:0031204 post-translational protein targeting to membrane, translocation",
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        "hit_score": 0.1,
        "record_id": "A0A8J8XD56-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8J8XQI4-1",
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        "protein_name": "Reproductive homeobox 8",
        "gene_name": "Rhoxf8",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Rhoxf8; Rhox8",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Reproductive homeobox 8",
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0001228 DNA-binding transcription activator activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus",
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        "hit_score": 0.1,
        "record_id": "A0A8J8XQI4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8J8YCD1-1",
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        "length": 263,
        "protein_name": "CEA cell adhesion molecule 12",
        "gene_name": "Ceacam12",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Ceacam12",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "CEA cell adhesion molecule 12",
        "protein_names_refseq": "",
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        "reported_c_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "biomarker_type": "",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0009897 external side of plasma membrane",
        "go_biological_process": "GO:0006955 immune response;GO:0042110 T cell activation",
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        "hit_score": 0.1,
        "record_id": "A0A8J8YCD1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8J8YFF8-1",
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        "length": 45,
        "protein_name": "Thymosin beta",
        "gene_name": "Tmsb15b2",
        "organism": "Rat",
        "refseq_name": "thymosin beta-15B",
        "refseq_ac": "NP_775435",
        "gene_names_uniprotkb": "Tmsb15b2",
        "gene_names_refseq": "Tmsb15b2; Tmsbl1",
        "protein_names_uniprotkb": "Thymosin beta",
        "protein_names_refseq": "thymosin beta-15B; thymosin beta-like protein 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:286978)",
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        "function": "Plays an important role in the organization of the cytoskeleton. Binds to and sequesters actin monomers (G actin) and therefore inhibits actin polymerization., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003785 actin monomer binding;GO:0140311 protein sequestering activity;GO:0003788 actin monomer sequestering activity",
        "go_cellular_component": "GO:0001725 stress fiber;GO:0031941 filamentous actin",
        "go_biological_process": "GO:0007015 actin filament organization;GO:0030335 positive regulation of cell migration;GO:0030334 regulation of cell migration;GO:0051497 negative regulation of stress fiber assembly;GO:0030837 negative regulation of actin filament polymerization",
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    {
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        "length": 559,
        "protein_name": "Carboxylic ester hydrolase",
        "gene_name": "LOC679368",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "LOC679368; Ces2el1; LOC688542",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Carboxylic ester hydrolase; 3.1.1.-",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0050253 retinyl-palmitate esterase activity;GO:0106435 carboxylesterase activity",
        "go_cellular_component": "",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8L2QWT9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7EM66-1",
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        "length": 758,
        "protein_name": "DNA repair and recombination protein RAD54-like",
        "gene_name": "Rad54l",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Rad54l",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "DNA repair and recombination protein RAD54-like; RAD54 homolog",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "non-Hodgkin lymphoma (Disease Ontology:DOID:0060060); sclerocornea (Disease Ontology:DOID:0060252); disease of cellular proliferation (Disease Ontology:DOID:14566); breast cancer (Disease Ontology:DOID:1612); pancreatic cancer (Disease Ontology:DOID:1793)",
        "pathway": "",
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        "function": "Multifunctional ATPase that plays a role in homologous recombination (HR) which is a major pathway for repairing DNA double-strand breaks (DSBs), single-stranded DNA (ssDNA) gaps, and stalled or collapsed replication forks. Acts as a molecular motor during the homology search and guides RAD51 ssDNA along a donor dsDNA thereby changing the homology search from the diffusion-based mechanism to a motor-guided mechanism. Also plays an essential role in RAD51-mediated synaptic complex formation which consists of three strands encased in a protein filament formed once homology is recognized. Once DNA strand exchange occured, dissociates RAD51 from nucleoprotein filaments formed on dsDNA., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "5.6.2.3;3.6.4.13;3.6.4.12;2.7.11.1;3.6.1.5;3.6.4.10;3.6.4.-;2.3.2.27;5.6.2.4;3.6.5.-;5.6.2.-;3.1.-.-;2.7.7.7;2.7.7.49;3.1.13.1;4.2.99.18;7.6.2.2;7.6.2.3;7.6.2.-;5.6.1.6;7.2.2.-;3.6.1.15;3.6.4.6;3.1.3.1;3.9.1.1;6.1.1.12;3.6.1.-;2.7.4.3;3.1.4.-;3.4.24.-;3.6.-.-;3.4.21.53;5.6.2.5",
        "go_molecular_function": "GO:0005524 ATP binding;GO:0016787 hydrolase activity;GO:0004386 helicase activity;GO:0036310 ATP-dependent DNA/DNA annealing activity;GO:0008094 ATP-dependent activity, acting on DNA",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0035861 site of double-strand break;GO:0032991 protein-containing complex",
        "go_biological_process": "GO:0006974 DNA damage response;GO:0006302 double-strand break repair;GO:0010212 response to ionizing radiation;GO:0000724 double-strand break repair via homologous recombination;GO:0009410 response to xenobiotic stimulus",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7F0H6-1",
        "uniprot_id": "F7F0H6_RAT",
        "mass": 48263.0,
        "length": 417,
        "protein_name": "Similar to interferon-inducible GTPase",
        "gene_name": "RGD1309362",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "RGD1309362; Ifgga2l1; LOC134483037",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Similar to interferon-inducible GTPase",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "metabolic dysfunction-associated steatotic liver disease (Disease Ontology:DOID:0080208)",
        "pathway": "",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0003924 GTPase activity;GO:0005525 GTP binding",
        "go_cellular_component": "GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0000045 autophagosome assembly;GO:0045087 innate immune response;GO:0035458 cellular response to interferon-beta",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F7F0H6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7F635-1",
        "uniprot_id": "F7F635_RAT",
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        "length": 258,
        "protein_name": "Alpha-hemoglobin-stabilizing protein",
        "gene_name": "Ahsp",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ahsp",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Alpha-hemoglobin-stabilizing protein; Erythroid differentiation-related factor; Erythroid-associated factor",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "HELLP syndrome (Disease Ontology:DOID:13133)",
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        "go_molecular_function": "GO:0030492 hemoglobin binding",
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    },
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        "refseq_name": "",
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        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Uncharacterized protein",
        "protein_names_refseq": "",
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        "pathway_count": 0,
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        "record_id": "F7FC52-1",
        "record_type": "protein"
    },
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        "length": 648,
        "protein_name": "Exonuclease 3'-5' domain-containing protein 2",
        "gene_name": "Exd2",
        "organism": "Rat",
        "refseq_name": "exonuclease 3'-5' domain-containing protein 2",
        "refseq_ac": "NP_001420937",
        "gene_names_uniprotkb": "Exd2",
        "gene_names_refseq": "Exd2; Exdl2; RGD1311087",
        "protein_names_uniprotkb": "Exonuclease 3'-5' domain-containing protein 2; 3'-5' exoribonuclease EXD2; 3.1.11.1; Exonuclease 3'-5' domain-like-containing protein 2",
        "protein_names_refseq": "exonuclease 3''-5'' domain-like 2; exonuclease 3'-5' domain-containing protein 2",
        "tax_id": 10116,
        "disease": "Werner syndrome (Disease Ontology:DOID:5688)",
        "pathway": " (rno:362759)",
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        "publication_id_list": "",
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        "missing_score": 10000,
        "biomarker_type": "",
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        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008296 3'-5'-DNA exonuclease activity;GO:0008310 single-stranded DNA 3'-5' DNA exonuclease activity;GO:0000287 magnesium ion binding;GO:0030145 manganese ion binding;GO:0042803 protein homodimerization activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005739 mitochondrion;GO:0005741 mitochondrial outer membrane;GO:0090734 site of DNA damage",
        "go_biological_process": "GO:0006302 double-strand break repair;GO:0000724 double-strand break repair via homologous recombination;GO:0000729 DNA double-strand break processing;GO:0031297 replication fork processing",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F7FEI8-1",
        "record_type": "protein"
    },
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        "uniprot_canonical_ac": "F7FFV6-1",
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        "length": 601,
        "protein_name": "PWWP domain containing 2B",
        "gene_name": "Pwwp2b",
        "organism": "Rat",
        "refseq_name": "PWWP domain-containing protein 2B isoform 2",
        "refseq_ac": "NP_001427202",
        "gene_names_uniprotkb": "Pwwp2b",
        "gene_names_refseq": "Pwwp2b; Pwwp2",
        "protein_names_uniprotkb": "PWWP domain containing 2B",
        "protein_names_refseq": "PWWP domain containing 2; PWWP domain-containing protein 2B isoform 2; PWWP domain-containing protein 2B",
        "tax_id": 10116,
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        "pathway_count": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "disease_count": 0,
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        "secondary_ac_list": "",
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        "go_molecular_function": "GO:0120325 NuRD complex binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0006338 chromatin remodeling;GO:0006351 DNA-templated transcription;GO:0032968 positive regulation of transcription elongation by RNA polymerase II;GO:0120161 regulation of cold-induced thermogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "F7FFV6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7FQB8-1",
        "uniprot_id": "F7FQB8_RAT",
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        "length": 621,
        "protein_name": "Karyopherin subunit alpha 4",
        "gene_name": "Kpna4",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Kpna4",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Karyopherin subunit alpha 4",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Functions in nuclear protein import., [UniProtKB, UniProtKB, UniProtKB]",
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        "total_o_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:0008139 nuclear localization sequence binding;GO:0061608 nuclear import signal receptor activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005643 nuclear pore;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0042564 NLS-dependent protein nuclear import complex",
        "go_biological_process": "GO:0042542 response to hydrogen peroxide;GO:0006607 NLS-bearing protein import into nucleus;GO:0006606 protein import into nucleus",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F7FQB8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "M0R864-1",
        "uniprot_id": "M0R864_RAT",
        "mass": 38847.0,
        "length": 343,
        "protein_name": "SH2 domain-containing adapter protein D",
        "gene_name": "Shd; Yju2",
        "organism": "Rat",
        "refseq_name": "SH2 domain-containing adapter protein D",
        "refseq_ac": "NP_001101693",
        "gene_names_uniprotkb": "Shd; Yju2; YJU2",
        "gene_names_refseq": "Shd",
        "protein_names_uniprotkb": "SH2 domain-containing adapter protein D",
        "protein_names_refseq": "SH2 domain-containing adapter protein D",
        "tax_id": 10116,
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        "pathway": " (rno:316507);  (R-RNO-72163)",
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        "class_list": "",
        "function": "May function as an adapter protein., [UniProtKB, UniProtKB]; Part of the spliceosome which catalyzes two sequential transesterification reactions, first the excision of the non-coding intron from pre-mRNA and then the ligation of the coding exons to form the mature mRNA. Plays a role in stabilizing the structure of the spliceosome catalytic core and docking of the branch helix into the active site, producing 5'-exon and lariat intron-3'-intermediates. May protect cells from TP53-dependent apoptosis upon dsDNA break damage through association with PRP19-CD5L complex., [UniProtKB, HAMAP, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0001784 phosphotyrosine residue binding;GO:0046872 metal ion binding",
        "go_cellular_component": "GO:0005681 spliceosomal complex;GO:0071006 U2-type catalytic step 1 spliceosome",
        "go_biological_process": "GO:0000349 generation of catalytic spliceosome for first transesterification step;GO:0045292 mRNA cis splicing, via spliceosome",
        "synthesized_glycan_count": 0,
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        "record_id": "M0R864-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZQU7-1",
        "uniprot_id": "A0A8I5ZQU7_RAT",
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        "length": 301,
        "protein_name": "Caspase 7",
        "gene_name": "Casp7",
        "organism": "Rat",
        "refseq_name": "caspase-7 isoform X1",
        "refseq_ac": "XP_008758769",
        "gene_names_uniprotkb": "Casp7",
        "gene_names_refseq": "Casp7",
        "protein_names_uniprotkb": "Caspase 7",
        "protein_names_refseq": "caspase-7 isoform X1",
        "tax_id": 10116,
        "disease": "endometritis (Disease Ontology:DOID:1002); Alzheimer's disease (Disease Ontology:DOID:10652); sciatic neuropathy (Disease Ontology:DOID:11446); breast cancer (Disease Ontology:DOID:1612); colon cancer (Disease Ontology:DOID:219); transient cerebral ischemia (Disease Ontology:DOID:224); lung non-small cell carcinoma (Disease Ontology:DOID:3908); ureteral obstruction (Disease Ontology:DOID:5199); rheumatoid arthritis (Disease Ontology:DOID:7148); type 2 diabetes mellitus (Disease Ontology:DOID:9352); acute myocardial infarction (Disease Ontology:DOID:9408)",
        "pathway": " (R-RNO-111459);  (R-RNO-111463);  (R-RNO-111464);  (R-RNO-111465);  (R-RNO-111469);  (R-RNO-264870)",
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        "go_molecular_function": "GO:0004197 cysteine-type endopeptidase activity;GO:0004190 aspartic-type endopeptidase activity;GO:0003723 RNA binding;GO:0008233 peptidase activity;GO:0008234 cysteine-type peptidase activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005615 extracellular space;GO:0005634 nucleus;GO:0005829 cytosol;GO:0008303 caspase complex",
        "go_biological_process": "GO:0006508 proteolysis;GO:0043065 positive regulation of apoptotic process;GO:0051402 neuron apoptotic process;GO:0042542 response to hydrogen peroxide;GO:0010212 response to ionizing radiation",
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        "length": 111,
        "protein_name": "Testis expressed 48",
        "gene_name": "Tex48",
        "organism": "Rat",
        "refseq_name": "testis-expressed protein 48",
        "refseq_ac": "NP_001386259",
        "gene_names_uniprotkb": "Tex48",
        "gene_names_refseq": "Tex48",
        "protein_names_uniprotkb": "Testis expressed 48",
        "protein_names_refseq": "testis-expressed protein 48",
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "",
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        "synthesized_glycan_count": 0,
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        "record_id": "A0A6B9RUI8-1",
        "record_type": "protein"
    },
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        "gene_name": "Vom1r1",
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        "refseq_name": "vomeronasal 1 receptor 1",
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        "protein_names_uniprotkb": "Vomeronasal type-1 receptor",
        "protein_names_refseq": "vomernasal 1 receptor Vom1r1; vomeronasal 1 receptor 1; vomeronasal 1 receptor, E5; vomeronasal V1r-type receptor V1re5; vomeronasal type-1 receptor 4",
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        "protein_name": "Atypical chemokine receptor 1",
        "gene_name": "Ackr1",
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        "refseq_name": "atypical chemokine receptor 1",
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        "protein_names_refseq": "Duffy blood group, atypical chemokine receptor; Duffy blood group, chemokine receptor; atypical chemokine receptor 1",
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        "disease": "sickle cell anemia (Disease Ontology:DOID:10923); malaria (Disease Ontology:DOID:12365); Plasmodium vivax malaria (Disease Ontology:DOID:12978)",
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        "protein_name": "Myc binding protein",
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        "protein_names_refseq": "C-Myc-binding protein; c-myc binding protein",
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        "protein_name": "Olfactory receptor",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:1990830 cellular response to leukemia inhibitory factor;GO:0060021 roof of mouth development;GO:0014707 branchiomeric skeletal muscle development;GO:0060539 diaphragm development",
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        "hit_score": 0.1,
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    },
    {
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        "length": 390,
        "protein_name": "SERTA domain containing 2",
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        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Sertad2",
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        "protein_names_uniprotkb": "SERTA domain containing 2",
        "protein_names_refseq": "",
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        "go_molecular_function": "GO:0003713 transcription coactivator activity",
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        "synthesized_glycan_count": 0,
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    },
    {
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        "protein_name": "3-ketodihydrosphingosine reductase",
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        "refseq_name": "3-ketodihydrosphingosine reductase isoform X1",
        "refseq_ac": "XP_038946804",
        "gene_names_uniprotkb": "Kdsr",
        "gene_names_refseq": "Fvt1; Kdsr",
        "protein_names_uniprotkb": "3-ketodihydrosphingosine reductase; 1.1.1.102; 3-dehydrosphinganine reductase",
        "protein_names_refseq": "3-ketodihydrosphingosine reductase isoform X1",
        "tax_id": 10116,
        "disease": "follicular lymphoma (Disease Ontology:DOID:0050873); erythrokeratodermia variabilis et progressiva 4 (Disease Ontology:DOID:0080250)",
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        "function": "Catalyzes the reduction of 3'-oxosphinganine (3-ketodihydrosphingosine/KDS) to sphinganine (dihydrosphingosine/DHS), the second step of de novo sphingolipid biosynthesis., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_biological_process": "GO:0006666 3-keto-sphinganine metabolic process;GO:0030148 sphingolipid biosynthetic process;GO:0006686 sphingomyelin biosynthetic process;GO:0006688 glycosphingolipid biosynthetic process;GO:0046513 ceramide biosynthetic process",
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    },
    {
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        "length": 258,
        "protein_name": "Protein FRG1",
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        "gene_names_uniprotkb": "Frg1-ps1; Frg1; Frg1-ps1; Frg1; LOC686103",
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        "tax_id": 10116,
        "disease": "facioscapulohumeral muscular dystrophy (Disease Ontology:DOID:11727)",
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        "function": "Binds to mRNA in a sequence-independent manner. May play a role in regulation of pre-mRNA splicing or in the assembly of rRNA into ribosomal subunits. May be involved in mRNA transport. May be involved in epigenetic regulation of muscle differentiation through regulation of activity of the histone-lysine N-methyltransferase KMT5B., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003723 RNA binding;GO:0003779 actin binding;GO:0051015 actin filament binding",
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        "length": 413,
        "protein_name": "Histone-lysine N-methyltransferase",
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        "refseq_name": "histone-lysine N-methyltransferase SUV39H1 isoform 1",
        "refseq_ac": "NP_001100426",
        "gene_names_uniprotkb": "Suv39h1",
        "gene_names_refseq": "RGD1565028; Suv39h1l1; Suv39h1",
        "protein_names_uniprotkb": "Histone-lysine N-methyltransferase; 2.1.1.-",
        "protein_names_refseq": "histone-lysine N-methyltransferase SUV39H1 isoform 1; histone-lysine N-methyltransferase SUV39H1; suppressor of variegation 3-9 homolog 1-like 1",
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        "disease": "pre-malignant neoplasm (Disease Ontology:DOID:0060071)",
        "pathway": " (rno:302553);  (R-RNO-3214841);  (R-RNO-427359)",
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        "publication_id_list": "16497704;19001366;21504832;24752040;27483126;28361889",
        "class_list": "",
        "function": "MRNA and protein expression of histone methyltransferases G9a and Suv39h1 were directly related to the availability of choline, [RefSeq, PubMed]; Overexpression of Suv39h1 results in the de-activation of proinflammatory pathways and reduced apoptosis and myocardial injury., [RefSeq, PubMed]; SUV39H augments intracellular reactive oxygen species levels in a SIRT1-dependent manner. Publication Status: Online-Only, [RefSeq, PubMed]; SUV39H1 plays a critical role in chromosome dynamics and development, neurite outgrowth, and ethanol-induced neuroadaptation through gene-specific silencing., [RefSeq, PubMed]; SirT1 preserves heterochromatin structure: it modulates Suv39h1 protein levels in stress conditions by preventing MDM2-mediated polyubiquitination at K87., [RefSeq, PubMed]; Suv4-20h2 and Suv-39h1 histone methyltransferases are expressed and Histone H3 lysine 9 and H4 lysine 20 are trimethylated in hepatocarcinogenesis induced by methyl deficiency in rats [Suv4-20h2 and Suv-39h1], [RefSeq, PubMed]",
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        "ec_number_list": "2.3.1.-;2.3.1.286;2.1.1.-;2.1.1.367;2.1.1.364;2.1.1.366",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0140947 histone H3K9me2 methyltransferase activity;GO:0140949 histone H3K9 trimethyltransferase activity;GO:0046974 histone H3K9 methyltransferase activity;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0000775 chromosome, centromeric region;GO:0005677 chromatin silencing complex;GO:0005652 nuclear lamina;GO:0000792 heterochromatin",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0030154 cell differentiation;GO:0045892 negative regulation of DNA-templated transcription;GO:0048511 rhythmic process;GO:0006364 rRNA processing",
        "synthesized_glycan_count": 0,
        "hit_score": 0.7,
        "record_id": "A0A8I6A3A4-1",
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    {
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        "length": 306,
        "protein_name": "Olfactory receptor",
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        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr1448",
        "refseq_ac": "NP_001000019",
        "gene_names_uniprotkb": "Or2ak4; Or2ak5d; Or2ak5e; Or2ak5; Or2ak4c; Or2ak4; Or2ak5d; Or2ak5e; Or2ak5",
        "gene_names_refseq": "Olr1448; Or2ak5",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 1448; olfactory receptor Olr1448; olfactory receptor gene Olr1448",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:287324);  (rno:287336);  (rno:405053)",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
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    {
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        "length": 1744,
        "protein_name": "Transient receptor potential cation channel subfamily M member 3",
        "gene_name": "Trpm3",
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        "gene_names_uniprotkb": "Trpm3",
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        "protein_names_uniprotkb": "Transient receptor potential cation channel subfamily M member 3",
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        "tax_id": 10116,
        "disease": "MASA syndrome (Disease Ontology:DOID:0060246); chromosome 15q13.3 microdeletion syndrome (Disease Ontology:DOID:0060394); microphthalmia (Disease Ontology:DOID:10629); cataract (Disease Ontology:DOID:83)",
        "pathway": " (R-RNO-3295583)",
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        "ec_number_list": "2.7.11.1",
        "go_molecular_function": "GO:0005262 calcium channel activity;GO:0005516 calmodulin binding;GO:0005261 monoatomic cation channel activity;GO:0005385 zinc ion transmembrane transporter activity;GO:0005546 phosphatidylinositol-4,5-bisphosphate binding",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane",
        "go_biological_process": "GO:0051262 protein tetramerization;GO:0071577 zinc ion transmembrane transport;GO:0051289 protein homotetramerization;GO:0006816 calcium ion transport;GO:0098655 monoatomic cation transmembrane transport",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A8I6ALW5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZLV1-1",
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        "length": 260,
        "protein_name": "Metaxin-2",
        "gene_name": "Mtx2",
        "organism": "Rat",
        "refseq_name": "metaxin-2 isoform 2",
        "refseq_ac": "NP_001416750",
        "gene_names_uniprotkb": "Mtx2",
        "gene_names_refseq": "Mtx2",
        "protein_names_uniprotkb": "Metaxin-2; Mitochondrial outer membrane import complex protein 2",
        "protein_names_refseq": "metaxin-2 isoform 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:288150)",
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        "class_list": "",
        "function": "Involved in transport of proteins into the mitochondrion., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0001401 SAM complex;GO:0005739 mitochondrion",
        "go_biological_process": "GO:0006839 mitochondrial transport;GO:0015031 protein transport;GO:0045040 protein insertion into mitochondrial outer membrane;GO:0070096 mitochondrial outer membrane translocase complex assembly",
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    },
    {
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        "gene_name": "Ap3s1",
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        "gene_names_uniprotkb": "Ap3s1",
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        "protein_names_uniprotkb": "Adaptor related protein complex 3 subunit sigma 1",
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        "function": "Part of the AP-3 complex, an adaptor-related complex which is not clathrin-associated. The complex is associated with the Golgi region as well as more peripheral structures. It facilitates the budding of vesicles from the Golgi membrane and may be directly involved in trafficking to lysosomes. In concert with the BLOC-1 complex, AP-3 is required to target cargos into vesicles assembled at cell bodies for delivery into neurites and nerve terminals., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005794 Golgi apparatus;GO:0030659 cytoplasmic vesicle membrane;GO:0030123 AP-3 adaptor complex;GO:0005802 trans-Golgi network;GO:1904115 axon cytoplasm",
        "go_biological_process": "GO:0006886 intracellular protein transport;GO:0006896 Golgi to vacuole transport;GO:0048490 anterograde synaptic vesicle transport;GO:0016192 vesicle-mediated transport;GO:0008089 anterograde axonal transport",
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    },
    {
        "uniprot_canonical_ac": "A0A8I6AJW1-1",
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        "length": 327,
        "protein_name": "Ring finger protein 121",
        "gene_name": "Rnf121",
        "organism": "Rat",
        "refseq_name": "E3 ubiquitin ligase RNF121",
        "refseq_ac": "NP_001101010",
        "gene_names_uniprotkb": "Rnf121",
        "gene_names_refseq": "Rnf121",
        "protein_names_uniprotkb": "Ring finger protein 121",
        "protein_names_refseq": "E3 ubiquitin ligase RNF121",
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        "disease": "",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0061630 ubiquitin protein ligase activity",
        "go_cellular_component": "GO:0016020 membrane;GO:0000139 Golgi membrane;GO:0005789 endoplasmic reticulum membrane",
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    },
    {
        "uniprot_canonical_ac": "B0BNF8-1",
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        "length": 242,
        "protein_name": "Protein HTATIP2",
        "gene_name": "Htatip2",
        "organism": "Rat",
        "refseq_name": "protein HTATIP2",
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        "gene_names_uniprotkb": "Htatip2",
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        "protein_names_uniprotkb": "Protein HTATIP2",
        "protein_names_refseq": "HIV-1 tat interactive protein 2, homolog; oxidoreductase HTATIP2; protein HTATIP2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:292935)",
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        "publication_id_list": "25312779;31468715",
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        "function": "Represses translation by preventing reactivation of elongation factor eEF1A (PubMed:31468715). May also inhibit nuclear import by competing with nuclear import substrates for binding to a subset of nuclear transport receptors (By similarity). Has additionally been proposed to act as a redox sensor involved in cellular oxidative stress surveillance (By similarity). May bind NADPH (By similarity)., [UniProtKB, PubMed, UniProtKB]; These results suggest that TIP30 expression is regulated by promoter methylation and miR-10b in ESCC., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0004674 protein serine/threonine kinase activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005739 mitochondrion;GO:0005829 cytosol",
        "go_biological_process": "GO:0006417 regulation of translation;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0046777 protein autophosphorylation;GO:0043068 positive regulation of programmed cell death",
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        "record_id": "B0BNF8-1",
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    },
    {
        "uniprot_canonical_ac": "A0A8I5ZZ81-1",
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        "length": 299,
        "protein_name": "SAP30 binding protein",
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        "gene_names_uniprotkb": "Sap30bp",
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        "protein_names_uniprotkb": "SAP30 binding protein",
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        "go_biological_process": "GO:0006355 regulation of DNA-templated transcription;GO:0009615 response to virus;GO:0048024 regulation of mRNA splicing, via spliceosome",
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        "record_id": "A0A8I5ZZ81-1",
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    },
    {
        "uniprot_canonical_ac": "A0A8I6ACY9-1",
        "uniprot_id": "A0A8I6ACY9_RAT",
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        "length": 290,
        "protein_name": "VPS37B subunit of ESCRT-I",
        "gene_name": "Vps37b",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Vps37b",
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        "protein_names_uniprotkb": "VPS37B subunit of ESCRT-I",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (rno:288659);  (R-RNO-917729)",
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        "class_list": "",
        "function": "Component of the ESCRT-I complex, a regulator of vesicular trafficking process. Required for the sorting of endocytic ubiquitinated cargos into multivesicular bodies. May be involved in cell growth and differentiation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0048306 calcium-dependent protein binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005768 endosome;GO:0005886 plasma membrane;GO:0031902 late endosome membrane;GO:0010008 endosome membrane",
        "go_biological_process": "GO:0015031 protein transport;GO:0036258 multivesicular body assembly;GO:0039702 viral budding via host ESCRT complex;GO:1903774 positive regulation of viral budding via host ESCRT complex;GO:0006612 protein targeting to membrane",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6ACY9-1",
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    },
    {
        "uniprot_canonical_ac": "A0A8I5ZLL5-1",
        "uniprot_id": "A0A8I5ZLL5_RAT",
        "mass": 60471.0,
        "length": 529,
        "protein_name": "Glycylpeptide N-tetradecanoyltransferase",
        "gene_name": "Nmt2",
        "organism": "Rat",
        "refseq_name": "glycylpeptide N-tetradecanoyltransferase 2 isoform 1",
        "refseq_ac": "NP_997473",
        "gene_names_uniprotkb": "Nmt2",
        "gene_names_refseq": "Nmt2",
        "protein_names_uniprotkb": "Glycylpeptide N-tetradecanoyltransferase; 2.3.1.97",
        "protein_names_refseq": "glycylpeptide N-tetradecanoyltransferase 2 isoform 1; glycylpeptide N-tetradecanoyltransferase 2",
        "tax_id": 10116,
        "disease": "muscular disease (Disease Ontology:DOID:0080000)",
        "pathway": " (rno:291318);  (R-RNO-2514859)",
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        "publication_id_list": "16538398;22673903;38852542",
        "class_list": "",
        "function": "Adds a myristoyl group to the N-terminal glycine residue of certain cellular proteins., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; NMT2 alleviates depression-like behavior in a rat model of chronic unpredictable stress: An integrated proteomic and phosphoproteomic analysis., [RefSeq, PubMed]; NMT2 protein exhibited functional myristoyltransferase activity, but appeared to be 4-time less active than NMT1., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "2.3.1.97",
        "go_molecular_function": "GO:0004379 glycylpeptide N-tetradecanoyltransferase activity;GO:0018030 peptidyl-lysine N6-myristoyltransferase activity",
        "go_cellular_component": "GO:0005794 Golgi apparatus;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0018008 N-terminal peptidyl-glycine N-myristoylation;GO:0072657 protein localization to membrane;GO:0006499 N-terminal protein myristoylation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "A0A8I5ZLL5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A0G2K2C4-1",
        "uniprot_id": "A0A0G2K2C4_RAT",
        "mass": 72332.0,
        "length": 679,
        "protein_name": "LIM domain binding 3",
        "gene_name": "Ldb3",
        "organism": "Rat",
        "refseq_name": "LIM domain-binding protein 3 isoform 2",
        "refseq_ac": "NP_001264095",
        "gene_names_uniprotkb": "Ldb3",
        "gene_names_refseq": "Ldb3; RGD1564875; ZASP",
        "protein_names_uniprotkb": "LIM domain binding 3",
        "protein_names_refseq": "Cypher; LIM domain-binding protein 3 isoform 2; LIM domain-binding protein 3",
        "tax_id": 10116,
        "disease": "cardiomyopathy (Disease Ontology:DOID:0050700); myofibrillar myopathy 1 (Disease Ontology:DOID:0080092); myofibrillar myopathy 4 (Disease Ontology:DOID:0080095); congenital myopathy (Disease Ontology:DOID:0081337); dilated cardiomyopathy 1C (Disease Ontology:DOID:0110423); distal myopathy (Disease Ontology:DOID:11720); myotonic dystrophy type 1 (Disease Ontology:DOID:11722); dilated cardiomyopathy (Disease Ontology:DOID:12930); myopathy (Disease Ontology:DOID:423)",
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        "publication_id_list": "22673903;32922198;34502162",
        "class_list": "",
        "function": "Downregulation of Cypher induces apoptosis in cardiomyocytes via Akt/p38 MAPK signaling pathway. Publication Status: Online-Only, [RefSeq, PubMed]",
        "predicted_glycosites": 2,
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        "reported_phosphosites": 0,
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        "reported_snv": 0,
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        "biomarker_type": "",
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        "disease_count": 9,
        "glyco_site_count": 2,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0051371 muscle alpha-actinin binding;GO:0003779 actin binding;GO:0046872 metal ion binding;GO:0005080 protein kinase C binding;GO:0019899 enzyme binding",
        "go_cellular_component": "GO:0005912 adherens junction;GO:0001725 stress fiber;GO:0030018 Z disc;GO:0031941 filamentous actin;GO:0005856 cytoskeleton",
        "go_biological_process": "GO:0007507 heart development;GO:0030036 actin cytoskeleton organization;GO:0061061 muscle structure development;GO:0045214 sarcomere organization",
        "synthesized_glycan_count": 0,
        "hit_score": 0.6,
        "record_id": "A0A0G2K2C4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q499Q0-1",
        "uniprot_id": "Q499Q0_RAT",
        "mass": 55669.0,
        "length": 498,
        "protein_name": "Thiamine transporter 1",
        "gene_name": "Slc19a2",
        "organism": "Rat",
        "refseq_name": "thiamine transporter 1",
        "refseq_ac": "NP_001025195",
        "gene_names_uniprotkb": "Slc19a2",
        "gene_names_refseq": "Slc19a2",
        "protein_names_uniprotkb": "Thiamine transporter 1; Solute carrier family 19 member 2; ThTr-1",
        "protein_names_refseq": "solute carrier family 19 (thiamine transporter), member 2; thiamine transporter 1",
        "tax_id": 10116,
        "disease": "biotin-responsive basal ganglia disease (Disease Ontology:DOID:0050659); thiamine-responsive megaloblastic anemia syndrome (Disease Ontology:DOID:0090117); megaloblastic anemia (Disease Ontology:DOID:13382); chronic kidney disease (Disease Ontology:DOID:784); diabetes mellitus (Disease Ontology:DOID:9351)",
        "pathway": " (rno:289175);  (R-RNO-196819)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "18762716",
        "class_list": "",
        "function": "High-affinity transporter for the intake of thiamine., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Involvement of RFC1 in the inner BRB transport of methyltetrahydrofolate., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0090482 vitamin transmembrane transporter activity;GO:0015234 thiamine transmembrane transporter activity",
        "go_cellular_component": "GO:0016020 membrane;GO:0005886 plasma membrane",
        "go_biological_process": "GO:0007283 spermatogenesis;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": 0.2,
        "record_id": "Q499Q0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6ADT9-1",
        "uniprot_id": "A0A8I6ADT9_RAT",
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        "length": 589,
        "protein_name": "Netrin G2",
        "gene_name": "Ntng2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ntng2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Netrin G2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:311836)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "38843836",
        "class_list": "",
        "function": "Involved in controlling patterning and neuronal circuit formation at the laminar, cellular, subcellular and synaptic levels. Promotes neurite outgrowth of both axons and dendrites., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0048787 presynaptic active zone membrane;GO:0098685 Schaffer collateral - CA1 synapse;GO:0098552 side of membrane;GO:0098978 glutamatergic synapse;GO:0030424 axon",
        "go_biological_process": "GO:0007409 axonogenesis;GO:0009887 animal organ morphogenesis;GO:0009888 tissue development;GO:2001222 regulation of neuron migration;GO:0150011 regulation of neuron projection arborization",
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        "record_id": "A0A8I6ADT9-1",
        "record_type": "protein"
    },
    {
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        "length": 727,
        "protein_name": "E3 ubiquitin-protein ligase LRSAM1",
        "gene_name": "Lrsam1",
        "organism": "Rat",
        "refseq_name": "E3 ubiquitin-protein ligase LRSAM1 isoform a",
        "refseq_ac": "NP_001101303",
        "gene_names_uniprotkb": "Lrsam1",
        "gene_names_refseq": "Lrsam1; RGD1564403",
        "protein_names_uniprotkb": "E3 ubiquitin-protein ligase LRSAM1; 2.3.2.27; Leucine-rich repeat and sterile alpha motif-containing protein 1; RING-type E3 ubiquitin transferase LRSAM1; Tsg101-associated ligase",
        "protein_names_refseq": "E3 ubiquitin-protein ligase LRSAM1 isoform a; E3 ubiquitin-protein ligase LRSAM1",
        "tax_id": 10116,
        "disease": "Charcot-Marie-Tooth disease axonal type 2P (Disease Ontology:DOID:0110169)",
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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:0004842 ubiquitin-protein transferase activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0016020 membrane",
        "go_biological_process": "GO:0045806 negative regulation of endocytosis;GO:0006914 autophagy;GO:0000209 protein polyubiquitination;GO:0051865 protein autoubiquitination;GO:0030163 protein catabolic process",
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        "hit_score": 0.1,
        "record_id": "A0A8I6AEY5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6ANY1-1",
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        "length": 749,
        "protein_name": "Activating signal cointegrator 1 complex subunit 2",
        "gene_name": "Ascc2",
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        "refseq_name": "activating signal cointegrator 1 complex subunit 2",
        "refseq_ac": "NP_001102561",
        "gene_names_uniprotkb": "Ascc2",
        "gene_names_refseq": "Ascc2; RGD1561422",
        "protein_names_uniprotkb": "Activating signal cointegrator 1 complex subunit 2",
        "protein_names_refseq": "activating signal cointegrator 1 complex subunit 2",
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        "pathway": " (rno:498402);  (R-RNO-9954716)",
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        "go_molecular_function": "GO:0043130 ubiquitin binding;GO:0070530 K63-linked polyubiquitin modification-dependent protein binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0022626 cytosolic ribosome;GO:1990391 DNA repair complex;GO:0180022 RQC-trigger complex",
        "go_biological_process": "GO:0072344 rescue of stalled ribosome;GO:0032790 ribosome disassembly;GO:0006355 regulation of DNA-templated transcription;GO:1990116 ribosome-associated ubiquitin-dependent protein catabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A8I6ANY1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6AD50-1",
        "uniprot_id": "A0A8I6AD50_RAT",
        "mass": 42200.0,
        "length": 371,
        "protein_name": "Aldo-keto reductase family 1, member C13",
        "gene_name": "Akr1c12l1; Akr1c13",
        "organism": "Rat",
        "refseq_name": "aldo-keto reductase family 1, member C12 isoform X1",
        "refseq_ac": "XP_006254252",
        "gene_names_uniprotkb": "Akr1c12l1; Akr1c13; Akr1c12; Akr1c13",
        "gene_names_refseq": "Akr1c12T; Akr1c12; Akr1c13",
        "protein_names_uniprotkb": "Aldo-keto reductase family 1, member C13",
        "protein_names_refseq": "aldo-keto reductase family 1, member C12 isoform X1",
        "tax_id": 10116,
        "disease": "alcohol dependence (Disease Ontology:DOID:0050741); ductal carcinoma in situ (Disease Ontology:DOID:0060074); B-lymphoblastic leukemia/lymphoma (Disease Ontology:DOID:0080630); castration-resistant prostate carcinoma (Disease Ontology:DOID:0080909); 46,XY sex reversal 8 (Disease Ontology:DOID:0111773); prostate cancer (Disease Ontology:DOID:10283); pre-eclampsia (Disease Ontology:DOID:10591); leukemia (Disease Ontology:DOID:1240); T-cell acute lymphoblastic leukemia (Disease Ontology:DOID:5603); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (rno:361266);  (R-RNO-193368);  (R-RNO-193775);  (R-RNO-193807);  (R-RNO-2162123);  (R-RNO-5365859);  (R-RNO-975634);  (R-RNO-9757110)",
        "pathway_count": 8,
        "publication_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0016491 oxidoreductase activity;GO:0004032 aldose reductase (NADPH) activity;GO:0047023 androsterone dehydrogenase [NAD(P)+] activity;GO:0032052 bile acid binding;GO:0047086 ketosteroid monooxygenase activity",
        "go_cellular_component": "GO:0005829 cytosol",
        "go_biological_process": "GO:0006693 prostaglandin metabolic process;GO:0044597 daunorubicin metabolic process;GO:0044598 doxorubicin metabolic process;GO:0042448 progesterone metabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6AD50-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5Y6B0-1",
        "uniprot_id": "A0A8I5Y6B0_RAT",
        "mass": 52478.0,
        "length": 461,
        "protein_name": "Protein-serine O-palmitoleoyltransferase porcupine",
        "gene_name": "Porcn",
        "organism": "Rat",
        "refseq_name": "protein-serine O-palmitoleoyltransferase porcupine",
        "refseq_ac": "NP_001166826",
        "gene_names_uniprotkb": "Porcn",
        "gene_names_refseq": "Porcn; RGD1564947",
        "protein_names_uniprotkb": "Protein-serine O-palmitoleoyltransferase porcupine; 2.3.1.250",
        "protein_names_refseq": "porcupine homolog; protein-cysteine N-palmitoyltransferase porcupine; protein-serine O-palmitoleoyltransferase porcupine",
        "tax_id": 10116,
        "disease": "focal dermal hypoplasia (Disease Ontology:DOID:2120)",
        "pathway": " (rno:317368)",
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        "publication_count": 1,
        "publication_id_list": "29393594",
        "class_list": "",
        "function": "",
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        "secondary_ac_list": "",
        "ec_number_list": "2.3.1.250",
        "go_molecular_function": "GO:0008374 O-acyltransferase activity;GO:1990698 palmitoleoyltransferase activity;GO:0017147 Wnt-protein binding",
        "go_cellular_component": "GO:0005789 endoplasmic reticulum membrane;GO:0098978 glutamatergic synapse;GO:0005783 endoplasmic reticulum;GO:0016020 membrane;GO:0032281 AMPA glutamate receptor complex",
        "go_biological_process": "GO:0016055 Wnt signaling pathway;GO:0045234 protein palmitoleylation;GO:0006497 protein lipidation;GO:0009100 glycoprotein metabolic process;GO:0030258 lipid modification",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A8I5Y6B0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6GJ20-1",
        "uniprot_id": "A0A8I6GJ20_RAT",
        "mass": 114596.0,
        "length": 1007,
        "protein_name": "Kinesin-like protein KIF23",
        "gene_name": "Kif23",
        "organism": "Rat",
        "refseq_name": "kinesin-like protein KIF23 isoform X4",
        "refseq_ac": "XP_038937412",
        "gene_names_uniprotkb": "Kif23",
        "gene_names_refseq": "Kif23",
        "protein_names_uniprotkb": "Kinesin-like protein KIF23",
        "protein_names_refseq": "kinesin-like protein KIF23 isoform X4",
        "tax_id": 10116,
        "disease": "congenital dyserythropoietic anemia type IIIa (Disease Ontology:DOID:0111399)",
        "pathway": " (rno:315740);  (R-RNO-2132295);  (R-RNO-6811434);  (R-RNO-68884);  (R-RNO-983189)",
        "pathway_count": 5,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Component of the centralspindlin complex that serves as a microtubule-dependent and Rho-mediated signaling required for the myosin contractile ring formation during the cell cycle cytokinesis. Essential for cytokinesis in Rho-mediated signaling. Required for the localization of ECT2 to the central spindle. Plus-end-directed motor enzyme that moves antiparallel microtubules in vitro., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "protein_name": "Thyroid hormone receptor interactor 11",
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        "gene_names_uniprotkb": "Trip11",
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        "protein_names_uniprotkb": "Thyroid hormone receptor interactor 11",
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        "protein_names_uniprotkb": "WD repeat domain 88",
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    {
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        "protein_name": "Lysine-specific demethylase 6B",
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        "gene_names_uniprotkb": "Kdm6b",
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        "protein_names_uniprotkb": "Lysine-specific demethylase 6B; 1.14.11.68; JmjC domain-containing protein 3; Jumonji domain-containing protein 3; [histone H3]-trimethyl-L-lysine(27) demethylase 6B",
        "protein_names_refseq": "jumonji domain-containing 3; lysine (K)-specific demethylase 6B; lysine-specific demethylase 6B isoform 2; lysine-specific demethylase 6B",
        "tax_id": 10116,
        "disease": "Stolerman neurodevelopmental syndrome (Disease Ontology:DOID:0081443); alcohol use disorder (Disease Ontology:DOID:1574); breast carcinoma (Disease Ontology:DOID:3459); renal cell carcinoma (Disease Ontology:DOID:4450)",
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        "function": "Histone demethylase that specifically demethylates 'Lys-27' of histone H3, thereby playing a central role in histone code. Demethylates trimethylated and dimethylated H3 'Lys-27'. Plays a central role in regulation of posterior development, by regulating HOX gene expression. Involved in inflammatory response by participating in macrophage differentiation in case of inflammation by regulating gene expression and macrophage differentiation. Plays a demethylase-independent role in chromatin remodeling to regulate T-box family member-dependent gene expression by acting as a link between T-box factors and the SMARCA4-containing SWI/SNF remodeling complex., [UniProtKB, UniProtKB, UniProtKB]; Jmjd3 Mediates Neuropathic Pain by Inducing Macrophage Infiltration and Activation in Lumbar Spinal Stenosis Animal Model. Publication Status: Online-Only, [RefSeq, PubMed]; KDM6B Negatively Regulates the Neurogenesis Potential of Apical Papilla Stem Cells via HES1. Publication Status: Online-Only, [RefSeq, PubMed]; Lysine demethylase KDM6B regulates HIF-1alpha-mediated systemic and cellular responses to intermittent hypoxia., [RefSeq, PubMed]; TRPM7 Mediates BSCB Disruption After Spinal Cord Injury by Regulating the mTOR/JMJD3 Axis in Rats., [RefSeq, PubMed]; Upregulation of lysine-specific demethylase 6B aggravates inflammatory pain through H3K27me3 demethylation-dependent production of TNF-alpha in the dorsal root ganglia and spinal dorsal horn in rats., [RefSeq, PubMed]",
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        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005634 nucleus;GO:0044666 MLL3/4 complex",
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        "protein_name": "Ankyrin repeat and SOCS box-containing 5",
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    {
        "uniprot_canonical_ac": "A0A8I6A0K6-1",
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        "length": 403,
        "protein_name": "Aminomethyltransferase",
        "gene_name": "Amt",
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        "refseq_name": "aminomethyltransferase, mitochondrial",
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        "gene_names_refseq": "Amt",
        "protein_names_uniprotkb": "Aminomethyltransferase; 2.1.2.10; Glycine cleavage system T protein",
        "protein_names_refseq": "aminomethyltransferase (glycine cleavage system protein T); aminomethyltransferase, mitochondrial",
        "tax_id": 10116,
        "disease": "glycine encephalopathy 2 (Disease Ontology:DOID:0061001); glycine encephalopathy (Disease Ontology:DOID:9268)",
        "pathway": " (rno:306586);  (R-RNO-6783984)",
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        "function": "The glycine cleavage system catalyzes the degradation of glycine., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005960 glycine cleavage complex",
        "go_biological_process": "GO:0006546 glycine catabolic process;GO:0019464 glycine decarboxylation via glycine cleavage system",
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        "record_type": "protein"
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        "uniprot_canonical_ac": "A0A8I6ASK1-1",
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        "length": 535,
        "protein_name": "procollagen-proline 4-dioxygenase",
        "gene_name": "P4ha2",
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        "refseq_name": "prolyl 4-hydroxylase subunit alpha-2 isoform 1 precursor",
        "refseq_ac": "NP_001101745",
        "gene_names_uniprotkb": "P4ha2",
        "gene_names_refseq": "P4ha2",
        "protein_names_uniprotkb": "procollagen-proline 4-dioxygenase; 1.14.11.2",
        "protein_names_refseq": "procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha II polypeptide; procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha polypeptide II; prolyl 4-hydroxylase subunit alpha-2 isoform 1 precursor; prolyl 4-hydroxylase, alpha polypeptide II",
        "tax_id": 10116,
        "disease": "myopia (Disease Ontology:DOID:11830)",
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        "class_list": "",
        "function": "Catalyzes the post-translational formation of 4-hydroxyproline in -Xaa-Pro-Gly- sequences in collagens and other proteins., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005506 iron ion binding;GO:0031418 L-ascorbic acid binding;GO:0004656 procollagen-proline 4-dioxygenase activity",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005788 endoplasmic reticulum lumen;GO:0016222 procollagen-proline 4-dioxygenase complex",
        "go_biological_process": "GO:0018401 peptidyl-proline hydroxylation to 4-hydroxy-L-proline",
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        "record_id": "A0A8I6ASK1-1",
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    {
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        "length": 2372,
        "protein_name": "Armadillo repeat containing, X-linked 4",
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        "organism": "Rat",
        "refseq_name": "armadillo repeat containing, X-linked 4 isoform 1",
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        "gene_names_uniprotkb": "Armcx4",
        "gene_names_refseq": "Armcx4",
        "protein_names_uniprotkb": "Armadillo repeat containing, X-linked 4",
        "protein_names_refseq": "armadillo repeat containing, X-linked 4 isoform 1; armadillo repeat-containing X-linked protein 4",
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        "protein_name": "Synaptopodin 2-like protein",
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        "gene_names_uniprotkb": "Synpo2l",
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        "protein_names_uniprotkb": "Synaptopodin 2-like protein",
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        "go_molecular_function": "GO:0003779 actin binding",
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        "protein_names_uniprotkb": "E3 ubiquitin-protein ligase RNF213; 2.3.2.27; E3 ubiquitin-lipopolysaccharide ligase RNF213; Mysterin; RING finger protein 213",
        "protein_names_refseq": "E3 ubiquitin-protein ligase RNF213 isoform X3",
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        "ec_number_list": "5.6.2.3;3.6.4.13;2.3.2.26;2.3.2.32;3.6.4.12;2.7.11.1;3.6.1.5;2.3.2.31;2.3.2.23;2.3.2.27;2.3.2.34;2.3.2.24;3.6.4.10;3.6.4.-;5.6.2.4;3.6.5.-;2.3.2.-;5.6.2.-;2.3.2.25;3.1.-.-;2.7.7.7;2.7.7.49;3.1.13.1;4.2.99.18;7.6.2.2;7.6.2.3;7.6.2.-;5.6.1.6;7.2.2.-;3.6.1.15;3.6.4.6;3.1.3.1;3.9.1.1;6.1.1.12;3.6.1.-;2.7.4.3;3.1.4.-;3.4.24.-;3.6.-.-;3.4.21.53;5.6.2.5",
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        "length": 831,
        "protein_name": "Cysteine--tRNA ligase, cytoplasmic",
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        "refseq_name": "cysteine--tRNA ligase, cytoplasmic isoform 1",
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        "protein_names_refseq": "cysteine--tRNA ligase, cytoplasmic isoform 1; cysteine--tRNA ligase, cytoplasmic; cysteinyl-tRNA synthetase, cytoplasmic",
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        "disease": "microcephaly (Disease Ontology:DOID:10907)",
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        "function": "Catalyzes the ATP-dependent ligation of cysteine to tRNA(Cys)., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "length": 1183,
        "protein_name": "Solute carrier family 9 member C1",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Slc9c1",
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        "protein_names_uniprotkb": "Solute carrier family 9 member C1; Na(+)/H(+) exchanger 10; Sodium/hydrogen exchanger 10; Sperm-specific Na(+)/H(+) exchanger",
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        "protein_name": "alpha-1,6-mannosyl-glycoprotein 6-beta-N-acetylglucosaminyltransferase",
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        "protein_names_uniprotkb": "alpha-1,6-mannosyl-glycoprotein 6-beta-N-acetylglucosaminyltransferase; 2.4.1.155",
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        "refseq_name": "EGF-like repeat and discoidin I-like domain-containing protein 3 isoform X1",
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        "protein_names_uniprotkb": "EGF like repeats and discoidin domains 3",
        "protein_names_refseq": "EGF-like repeat and discoidin I-like domain-containing protein 3 isoform X1",
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        "function": "Promotes adhesion of endothelial cells through interaction with the alpha-v/beta-3 integrin receptor. Inhibits formation of vascular-like structures. May be involved in regulation of vascular morphogenesis of remodeling in embryonic development., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005509 calcium ion binding",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005576 extracellular region",
        "go_biological_process": "GO:0007155 cell adhesion;GO:0010811 positive regulation of cell-substrate adhesion",
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        "hit_score": 0.4,
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6AIG5-1",
        "uniprot_id": "A0A8I6AIG5_RAT",
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        "length": 738,
        "protein_name": "SUZ12 polycomb repressive complex 2 subunit",
        "gene_name": "Suz12",
        "organism": "Rat",
        "refseq_name": "polycomb protein SUZ12",
        "refseq_ac": "NP_001414588",
        "gene_names_uniprotkb": "Suz12",
        "gene_names_refseq": "Suz12",
        "protein_names_uniprotkb": "SUZ12 polycomb repressive complex 2 subunit",
        "protein_names_refseq": "polycomb protein SUZ12",
        "tax_id": 10116,
        "disease": "spina bifida (Disease Ontology:DOID:0080016); renal Wilms' tumor (Disease Ontology:DOID:5176)",
        "pathway": " (rno:688041);  (R-RNO-212300);  (R-RNO-2559580);  (R-RNO-3214841);  (R-RNO-4551638);  (R-RNO-8943724);  (R-RNO-8953750);  (R-RNO-9764725);  (R-RNO-9909649)",
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        "publication_id_list": "22673903;28041882",
        "class_list": "",
        "function": "LncRNA OL1 interacts with Suz12-PRC2 complex to orchestrate the oligodendrocyte differentiation program., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0003682 chromatin binding;GO:0003723 RNA binding;GO:0008047 enzyme activator activity;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0016604 nuclear body;GO:0035098 ESC/E(Z) complex",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006325 chromatin organization;GO:0060816 random inactivation of X chromosome;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0008284 positive regulation of cell population proliferation",
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    },
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        "uniprot_canonical_ac": "A0A8I5ZPV1-1",
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        "length": 522,
        "protein_name": "TBC1 domain family, member 22a",
        "gene_name": "Tbc1d22a",
        "organism": "Rat",
        "refseq_name": "TBC1 domain family member 22A isoform X1",
        "refseq_ac": "XP_038936251",
        "gene_names_uniprotkb": "Tbc1d22a",
        "gene_names_refseq": "RGD1306588; Tbc1d22a",
        "protein_names_uniprotkb": "TBC1 domain family, member 22a",
        "protein_names_refseq": "TBC1 domain family member 22A isoform X1",
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        "class_list": "",
        "function": "May act as a GTPase-activating protein for Rab family protein(s)., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005096 GTPase activator activity;GO:0042803 protein homodimerization activity;GO:0071889 14-3-3 protein binding",
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    {
        "uniprot_canonical_ac": "A0A8I6AAA4-1",
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        "length": 308,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or5af1b; Or5af1; Or9e1",
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        "refseq_name": "olfactory receptor Olr1457",
        "refseq_ac": "NP_001000526",
        "gene_names_uniprotkb": "Or5af1b; Or5af1; Or9e1; Olr1460; Or5af1b; Or5af1c; Or5af1; Or9e1b",
        "gene_names_refseq": "Olr1457; Or5af1b",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 1457; olfactory receptor Olr1457; olfactory receptor gene Olr1457",
        "tax_id": 10116,
        "disease": "hypertrophic cardiomyopathy (Disease Ontology:DOID:11984)",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding",
        "go_cellular_component": "GO:0005886 plasma membrane",
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        "record_id": "A0A8I6AAA4-1",
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    {
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        "length": 454,
        "protein_name": "Mitochondrial dynamics protein MID49",
        "gene_name": "Mief2",
        "organism": "Rat",
        "refseq_name": "mitochondrial dynamics protein MID49",
        "refseq_ac": "NP_001385773",
        "gene_names_uniprotkb": "Mief2; Smcr7",
        "gene_names_refseq": "Mief2; RGD1560728; Smcr7",
        "protein_names_uniprotkb": "Mitochondrial dynamics protein MID49; Mitochondrial elongation factor 2",
        "protein_names_refseq": "Smith-Magenis syndrome chromosome region, candidate 7 homolog; mitochondrial dynamic protein MID49; mitochondrial dynamics protein MID49",
        "tax_id": 10116,
        "disease": "combined oxidative phosphorylation deficiency 49 (Disease Ontology:DOID:0112110)",
        "pathway": " (rno:497916)",
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005741 mitochondrial outer membrane;GO:0005739 mitochondrion",
        "go_biological_process": "GO:0007005 mitochondrion organization;GO:0090314 positive regulation of protein targeting to membrane;GO:0090141 positive regulation of mitochondrial fission;GO:0010821 regulation of mitochondrion organization",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6GLF2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZUN3-1",
        "uniprot_id": "A0A8I5ZUN3_RAT",
        "mass": 3752315.0,
        "length": 33800,
        "protein_name": "Titin",
        "gene_name": "Ttn",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ttn",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Titin; 2.7.11.1; Connectin",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "atrial fibrillation (Disease Ontology:DOID:0060224); congenital myopathy 5 (Disease Ontology:DOID:0081341); autosomal recessive limb-girdle muscular dystrophy type 2J (Disease Ontology:DOID:0110283); hypertrophic cardiomyopathy 9 (Disease Ontology:DOID:0110315); dilated cardiomyopathy 1G (Disease Ontology:DOID:0110430); tibial muscular dystrophy (Disease Ontology:DOID:0111078); myofibrillar myopathy 9 (Disease Ontology:DOID:0111188); dilated cardiomyopathy (Disease Ontology:DOID:12930); coronary artery disease (Disease Ontology:DOID:3393); myocardial infarction (Disease Ontology:DOID:5844)",
        "pathway": "",
        "pathway_count": 0,
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        "publication_id_list": "22673903",
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        "function": "Key component in the assembly and functioning of vertebrate striated muscles. By providing connections at the level of individual microfilaments, it contributes to the fine balance of forces between the two halves of the sarcomere. The size and extensibility of the cross-links are the main determinants of sarcomere extensibility properties of muscle. In non-muscle cells, seems to play a role in chromosome condensation and chromosome segregation during mitosis. Might link the lamina network to chromatin or nuclear actin, or both during interphase., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 14,
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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:0051371 muscle alpha-actinin binding;GO:0002020 protease binding;GO:0003713 transcription coactivator activity;GO:0004674 protein serine/threonine kinase activity;GO:0004713 protein tyrosine kinase activity",
        "go_cellular_component": "GO:0000794 condensed nuclear chromosome;GO:0005865 striated muscle thin filament;GO:0030017 sarcomere;GO:0031674 I band;GO:0030018 Z disc",
        "go_biological_process": "GO:0035995 detection of muscle stretch;GO:1901897 regulation of relaxation of cardiac muscle;GO:0001701 in utero embryonic development;GO:0006338 chromatin remodeling;GO:0006936 muscle contraction",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A8I5ZUN3-1",
        "record_type": "protein"
    },
    {
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        "length": 722,
        "protein_name": "La ribonucleoprotein 4",
        "gene_name": "Larp4",
        "organism": "Rat",
        "refseq_name": "La ribonucleoprotein 4 isoform 1",
        "refseq_ac": "NP_001419165",
        "gene_names_uniprotkb": "Larp4",
        "gene_names_refseq": "Larp4",
        "protein_names_uniprotkb": "La ribonucleoprotein 4",
        "protein_names_refseq": "La ribonucleoprotein 4 isoform 1; La ribonucleoprotein domain family, member 4; la-related protein 4-like",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
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        "go_molecular_function": "GO:0003723 RNA binding;GO:0003730 mRNA 3'-UTR binding;GO:0008143 poly(A) binding",
        "go_cellular_component": "GO:0005829 cytosol;GO:0010494 cytoplasmic stress granule;GO:0022627 cytosolic small ribosomal subunit",
        "go_biological_process": "GO:0045727 positive regulation of translation;GO:0010608 post-transcriptional regulation of gene expression",
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        "hit_score": 0.1,
        "record_id": "A0A8I6A7G2-1",
        "record_type": "protein"
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        "go_biological_process": "GO:0016197 endosomal transport;GO:0007029 endoplasmic reticulum organization;GO:0090148 membrane fission;GO:0097750 endosome membrane tubulation;GO:0140285 endosome fission",
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        "protein_names_refseq": "sphingomyelin phosphodiesterase 5 isoform X2",
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        "go_biological_process": "GO:0006665 sphingolipid metabolic process;GO:0046513 ceramide biosynthetic process;GO:0006672 ceramide metabolic process;GO:0006685 sphingomyelin catabolic process;GO:0006684 sphingomyelin metabolic process",
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    {
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        "protein_names_uniprotkb": "FERM and PDZ domain-containing protein 4; PDZ domain-containing protein 10; PSD-95-interacting regulator of spine morphogenesis",
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        "function": "Positive regulator of dendritic spine morphogenesis and density. Required for the maintenance of excitatory synaptic transmission. Binds phosphatidylinositol 4,5-bisphosphate., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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    {
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        "protein_name": "CAP-GLY domain containing linker protein 3",
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        "refseq_name": "CAP-Gly domain-containing linker protein 3",
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        "gene_names_refseq": "Clip3; RGD1306245",
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        "function": "CLIP3 and PCNA expression during early myelination may be related to the direct uptake and transport of lipids and cholesterol, by Schwann cells to prepare for the formation of myelin sheath-like structures around regenerated axons after SNI., [RefSeq, PubMed]; CLIP3 up-regulation following spinal cord injury is associated with astrocyte proliferation.  CLIP3 interacted with STAT3 in the injured spinal cord., [RefSeq, PubMed]",
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        "protein_name": "Adenosine 3'-phospho 5'-phosphosulfate transporter 2",
        "gene_name": "Slc35b3",
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        "refseq_name": "adenosine 3'-phospho 5'-phosphosulfate transporter 2",
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        "gene_names_refseq": "Slc35b3",
        "protein_names_uniprotkb": "Adenosine 3'-phospho 5'-phosphosulfate transporter 2",
        "protein_names_refseq": "adenosine 3'-phospho 5'-phosphosulfate transporter 2; solute carrier family 35 (adenosine 3'-phospho 5'-phosphosulfate transporter), member B3",
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        "pathway": " (rno:306866);  (R-RNO-174362);  (R-RNO-727802)",
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        "go_molecular_function": "GO:0046964 3'-phosphoadenosine 5'-phosphosulfate transmembrane transporter activity",
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        "go_biological_process": "GO:1902558 5'-adenylyl sulfate transmembrane transport;GO:0055085 transmembrane transport;GO:0046963 3'-phosphoadenosine 5'-phosphosulfate transport;GO:0006478 peptidyl-tyrosine sulfation",
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    {
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        "length": 1257,
        "protein_name": "TBC1 domain family member 1",
        "gene_name": "Tbc1d1",
        "organism": "Rat",
        "refseq_name": "TBC1 domain family member 1",
        "refseq_ac": "NP_001414246",
        "gene_names_uniprotkb": "Tbc1d1",
        "gene_names_refseq": "Tbc1d1",
        "protein_names_uniprotkb": "TBC1 domain family member 1",
        "protein_names_refseq": "TBC1 (tre-2/USP6, BUB2, cdc16) domain family, member 1; TBC1 domain family member 1",
        "tax_id": 10116,
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        "pathway": " (rno:360937)",
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        "function": "Data show that TBC1D1 is expressed and phosphorylated in response to glucose in these cells., [RefSeq, PubMed]; EPI64 acted as a physiological Rab27-GAP that enhanced GTPase activity of Rab27 in response to IPR stimulation, and that this activity is required for IPR-induced amylase release., [RefSeq, PubMed]; Fundamental role for TBC1D1 in maintaining in vivo beta-cell mass, [RefSeq, PubMed]; Increased TBC1D1 phosphorylation may play a role in the insulin-independent increase in glucose transport postexercise., [RefSeq, PubMed]; May act as a GTPase-activating protein for Rab family protein(s). May play a role in the cell cycle and differentiation of various tissues. Involved in the trafficking and translocation of GLUT4-containing vesicles and insulin-stimulated glucose uptake into cells., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Results highlight a critical role for TBC1D1 in exercise tolerance and contraction-mediated translocation of GLUT4 to the plasma membrane in skeletal muscle., [RefSeq, PubMed]; Significant differences found among the muscles for GLUT4 (2.5-fold), TUG (1.7-fold), RUVBL2 (2.0-fold), and TBC1D1 (2.7-fold), but not AS160., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0005096 GTPase activator activity",
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        "go_biological_process": "GO:0032880 regulation of protein localization;GO:0061179 negative regulation of insulin secretion involved in cellular response to glucose stimulus",
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        "protein_names_refseq": "TBC1 domain family member 15 isoform 2",
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    },
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        "protein_name": "RALY RNA binding protein-like",
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        "protein_names_refseq": "RNA-binding Raly-like protein isoform X3",
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        "protein_name": "Enhancer trap locus 4",
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        "refseq_name": "sickle tail protein homolog",
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        "gene_names_refseq": "Ptges3l",
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        "protein_names_refseq": "putative protein PTGES3L isoform X2",
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        "protein_name": "small monomeric GTPase",
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        "protein_names_uniprotkb": "small monomeric GTPase; 3.6.5.2",
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    },
    {
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        "uniprot_id": "A0A8I5ZRZ8_RAT",
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        "length": 1048,
        "protein_name": "Multifunctional ROCO family signaling regulator 1",
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        "refseq_name": "malignant fibrous histiocytoma-amplified sequence 1 isoform 1",
        "refseq_ac": "NP_001423493",
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        "protein_names_uniprotkb": "Multifunctional ROCO family signaling regulator 1",
        "protein_names_refseq": "malignant fibrous histiocytoma amplified sequence 1; malignant fibrous histiocytoma-amplified sequence 1 isoform 1",
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        "disease": "fibrous histiocytoma (Disease Ontology:DOID:4415)",
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        "go_molecular_function": "GO:0005525 GTP binding;GO:0031625 ubiquitin protein ligase binding;GO:0051721 protein phosphatase 2A binding",
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    {
        "uniprot_canonical_ac": "A0A8I6A9T2-1",
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        "protein_name": "Solute carrier family 2, facilitated glucose transporter member 12",
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        "gene_names_uniprotkb": "Slc2a12",
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        "protein_names_uniprotkb": "Solute carrier family 2, facilitated glucose transporter member 12; Glucose transporter type 12",
        "protein_names_refseq": "",
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        "function": "Insulin-independent facilitative glucose transporter., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0055056 D-glucose transmembrane transporter activity;GO:0022857 transmembrane transporter activity",
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        "go_biological_process": "GO:0072359 circulatory system development;GO:1904659 D-glucose transmembrane transport",
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        "length": 195,
        "protein_name": "LSM12 homolog",
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        "refseq_name": "protein LSM12",
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        "protein_names_uniprotkb": "LSM12 homolog",
        "protein_names_refseq": "protein LSM12 homolog; protein LSM12",
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        "function": "Plays a role in the regulation of the mitochondrial ribosome assembly and of translational activity. Displays GTPase activity. Involved in the ribosome maturation process., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "refseq_name": "protein canopy homolog 1 isoform X1",
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        "go_molecular_function": "GO:0035925 mRNA 3'-UTR AU-rich region binding;GO:0003723 RNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005730 nucleolus;GO:0005829 cytosol;GO:0016607 nuclear speck;GO:0000176 nuclear exosome (RNase complex)",
        "go_biological_process": "GO:0071028 nuclear mRNA surveillance;GO:0034473 U1 snRNA 3'-end processing;GO:0034476 U5 snRNA 3'-end processing;GO:0006396 RNA processing;GO:0016075 rRNA catabolic process",
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    },
    {
        "uniprot_canonical_ac": "A0A8I5ZPJ9-1",
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        "length": 639,
        "protein_name": "U3 small nucleolar RNA-associated protein 18 homolog",
        "gene_name": "Utp18",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Utp18",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "U3 small nucleolar RNA-associated protein 18 homolog; WD repeat-containing protein 50",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-6791226)",
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        "publication_id_list": "22673903",
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        "function": "Part of the small subunit (SSU) processome, first precursor of the small eukaryotic ribosomal subunit. During the assembly of the SSU processome in the nucleolus, many ribosome biogenesis factors, an RNA chaperone and ribosomal proteins associate with the nascent pre-rRNA and work in concert to generate RNA folding, modifications, rearrangements and cleavage as well as targeted degradation of pre-ribosomal RNA by the RNA exosome. Involved in nucleolar processing of pre-18S ribosomal RNA., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005730 nucleolus;GO:0034388 Pwp2p-containing subcomplex of 90S preribosome;GO:0005634 nucleus;GO:0032040 small-subunit processome",
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    },
    {
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        "length": 1600,
        "protein_name": "GATOR1 complex protein DEPDC5",
        "gene_name": "Depdc5",
        "organism": "Rat",
        "refseq_name": "GATOR1 complex protein DEPDC5 isoform 2",
        "refseq_ac": "NP_001423834",
        "gene_names_uniprotkb": "Depdc5",
        "gene_names_refseq": "Depdc5",
        "protein_names_uniprotkb": "GATOR1 complex protein DEPDC5; DEP domain-containing protein 5",
        "protein_names_refseq": "DEP domain-containing protein 5; GATOR complex protein DEPDC5; GATOR1 complex protein DEPDC5 isoform 2; GATOR1 complex protein DEPDC5",
        "tax_id": 10116,
        "disease": "familial focal epilepsy with variable foci 1 (Disease Ontology:DOID:0081421); developmental and epileptic encephalopathy (Disease Ontology:DOID:0112202); cancer (Disease Ontology:DOID:162); epilepsy (Disease Ontology:DOID:1826); focal epilepsy (Disease Ontology:DOID:2234)",
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        "publication_id_list": "26873552",
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        "function": "DEP-domain containing 5 knockout rats exhibit multiple features of rodent models of mechanistic target of rapamycin complex 1 (mTOR) mTORopathies, and thus, stand as a relevant model to study their underlying pathogenic mechanisms., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0005096 GTPase activator activity;GO:0044877 protein-containing complex binding;GO:0031267 small GTPase binding",
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    },
    {
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        "gene_names_uniprotkb": "Ankrd23",
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        "protein_names_uniprotkb": "Ankyrin repeat domain-containing protein 23; Diabetes-related ankyrin repeat protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "congestive heart failure (Disease Ontology:DOID:6000); type 2 diabetes mellitus (Disease Ontology:DOID:9352)",
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        "class_list": "",
        "function": "May be involved in the energy metabolism. Could be a molecular link between myofibrillar stretch-induced signaling pathways and muscle gene expression., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0000976 transcription cis-regulatory region binding;GO:0031432 titin binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0031674 I band;GO:0005654 nucleoplasm;GO:0014704 intercalated disc;GO:0030016 myofibril",
        "go_biological_process": "GO:0035994 response to muscle stretch;GO:0006631 fatty acid metabolic process;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0009612 response to mechanical stimulus;GO:0060297 regulation of sarcomere organization",
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        "length": 1122,
        "protein_name": "Family with sequence similarity 184, member A",
        "gene_name": "Fam184a",
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        "refseq_name": "protein FAM184A isoform X2",
        "refseq_ac": "XP_038955241",
        "gene_names_uniprotkb": "Fam184a",
        "gene_names_refseq": "Fam184a-ps1; Fam184a; RGD1311294",
        "protein_names_uniprotkb": "Family with sequence similarity 184, member A",
        "protein_names_refseq": "protein FAM184A isoform X2",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0000932 P-body;GO:0034451 centriolar satellite;GO:0036064 ciliary basal body",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZR45-1",
        "uniprot_id": "A0A8I5ZR45_RAT",
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        "length": 430,
        "protein_name": "Pre-B-cell leukemia transcription factor 1",
        "gene_name": "Pbx1",
        "organism": "Rat",
        "refseq_name": "pre-B-cell leukemia transcription factor 1 isoform a",
        "refseq_ac": "NP_001128334",
        "gene_names_uniprotkb": "Pbx1",
        "gene_names_refseq": "Pbx1",
        "protein_names_uniprotkb": "Pre-B-cell leukemia transcription factor 1; Homeobox protein PBX1",
        "protein_names_refseq": "pre-B-cell leukemia homeobox 1; pre-B-cell leukemia transcription factor 1 isoform a; pre-B-cell leukemia transcription factor 1",
        "tax_id": 10116,
        "disease": "congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay (Disease Ontology:DOID:0112359); glaucoma (Disease Ontology:DOID:1686); brain infarction (Disease Ontology:DOID:3454)",
        "pathway": " (rno:304947)",
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        "publication_id_list": "37673222",
        "class_list": "",
        "function": "As part of a PDX1:PBX1b:MEIS2B complex in pancreatic acinar cells, is involved in the transcriptional activation of the ELA1 enhancer; the complex binds to the enhancer B element and cooperates with the transcription factor 1 complex (PTF1) bound to the enhancer A element., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Mesenchymal stem cells overexpressing PBX1 alleviates haemorrhagic shock-induced kidney damage by inhibiting NF-kappaB activation., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0043565 sequence-specific DNA binding;GO:0003677 DNA 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:0005667 transcription regulator complex;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0016604 nuclear body",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0030154 cell differentiation;GO:0006694 steroid biosynthetic process;GO:0007548 sex differentiation;GO:0001779 natural killer cell differentiation",
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        "hit_score": 0.2,
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        "record_type": "protein"
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    {
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        "length": 312,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or13a23; Or13a26; Or13a27b",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Or13a23; Or13a26; Or13a27b; Or13a23; Or13a27c; Or13a27e; Or13a27",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:405040);  (rno:405925)",
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        "function": "Possible taste receptor., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding",
        "go_cellular_component": "GO:0005886 plasma membrane",
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        "record_id": "A0A8I6GHW5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6AAD5-1",
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        "length": 436,
        "protein_name": "26S proteasome non-ATPase regulatory subunit 12",
        "gene_name": "Psmd12",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Psmd12",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "26S proteasome non-ATPase regulatory subunit 12; 26S proteasome regulatory subunit RPN5; 26S proteasome regulatory subunit p55",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "cancer (Disease Ontology:DOID:162)",
        "pathway": "",
        "pathway_count": 0,
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        "class_list": "",
        "function": "Component of the 26S proteasome, a multiprotein complex involved in the ATP-dependent degradation of ubiquitinated proteins. This complex plays a key role in the maintenance of protein homeostasis by removing misfolded or damaged proteins, which could impair cellular functions, and by removing proteins whose functions are no longer required. Therefore, the proteasome participates in numerous cellular processes, including cell cycle progression, apoptosis, or DNA damage repair., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005838 proteasome regulatory particle;GO:0022624 proteasome accessory complex;GO:0000502 proteasome complex",
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        "synthesized_glycan_count": 0,
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZYH1-1",
        "uniprot_id": "A0A8I5ZYH1_RAT",
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        "length": 403,
        "protein_name": "Poly(rC)-binding protein 4",
        "gene_name": "Pcbp4",
        "organism": "Rat",
        "refseq_name": "poly(rC)-binding protein 4",
        "refseq_ac": "NP_001178812",
        "gene_names_uniprotkb": "Pcbp4",
        "gene_names_refseq": "Pcbp4",
        "protein_names_uniprotkb": "Poly(rC)-binding protein 4; Alpha-CP4",
        "protein_names_refseq": "poly(rC)-binding protein 4",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:363133)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Single-stranded nucleic acid binding protein that binds preferentially to oligo dC., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "ec_number_list": "",
        "go_molecular_function": "GO:0003723 RNA binding;GO:0003730 mRNA 3'-UTR binding",
        "go_cellular_component": "GO:0005829 cytosol",
        "go_biological_process": "GO:0043488 regulation of mRNA stability;GO:0008630 intrinsic apoptotic signaling pathway in response to DNA damage;GO:0048025 negative regulation of mRNA splicing, via spliceosome;GO:0030330 DNA damage response, signal transduction by p53 class mediator;GO:0043518 negative regulation of DNA damage response, signal transduction by p53 class mediator",
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        "hit_score": 0.1,
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZL15-1",
        "uniprot_id": "A0A8I5ZL15_RAT",
        "mass": 57512.0,
        "length": 498,
        "protein_name": "PRAME like 36 like 1",
        "gene_name": "Pramel36l1; Pramel53",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Pramel36l1; Pramel53; LOC100909497; LOC100910292; LOC134481896",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "PRAME like 36 like 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:100909497)",
        "pathway_count": 1,
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        "biomarker_type": "",
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        "go_molecular_function": "GO:1990756 ubiquitin-like ligase-substrate adaptor activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0031462 Cul2-RING ubiquitin ligase complex",
        "go_biological_process": "GO:0008284 positive regulation of cell population proliferation;GO:0043066 negative regulation of apoptotic process;GO:0045892 negative regulation of DNA-templated transcription;GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process;GO:0045596 negative regulation of cell differentiation",
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        "record_id": "A0A8I5ZL15-1",
        "record_type": "protein"
    },
    {
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        "uniprot_id": "A0A8I6AKF3_RAT",
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        "length": 204,
        "protein_name": "Glucosamine 6-phosphate N-acetyltransferase",
        "gene_name": "Gnpnat1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Gnpnat1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Glucosamine 6-phosphate N-acetyltransferase; 2.3.1.4",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "keratosis follicularis spinulosa decalvans (Disease Ontology:DOID:0080753); cancer (Disease Ontology:DOID:162)",
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        "secondary_ac_list": "",
        "ec_number_list": "2.3.1.4",
        "go_molecular_function": "GO:0042802 identical protein binding;GO:0004343 glucosamine 6-phosphate N-acetyltransferase activity;GO:0048029 monosaccharide binding",
        "go_cellular_component": "GO:0005794 Golgi apparatus;GO:0005770 late endosome;GO:0005793 endoplasmic reticulum-Golgi intermediate compartment",
        "go_biological_process": "GO:0006044 N-acetylglucosamine metabolic process;GO:0001889 liver development;GO:1990830 cellular response to leukemia inhibitory factor;GO:0006041 glucosamine metabolic process;GO:0006048 UDP-N-acetylglucosamine biosynthetic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6AKF3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6ARN3-1",
        "uniprot_id": "A0A8I6ARN3_RAT",
        "mass": 78901.0,
        "length": 711,
        "protein_name": "Zinc finger and BTB domain containing 39",
        "gene_name": "Zbtb39",
        "organism": "Rat",
        "refseq_name": "zinc finger and BTB domain-containing protein 39",
        "refseq_ac": "NP_001124009",
        "gene_names_uniprotkb": "Zbtb39",
        "gene_names_refseq": "RGD1306532; Zbtb39",
        "protein_names_uniprotkb": "Zinc finger and BTB domain containing 39",
        "protein_names_refseq": "zinc finger and BTB domain-containing protein 39",
        "tax_id": 10116,
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        "pathway": " (rno:299510)",
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        "class_list": "",
        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0008270 zinc ion binding",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0006351 DNA-templated transcription",
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        "hit_score": 0.1,
        "record_id": "A0A8I6ARN3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "B4F767-1",
        "uniprot_id": "B4F767_RAT",
        "mass": 98778.0,
        "length": 870,
        "protein_name": "E3 ubiquitin-protein ligase",
        "gene_name": "Wwp2",
        "organism": "Rat",
        "refseq_name": "NEDD4-like E3 ubiquitin-protein ligase WWP2",
        "refseq_ac": "NP_001099654",
        "gene_names_uniprotkb": "Wwp2",
        "gene_names_refseq": "Wwp2",
        "protein_names_uniprotkb": "E3 ubiquitin-protein ligase; 2.3.2.26",
        "protein_names_refseq": "NEDD4-like E3 ubiquitin-protein ligase WWP2",
        "tax_id": 10116,
        "disease": "Liddle syndrome (Disease Ontology:DOID:0050477)",
        "pathway": " (rno:291999);  (R-RNO-8948751);  (R-RNO-9013406);  (R-RNO-9013420);  (R-RNO-9013507)",
        "pathway_count": 5,
        "publication_count": 1,
        "publication_id_list": "35545948",
        "class_list": "",
        "function": "Hypoxia-induced mesenchymal stem cells inhibit corneal fibroblast proliferation by regulating the WWP2/Notch1 axis., [RefSeq, PubMed]",
        "predicted_glycosites": 1,
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        "biomarker_type": "",
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        "secondary_ac_list": "F7EYF1",
        "ec_number_list": "3.4.19.12;2.3.2.26;2.7.11.1;2.7.10.1;3.1.3.67;3.1.3.-;3.1.3.16;3.1.3.48;3.6.5.2;2.7.10.2;1.16.1.-;2.3.2.27",
        "go_molecular_function": "GO:0061630 ubiquitin protein ligase activity;GO:0061629 RNA polymerase II-specific DNA-binding transcription factor binding;GO:0140678 molecular function inhibitor activity;GO:0016874 ligase activity;GO:0019870 potassium channel inhibitor activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005576 extracellular region",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process;GO:0016567 protein ubiquitination;GO:0034765 regulation of monoatomic ion transmembrane transport;GO:1903765 negative regulation of potassium ion export across plasma membrane",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "B4F767-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6AAJ7-1",
        "uniprot_id": "A0A8I6AAJ7_RAT",
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        "length": 621,
        "protein_name": "Rab proteins geranylgeranyltransferase component A",
        "gene_name": "Chml",
        "organism": "Rat",
        "refseq_name": "rab proteins geranylgeranyltransferase component A 2",
        "refseq_ac": "NP_001102994",
        "gene_names_uniprotkb": "Chml",
        "gene_names_refseq": "Chml",
        "protein_names_uniprotkb": "Rab proteins geranylgeranyltransferase component A",
        "protein_names_refseq": "CHM like, Rab escort protein 2; choroideremia-like (Rab escort protein 2); rab proteins geranylgeranyltransferase component A 2",
        "tax_id": 10116,
        "disease": "asthma (Disease Ontology:DOID:2841); choroideremia (Disease Ontology:DOID:9821)",
        "pathway": " (rno:689102);  (R-RNO-8873719);  (R-RNO-8876198)",
        "pathway_count": 3,
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        "publication_id_list": "",
        "class_list": "",
        "function": "Substrate-binding subunit (component A) of the Rab geranylgeranyltransferase (GGTase) complex. Binds unprenylated Rab proteins and presents the substrate peptide to the catalytic component B. The component A is thought to be regenerated by transferring its prenylated Rab back to the donor membrane., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "ec_number_list": "",
        "go_molecular_function": "GO:0005096 GTPase activator activity;GO:0031267 small GTPase binding;GO:0005092 GDP-dissociation inhibitor activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005829 cytosol;GO:0005968 Rab-protein geranylgeranyltransferase complex",
        "go_biological_process": "GO:0006886 intracellular protein transport;GO:0006612 protein targeting to membrane;GO:0007264 small GTPase-mediated signal transduction;GO:0016192 vesicle-mediated transport;GO:0018344 protein geranylgeranylation",
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        "hit_score": 0.1,
        "record_id": "A0A8I6AAJ7-1",
        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "A0A8I6AD76-1",
        "uniprot_id": "A0A8I6AD76_RAT",
        "mass": 47162.0,
        "length": 415,
        "protein_name": "Pyroglutamylated RF-amide peptide receptor",
        "gene_name": "Qrfprl",
        "organism": "Rat",
        "refseq_name": "uncharacterized protein LOC500157",
        "refseq_ac": "NP_001102709",
        "gene_names_uniprotkb": "Qrfprl; RGD1560028",
        "gene_names_refseq": "Qrfprl; RGD1560028",
        "protein_names_uniprotkb": "Pyroglutamylated RF-amide peptide receptor; AQ27; G-protein coupled receptor 103; Orexigenic neuropeptide QRFP receptor; SP9155",
        "protein_names_refseq": "uncharacterized protein LOC500157",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:500157);  (R-RNO-389397);  (R-RNO-416476)",
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        "publication_count": 1,
        "publication_id_list": "16996040",
        "class_list": "",
        "function": "QRFP-r2 when expressed in COS-7 cells was activated by the QRFP peptide with an EC50 similar to that for rat GPR103 (QRFP-r1). In situ hybridization showed little overlap of QFRP-r2 mRNA with rat QRFP-r1., [RefSeq, PubMed]; Receptor for the orexigenic neuropeptide QRFP. The activity of this receptor is mediated by G proteins that modulate adenylate cyclase activity and intracellular calcium levels., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "protein_names_refseq": "melanoma-associated antigen B3; melanoma-associated antigen B5; uncharacterized protein LOC503444",
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        "protein_name": "Toll-like receptor 7",
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        "refseq_name": "toll-like receptor 7 isoform X1",
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        "disease": "COVID-19 (Disease Ontology:DOID:0080600); severe COVID-19 (Disease Ontology:DOID:0081013); X-Linked immunodeficiency 74 (Disease Ontology:DOID:0112063); anogenital venereal wart (Disease Ontology:DOID:11168); respiratory syncytial virus infectious disease (Disease Ontology:DOID:1273); alcohol use disorder (Disease Ontology:DOID:1574); asthma (Disease Ontology:DOID:2841); atopic dermatitis (Disease Ontology:DOID:3310); allergic rhinitis (Disease Ontology:DOID:4481); rhinitis (Disease Ontology:DOID:4483); perinatal necrotizing enterocolitis (Disease Ontology:DOID:8677); systemic lupus erythematosus (Disease Ontology:DOID:9074)",
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        "go_molecular_function": "GO:0003725 double-stranded RNA binding;GO:0003727 single-stranded RNA binding;GO:0035197 siRNA binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005768 endosome;GO:0005783 endoplasmic reticulum;GO:0005886 plasma membrane;GO:0043235 receptor complex",
        "go_biological_process": "GO:0032727 positive regulation of interferon-alpha production;GO:0006954 inflammatory response;GO:0045087 innate immune response;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0051607 defense response to virus",
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    {
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        "length": 309,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or4x11c",
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        "refseq_name": "olfactory receptor Olr734",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
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    {
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        "protein_name": "Molybdenum cofactor biosynthesis protein 1",
        "gene_name": "Mocs1",
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        "protein_names_uniprotkb": "Molybdenum cofactor biosynthesis protein 1; 4.1.99.22; 4.6.1.17",
        "protein_names_refseq": "molybdenum cofactor biosynthesis protein 1",
        "tax_id": 10116,
        "disease": "molybdenum cofactor deficiency type A (Disease Ontology:DOID:0111164)",
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        "function": "Isoform MOCS1A and isoform MOCS1B probably form a complex that catalyzes the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP). MOCS1A catalyzes the cyclization of GTP to (8S)-3',8-cyclo-7,8-dihydroguanosine 5'-triphosphate and MOCS1B catalyzes the subsequent conversion of (8S)-3',8-cyclo-7,8-dihydroguanosine 5'-triphosphate to cPMP., [UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005759 mitochondrial matrix;GO:0005829 cytosol",
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        "protein_name": "Olfactory receptor",
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        "secondary_ac_list": "",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
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        "length": 718,
        "protein_name": "Sodium/myo-inositol cotransporter",
        "gene_name": "Slc5a3",
        "organism": "Rat",
        "refseq_name": "sodium/myo-inositol cotransporter",
        "refseq_ac": "NP_446167",
        "gene_names_uniprotkb": "Slc5a3",
        "gene_names_refseq": "Slc5a3; Smit",
        "protein_names_uniprotkb": "Sodium/myo-inositol cotransporter; Sodium/myo-inositol transporter 1; Solute carrier family 5 member 3",
        "protein_names_refseq": "sodium/myo-inositol cotransporter; solute carrier family 5 (inositol transporters), member 3; solute carrier family 5 (sodium/myo-inositol cotransporter), member 3",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:114507);  (R-RNO-429593)",
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        "publication_count": 5,
        "publication_id_list": "12098491;12427139;28202581;29551423;32787517",
        "class_list": "",
        "function": "Basolateral Na+-MI cotransporter activity is maximal at physiological pH values of MTAL cells and interstitium, and a powerful modulation of the transporter activity may be exerted by pHe and pHi., [RefSeq, PubMed]; Intracerebral hemorrhage upregulates Na(+)/myo-inositol cotransporter in the rat brain., [RefSeq, PubMed]; Myo-inositol transporter SMIT1 is required to maintain a stable phosphoinositide pool in beta-cells in order that phosphoinositide remains available despite its rapid turnover., [RefSeq, PubMed]; Results indicate that H(+)/myo-inositol cotransporter (HMIT) is expressed in marginal cells and basal cells of the stria vascularis, while Na(+)/myo-inositol cotransporter 1 (SMIT1) expression is enriched in basal cells. Study speculates that HMIT and SMIT1 may play important roles in the homeostasis of cochlear fluids., [RefSeq, PubMed]; SMIT (Sodium-Myo-Inositol Transporter) 1 Regulates Arterial Contractility Through the Modulation of Vascular Kv7 Channels., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005367 myo-inositol:sodium symporter activity;GO:0005412 D-glucose:sodium symporter activity;GO:0015459 potassium channel regulator activity;GO:0044325 transmembrane transporter binding;GO:0015166 polyol transmembrane transporter activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0016323 basolateral plasma membrane;GO:0048471 perinuclear region of cytoplasm;GO:0016324 apical plasma membrane;GO:0008076 voltage-gated potassium channel complex",
        "go_biological_process": "GO:0006020 inositol metabolic process;GO:1904659 D-glucose transmembrane transport;GO:0007422 peripheral nervous system development;GO:1903428 positive regulation of reactive oxygen species biosynthetic process;GO:0043576 regulation of respiratory gaseous exchange",
        "synthesized_glycan_count": 0,
        "hit_score": 0.6,
        "record_id": "A0A8I6GM79-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8J8XB91-1",
        "uniprot_id": "A0A8J8XB91_RAT",
        "mass": 38800.0,
        "length": 343,
        "protein_name": "Tribbles homolog 2",
        "gene_name": "Trib2",
        "organism": "Rat",
        "refseq_name": "tribbles homolog 2",
        "refseq_ac": "NP_001101485",
        "gene_names_uniprotkb": "Trib2",
        "gene_names_refseq": "RGD1564451; Trib2",
        "protein_names_uniprotkb": "Tribbles homolog 2",
        "protein_names_refseq": "tribbles homolog 2",
        "tax_id": 10116,
        "disease": "glucose metabolism disease (Disease Ontology:DOID:4194)",
        "pathway": " (rno:313974)",
        "pathway_count": 1,
        "publication_count": 3,
        "publication_id_list": "22012613;28364459;36626273",
        "class_list": "",
        "function": "Interacts with MAPK kinases and regulates activation of MAP kinases. Does not display kinase activity., [UniProtKB, UniProtKB]; TRB2 plays important roles in the pathogenesis of diabetic-2 large artery complications at early stage, and these effects may be modulated by miR-98, [RefSeq, PubMed]; The absence of a change in hypocretin cell populations suggested that factors other than anti-TRIB2 antibody play a part in the loss of hypocretin neurons in narcolepsy. The increased anti-TRIB2 antibody after the destruction of hypocretin neurons suggest that anti-TRIB2 antibody in narcolepsy patients is the consequence rather than the inciting cause of hypocretin cell destruction., [RefSeq, PubMed]; The role of tribbles homolog 2 in vascular smooth muscle cell proliferation., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "secondary_ac_list": "",
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        "go_molecular_function": "GO:0055106 ubiquitin-protein transferase regulator activity;GO:0031434 mitogen-activated protein kinase kinase binding;GO:0031625 ubiquitin protein ligase binding;GO:0004860 protein kinase inhibitor activity;GO:0061629 RNA polymerase II-specific DNA-binding transcription factor binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005856 cytoskeleton",
        "go_biological_process": "GO:0032693 negative regulation of interleukin-10 production;GO:0032436 positive regulation of proteasomal ubiquitin-dependent protein catabolic process;GO:0045599 negative regulation of fat cell differentiation",
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    },
    {
        "uniprot_canonical_ac": "A0A8J8XCE4-1",
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        "mass": 45129.0,
        "length": 409,
        "protein_name": "Zona pellucida binding protein",
        "gene_name": "Zpbp",
        "organism": "Rat",
        "refseq_name": "zona pellucida-binding protein 1",
        "refseq_ac": "NP_001020310",
        "gene_names_uniprotkb": "Zpbp",
        "gene_names_refseq": "Zpbp",
        "protein_names_uniprotkb": "Zona pellucida binding protein",
        "protein_names_refseq": "zona pellucida-binding protein 1",
        "tax_id": 10116,
        "disease": "spermatogenic failure 66 (Disease Ontology:DOID:0070565)",
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        "publication_id_list": "19204925",
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        "function": "The localization of IAM38 on the extracellular side of both the inner and outer acrosomal membrane during the cap phase of acrosomal development supports the role of this prominent protein in acrosomal compaction., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0001669 acrosomal vesicle;GO:0044297 cell body;GO:0002199 zona pellucida receptor complex",
        "go_biological_process": "GO:0007339 binding of sperm to zona pellucida;GO:0001675 acrosome assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A8J8XCE4-1",
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    },
    {
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        "length": 264,
        "protein_name": "Transmembrane protein 41a",
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        "organism": "Rat",
        "refseq_name": "transmembrane protein 41A",
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        "gene_names_uniprotkb": "Tmem41a",
        "gene_names_refseq": "Tmem41a",
        "protein_names_uniprotkb": "Transmembrane protein 41a",
        "protein_names_refseq": "transmembrane protein 41A",
        "tax_id": 10116,
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        "pathway": " (rno:681708)",
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        "go_cellular_component": "GO:0016020 membrane",
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        "record_id": "B1WC43-1",
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        "length": 416,
        "protein_name": "Ankyrin repeat and sterile alpha motif domain containing 4B",
        "gene_name": "Anks4b",
        "organism": "Rat",
        "refseq_name": "ankyrin repeat and SAM domain-containing protein 4B",
        "refseq_ac": "NP_001121122",
        "gene_names_uniprotkb": "Anks4b",
        "gene_names_refseq": "Anks4b",
        "protein_names_uniprotkb": "Ankyrin repeat and sterile alpha motif domain containing 4B",
        "protein_names_refseq": "ankyrin repeat and SAM domain-containing protein 4B; harmonin-interacting ankyrin repeat-containing",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:687561)",
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        "secondary_ac_list": "M0RBX2",
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        "go_molecular_function": "GO:0017022 myosin binding",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0005903 brush border;GO:0005789 endoplasmic reticulum membrane;GO:0005902 microvillus;GO:0002141 stereocilia ankle link",
        "go_biological_process": "GO:0034976 response to endoplasmic reticulum stress;GO:1904106 protein localization to microvillus;GO:1904970 brush border assembly;GO:0065003 protein-containing complex assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "B2GV19-1",
        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "B5DFA6-1",
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        "length": 295,
        "protein_name": "GTP-binding protein",
        "gene_name": "Gem",
        "organism": "Rat",
        "refseq_name": "GTP-binding protein GEM",
        "refseq_ac": "NP_001100107",
        "gene_names_uniprotkb": "Gem",
        "gene_names_refseq": "Gem",
        "protein_names_uniprotkb": "GTP-binding protein",
        "protein_names_refseq": "GTP binding protein (gene overexpressed in skeletal muscle); GTP-binding protein GEM",
        "tax_id": 10116,
        "disease": "glaucoma (Disease Ontology:DOID:1686)",
        "pathway": " (rno:297902)",
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        "publication_count": 4,
        "publication_id_list": "15860732;23076376;23602967;24948002",
        "class_list": "",
        "function": "Binding of 14-3-3, calmodulin and calcium channel beta-subunits to Kir/Gem is mutually exclusive, [RefSeq, PubMed]; Data suggest that GTP-binding protein Gem might play a crucial role in retinal ganglion cells (RGCs) apoptosis after nerve crush (ONC)., [RefSeq, PubMed]; Increased expression of Gem after rat sciatic nerve injury., [RefSeq, PubMed]; The results of tjis study suggested that Gem may be implicated in the proliferation of microglia and astrocytes after spinal cord injury., [RefSeq, PubMed]",
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        "secondary_ac_list": "E9PT99",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005886 plasma membrane;GO:0051233 spindle midzone;GO:0009898 cytoplasmic side of plasma membrane;GO:0030496 midbody",
        "go_biological_process": "GO:0051310 metaphase chromosome alignment;GO:0000278 mitotic cell cycle;GO:0051276 chromosome organization",
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    },
    {
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        "uniprot_id": "F7EZP5_RAT",
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        "length": 251,
        "protein_name": "Protease, serine 59",
        "gene_name": "Prss59",
        "organism": "Rat",
        "refseq_name": "protease, serine 59 isoform X1",
        "refseq_ac": "XP_006236430",
        "gene_names_uniprotkb": "Prss59",
        "gene_names_refseq": "Prss59; Tryx5",
        "protein_names_uniprotkb": "Protease, serine 59",
        "protein_names_refseq": "protease, serine 59 isoform X1",
        "tax_id": 10116,
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        "go_molecular_function": "GO:0004252 serine-type endopeptidase activity",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005794 Golgi apparatus;GO:0030141 secretory granule",
        "go_biological_process": "GO:0006508 proteolysis;GO:0051604 protein maturation;GO:2000243 positive regulation of reproductive process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F7EZP5-1",
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    },
    {
        "uniprot_canonical_ac": "F7F4L4-1",
        "uniprot_id": "F7F4L4_RAT",
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        "length": 376,
        "protein_name": "DnaJ heat shock protein family (Hsp40) member B12",
        "gene_name": "Dnajb12",
        "organism": "Rat",
        "refseq_name": "dnaJ homolog subfamily B member 12 isoform X1",
        "refseq_ac": "XP_038954544",
        "gene_names_uniprotkb": "Dnajb12",
        "gene_names_refseq": "Dnajb12",
        "protein_names_uniprotkb": "DnaJ heat shock protein family (Hsp40) member B12",
        "protein_names_refseq": "dnaJ homolog subfamily B member 12 isoform X1",
        "tax_id": 10116,
        "disease": "Huntington's disease (Disease Ontology:DOID:12858)",
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        "pathway_count": 0,
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        "go_molecular_function": "GO:0030544 Hsp70 protein binding",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0031965 nuclear membrane;GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0006457 protein folding;GO:0036503 ERAD pathway;GO:0071218 cellular response to misfolded protein;GO:0065003 protein-containing complex assembly",
        "synthesized_glycan_count": 0,
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    },
    {
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        "length": 375,
        "protein_name": "INO80 complex subunit B",
        "gene_name": "Ino80b",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ino80b",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "INO80 complex subunit B",
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        "tax_id": 10116,
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        "pathway": " (R-RNO-5689603);  (R-RNO-5696394)",
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0031011 Ino80 complex;GO:0016604 nuclear body",
        "go_biological_process": "GO:0060382 regulation of DNA strand elongation;GO:0033044 regulation of chromosome organization;GO:0006338 chromatin remodeling;GO:0000723 telomere maintenance;GO:0045893 positive regulation of DNA-templated transcription",
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    },
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        "length": 313,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or8b54b",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr1261",
        "refseq_ac": "NP_001000804",
        "gene_names_uniprotkb": "Or8b54b",
        "gene_names_refseq": "Olr1261; Or8b54b",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 1261; olfactory receptor 8B3-like; olfactory receptor Olr1261; olfactory receptor gene Olr1261",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:405090)",
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        "function": "Odorant receptor., [UniProtKB, UniProtKB]; Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "go_cellular_component": "GO:0005886 plasma membrane",
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        "protein_name": "Arylsulfatase family, member J",
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        "refseq_name": "arylsulfatase J",
        "refseq_ac": "NP_001041352",
        "gene_names_uniprotkb": "Arsj; AABR07013255.1",
        "gene_names_refseq": "Arsj; RGD1307640",
        "protein_names_uniprotkb": "Arylsulfatase family, member J",
        "protein_names_refseq": "arylsulfatase J",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:311013);  (R-RNO-1663150);  (R-RNO-9840310)",
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        "go_molecular_function": "GO:0046872 metal ion binding;GO:0008484 sulfuric ester hydrolase activity",
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        "synthesized_glycan_count": 0,
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        "record_id": "Q32KJ7-1",
        "record_type": "protein"
    },
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        "length": 373,
        "protein_name": "Uncharacterized protein",
        "gene_name": "AABR07039936.1",
        "organism": "Rat",
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        "gene_names_uniprotkb": "AABR07039936.1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Uncharacterized protein",
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        "secondary_ac_list": "F7FDC8",
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        "go_molecular_function": "GO:0047057 vitamin-K-epoxide reductase (warfarin-sensitive) activity",
        "go_cellular_component": "",
        "go_biological_process": "GO:0042373 vitamin K metabolic process",
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        "hit_score": 0.1,
        "record_id": "Q6TUH2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q9ERV4-1",
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        "length": 169,
        "protein_name": "Sex-determining region Y protein",
        "gene_name": "LOC134484451",
        "organism": "Rat",
        "refseq_name": "sex-determining region Y protein-like",
        "refseq_ac": "NP_001403668",
        "gene_names_uniprotkb": "LOC134484451; Sry3A; Sry3B1; Sry3C; Sry3a; Sry3b1; Sry3c; Sry3",
        "gene_names_refseq": "Sry3",
        "protein_names_uniprotkb": "Sex-determining region Y protein; Testis-determining factor",
        "protein_names_refseq": "HMG box transcription factor Sry3; sex-determining region Y protein-like",
        "tax_id": 10116,
        "disease": "46,XX sex reversal 1 (Disease Ontology:DOID:0111761); 46,XY sex reversal 1 (Disease Ontology:DOID:0111778); 46,XY complete gonadal dysgenesis (Disease Ontology:DOID:14448)",
        "pathway": " (rno:120099577);  (rno:134484451);  (R-RNO-3769402)",
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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]",
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        "secondary_ac_list": "A0A8I6ASY9",
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        "go_molecular_function": "GO:0005516 calmodulin binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0001228 DNA-binding transcription activator activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus;GO:0016607 nuclear speck",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0030154 cell differentiation;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0007548 sex differentiation;GO:0030238 male sex determination",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "Q9ERV4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A0G2JUS3-1",
        "uniprot_id": "A0A0G2JUS3_RAT",
        "mass": 64384.0,
        "length": 561,
        "protein_name": "Zinc finger protein 790 like 2",
        "gene_name": "Zfp790l2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Zfp790l2; AABR07002893.1; LOC100912787",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger protein 790 like 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (rno:100912787);  (R-RNO-212436)",
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        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0006357 regulation of transcription by RNA polymerase II",
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        "length": 914,
        "protein_name": "Catenin alpha 3",
        "gene_name": "Ctnna3",
        "organism": "Rat",
        "refseq_name": "catenin alpha-3 isoform X1",
        "refseq_ac": "XP_038955205",
        "gene_names_uniprotkb": "Ctnna3",
        "gene_names_refseq": "AABR07044900.1; Catna3; Ctnna3; RGD1559455; RGD1562230",
        "protein_names_uniprotkb": "Catenin alpha 3",
        "protein_names_refseq": "catenin alpha-3 isoform X1",
        "tax_id": 10116,
        "disease": "esophageal atresia/tracheoesophageal fistula (Disease Ontology:DOID:0080171); childhood-onset asthma (Disease Ontology:DOID:0080815); occupational asthma (Disease Ontology:DOID:0080820); arrhythmogenic right ventricular dysplasia 13 (Disease Ontology:DOID:0110084); asthma (Disease Ontology:DOID:2841)",
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        "go_molecular_function": "GO:0051015 actin filament binding;GO:0045296 cadherin binding;GO:0008013 beta-catenin binding",
        "go_cellular_component": "GO:0005856 cytoskeleton;GO:0005912 adherens junction;GO:0030027 lamellipodium;GO:0005916 fascia adherens;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0016477 cell migration;GO:0086091 regulation of heart rate by cardiac conduction;GO:0098609 cell-cell adhesion;GO:0098911 regulation of ventricular cardiac muscle cell action potential;GO:0086073 bundle of His cell-Purkinje myocyte adhesion involved in cell communication",
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        "length": 846,
        "protein_name": "Tubulin tyrosine ligase like 13",
        "gene_name": "Ttll13",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ttll13",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Tubulin tyrosine ligase like 13",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "go_molecular_function": "GO:0070740 tubulin-glutamic acid ligase activity;GO:0005524 ATP binding;GO:0015631 tubulin binding",
        "go_cellular_component": "GO:0036064 ciliary basal body",
        "go_biological_process": "GO:0001578 microtubule bundle formation",
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    {
        "uniprot_canonical_ac": "A0A8I5Y5L8-1",
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        "length": 730,
        "protein_name": "Sorbin and SH3 domain containing 3",
        "gene_name": "Sorbs3",
        "organism": "Rat",
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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,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0006357 regulation of transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I5ZWW3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZYE5-1",
        "uniprot_id": "A0A8I5ZYE5_RAT",
        "mass": 17314.0,
        "length": 153,
        "protein_name": "Oligosaccharyltransferase complex subunit",
        "gene_name": "Ostcl1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ostcl1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Oligosaccharyltransferase complex subunit",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Subunit of STT3A-containing oligosaccharyl transferase (OST-A) 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). Within the OST-A complex, acts as an adapter that anchors the OST-A complex to the Sec61 complex. May be involved in N-glycosylation of APP (amyloid-beta precursor protein). Can modulate gamma-secretase cleavage of APP by enhancing endoprotelysis of PSEN1., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0030674 protein-macromolecule adaptor activity",
        "go_cellular_component": "GO:0008250 oligosaccharyltransferase complex",
        "go_biological_process": "GO:0009101 glycoprotein biosynthetic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I5ZYE5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZZ93-1",
        "uniprot_id": "A0A8I5ZZ93_RAT",
        "mass": 19530.0,
        "length": 181,
        "protein_name": "Peptidyl-tRNA hydrolase 2, mitochondrial",
        "gene_name": "Ptrh2",
        "organism": "Rat",
        "refseq_name": "peptidyl-tRNA hydrolase 2, mitochondrial",
        "refseq_ac": "NP_001013882",
        "gene_names_uniprotkb": "Ptrh2",
        "gene_names_refseq": "Ptrh2; RGD1306819",
        "protein_names_uniprotkb": "Peptidyl-tRNA hydrolase 2, mitochondrial; 3.1.1.29",
        "protein_names_refseq": "Bcl-2 inhibitor of transcription; peptidyl-tRNA hydrolase 2, mitochondrial",
        "tax_id": 10116,
        "disease": "invasive aspergillosis (Disease Ontology:DOID:0050073); Keshan disease (Disease Ontology:DOID:0050083); alcohol dependence (Disease Ontology:DOID:0050741); warfarin resistance (Disease Ontology:DOID:0080665); hypertension (Disease Ontology:DOID:10763); sickle cell anemia (Disease Ontology:DOID:10923); urinary bladder cancer (Disease Ontology:DOID:11054); dilated cardiomyopathy (Disease Ontology:DOID:12930); eosinophilic esophagitis (Disease Ontology:DOID:13922); Plasmodium falciparum malaria (Disease Ontology:DOID:14067); breast cancer (Disease Ontology:DOID:1612); tuberculosis (Disease Ontology:DOID:399); hyperglycemia (Disease Ontology:DOID:4195); multiple chemical sensitivity (Disease Ontology:DOID:4661); head and neck squamous cell carcinoma (Disease Ontology:DOID:5520); hepatocellular carcinoma (Disease Ontology:DOID:684); peptic ulcer disease (Disease Ontology:DOID:750); diabetes mellitus (Disease Ontology:DOID:9351); type 2 diabetes mellitus (Disease Ontology:DOID:9352); multiple myeloma (Disease Ontology:DOID:9538); heroin dependence (Disease Ontology:DOID:9976); hypoglycemia (Disease Ontology:DOID:9993)",
        "pathway": " (rno:287593)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Peptidyl-tRNA hydrolase which releases tRNAs from the ribosome during protein synthesis. Promotes caspase-independent apoptosis by regulating the function of two transcriptional regulators, AES and TLE1., [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": 22,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "3.1.1.29",
        "go_molecular_function": "GO:0004045 peptidyl-tRNA hydrolase activity",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005741 mitochondrial outer membrane;GO:0005829 cytosol",
        "go_biological_process": "GO:0010629 negative regulation of gene expression;GO:2000210 positive regulation of anoikis;GO:2000811 negative regulation of anoikis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I5ZZ93-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZZB2-1",
        "uniprot_id": "A0A8I5ZZB2_RAT",
        "mass": 46592.0,
        "length": 420,
        "protein_name": "Tubulin epsilon and delta complex 1",
        "gene_name": "Tedc1",
        "organism": "Rat",
        "refseq_name": "tubulin epsilon and delta complex protein 1",
        "refseq_ac": "NP_001386073",
        "gene_names_uniprotkb": "Tedc1",
        "gene_names_refseq": "Tedc1",
        "protein_names_uniprotkb": "Tubulin epsilon and delta complex 1",
        "protein_names_refseq": "tubulin epsilon and delta complex protein 1; uncharacterized protein C14orf80 homolog",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:690422)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005813 centrosome;GO:0005929 cilium;GO:0005814 centriole",
        "go_biological_process": "GO:0045880 positive regulation of smoothened signaling pathway;GO:0007010 cytoskeleton organization;GO:0000226 microtubule cytoskeleton organization",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I5ZZB2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6A1A7-1",
        "uniprot_id": "A0A8I6A1A7_RAT",
        "mass": 58741.0,
        "length": 510,
        "protein_name": "Alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase A",
        "gene_name": "ENSRNOG00000069701",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "ENSRNOG00000069701",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase A; 2.4.1.145; N-glycosyl-oligosaccharide-glycoprotein N-acetylglucosaminyltransferase IVa; UDP-N-acetylglucosamine: alpha-1,3-D-mannoside beta-1,4-N-acetylglucosaminyltransferase IVa",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Glycosyltransferase that catalyze the transfer of GlcNAc from UDP-GlcNAc to the GlcNAcbeta1-2Manalpha1-3 arm of the core structure of N-linked glycans through a beta1-4 linkage and participates in the production of tri- and tetra-antennary N-linked sugar chains. Involved in glucose transport by mediating SLC2A2/GLUT2 glycosylation, thereby controlling cell-surface expression of SLC2A2 in pancreatic beta cells., [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": "2.4.1.145",
        "go_molecular_function": "GO:0046872 metal ion binding;GO:0008375 acetylglucosaminyltransferase activity;GO:0008454 alpha-1,3-mannosylglycoprotein 4-beta-N-acetylglucosaminyltransferase activity",
        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005576 extracellular region;GO:0005783 endoplasmic reticulum;GO:0005795 Golgi stack;GO:0005793 endoplasmic reticulum-Golgi intermediate compartment",
        "go_biological_process": "GO:0006487 protein N-linked glycosylation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6A1A7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6A2B8-1",
        "uniprot_id": "A0A8I6A2B8_RAT",
        "mass": 155844.0,
        "length": 1404,
        "protein_name": "Mediator of RNA polymerase II transcription subunit 14",
        "gene_name": "LOC103694537",
        "organism": "Rat",
        "refseq_name": "mediator of RNA polymerase II transcription subunit 14-like",
        "refseq_ac": "NP_001416314",
        "gene_names_uniprotkb": "LOC103694537; AC239701.1",
        "gene_names_refseq": "LOC103694537; MED14Y; MED14",
        "protein_names_uniprotkb": "Mediator of RNA polymerase II transcription subunit 14; Mediator complex subunit 14",
        "protein_names_refseq": "mediator complex subunit 14; mediator of RNA polymerase II transcription subunit 14-like",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Component of the Mediator complex, a coactivator involved in the regulated transcription of nearly all RNA polymerase II-dependent genes. Mediator functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery. Mediator is recruited to promoters by direct interactions with regulatory proteins and serves as a scaffold for the assembly of a functional preinitiation complex with RNA polymerase II and the general transcription factors., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_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_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003712 transcription coregulator activity",
        "go_cellular_component": "GO:0016592 mediator complex;GO:0070847 core mediator complex",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6A2B8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6A377-1",
        "uniprot_id": "A0A8I6A377_RAT",
        "mass": 15889.0,
        "length": 151,
        "protein_name": "Lymphocyte antigen 6 complex, locus A like 1",
        "gene_name": "Ly6al1",
        "organism": "Rat",
        "refseq_name": "lymphocyte antigen 6B isoform X1",
        "refseq_ac": "XP_017450736",
        "gene_names_uniprotkb": "Ly6al1; AABR07058441.1; LOC300024",
        "gene_names_refseq": "Ly6al1",
        "protein_names_uniprotkb": "Lymphocyte antigen 6 complex, locus A like 1",
        "protein_names_refseq": "lymphocyte antigen 6B isoform X1",
        "tax_id": 10116,
        "disease": "osteoporosis (Disease Ontology:DOID:11476)",
        "pathway": " (rno:300024)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 2,
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        "predicted_o_glycosites": 2,
        "predicted_c_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
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        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 2,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0033130 acetylcholine receptor binding;GO:0030550 acetylcholine receptor inhibitor activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0045202 synapse;GO:0098552 side of membrane",
        "go_biological_process": "GO:0095500 acetylcholine receptor signaling pathway",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6A377-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6A3K8-1",
        "uniprot_id": "A0A8I6A3K8_RAT",
        "mass": 33907.0,
        "length": 299,
        "protein_name": "Testis expressed 51",
        "gene_name": "Tex51",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Tex51",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Testis expressed 51",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
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        "predicted_glycosites": 0,
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        "protein_names_refseq": "large ribosomal subunit protein eL21-like",
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        "protein_name": "Olfactory receptor",
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        "pathway": " (R-RNO-173623);  (R-RNO-198933);  (R-RNO-202733);  (R-RNO-2029481);  (R-RNO-2029482);  (R-RNO-2029485);  (R-RNO-2168880);  (R-RNO-2454202);  (R-RNO-2730905);  (R-RNO-2871796);  (R-RNO-2871809);  (R-RNO-2871837);  (R-RNO-5690714);  (R-RNO-977606);  (R-RNO-983695)",
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        "refseq_ac": "NP_001414221",
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        "gene_names_refseq": "Gal3st2",
        "protein_names_uniprotkb": "Galactose-3-O-sulfotransferase 2C",
        "protein_names_refseq": "galactose-3-O-sulfotransferase 2",
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        "go_molecular_function": "GO:0050694 galactose 3-O-sulfotransferase activity;GO:0001733 galactosylceramide sulfotransferase activity",
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        "refseq_name": "tubulin polyglutamylase TTLL11 isoform X1",
        "refseq_ac": "XP_017447625",
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        "gene_names_refseq": "Ttll11",
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        "protein_names_refseq": "tubulin polyglutamylase TTLL11 isoform X1",
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        "protein_name": "Vomeronasal type-1 receptor",
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        "protein_names_refseq": "vomernasal 1 receptor Vom1r76; vomeronasal 1 receptor 76; vomeronasal 1 receptor, C27; vomeronasal V1r-type receptor V1rc27; vomeronasal type-1 receptor 100",
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        "protein_name": "Progestin and adipoQ receptor family member 5",
        "gene_name": "Paqr5",
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        "protein_names_uniprotkb": "Progestin and adipoQ receptor family member 5",
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        "go_molecular_function": "GO:0046872 metal ion binding",
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        "uniprot_canonical_ac": "A0A8I6AFM0-1",
        "uniprot_id": "A0A8I6AFM0_RAT",
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        "length": 1938,
        "protein_name": "Myosin heavy chain 13",
        "gene_name": "Myh13",
        "organism": "Rat",
        "refseq_name": "myosin-13",
        "refseq_ac": "NP_001414391",
        "gene_names_uniprotkb": "Myh13",
        "gene_names_refseq": "MHCEO; MyHC; Myh13",
        "protein_names_uniprotkb": "Myosin heavy chain 13",
        "protein_names_refseq": "myosin heavy polypeptide 13; myosin, heavy chain 13, skeletal muscle; myosin, heavy polypeptide 13, skeletal muscle; myosin-13",
        "tax_id": 10116,
        "disease": "distal arthrogryposis (Disease Ontology:DOID:0050646); cardiomyopathy (Disease Ontology:DOID:0050700); familial hypertrophic cardiomyopathy (Disease Ontology:DOID:0080326); congenital myopathy 6 (Disease Ontology:DOID:0080719); dilated cardiomyopathy 1S (Disease Ontology:DOID:0110454); autosomal dominant hyaline body myopathy (Disease Ontology:DOID:0111269); distal arthrogryposis type 1 (Disease Ontology:DOID:0111596); distal arthrogryposis type 2B3 (Disease Ontology:DOID:0111602); distal arthrogryposis type 2A (Disease Ontology:DOID:0111605); distal myopathy (Disease Ontology:DOID:11720); dilated cardiomyopathy (Disease Ontology:DOID:12930); myotonia congenita (Disease Ontology:DOID:2106); inclusion body myositis (Disease Ontology:DOID:3429); restrictive cardiomyopathy (Disease Ontology:DOID:397); myopathy (Disease Ontology:DOID:423)",
        "pathway": " (rno:103693367)",
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        "function": "Muscle contraction., [UniProtKB, UniProtKB, UniProtKB]",
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        "length": 308,
        "protein_name": "Olfactory receptor",
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        "refseq_ac": "NP_001414359",
        "gene_names_uniprotkb": "Tcf7",
        "gene_names_refseq": "Tcf7",
        "protein_names_uniprotkb": "Transcription factor 7; T-cell-specific transcription factor 1",
        "protein_names_refseq": "transcription factor 7 (T-cell specific, HMG-box); transcription factor 7, T-cell specific; transcription factor 7",
        "tax_id": 10116,
        "disease": "prostate cancer (Disease Ontology:DOID:10283); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (rno:363595);  (R-RNO-201722);  (R-RNO-3769402);  (R-RNO-4641265);  (R-RNO-8951430);  (R-RNO-9825892)",
        "pathway_count": 6,
        "publication_count": 1,
        "publication_id_list": "22673903",
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        "function": "",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0000976 transcription cis-regulatory region binding;GO:0008013 beta-catenin binding;GO:0003677 DNA binding;GO:0003700 DNA-binding transcription factor activity;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005634 nucleus;GO:0000785 chromatin;GO:0000791 euchromatin;GO:1990907 beta-catenin-TCF complex",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0016055 Wnt signaling pathway;GO:0009888 tissue development;GO:0071353 cellular response to interleukin-4;GO:0048619 embryonic hindgut morphogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A8I6ASU6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6A165-1",
        "uniprot_id": "A0A8I6A165_RAT",
        "mass": 55346.0,
        "length": 493,
        "protein_name": "non-specific serine/threonine protein kinase",
        "gene_name": "LOC134479830; Smokl4; Smokl8",
        "organism": "Rat",
        "refseq_name": "putative sperm motility kinase W",
        "refseq_ac": "XP_063120642",
        "gene_names_uniprotkb": "LOC134479830; Smokl4; Smokl8; LOC120093114; Smokl8",
        "gene_names_refseq": "Smokl4",
        "protein_names_uniprotkb": "non-specific serine/threonine protein kinase; 2.7.11.1",
        "protein_names_refseq": "putative sperm motility kinase W",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:120093114)",
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        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "May play a role in sperm motility, especially in the regulation of flagellar function., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "ec_number_list": "2.7.11.1;2.7.12.1;2.7.1.153;2.7.1.137;2.7.11.24;2.7.11.25;2.7.11.22;2.7.11.23;2.7.4.6;2.7.1.154;2.7.11.38;2.7.11.17;2.7.11.21;2.7.12.2;2.7.1.40;2.7.11.12;2.7.11.26;2.7.11.34;2.7.10.2;2.7.1.150;2.7.11.13;4.1.1.32;2.7.11.19;2.7.2.3;2.7.11.11;2.7.11.31;3.1.3.16;2.7.11.4;2.3.1.48;3.1.11.-;2.7.13.3;2.7.4.18;3.1.24.-;3.4.19.12;2.7.11.39;2.4.99.18;2.7.11.10",
        "go_molecular_function": "GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding;GO:0050321 tau-protein kinase activity",
        "go_cellular_component": "GO:0005737 cytoplasm",
        "go_biological_process": "GO:0035556 intracellular signal transduction;GO:0000226 microtubule cytoskeleton organization",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6A165-1",
        "record_type": "protein"
    },
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        "uniprot_canonical_ac": "M0R4Z8-1",
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        "length": 284,
        "protein_name": "Glutamine amidotransferase-like class 1 domain-containing protein 1",
        "gene_name": "Gatd1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Gatd1; Pddc1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Glutamine amidotransferase-like class 1 domain-containing protein 1; Ferry endosomal RAB5 effector complex subunit 5; Parkinson disease 7 domain-containing protein 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
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        "publication_id_list": "",
        "class_list": "",
        "function": "Component of the FERRY complex (Five-subunit Endosomal Rab5 and RNA/ribosome intermediary). The FERRY complex directly interacts with mRNAs and RAB5A, and functions as a RAB5A effector involved in the localization and the distribution of specific mRNAs most likely by mediating their endosomal transport. The complex recruits mRNAs and ribosomes to early endosomes through direct mRNA-interaction., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
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        "ec_number_list": "",
        "go_molecular_function": "GO:0019172 glyoxalase III activity",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0005769 early endosome;GO:0005654 nucleoplasm;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0019243 methylglyoxal catabolic process to D-lactate via S-lactoyl-glutathione",
        "synthesized_glycan_count": 0,
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        "record_id": "M0R4Z8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6A0A7-1",
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        "protein_name": "ZNRD1 antisense RNA 1",
        "gene_name": "Znrd1as1",
        "organism": "Rat",
        "refseq_name": "ZNRD1 antisense RNA 1 isoform X1",
        "refseq_ac": "XP_006255939",
        "gene_names_uniprotkb": "Znrd1as1",
        "gene_names_refseq": "RGD1564067; Tcte4; Tctex4; Znrd1as1; Znrd1as",
        "protein_names_uniprotkb": "ZNRD1 antisense RNA 1",
        "protein_names_refseq": "ZNRD1 antisense RNA 1 isoform X1",
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    },
    {
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        "length": 1050,
        "protein_name": "FHF complex subunit HOOK interacting protein 1A",
        "gene_name": "Fhip1a",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Fhip1a",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "FHF complex subunit HOOK interacting protein 1A",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (rno:365834)",
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        "go_molecular_function": "",
        "go_cellular_component": "",
        "go_biological_process": "GO:1905719 protein localization to perinuclear region of cytoplasm",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6GM32-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6AS56-1",
        "uniprot_id": "A0A8I6AS56_RAT",
        "mass": 37379.0,
        "length": 342,
        "protein_name": "sn-1-specific diacylglycerol lipase ABHD11",
        "gene_name": "Abhd11",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Abhd11; Abhd11l1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "sn-1-specific diacylglycerol lipase ABHD11; 3.1.1.116; Alpha/beta hydrolase domain-containing protein 11",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:360831)",
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        "function": "Catalyzes the hydrolysis of diacylglycerol in vitro and may function as a key regulator in lipid metabolism, namely by regulating the intracellular levels of diacylglycerol. 1,2-diacyl-sn-glycerols are the preferred substrate over 1,3-diacyl-sn-glycerols. The enzyme hydrolyzes stearate in preference to palmitate from the sn-1 position of 1,2-diacyl-sn-glycerols. Maintains the functional lipoylation of the 2-oxoglutarate dehydrogenase complex (OGDHc) through its interaction with the OGDHc by preventing the formation of lipoyl adducts. In addition, is also required for the expansion and differentiation of embryonic stem cells (ESCs)., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "ec_number_list": "3.1.1.116;3.1.1.3;3.1.1.26",
        "go_molecular_function": "GO:0016298 lipase activity;GO:0052689 carboxylic ester hydrolase activity",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005759 mitochondrial matrix;GO:0045252 oxoglutarate dehydrogenase complex",
        "go_biological_process": "GO:0006629 lipid metabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6AS56-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5Y6C5-1",
        "uniprot_id": "A0A8I5Y6C5_RAT",
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        "length": 537,
        "protein_name": "SH2 domain-containing adapter protein E",
        "gene_name": "She",
        "organism": "Rat",
        "refseq_name": "SH2 domain-containing adapter protein E isoform X1",
        "refseq_ac": "XP_063138791",
        "gene_names_uniprotkb": "She",
        "gene_names_refseq": "She",
        "protein_names_uniprotkb": "SH2 domain-containing adapter protein E",
        "protein_names_refseq": "SH2 domain-containing adapter protein E isoform X1",
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        "pathway": " (rno:685088)",
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        "go_molecular_function": "GO:0001784 phosphotyrosine residue binding",
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    },
    {
        "uniprot_canonical_ac": "A0A8I6GC89-1",
        "uniprot_id": "A0A8I6GC89_RAT",
        "mass": 21603.0,
        "length": 201,
        "protein_name": "Cripto, FRL-1, cryptic family 1",
        "gene_name": "Cfc1",
        "organism": "Rat",
        "refseq_name": "cryptic protein",
        "refseq_ac": "NP_001102774",
        "gene_names_uniprotkb": "Cfc1",
        "gene_names_refseq": "Cfc1; RGD1562188",
        "protein_names_uniprotkb": "Cripto, FRL-1, cryptic family 1",
        "protein_names_refseq": "cripto, FRL-1, cryptic family 1; cryptic protein",
        "tax_id": 10116,
        "disease": "visceral heterotaxy (Disease Ontology:DOID:0050545); visceral heterotaxy 2 (Disease Ontology:DOID:0051017); dextro-looped transposition of the great arteries (Disease Ontology:DOID:0060770); right atrial isomerism (Disease Ontology:DOID:0060856); double outlet right ventricle (Disease Ontology:DOID:6406); tetralogy of Fallot (Disease Ontology:DOID:6419)",
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        "disease": "Alzheimer's disease (Disease Ontology:DOID:10652); cystic fibrosis (Disease Ontology:DOID:1485); multiple sclerosis (Disease Ontology:DOID:2377); larynx cancer (Disease Ontology:DOID:2596); asthma (Disease Ontology:DOID:2841); high grade glioma (Disease Ontology:DOID:3070); osteosarcoma (Disease Ontology:DOID:3347); meningioma (Disease Ontology:DOID:3565); macular degeneration (Disease Ontology:DOID:4448); pulmonary emphysema (Disease Ontology:DOID:9675); obesity (Disease Ontology:DOID:9970)",
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        "biomarker_type": "",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005776 autophagosome",
        "go_biological_process": "GO:0006915 apoptotic process;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006357 regulation of transcription by RNA polymerase II;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0010468 regulation of gene expression",
        "synthesized_glycan_count": 0,
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    },
    {
        "uniprot_canonical_ac": "A0A8I5ZND3-1",
        "uniprot_id": "A0A8I5ZND3_RAT",
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        "length": 837,
        "protein_name": "V-type proton ATPase subunit a",
        "gene_name": "Tcirg1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Tcirg1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "V-type proton ATPase subunit a",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "autosomal recessive osteopetrosis 1 (Disease Ontology:DOID:0110942); clubfoot (Disease Ontology:DOID:11836); renal tubular acidosis (Disease Ontology:DOID:14219); Parkinson's disease (Disease Ontology:DOID:14330)",
        "pathway": " (R-RNO-1222556);  (R-RNO-6798695);  (R-RNO-77387);  (R-RNO-917977);  (R-RNO-9639288);  (R-RNO-983712)",
        "pathway_count": 6,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Essential component of the vacuolar proton pump (V-ATPase), a multimeric enzyme that catalyzes the translocation of protons across the membranes. Required for assembly and activity of the V-ATPase., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 2,
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        "go_molecular_function": "GO:0046961 proton-transporting ATPase activity, rotational mechanism;GO:0051117 ATPase binding;GO:0015078 proton transmembrane transporter activity",
        "go_cellular_component": "GO:0000220 vacuolar proton-transporting V-type ATPase, V0 domain;GO:0005634 nucleus;GO:0005886 plasma membrane;GO:0005764 lysosome;GO:0016324 apical plasma membrane",
        "go_biological_process": "GO:0030316 osteoclast differentiation;GO:0035711 T-helper 1 cell activation;GO:0010155 regulation of proton transport;GO:0090383 phagosome acidification;GO:0000045 autophagosome assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
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    },
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        "uniprot_canonical_ac": "M0R3J8-1",
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        "length": 481,
        "protein_name": "REST corepressor 1",
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        "organism": "Rat",
        "refseq_name": "REST corepressor 1",
        "refseq_ac": "NP_001402060",
        "gene_names_uniprotkb": "Rcor1; LOC102554884",
        "gene_names_refseq": "RGD1305743; Rcor1",
        "protein_names_uniprotkb": "REST corepressor 1",
        "protein_names_refseq": "Mtfp1-like proline rich protein; REST corepressor 1",
        "tax_id": 10116,
        "disease": "Alzheimer's disease (Disease Ontology:DOID:10652)",
        "pathway": " (rno:102554884);  (R-RNO-3214815);  (R-RNO-983231)",
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        "publication_count": 2,
        "publication_id_list": "22673903;37978036",
        "class_list": "",
        "function": "RCOR1 improves neurobehaviors and neuron injury in rat cerebral palsy by Endothelin-1 targeting-induced Akt/GSK-3beta pathway upregulation., [RefSeq, PubMed]",
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        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0045892 negative regulation of DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0010629 negative regulation of gene expression;GO:0030218 erythrocyte differentiation",
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        "length": 678,
        "protein_name": "Cation channel sperm-associated protein 1",
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        "refseq_name": "cation channel sperm-associated protein 1 isoform 1",
        "refseq_ac": "NP_001419527",
        "gene_names_uniprotkb": "Catsper1",
        "gene_names_refseq": "Catsper1",
        "protein_names_uniprotkb": "Cation channel sperm-associated protein 1",
        "protein_names_refseq": "cation channel of sperm 1; cation channel sperm-associated protein 1 isoform 1; cation channel sperm-associated protein 1",
        "tax_id": 10116,
        "disease": "spermatogenic failure 7 (Disease Ontology:DOID:0070173)",
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        "publication_id_list": "22673903;23148924;31041823;33456575",
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        "function": "Down-regulation of the CatSper1 channel in epididymal spermatozoa likely contributes to the pathogenesis of asthenozoospermia, whereas up-regulation of the channel by SJS improves sperm motility., [RefSeq, PubMed]; Roles of CatSper channels in the pathogenesis of asthenozoospermia and the therapeutic effects of acupuncture-like treatment on asthenozoospermia. Publication Status: Online-Only, [RefSeq, PubMed]; The effect of clomiphene citrate and human chorionic gonadotropin on the expression of CatSper1, CatSper2, LHCGR, and SF1 genes, as well as the structural changes in testicular tissue of adult rats., [RefSeq, PubMed]",
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        "go_biological_process": "GO:0007283 spermatogenesis;GO:0030154 cell differentiation;GO:0030317 flagellated sperm motility;GO:0007342 fusion of sperm to egg plasma membrane involved in single fertilization;GO:0006816 calcium ion transport",
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        "record_type": "protein"
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        "length": 726,
        "protein_name": "small monomeric GTPase",
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        "refseq_name": "EF-hand calcium-binding domain-containing protein 4B isoform a",
        "refseq_ac": "NP_001418775",
        "gene_names_uniprotkb": "Cracr2a",
        "gene_names_refseq": "Cracr2a; Efcab4b; RGD1563719",
        "protein_names_uniprotkb": "small monomeric GTPase; 3.6.5.2",
        "protein_names_refseq": "EF-hand calcium binding domain 4B; EF-hand calcium-binding domain-containing protein 4B isoform a; EF-hand calcium-binding domain-containing protein 4B",
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        "ec_number_list": "3.6.5.2;3.6.1.1;3.6.5.-;3.6.5.3;2.3.2.27;2.3.2.5;2.7.11.1;3.6.5.5;2.7.1.35;3.6.1.5;3.4.24.34;3.2.1.17;3.5.3.1;2.3.1.16;2.3.1.9;2.3.1.155;3.4.23.5;1.4.3.22;1.4.3.-;3.1.3.48;3.1.21.-;3.5.1.3;3.6.1.-;2.7.10.2;3.4.19.9;3.6.5.4;1.8.3.2;3.2.1.166;3.6.1.6;3.2.1.18;3.4.18.1",
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        "go_biological_process": "GO:0051928 positive regulation of calcium ion transport;GO:0032237 activation of store-operated calcium channel activity;GO:0002115 store-operated calcium entry;GO:0016192 vesicle-mediated transport;GO:0045063 T-helper 1 cell differentiation",
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        "protein_name": "Vacuolar protein sorting 13 homolog C",
        "gene_name": "Vps13c",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Vps13c",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Vacuolar protein sorting 13 homolog C",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "cerebellar ataxia (Disease Ontology:DOID:0050753); choreaacanthocytosis (Disease Ontology:DOID:0050766); Parkinson's disease 23 (Disease Ontology:DOID:0060896); Cohen syndrome (Disease Ontology:DOID:0111590); autosomal recessive spinocerebellar ataxia 4 (Disease Ontology:DOID:0111611); Parkinson's disease (Disease Ontology:DOID:14330)",
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        "go_cellular_component": "GO:0005811 lipid droplet;GO:0005741 mitochondrial outer membrane;GO:0005829 cytosol;GO:0005764 lysosome;GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0006869 lipid transport;GO:1905090 negative regulation of type 2 mitophagy;GO:0045053 protein retention in Golgi apparatus;GO:0032868 response to insulin;GO:0007005 mitochondrion organization",
        "synthesized_glycan_count": 0,
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        "record_id": "A0A8I5ZMR7-1",
        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "A0A8I6GJC6-1",
        "uniprot_id": "A0A8I6GJC6_RAT",
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        "length": 1261,
        "protein_name": "Phospholipid-transporting ATPase",
        "gene_name": "Atp8b2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Atp8b2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Phospholipid-transporting ATPase; 7.6.2.1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "progressive familial intrahepatic cholestasis (Disease Ontology:DOID:0070221)",
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        "ec_number_list": "7.6.2.1",
        "go_molecular_function": "GO:0000287 magnesium ion binding;GO:0005524 ATP binding;GO:0016887 ATP hydrolysis activity;GO:0140345 phosphatidylcholine flippase activity;GO:0140326 ATPase-coupled intramembrane lipid transporter activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0016020 membrane;GO:0012505 endomembrane system;GO:0005794 Golgi apparatus;GO:0005886 plasma membrane",
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        "record_id": "A0A8I6GJC6-1",
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    {
        "uniprot_canonical_ac": "A0A8I6ASV5-1",
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        "length": 421,
        "protein_name": "Solute carrier family 35, member F3",
        "gene_name": "Slc35f3",
        "organism": "Rat",
        "refseq_name": "solute carrier family 35, member F3 isoform 2",
        "refseq_ac": "NP_001418897",
        "gene_names_uniprotkb": "Slc35f3; LOC679321",
        "gene_names_refseq": "Slc35f3",
        "protein_names_uniprotkb": "Solute carrier family 35, member F3",
        "protein_names_refseq": "putative thiamine transporter SLC35F3; solute carrier family 35, member F3 isoform 2",
        "tax_id": 10116,
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        "gene_names_uniprotkb": "ENSRNOG00000065205; Zfp715-ps1; Zfp715-ps1",
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    },
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        "protein_name": "Guanine nucleotide-binding protein subunit alpha",
        "gene_name": "Gna14",
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        "gene_names_uniprotkb": "Gna14",
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        "protein_names_uniprotkb": "Guanine nucleotide-binding protein subunit alpha",
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        "tax_id": 10116,
        "disease": "McCune Albright syndrome (Disease Ontology:DOID:1858); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (R-RNO-112043);  (R-RNO-202040);  (R-RNO-399997);  (R-RNO-416476);  (R-RNO-418592);  (R-RNO-428930);  (R-RNO-434316);  (R-RNO-456926)",
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        "class_list": "",
        "function": "Guanine nucleotide-binding proteins (G proteins) are involved as modulators or transducers in various transmembrane signaling systems., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005834 heterotrimeric G-protein complex",
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    {
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        "length": 2215,
        "protein_name": "Myosin VIIA",
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        "refseq_name": "unconventional myosin-VIIa isoform X2",
        "refseq_ac": "XP_006229806",
        "gene_names_uniprotkb": "Myo7a",
        "gene_names_refseq": "Myo7a",
        "protein_names_uniprotkb": "Myosin VIIA",
        "protein_names_refseq": "unconventional myosin-VIIa isoform X2",
        "tax_id": 10116,
        "disease": "Usher syndrome type 1B (Disease Ontology:DOID:0070655); autosomal recessive nonsyndromic deafness 2 (Disease Ontology:DOID:0110477); autosomal dominant nonsyndromic deafness 11 (Disease Ontology:DOID:0110543); Usher syndrome type 1 (Disease Ontology:DOID:0110826); sensorineural hearing loss (Disease Ontology:DOID:10003); Leber congenital amaurosis (Disease Ontology:DOID:14791); auditory system disease (Disease Ontology:DOID:2742); congenital nystagmus (Disease Ontology:DOID:9649)",
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        "protein_names_uniprotkb": "Lymphocyte cytosolic protein 2; SH2 domain-containing leukocyte protein of 76 kDa; SLP-76 tyrosine phosphoprotein",
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        "tax_id": 10116,
        "disease": "immunodeficiency 81 (Disease Ontology:DOID:0061052)",
        "pathway": " (R-RNO-114604);  (R-RNO-202433);  (R-RNO-2424491);  (R-RNO-2871796);  (R-RNO-2871809)",
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        "go_molecular_function": "GO:0030674 protein-macromolecule adaptor activity",
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        "length": 440,
        "protein_name": "Palmitoyltransferase",
        "gene_name": "Zdhhc1",
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        "refseq_name": "palmitoyltransferase ZDHHC1 isoform 4",
        "refseq_ac": "NP_001421106",
        "gene_names_uniprotkb": "Zdhhc1",
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        "protein_names_uniprotkb": "Palmitoyltransferase; 2.3.1.225",
        "protein_names_refseq": "membrane-associated DHHC1 zinc finger protein; palmitoyltransferase ZDHHC1 isoform 4; probable palmitoyltransferase ZDHHC1; zinc finger, DHHC domain containing 1; zinc finger, DHHC-type containing 1",
        "tax_id": 10116,
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        "publication_id_list": "23687301",
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        "function": "In silico screening for palmitoyl substrates reveals a role for DHHC1/3/10 (zDHHC1/3/11)-mediated neurochondrin palmitoylation in its targeting to Rab5-positive endosomes., [RefSeq, PubMed]",
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        "ec_number_list": "2.3.1.225;2.3.1.-;6.3.1.2",
        "go_molecular_function": "GO:0019706 protein-cysteine S-palmitoyltransferase activity;GO:0016409 palmitoyltransferase activity",
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        "go_biological_process": "GO:1905668 positive regulation of protein localization to endosome;GO:0006612 protein targeting to membrane;GO:0002230 positive regulation of defense response to virus by host;GO:0032461 positive regulation of protein oligomerization;GO:1900227 positive regulation of NLRP3 inflammasome complex assembly",
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        "protein_name": "Hematopoietic lineage cell-specific protein",
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        "organism": "Rat",
        "refseq_name": "hematopoietic lineage cell-specific protein",
        "refseq_ac": "NP_001011898",
        "gene_names_uniprotkb": "Hcls1",
        "gene_names_refseq": "Hcls1",
        "protein_names_uniprotkb": "Hematopoietic lineage cell-specific protein; Hematopoietic cell-specific LYN substrate 1; LckBP1",
        "protein_names_refseq": "hematopoietic lineage cell-specific protein",
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        "function": "Substrate of the antigen receptor-coupled tyrosine kinase. Plays a role in antigen receptor signaling for both clonal expansion and deletion in lymphoid cells. May also be involved in the regulation of gene expression., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0017124 SH3 domain binding;GO:0019901 protein kinase binding;GO:0051015 actin filament binding;GO:0044877 protein-containing complex binding;GO:0035591 signaling adaptor activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0005667 transcription regulator complex",
        "go_biological_process": "GO:0030854 positive regulation of granulocyte differentiation;GO:0042307 positive regulation of protein import into nucleus;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0007015 actin filament organization;GO:0008284 positive regulation of cell population proliferation",
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        "refseq_name": "transmembrane protein 128",
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        "gene_names_uniprotkb": "Tmem128",
        "gene_names_refseq": "RGD1310481; Tmem128",
        "protein_names_uniprotkb": "Transmembrane protein 128",
        "protein_names_refseq": "transmembrane protein 128",
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    {
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        "length": 538,
        "protein_name": "RING finger protein 37",
        "gene_name": "Ubox5",
        "organism": "Rat",
        "refseq_name": "RING finger protein 37",
        "refseq_ac": "NP_001029169",
        "gene_names_uniprotkb": "Ubox5",
        "gene_names_refseq": "RGD1305440; Ubox5",
        "protein_names_uniprotkb": "RING finger protein 37; 2.3.2.27; RING-type E3 ubiquitin transferase RNF37; U-box domain-containing protein 5; UbcM4-interacting protein 5",
        "protein_names_refseq": "RING finger protein 37",
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        "function": "May have a ubiquitin-protein ligase activity acting as an E3 ubiquitin-protein ligase or as a ubiquitin-ubiquitin ligase promoting elongation of ubiquitin chains on substrates., [UniProtKB, UniProtKB]",
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        "protein_name": "Leucine-rich alpha-2-glycoprotein 1",
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        "gene_names_uniprotkb": "Lrg1",
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        "gene_names_refseq": "Dmwd; Hn1-ps1; Rshl1; Rsph6a",
        "protein_names_uniprotkb": "Radial spoke head 6 homolog A",
        "protein_names_refseq": "dystrophia myotonica-containing WD repeat motif; hematological and neurological expressed 1 (Hn1-ps1) pseudogene; radial spoke head protein 6 homolog A isoform 1; radial spoke head protein 6 homolog A; radial spoke head-like protein 1; radial spokehead-like 1",
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        "mass": 38055.0,
        "length": 347,
        "protein_name": "Sirtuin 3",
        "gene_name": "Sirt3",
        "organism": "Rat",
        "refseq_name": "NAD-dependent protein deacetylase sirtuin-3, mitochondrial isoform X1",
        "refseq_ac": "XP_063142583",
        "gene_names_uniprotkb": "Sirt3",
        "gene_names_refseq": "Sirt3",
        "protein_names_uniprotkb": "Sirtuin 3",
        "protein_names_refseq": "NAD-dependent protein deacetylase sirtuin-3, mitochondrial isoform X1",
        "tax_id": 10116,
        "disease": "abdominal obesity-metabolic syndrome (Disease Ontology:DOID:0060611); metabolic dysfunction-associated steatotic liver disease (Disease Ontology:DOID:0080208); Alzheimer's disease (Disease Ontology:DOID:10652); prediabetes syndrome (Disease Ontology:DOID:11716); myocardial infarction (Disease Ontology:DOID:5844); congestive heart failure (Disease Ontology:DOID:6000); type 2 diabetes mellitus (Disease Ontology:DOID:9352); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (R-RNO-2151201);  (R-RNO-9617629);  (R-RNO-9841251);  (R-RNO-9854311)",
        "pathway_count": 4,
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        "publication_id_list": "39261577",
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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:0019899 enzyme binding;GO:0070403 NAD+ binding;GO:0043565 sequence-specific DNA binding;GO:0017136 histone deacetylase activity, NAD-dependent",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005739 mitochondrion;GO:0005743 mitochondrial inner membrane;GO:0005759 mitochondrial matrix",
        "go_biological_process": "GO:1902553 positive regulation of catalase activity;GO:0032024 positive regulation of insulin secretion;GO:2000378 negative regulation of reactive oxygen species metabolic process;GO:0070373 negative regulation of ERK1 and ERK2 cascade;GO:1903862 positive regulation of oxidative phosphorylation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "A0A8I5XWT5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5Y0D9-1",
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        "length": 101,
        "protein_name": "ATPase inhibitor, mitochondrial",
        "gene_name": "ENSRNOG00000062699",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "ENSRNOG00000062699",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "ATPase inhibitor, mitochondrial; ATP synthase F1 subunit epsilon",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
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        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Endogenous F(1)F(o)-ATPase inhibitor limiting ATP depletion when the mitochondrial membrane potential falls below a threshold and the F(1)F(o)-ATP synthase starts hydrolyzing ATP to pump protons out of the mitochondrial matrix. Required to avoid the consumption of cellular ATP when the F(1)F(o)-ATP synthase enzyme acts as an ATP hydrolase. Indirectly acts as a regulator of heme synthesis in erythroid tissues: regulates heme synthesis by modulating the mitochondrial pH and redox potential, allowing FECH to efficiently catalyze the incorporation of iron into protoporphyrin IX to produce heme., [UniProtKB, UniProtKB]; Indirectly acts as a regulator of heme synthesis in erythroid tissues: regulates heme synthesis by modulating the mitochondrial pH and redox potential, allowing fech to efficiently catalyze the incorporation of iron into protoporphyrin IX to produce heme., [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:0042030 ATPase inhibitor activity",
        "go_cellular_component": "GO:0005739 mitochondrion",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I5Y0D9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5Y0R4-1",
        "uniprot_id": "A0A8I5Y0R4_RAT",
        "mass": 69974.0,
        "length": 615,
        "protein_name": "EF-hand calcium-binding domain-containing protein 7",
        "gene_name": "Efcab7",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Efcab7",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "EF-hand calcium-binding domain-containing protein 7",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
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        "publication_id_list": "",
        "class_list": "",
        "function": "Component of the EvC complex that positively regulates ciliary Hedgehog (Hh) signaling. Required for the localization of the EVC2:EVC subcomplex at the base of primary cilia., [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:0005509 calcium ion binding",
        "go_cellular_component": "GO:0009898 cytoplasmic side of plasma membrane;GO:0060170 ciliary membrane;GO:0098797 plasma membrane protein complex",
        "go_biological_process": "GO:0042307 positive regulation of protein import into nucleus;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0008589 regulation of smoothened signaling pathway;GO:1903569 positive regulation of protein localization to ciliary membrane;GO:0120229 protein localization to motile cilium",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I5Y0R4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5Y101-1",
        "uniprot_id": "A0A8I5Y101_RAT",
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        "length": 315,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or8h7",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr522",
        "refseq_ac": "NP_001000562",
        "gene_names_uniprotkb": "Or8h7; Or8h7b",
        "gene_names_refseq": "Olr522; Or8h7b; ratchr3-70010454-70009507_ORF",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 522; olfactory receptor Olr522; olfactory receptor gene Olr522",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:295776);  (rno:366100)",
        "pathway_count": 2,
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        "publication_id_list": "",
        "class_list": "",
        "function": "Odorant receptor., [UniProtKB, UniProtKB, UniProtKB]; Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell",
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        "hit_score": 0.1,
        "record_id": "A0A8I5Y101-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5Y1U6-1",
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        "length": 360,
        "protein_name": "TDPOZ2",
        "gene_name": "LOC134485749",
        "organism": "Rat",
        "refseq_name": "TD and POZ domain-containing protein 5-like",
        "refseq_ac": "XP_063138845",
        "gene_names_uniprotkb": "LOC134485749",
        "gene_names_refseq": "LOC134485749",
        "protein_names_uniprotkb": "TDPOZ2",
        "protein_names_refseq": "TD and POZ domain-containing protein 5-like",
        "tax_id": 10116,
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        "pathway": " (rno:134485749)",
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        "secondary_ac_list": "",
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        "go_molecular_function": "GO:0031625 ubiquitin protein ligase binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process;GO:0030162 regulation of proteolysis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I5Y1U6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5Y6U5-1",
        "uniprot_id": "A0A8I5Y6U5_RAT",
        "mass": 19551.0,
        "length": 174,
        "protein_name": "Signal recognition particle 14 kDa protein",
        "gene_name": "Srp14",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Srp14",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Signal recognition particle 14 kDa protein; SRP14",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-1799339);  (R-RNO-6798695)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Component of the signal recognition particle (SRP) complex, a ribonucleoprotein complex that mediates the cotranslational targeting of secretory and membrane proteins to the endoplasmic reticulum (ER). SRP9 together with SRP14 and the Alu portion of the SRP RNA, constitutes the elongation arrest domain of SRP. The complex of SRP9 and SRP14 is required for SRP RNA binding., [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:0030942 endoplasmic reticulum signal peptide binding;GO:0008312 7S RNA binding",
        "go_cellular_component": "GO:0005786 signal recognition particle, endoplasmic reticulum targeting;GO:0005634 nucleus",
        "go_biological_process": "GO:0006614 SRP-dependent cotranslational protein targeting to membrane;GO:0045047 protein targeting to ER",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A8I5Y6U5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5Y7E5-1",
        "uniprot_id": "A0A8I5Y7E5_RAT",
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        "length": 89,
        "protein_name": "40S ribosomal protein S27-like",
        "gene_name": "ENSRNOG00000070133",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "ENSRNOG00000070133",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "40S ribosomal protein S27-like",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003723 RNA binding;GO:0008270 zinc ion binding;GO:0003735 structural constituent of ribosome",
        "go_cellular_component": "GO:0022627 cytosolic small ribosomal subunit",
        "go_biological_process": "GO:0006412 translation;GO:0000028 ribosomal small subunit assembly",
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        "hit_score": 0.1,
        "record_id": "A0A8I5Y7E5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5Y7L4-1",
        "uniprot_id": "A0A8I5Y7L4_RAT",
        "mass": 181993.0,
        "length": 1614,
        "protein_name": "DNA topoisomerase 2",
        "gene_name": "Top2b",
        "organism": "Rat",
        "refseq_name": "DNA topoisomerase 2-beta",
        "refseq_ac": "NP_001094328",
        "gene_names_uniprotkb": "Top2b",
        "gene_names_refseq": "Top2b",
        "protein_names_uniprotkb": "DNA topoisomerase 2; 5.6.2.2",
        "protein_names_refseq": "DNA topoisomerase 2-beta; topoisomerase (DNA) II beta; topoisomerase II beta",
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    },
    {
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        "protein_name": "60 kDa heat shock protein, mitochondrial",
        "gene_name": "ENSRNOG00000065699",
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        "gene_names_uniprotkb": "ENSRNOG00000065699",
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        "protein_names_uniprotkb": "60 kDa heat shock protein, mitochondrial; 5.6.1.7; 60 kDa chaperonin; Chaperonin 60; Heat shock protein 60",
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        "protein_names_refseq": "family with sequence similarity 128, member B; mitotic spindle organizing protein 2B; mitotic-spindle organizing protein 2B",
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        "protein_name": "DNA (cytosine-5-)-methyltransferase",
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        "protein_names_uniprotkb": "DNA (cytosine-5-)-methyltransferase; 2.1.1.37",
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        "protein_name": "RecQ-mediated genome instability protein 2",
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        "refseq_name": "RecQ mediated genome instability 2",
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        "gene_names_refseq": "RGD1563163; Rmi2",
        "protein_names_uniprotkb": "RecQ-mediated genome instability protein 2",
        "protein_names_refseq": "RMI2, RecQ mediated genome instability 2, homolog; RecQ mediated genome instability 2; recQ-mediated genome instability protein 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:497856);  (R-RNO-5685938);  (R-RNO-5685942);  (R-RNO-5693537);  (R-RNO-5693568);  (R-RNO-5693579);  (R-RNO-5693607);  (R-RNO-5693616);  (R-RNO-6804756);  (R-RNO-69473)",
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        "function": "Essential component of the RMI complex, a complex that plays an important role in the processing of homologous recombination intermediates. It is required to regulate sister chromatid segregation and to limit DNA crossover. Essential for the stability, localization, and function of BLM, TOP3A, and complexes containing BLM. In the RMI complex, it is required to target BLM to chromatin and stress-induced nuclear foci and mitotic phosphorylation of BLM., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003677 DNA binding",
        "go_cellular_component": "GO:0005829 cytosol;GO:0016607 nuclear speck;GO:0031422 RecQ family helicase-topoisomerase III complex",
        "go_biological_process": "GO:2000042 negative regulation of double-strand break repair via homologous recombination;GO:0006281 DNA repair;GO:0006260 DNA replication;GO:0000724 double-strand break repair via homologous recombination;GO:0033045 regulation of sister chromatid segregation",
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        "uniprot_canonical_ac": "A0A8I6A0G6-1",
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        "length": 404,
        "protein_name": "Keratin 33A",
        "gene_name": "Krt33a",
        "organism": "Rat",
        "refseq_name": "keratin, type I cuticular Ha3-I",
        "refseq_ac": "NP_001008757",
        "gene_names_uniprotkb": "Krt33a",
        "gene_names_refseq": "Ka27; Krt33a; RGD1306249",
        "protein_names_uniprotkb": "Keratin 33A",
        "protein_names_refseq": "keratin, type I cuticular Ha3-I; type I hair keratin KA27",
        "tax_id": 10116,
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        "pathway": " (rno:303527);  (R-RNO-6805567);  (R-RNO-6809371)",
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        "protein_names_refseq": "zinc finger protein 664; zinc finger protein 7; zinc finger protein Zfoc1",
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        "gene_names_uniprotkb": "ENSRNOG00000064141; LOC134482080",
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        "biomarker_type": "",
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane",
        "go_biological_process": "GO:0006644 phospholipid metabolic process;GO:0010976 positive regulation of neuron projection development;GO:0051491 positive regulation of filopodium assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6B5V9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZRZ0-1",
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        "length": 539,
        "protein_name": "Vang-like protein",
        "gene_name": "Vangl1",
        "organism": "Rat",
        "refseq_name": "vang-like protein 1 isoform X1",
        "refseq_ac": "XP_006233116",
        "gene_names_uniprotkb": "Vangl1",
        "gene_names_refseq": "Vangl1",
        "protein_names_uniprotkb": "Vang-like protein",
        "protein_names_refseq": "vang-like protein 1 isoform X1",
        "tax_id": 10116,
        "disease": "neural tube defect (Disease Ontology:DOID:0080074); caudal regression syndrome (Disease Ontology:DOID:0080700)",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0016328 lateral plasma membrane;GO:0005886 plasma membrane",
        "go_biological_process": "GO:0043473 pigmentation;GO:0120197 mucociliary clearance",
        "synthesized_glycan_count": 0,
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    },
    {
        "uniprot_canonical_ac": "A0A8I6AA59-1",
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        "length": 76,
        "protein_name": "Liver-expressed antimicrobial peptide 2",
        "gene_name": "Leap2",
        "organism": "Rat",
        "refseq_name": "liver-expressed antimicrobial peptide 2 precursor",
        "refseq_ac": "NP_001380270",
        "gene_names_uniprotkb": "Leap2",
        "gene_names_refseq": "Ac1177; Leap2",
        "protein_names_uniprotkb": "Liver-expressed antimicrobial peptide 2",
        "protein_names_refseq": "liver-expressed antimicrobial peptide 2 precursor; liver-expressed antimicrobial peptide 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:497901)",
        "pathway_count": 1,
        "publication_count": 2,
        "publication_id_list": "35159134;36076912",
        "class_list": "",
        "function": "Has an antimicrobial activity., [UniProtKB, UniProtKB]; LEAP-2 Counteracts Ghrelin-Induced Food Intake in a Nutrient, Growth Hormone and Age Independent Manner. Publication Status: Online-Only, [RefSeq, PubMed]; Study of the Ghrelin/LEAP-2 Ratio in Humans and Rats during Different Phases of Pregnancy. Publication Status: Online-Only, [RefSeq, PubMed]",
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005576 extracellular region",
        "go_biological_process": "GO:0061844 antimicrobial humoral immune response mediated by antimicrobial peptide;GO:0042742 defense response to bacterium",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "A0A8I6AA59-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A0G2JT75-1",
        "uniprot_id": "A0A0G2JT75_RAT",
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        "length": 235,
        "protein_name": "STARD3 N-terminal like",
        "gene_name": "Stard3nl",
        "organism": "Rat",
        "refseq_name": "STARD3 N-terminal-like protein",
        "refseq_ac": "NP_001008299",
        "gene_names_uniprotkb": "Stard3nl",
        "gene_names_refseq": "Stard3nl",
        "protein_names_uniprotkb": "STARD3 N-terminal like",
        "protein_names_refseq": "MLN64 N-terminal domain homolog; MLN64 N-terminal homolog; STARD3 N-terminal-like protein",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:291182)",
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        "publication_count": 2,
        "publication_id_list": "15342684;22673903",
        "class_list": "",
        "function": "MLN64 has roles with StAR, and SCP-2 in regulating bile acid synthesis, [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0042803 protein homodimerization activity;GO:0015485 cholesterol binding",
        "go_cellular_component": "GO:0044232 organelle membrane contact site;GO:0005768 endosome;GO:0005789 endoplasmic reticulum membrane;GO:0031902 late endosome membrane;GO:0140284 endoplasmic reticulum-endosome membrane contact site",
        "go_biological_process": "GO:0099044 vesicle tethering to endoplasmic reticulum",
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        "record_id": "A0A0G2JT75-1",
        "record_type": "protein"
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        "length": 973,
        "protein_name": "Nonsense-mediated mRNA decay factor",
        "gene_name": "Smg5l1",
        "organism": "Rat",
        "refseq_name": "similar to Est1p-like protein B isoform 2",
        "refseq_ac": "NP_001333232",
        "gene_names_uniprotkb": "Smg5l1; AABR07057678.1; RGD1309489",
        "gene_names_refseq": "RGD1309489; Smg5l1",
        "protein_names_uniprotkb": "Nonsense-mediated mRNA decay factor",
        "protein_names_refseq": "similar to Est1p-like protein B isoform 2",
        "tax_id": 10116,
        "disease": "autism spectrum disorder (Disease Ontology:DOID:0060041); syndromic X-linked intellectual disability (Disease Ontology:DOID:0060309); syndromic X-linked intellectual disability Najm type (Disease Ontology:DOID:0060807); FG syndrome (Disease Ontology:DOID:14711)",
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        "function": "Plays a role in nonsense-mediated mRNA decay. Does not have RNase activity by itself. Promotes dephosphorylation of UPF1. Together with SMG7 is thought to provide a link to the mRNA degradation machinery involving exonucleolytic pathways, and to serve as an adapter for UPF1 to protein phosphatase 2A (PP2A), thereby triggering UPF1 dephosphorylation. Necessary for TERT activity., [UniProtKB, UniProtKB]",
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        "secondary_ac_list": "A0A8I6ADQ4",
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        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0000184 nuclear-transcribed mRNA catabolic process, nonsense-mediated decay",
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        "record_id": "A0A8I5ZUK4-1",
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    {
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        "length": 904,
        "protein_name": "Toll-like receptor 12",
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        "organism": "Rat",
        "refseq_name": "toll-like receptor 12 precursor",
        "refseq_ac": "NP_001102152",
        "gene_names_uniprotkb": "Tlr12",
        "gene_names_refseq": "RGD1559145; Tlr12",
        "protein_names_uniprotkb": "Toll-like receptor 12",
        "protein_names_refseq": "toll-like receptor 12 precursor",
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        "pathway": " (rno:362604)",
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0016020 membrane",
        "go_biological_process": "GO:0006954 inflammatory response;GO:0007165 signal transduction;GO:0045087 innate immune response",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6AUA9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZQG2-1",
        "uniprot_id": "A0A8I5ZQG2_RAT",
        "mass": 46859.0,
        "length": 423,
        "protein_name": "Testican-2",
        "gene_name": "Spock2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Spock2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Testican-2; SPARC/osteonectin, CWCV, and Kazal-like domains proteoglycan 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:361840)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "May participate in diverse steps of neurogenesis. Binds calcium., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "go_molecular_function": "GO:0005509 calcium ion binding;GO:0005539 glycosaminoglycan binding;GO:0008191 metalloendopeptidase inhibitor activity;GO:0050840 extracellular matrix binding",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0031012 extracellular matrix",
        "go_biological_process": "GO:0010810 regulation of cell-substrate adhesion;GO:0030198 extracellular matrix organization;GO:1990830 cellular response to leukemia inhibitory factor;GO:0010811 positive regulation of cell-substrate adhesion",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A8I5ZQG2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6AF06-1",
        "uniprot_id": "A0A8I6AF06_RAT",
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        "length": 810,
        "protein_name": "Family with sequence similarity 193, member B",
        "gene_name": "Fam193b",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Fam193b",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Family with sequence similarity 193, member B",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway": " (rno:498703)",
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        "biomarker_type": "",
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005737 cytoplasm",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6AF06-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZVY3-1",
        "uniprot_id": "A0A8I5ZVY3_RAT",
        "mass": 24898.0,
        "length": 224,
        "protein_name": "GrpE protein homolog",
        "gene_name": "Grpel2",
        "organism": "Rat",
        "refseq_name": "grpE protein homolog 2, mitochondrial",
        "refseq_ac": "NP_001102983",
        "gene_names_uniprotkb": "Grpel2",
        "gene_names_refseq": "Afap1l1; Grpel2",
        "protein_names_uniprotkb": "GrpE protein homolog",
        "protein_names_refseq": "AFAP1-like protein 1; actin filament-associated protein 1-like 1; grpE protein homolog 2, mitochondrial",
        "tax_id": 10116,
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        "pathway": " (rno:688777)",
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        "publication_id_list": "",
        "class_list": "",
        "function": "Essential component of the PAM complex, a complex required for the translocation of transit peptide-containing proteins from the inner membrane into the mitochondrial matrix in an ATP-dependent manner. Seems to control the nucleotide-dependent binding of mitochondrial HSP70 to substrate proteins. Stimulates ATPase activity of mt-HSP70. May also serve to modulate the interconversion of oligomeric (inactive) and monomeric (active) forms of mt-HSP70., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
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        "predicted_s_glycosites": 0,
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        "mined_s_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0042803 protein homodimerization activity;GO:0051087 protein-folding chaperone binding;GO:0000774 adenyl-nucleotide exchange factor activity;GO:0051082 unfolded protein binding",
        "go_cellular_component": "GO:0005759 mitochondrial matrix;GO:0001405 PAM complex, Tim23 associated import motor;GO:0005739 mitochondrion",
        "go_biological_process": "GO:0006457 protein folding;GO:0030150 protein import into mitochondrial matrix",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I5ZVY3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6AG30-1",
        "uniprot_id": "A0A8I6AG30_RAT",
        "mass": 13050.0,
        "length": 126,
        "protein_name": "Cyclin-dependent kinase 2 associated protein 2",
        "gene_name": "Cdk2ap2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Cdk2ap2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Cyclin-dependent kinase 2 associated protein 2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
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        "predicted_glycosites": 3,
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        "predicted_o_glycosites": 3,
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        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
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        "reported_c_glycosites_with_glycan": 0,
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        "total_n_glycosites": 0,
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        "total_c_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 3,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005874 microtubule;GO:0016581 NuRD complex",
        "go_biological_process": "GO:2000134 negative regulation of G1/S transition of mitotic cell cycle;GO:2000035 regulation of stem cell division;GO:0070507 regulation of microtubule cytoskeleton organization",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6AG30-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A0G2JYX9-1",
        "uniprot_id": "A0A0G2JYX9_RAT",
        "mass": 77987.0,
        "length": 711,
        "protein_name": "Interleukin-1 receptor-associated kinase 1",
        "gene_name": "Irak1",
        "organism": "Rat",
        "refseq_name": "interleukin-1 receptor-associated kinase 1 isoform X1",
        "refseq_ac": "XP_006229660",
        "gene_names_uniprotkb": "Irak1",
        "gene_names_refseq": "Irak1; RGD1563841",
        "protein_names_uniprotkb": "Interleukin-1 receptor-associated kinase 1; 2.7.11.1",
        "protein_names_refseq": "interleukin-1 receptor-associated kinase 1 isoform X1",
        "tax_id": 10116,
        "disease": "cognitive disorder (Disease Ontology:DOID:1561); diffuse scleroderma (Disease Ontology:DOID:1580); squamous cell carcinoma (Disease Ontology:DOID:1749); brain ischemia (Disease Ontology:DOID:2316); asthma (Disease Ontology:DOID:2841); pulmonary tuberculosis (Disease Ontology:DOID:2957); primary immunodeficiency disease (Disease Ontology:DOID:612); ankylosing spondylitis (Disease Ontology:DOID:7147); psoriasis (Disease Ontology:DOID:8893); psoriatic arthritis (Disease Ontology:DOID:9008)",
        "pathway": " (R-RNO-1257604);  (R-RNO-209543);  (R-RNO-209560);  (R-RNO-445989);  (R-RNO-450302);  (R-RNO-450321);  (R-RNO-6811558);  (R-RNO-9020702);  (R-RNO-937039);  (R-RNO-975144)",
        "pathway_count": 10,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
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        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
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        "total_reported_o_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 10,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "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;2.7.11.24;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;2.7.11.10;2.7.11.19;2.7.2.3;2.7.11.11;3.1.3.48;2.7.11.31;3.1.3.16;2.7.11.4;2.3.1.48;3.2.2.6;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;2.3.2.23;3.2.1.31",
        "go_molecular_function": "GO:0004674 protein serine/threonine kinase activity;GO:0005524 ATP binding;GO:0004672 protein kinase activity;GO:0019901 protein kinase binding;GO:0042802 identical protein binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005811 lipid droplet;GO:0005829 cytosol;GO:0016020 membrane;GO:0032991 protein-containing complex",
        "go_biological_process": "GO:0070498 interleukin-1-mediated signaling pathway;GO:0045087 innate immune response;GO:0006355 regulation of DNA-templated transcription;GO:0031663 lipopolysaccharide-mediated signaling pathway;GO:1902533 positive regulation of intracellular signal transduction",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A0G2JYX9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8J8XT05-1",
        "uniprot_id": "A0A8J8XT05_RAT",
        "mass": 61818.0,
        "length": 544,
        "protein_name": "Butyrophilin-like 8",
        "gene_name": "Btnl8",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Btnl8",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Butyrophilin-like 8",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
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        "pathway_count": 0,
        "publication_count": 0,
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        "class_list": "",
        "function": "",
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        "predicted_o_glycosites": 0,
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        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "reported_phosphosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0016020 membrane",
        "go_biological_process": "GO:0050776 regulation of immune response",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8J8XT05-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6ALT7-1",
        "uniprot_id": "A0A8I6ALT7_RAT",
        "mass": 106814.0,
        "length": 991,
        "protein_name": "Collagen alpha-2(VI) chain",
        "gene_name": "Col6a2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Col6a2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Collagen alpha-2(VI) chain",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "Ullrich congenital muscular dystrophy 1B (Disease Ontology:DOID:0060942); Bethlem myopathy 1A (Disease Ontology:DOID:0061198); Bethlem myopathy 1B (Disease Ontology:DOID:0061199); myocardial infarction (Disease Ontology:DOID:5844)",
        "pathway": " (R-RNO-1650814)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Collagen VI acts as a cell-binding protein., [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,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 4,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005518 collagen binding",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0005886 plasma membrane;GO:0031012 extracellular matrix;GO:0042383 sarcolemma;GO:0032991 protein-containing complex",
        "go_biological_process": "GO:0007155 cell adhesion;GO:0051402 neuron apoptotic process;GO:0009411 response to UV;GO:0009749 response to glucose;GO:0043491 phosphatidylinositol 3-kinase/protein kinase B signal transduction",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6ALT7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7ESG0-1",
        "uniprot_id": "F7ESG0_RAT",
        "mass": 47111.0,
        "length": 421,
        "protein_name": "Endonuclease 8-like 1",
        "gene_name": "Neil1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Neil1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Endonuclease 8-like 1; 4.2.99.18; DNA glycosylase/AP lyase Neil1; DNA-(apurinic or apyrimidinic site) lyase Neil1; Endonuclease VIII-like 1; Nei homolog 1; Nei-like protein 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "abdominal obesity-metabolic syndrome (Disease Ontology:DOID:0060611); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (rno:367090)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as a DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized pyrimidines, such as thymine glycol, formamidopyrimidine (Fapy) and 5-hydroxyuracil. Has marginal activity towards 8-oxoguanine. Has AP (apurinic/apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates. Has DNA glycosylase/lyase activity towards mismatched uracil and thymine, in particular in U:C and T:C mismatches. Specifically binds 5-hydroxymethylcytosine (5hmC), suggesting that it acts as a specific reader of 5hmC., [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_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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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 2,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0003684 damaged DNA binding;GO:0019104 DNA N-glycosylase activity;GO:0140078 class I DNA-(apurinic or apyrimidinic site) endonuclease activity;GO:0003906 DNA-(apurinic or apyrimidinic site) endonuclease activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0006284 base-excision repair;GO:0006281 DNA repair",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F7ESG0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6ASH2-1",
        "uniprot_id": "A0A8I6ASH2_RAT",
        "mass": 470266.0,
        "length": 4387,
        "protein_name": "Basement membrane-specific heparan sulfate proteoglycan core protein",
        "gene_name": "Hspg2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Hspg2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Basement membrane-specific heparan sulfate proteoglycan core protein; Perlecan",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "dextro-looped transposition of the great arteries (Disease Ontology:DOID:0060770); Schwartz-Jampel syndrome 1 (Disease Ontology:DOID:0090005); Silverman-Handmaker type dyssegmental dysplasia (Disease Ontology:DOID:0090032); hypertension (Disease Ontology:DOID:10763); thanatophoric dysplasia (Disease Ontology:DOID:13481); osteochondrodysplasia (Disease Ontology:DOID:2256); carotid artery disease (Disease Ontology:DOID:3407); hyperglycemia (Disease Ontology:DOID:4195)",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Anti-angiogenic and anti-tumor peptide that inhibits endothelial cell migration, collagen-induced endothelial tube morphogenesis and blood vessel growth in the chorioallantoic membrane. Blocks endothelial cell adhesion to fibronectin and type I collagen. Anti-tumor agent in neovascularization. Interaction with its ligand, integrin alpha2/beta1, is required for the anti-angiogenic properties. Evokes a reduction in phosphorylation of receptor tyrosine kinases via alpha2/beta1 integrin-mediated activation of the tyrosine phosphatase, PTPN6., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Has anti-angiogenic properties that require binding of calcium ions for full activity., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 5,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 5,
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        "mined_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,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 8,
        "glyco_site_count": 5,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005509 calcium ion binding;GO:0002020 protease binding;GO:0002162 dystroglycan binding;GO:0070052 collagen V binding;GO:0008046 axon guidance receptor activity",
        "go_cellular_component": "GO:0005796 Golgi lumen;GO:0005604 basement membrane;GO:0005886 plasma membrane;GO:0030424 axon;GO:0031012 extracellular matrix",
        "go_biological_process": "GO:0001525 angiogenesis;GO:0030154 cell differentiation;GO:0007420 brain development;GO:0007162 negative regulation of cell adhesion;GO:0008285 negative regulation of cell population proliferation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6ASH2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6AKV2-1",
        "uniprot_id": "A0A8I6AKV2_RAT",
        "mass": 208480.0,
        "length": 1932,
        "protein_name": "TP53-binding protein 1",
        "gene_name": "Tp53bp1",
        "organism": "Rat",
        "refseq_name": "TP53-binding protein 1",
        "refseq_ac": "NP_001358188",
        "gene_names_uniprotkb": "Tp53bp1",
        "gene_names_refseq": "Tp53bp1; Trp53bp1",
        "protein_names_uniprotkb": "TP53-binding protein 1",
        "protein_names_refseq": "TP53-binding protein 1; transformation related protein 53 binding protein 1; tumor suppressor p53-binding protein 1",
        "tax_id": 10116,
        "disease": "pulmonary hypertension (Disease Ontology:DOID:6432)",
        "pathway": " (rno:296099);  (R-RNO-3232118);  (R-RNO-5693565);  (R-RNO-5693571);  (R-RNO-5693607);  (R-RNO-69473)",
        "pathway_count": 6,
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        "publication_id_list": "22673903",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 2,
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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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        "disease_count": 1,
        "glyco_site_count": 2,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0140005 histone H4K20me2 reader activity;GO:0061649 ubiquitin-modified histone reader activity;GO:0003713 transcription coactivator activity;GO:0042393 histone binding",
        "go_cellular_component": "GO:0016604 nuclear body;GO:0000776 kinetochore;GO:0035861 site of double-strand break;GO:0005634 nucleus;GO:0005737 cytoplasm",
        "go_biological_process": "GO:2000042 negative regulation of double-strand break repair via homologous recombination;GO:0006351 DNA-templated transcription;GO:0006355 regulation of DNA-templated transcription;GO:0006303 double-strand break repair via nonhomologous end joining;GO:0045830 positive regulation of isotype switching",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A8I6AKV2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6GHT1-1",
        "uniprot_id": "A0A8I6GHT1_RAT",
        "mass": 24234.0,
        "length": 208,
        "protein_name": "Calcyphosine-like",
        "gene_name": "Capsl",
        "organism": "Rat",
        "refseq_name": "calcyphosin-like protein isoform X1",
        "refseq_ac": "XP_008758985",
        "gene_names_uniprotkb": "Capsl",
        "gene_names_refseq": "Capsl; RGD1308776",
        "protein_names_uniprotkb": "Calcyphosine-like",
        "protein_names_refseq": "calcyphosin-like protein isoform X1",
        "tax_id": 10116,
        "disease": "exudative vitreoretinopathy (Disease Ontology:DOID:0050535)",
        "pathway": " (rno:294795)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
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        "mined_s_glycosites": 0,
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        "reported_snv": 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:0005509 calcium ion binding",
        "go_cellular_component": "GO:0043226 organelle",
        "go_biological_process": "GO:0001525 angiogenesis;GO:0001570 vasculogenesis;GO:0060041 retina development in camera-type eye;GO:0043542 endothelial cell migration;GO:0001935 endothelial cell proliferation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6GHT1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZP99-1",
        "uniprot_id": "A0A8I5ZP99_RAT",
        "mass": 51149.0,
        "length": 463,
        "protein_name": "HEPACAM family member 2",
        "gene_name": "Hepacam2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Hepacam2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "HEPACAM family member 2; Mitotic kinetics regulator",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Required during prometaphase for centrosome maturation. Following poly-ADP-ribosylation (PARsylation) by TNKS, translocates from the Golgi apparatus to mitotic centrosomes and plays a key role in the formation of robust microtubules for prompt movement of chromosomes: anchors AKAP9/CG-NAP, a scaffold protein of the gamma-tubulin ring complex and promotes centrosome maturation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "reported_o_glycosites": 0,
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        "total_reported_n_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0012505 endomembrane system;GO:0005794 Golgi apparatus;GO:0005813 centrosome;GO:0005819 spindle",
        "go_biological_process": "GO:0007098 centrosome cycle",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I5ZP99-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8J8Y678-1",
        "uniprot_id": "A0A8J8Y678_RAT",
        "mass": 18416.0,
        "length": 161,
        "protein_name": "Ubiquitin-conjugating enzyme E2 G2",
        "gene_name": "Ube2g2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ube2g2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ubiquitin-conjugating enzyme E2 G2; 2.3.2.23; E2 ubiquitin-conjugating enzyme G2; Ubiquitin carrier protein G2; Ubiquitin-protein ligase G2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:294331);  (R-RNO-8866652);  (R-RNO-983168)",
        "pathway_count": 3,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Accepts ubiquitin from the E1 complex and catalyzes its covalent attachment to other proteins. In vitro catalyzes 'Lys-48'-linked polyubiquitination. Involved in endoplasmic reticulum-associated degradation (ERAD). Required for sterol-induced ubiquitination of 3-hydroxy-3-methylglutaryl coenzyme A reductase and its subsequent proteasomal degradation., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "total_reported_n_glycosites": 0,
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        "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;2.3.2.34;2.3.2.24;2.3.2.-;2.3.2.25;6.2.1.45;6.2.1.64",
        "go_molecular_function": "GO:0005524 ATP binding;GO:0042802 identical protein binding;GO:0004842 ubiquitin-protein transferase activity;GO:0061631 ubiquitin conjugating enzyme activity;GO:0016740 transferase activity",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005811 lipid droplet;GO:0005829 cytosol",
        "go_biological_process": "GO:0000209 protein polyubiquitination;GO:0006511 ubiquitin-dependent protein catabolic process;GO:0036503 ERAD pathway;GO:0070936 protein K48-linked ubiquitination;GO:0035458 cellular response to interferon-beta",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8J8Y678-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5YC43-1",
        "uniprot_id": "A0A8I5YC43_RAT",
        "mass": 133888.0,
        "length": 1191,
        "protein_name": "Zinc finger E-box-binding homeobox 2",
        "gene_name": "Zeb2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Zeb2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger E-box-binding homeobox 2; Smad-interacting protein 1; Zinc finger homeobox protein 1b",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "rheumatic heart disease (Disease Ontology:DOID:0050827); Mowat-Wilson syndrome (Disease Ontology:DOID:0060485); Hirschsprung's disease (Disease Ontology:DOID:10487); T-cell adult acute lymphocytic leukemia (Disease Ontology:DOID:5602); proteinuria (Disease Ontology:DOID:576); myocardial infarction (Disease Ontology:DOID:5844)",
        "pathway": " (rno:311071);  (R-RNO-9762293)",
        "pathway_count": 2,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Transcriptional inhibitor that binds to DNA sequence 5'-CACCT-3' in different promoters. Represses transcription of E-cadherin. Represses expression of MEOX2., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0003700 DNA-binding transcription factor activity;GO:0008270 zinc ion binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005694 chromosome;GO:0005730 nucleolus;GO:0000785 chromatin",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0048023 positive regulation of melanin biosynthetic process;GO:0030177 positive regulation of Wnt signaling pathway",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A8I5YC43-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F6PU86-1",
        "uniprot_id": "F6PU86_RAT",
        "mass": 39314.0,
        "length": 366,
        "protein_name": "RNA 3'-terminal phosphate cyclase",
        "gene_name": "Rtca",
        "organism": "Rat",
        "refseq_name": "RNA 3'-terminal phosphate cyclase",
        "refseq_ac": "NP_001004227",
        "gene_names_uniprotkb": "Rtca",
        "gene_names_refseq": "Rtca; Rtcd1",
        "protein_names_uniprotkb": "RNA 3'-terminal phosphate cyclase; 6.5.1.4; RNA terminal phosphate cyclase domain-containing protein 1",
        "protein_names_refseq": "RNA 3'-terminal phosphate cyclase; RNA terminal phosphate cyclase domain 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:295395)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Catalyzes the conversion of 3'-phosphate to a 2',3'-cyclic phosphodiester at the end of RNA. The mechanism of action of the enzyme occurs in 3 steps: (A) adenylation of the enzyme by ATP; (B) transfer of adenylate to an RNA-N3'P to produce RNA-N3'PP5'A; (C) and attack of the adjacent 2'-hydroxyl on the 3'-phosphorus in the diester linkage to produce the cyclic end product. Likely functions in some aspects of cellular RNA processing. Function plays an important role in regulating axon regeneration by inhibiting central nervous system (CNS) axon regeneration following optic nerve injury., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "6.5.1.4",
        "go_molecular_function": "GO:0005524 ATP binding;GO:0003963 RNA-3'-phosphate cyclase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0006396 RNA processing;GO:1905592 negative regulation of optical nerve axon regeneration",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F6PU86-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6B3Z0-1",
        "uniprot_id": "A0A8I6B3Z0_RAT",
        "mass": 115841.0,
        "length": 996,
        "protein_name": "TBC1 domain family member 31",
        "gene_name": "Tbc1d31",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Tbc1d31; Wdr67",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "TBC1 domain family member 31; WD repeat-containing protein 67",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:299949)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Molecular adapter which is involved in cilium biogenesis. Part of a functional complex including OFD1 a centriolar protein involved in cilium assembly. Could regulate the cAMP-dependent phosphorylation of OFD1, and its subsequent ubiquitination by PJA2 which ultimately leads to its proteasomal degradation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "function": "E3 ubiquitin ligase catalyzing the covalent attachment of ubiquitin moieties onto substrate proteins., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005829 cytosol;GO:0016020 membrane",
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    },
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        "length": 955,
        "protein_name": "Anoctamin",
        "gene_name": "Ano4",
        "organism": "Rat",
        "refseq_name": "anoctamin-4 isoform 1",
        "refseq_ac": "NP_001382654",
        "gene_names_uniprotkb": "Ano4",
        "gene_names_refseq": "Ano4; Tmem16d",
        "protein_names_uniprotkb": "Anoctamin",
        "protein_names_refseq": "anoctamin-4 isoform 1; chromosome alignment-maintaining phosphoprotein 1-like; transmembrane protein 16D (eight membrane-spanning domains)",
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        "go_molecular_function": "GO:0046983 protein dimerization activity;GO:0005229 intracellularly calcium-gated chloride channel activity;GO:0017128 phospholipid scramblase activity",
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        "go_biological_process": "GO:0045332 phospholipid translocation;GO:1902476 chloride transmembrane transport;GO:0061589 calcium activated phosphatidylserine scrambling;GO:0061590 calcium activated phosphatidylcholine scrambling;GO:0061591 calcium activated galactosylceramide scrambling",
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        "gene_names_refseq": "Celf3; RGD1563168; Tnrc4",
        "protein_names_uniprotkb": "CUGBP Elav-like family member 3; Bruno-like protein 1; CUG-BP- and ETR-3-like factor 3; ELAV-type RNA-binding protein 1; RNA-binding protein BRUNOL-1; Trinucleotide repeat-containing gene 4 protein",
        "protein_names_refseq": "CUGBP Elav-like family member 3 isoform X1",
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        "protein_name": "Protein unc-93 homolog B1",
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        "protein_names_uniprotkb": "Protein unc-93 homolog B1",
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        "function": "Plays an important role in innate and adaptive immunity by regulating nucleotide-sensing Toll-like receptor (TLR) signaling. Required for the transport of a subset of TLRs (including TLR3, TLR7 and TLR9) from the endoplasmic reticulum to endolysosomes where they can engage pathogen nucleotides and activate signaling cascades. May play a role in autoreactive B-cells removal., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "protein_name": "Forkhead box J3",
        "gene_name": "Foxj3",
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        "refseq_name": "forkhead box protein J3",
        "refseq_ac": "NP_001101441",
        "gene_names_uniprotkb": "Foxj3",
        "gene_names_refseq": "Foxj3",
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        "protein_names_refseq": "forkhead box protein J3",
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        "go_molecular_function": "GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0003700 DNA-binding transcription factor activity;GO:0043565 sequence-specific DNA binding;GO:0001228 DNA-binding transcription activator activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0007141 male meiosis I;GO:0007283 spermatogenesis;GO:0045944 positive regulation of transcription by RNA polymerase II",
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        "length": 1086,
        "protein_name": "Atos homolog protein A",
        "gene_name": "Atosa",
        "organism": "Rat",
        "refseq_name": "atos homolog protein A isoform 3",
        "refseq_ac": "NP_001423403",
        "gene_names_uniprotkb": "Atosa; Fam214a",
        "gene_names_refseq": "Atosa; Fam214a; RGD1310552",
        "protein_names_uniprotkb": "Atos homolog protein A",
        "protein_names_refseq": "atos homolog protein A isoform 3; atos homolog protein A; family with sequence similarity 214, member A",
        "tax_id": 10116,
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        "publication_id_list": "38843836",
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        "function": "Transcription regulator that syncronizes transcriptional and translational programs to promote macrophage invasion of tissues., [UniProtKB, UniProtKB, UniProtKB]",
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    {
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        "length": 400,
        "protein_name": "PHD finger protein 24",
        "gene_name": "Phf24",
        "organism": "Rat",
        "refseq_name": "PHD finger protein 24",
        "refseq_ac": "NP_001385764",
        "gene_names_uniprotkb": "Phf24; RGD1559864",
        "gene_names_refseq": "Phf24; RGD1559864",
        "protein_names_uniprotkb": "PHD finger protein 24",
        "protein_names_refseq": "Gai-interacting protein; PHD finger protein 24",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:500446)",
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        "publication_count": 2,
        "publication_id_list": "22673903;33115988",
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        "function": "PHF24 is expressed in the inhibitory interneurons in rats., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0008270 zinc ion binding",
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        "go_biological_process": "GO:0007214 gamma-aminobutyric acid signaling pathway;GO:0050966 detection of mechanical stimulus involved in sensory perception of pain;GO:0032228 regulation of synaptic transmission, GABAergic;GO:0008277 regulation of G protein-coupled receptor signaling pathway",
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    {
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        "uniprot_id": "A0A8I6GEJ2_RAT",
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        "length": 503,
        "protein_name": "Chromodomain Y-like protein 2",
        "gene_name": "Cdyl2",
        "organism": "Rat",
        "refseq_name": "chromodomain Y-like protein 2",
        "refseq_ac": "NP_001099659",
        "gene_names_uniprotkb": "Cdyl2",
        "gene_names_refseq": "Cdyl2",
        "protein_names_uniprotkb": "Chromodomain Y-like protein 2",
        "protein_names_refseq": "chromodomain Y-like protein 2; chromodomain protein, Y chromosome-like 2; chromodomain protein, Y-like 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:292044)",
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        "publication_id_list": "21536231;22673903",
        "class_list": "",
        "function": "The researchers found evidence that Sry3 is one of the genes associated with the increased risk of spontaneous hypertension Y chromosome phenotype in Wistar Kyoto rats, [RefSeq, PubMed]",
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        "gene_name": "Nipal3",
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        "protein_names_refseq": "NIPA-like protein 3",
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        "gene_names_refseq": "LOC120093759",
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        "protein_names_refseq": "olfactory receptor 10H28-like",
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        "refseq_name": "ankyrin repeat and MYND domain-containing protein 1 isoform X1",
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        "gene_names_refseq": "Ankmy1",
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        "protein_names_refseq": "ankyrin repeat and MYND domain-containing protein 1 isoform X1",
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        "protein_name": "Olfactory receptor",
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        "protein_names_uniprotkb": "Olfactory receptor",
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        "protein_name": "Cytoplasmic protein",
        "gene_name": "Nck1",
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        "refseq_name": "SH2/SH3 adapter protein NCK1",
        "refseq_ac": "NP_001100321",
        "gene_names_uniprotkb": "Nck1",
        "gene_names_refseq": "Nck1",
        "protein_names_uniprotkb": "Cytoplasmic protein",
        "protein_names_refseq": "SH2/SH3 adapter protein NCK1; cytoplasmic protein NCK1; non-catalytic region of tyrosine kinase adaptor protein 1",
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        "pathway": " (rno:300955);  (R-RNO-186763);  (R-RNO-202433);  (R-RNO-2029482);  (R-RNO-373753);  (R-RNO-418885);  (R-RNO-4420097);  (R-RNO-5663213);  (R-RNO-9013420);  (R-RNO-9013424);  (R-RNO-9833482);  (R-RNO-983695)",
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    {
        "uniprot_canonical_ac": "A0A8I5Y075-1",
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        "length": 443,
        "protein_name": "Intraflagellar transport 52",
        "gene_name": "Ift52",
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        "refseq_name": "intraflagellar transport protein 52 homolog isoform X1",
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        "gene_names_refseq": "Ift52; RGD1311004",
        "protein_names_uniprotkb": "Intraflagellar transport 52",
        "protein_names_refseq": "intraflagellar transport protein 52 homolog isoform X1",
        "tax_id": 10116,
        "disease": "asphyxiating thoracic dystrophy (Disease Ontology:DOID:0050592)",
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        "go_cellular_component": "GO:0005813 centrosome;GO:0005814 centriole;GO:0036064 ciliary basal body;GO:0032391 photoreceptor connecting cilium;GO:0097546 ciliary base",
        "go_biological_process": "GO:0060271 cilium assembly;GO:0035720 intraciliary anterograde transport;GO:0050680 negative regulation of epithelial cell proliferation;GO:0007368 determination of left/right symmetry;GO:0001947 heart looping",
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    {
        "uniprot_canonical_ac": "A0A8J8YNL9-1",
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        "protein_name": "Translin",
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        "protein_names_uniprotkb": "Translin; Component 3 of promoter of RISC",
        "protein_names_refseq": "translin",
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        "function": "DNA-binding protein that specifically recognizes consensus sequences at the breakpoint junctions in chromosomal translocations, mostly involving immunoglobulin (Ig)/T-cell receptor gene segments. Seems to recognize single-stranded DNA ends generated by staggered breaks occurring at recombination hot spots., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Exhibits both single-stranded and double-stranded endoribonuclease activity. May act as an activator of RNA-induced silencing complex (RISC) by facilitating endonucleolytic cleavage of the siRNA passenger strand., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Findings implicate abnormal dendritic trafficking of BDNF mRNA in the pathophysiology of neuropsychiatric disorders linked to the translin G196A mutation., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0003723 RNA binding;GO:0016787 hydrolase activity;GO:0046872 metal ion binding;GO:0004519 endonuclease activity;GO:0043565 sequence-specific DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005654 nucleoplasm;GO:1902555 endoribonuclease complex",
        "go_biological_process": "GO:0016070 RNA metabolic process;GO:0030422 siRNA processing",
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        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "M0R3U0-1",
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        "length": 2143,
        "protein_name": "HEAT repeat-containing protein 1",
        "gene_name": "Heatr1",
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        "refseq_name": "HEAT repeat-containing protein 1",
        "refseq_ac": "NP_001101888",
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        "gene_names_refseq": "Heatr1l1; Heatr1; RGD1564769",
        "protein_names_uniprotkb": "HEAT repeat-containing protein 1",
        "protein_names_refseq": "HEAT repeat containing 1-like 1; HEAT repeat-containing protein 1",
        "tax_id": 10116,
        "disease": "glioblastoma (Disease Ontology:DOID:3068); pancreatic ductal carcinoma (Disease Ontology:DOID:3587)",
        "pathway": " (rno:361262);  (R-RNO-6791226)",
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        "function": "Involved in nucleolar processing of pre-18S ribosomal RNA., [UniProtKB, UniProtKB, UniProtKB]; Ribosome biogenesis factor; required for recruitment of Myc to nucleoli. Involved in nucleolar processing of pre-18S ribosomal RNA. Required for optimal pre-ribosomal RNA transcription by RNA polymerase I. 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. Involved in neuronal-lineage cell proliferation., [UniProtKB, UniProtKB, UniProtKB]",
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        "biomarker_type": "",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0030515 snoRNA binding",
        "go_cellular_component": "GO:0005730 nucleolus;GO:1990904 ribonucleoprotein complex;GO:0005739 mitochondrion;GO:0001650 fibrillar center;GO:0034455 t-UTP complex",
        "go_biological_process": "GO:0006364 rRNA processing;GO:2000234 positive regulation of rRNA processing;GO:1902570 protein localization to nucleolus;GO:0006351 DNA-templated transcription;GO:0045943 positive regulation of transcription by RNA polymerase I",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6GHR1-1",
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        "length": 525,
        "protein_name": "Gamma-aminobutyric acid receptor subunit theta",
        "gene_name": "Gabrq",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Gabrq",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Gamma-aminobutyric acid receptor subunit theta; GABA(A) receptor subunit theta",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "developmental disorder of mental health (Disease Ontology:DOID:0060037)",
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        "class_list": "",
        "function": "Theta subunit of the heteropentameric ligand-gated chloride channel gated by gamma-aminobutyric acid (GABA), a major inhibitory neurotransmitter in the brain. GABA-gated chloride channels, also named GABA(A) receptors (GABAAR), consist of five subunits arranged around a central pore and contain GABA active binding site(s) located at the alpha and beta subunit interfaces. When activated by GABA, GABAARs selectively allow the flow of chloride anions across the cell membrane down their electrochemical gradient., [UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "7.6.2.2;7.6.2.3;7.6.2.-;5.6.1.6;1.11.1.-;1.8.-.-;1.8.5.1",
        "go_molecular_function": "GO:0004890 GABA-A receptor activity;GO:0022851 GABA-gated chloride ion channel activity",
        "go_cellular_component": "GO:0045211 postsynaptic membrane;GO:0034707 chloride channel complex;GO:1902711 GABA-A receptor complex;GO:0043235 receptor complex",
        "go_biological_process": "GO:1902476 chloride transmembrane transport;GO:0051932 synaptic transmission, GABAergic",
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        "record_type": "protein"
    },
    {
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        "length": 1045,
        "protein_name": "Polyhomeotic homolog 1",
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        "organism": "Rat",
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        "gene_names_uniprotkb": "Phc1",
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        "protein_names_uniprotkb": "Polyhomeotic homolog 1",
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        "tax_id": 10116,
        "disease": "primary autosomal recessive microcephaly 11 (Disease Ontology:DOID:0070287); dilated cardiomyopathy (Disease Ontology:DOID:12930); cancer (Disease Ontology:DOID:162); tetralogy of Fallot (Disease Ontology:DOID:6419)",
        "pathway": " (rno:312690);  (R-RNO-2559580);  (R-RNO-3108214);  (R-RNO-3899300);  (R-RNO-4551638);  (R-RNO-4570464);  (R-RNO-8939243);  (R-RNO-8943724);  (R-RNO-8953750)",
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0008270 zinc ion binding;GO:0003682 chromatin binding;GO:0042393 histone binding",
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        "go_molecular_function": "GO:0008270 zinc ion binding",
        "go_cellular_component": "GO:0036126 sperm flagellum",
        "go_biological_process": "GO:0030317 flagellated sperm motility;GO:0007288 sperm axoneme assembly",
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        "record_type": "protein"
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    {
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        "protein_name": "Nucleoporin 205",
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        "organism": "Rat",
        "refseq_name": "nuclear pore complex protein Nup205 isoform X1",
        "refseq_ac": "XP_038963704",
        "gene_names_uniprotkb": "Nup205",
        "gene_names_refseq": "Nup205",
        "protein_names_uniprotkb": "Nucleoporin 205",
        "protein_names_refseq": "nuclear pore complex protein Nup205 isoform X1",
        "tax_id": 10116,
        "disease": "nephrotic syndrome type 13 (Disease Ontology:DOID:0080381)",
        "pathway": " (R-RNO-159227);  (R-RNO-159230);  (R-RNO-159231);  (R-RNO-159236);  (R-RNO-170822);  (R-RNO-1855170);  (R-RNO-1855196);  (R-RNO-1855229);  (R-RNO-191859);  (R-RNO-3108214);  (R-RNO-3232142);  (R-RNO-3301854);  (R-RNO-3371453);  (R-RNO-4085377);  (R-RNO-4551638);  (R-RNO-4570464);  (R-RNO-4615885);  (R-RNO-9615933)",
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        "go_molecular_function": "GO:0017056 structural constituent of nuclear pore",
        "go_cellular_component": "GO:0005635 nuclear envelope;GO:0005643 nuclear pore;GO:0031965 nuclear membrane;GO:0034399 nuclear periphery;GO:0044611 nuclear pore inner ring",
        "go_biological_process": "GO:0006999 nuclear pore organization;GO:0051292 nuclear pore complex assembly",
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        "hit_score": 0.1,
        "record_id": "A0A8I5ZJ67-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8J8XD91-1",
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        "length": 199,
        "protein_name": "Translocase of inner mitochondrial membrane 17b",
        "gene_name": "Timm17b",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Timm17b",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Translocase of inner mitochondrial membrane 17b",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "pathway_count": 0,
        "publication_count": 0,
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        "class_list": "",
        "function": "Essential component of the TIM23 complex, a complex that mediates the translocation of transit peptide-containing proteins across the mitochondrial inner membrane., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0005743 mitochondrial inner membrane;GO:0005744 TIM23 mitochondrial import inner membrane translocase complex",
        "go_biological_process": "GO:0030150 protein import into mitochondrial matrix",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6G699-1",
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        "length": 927,
        "protein_name": "FERM domain containing kindlin 2",
        "gene_name": "Fermt2",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Fermt2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "FERM domain containing kindlin 2",
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        "tax_id": 10116,
        "disease": "Kindler syndrome (Disease Ontology:DOID:0060472); acute myeloid leukemia (Disease Ontology:DOID:9119)",
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        "go_molecular_function": "GO:0044877 protein-containing complex binding;GO:0003779 actin binding;GO:0005178 integrin binding;GO:0005547 phosphatidylinositol-3,4,5-trisphosphate binding;GO:0019901 protein kinase binding",
        "go_cellular_component": "GO:0042995 cell projection;GO:0070161 anchoring junction;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0007155 cell adhesion;GO:0007229 integrin-mediated signaling pathway;GO:0030335 positive regulation of cell migration;GO:0051897 positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction;GO:0070374 positive regulation of ERK1 and ERK2 cascade",
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    {
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        "uniprot_id": "A0A8I6GFX3_RAT",
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        "length": 1652,
        "protein_name": "RNA uridylyltransferase",
        "gene_name": "Tut4",
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        "refseq_name": "terminal uridylyltransferase 4 isoform X4",
        "refseq_ac": "XP_063143792",
        "gene_names_uniprotkb": "Tut4",
        "gene_names_refseq": "Tut4; Zcchc11",
        "protein_names_uniprotkb": "RNA uridylyltransferase; 2.7.7.52",
        "protein_names_refseq": "terminal uridylyltransferase 4 isoform X4",
        "tax_id": 10116,
        "disease": "breast cancer (Disease Ontology:DOID:1612); liver benign neoplasm (Disease Ontology:DOID:916)",
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        "function": "May play a role in differentiating skeletal muscle., [UniProtKB, UniProtKB, UniProtKB]",
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        "protein_name": "DDB1- and CUL4-associated factor 6",
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        "function": "Ligand-dependent coactivator of nuclear receptors. Enhance transcriptional activity of the nuclear receptors NR3C1 and AR. May function as a substrate receptor for CUL4-DDB1 E3 ubiquitin-protein ligase complex., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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    {
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        "protein_names_refseq": "SFRS2-interacting protein; protein SCAF11; serine/arginine-rich splicing factor 2, interacting protein; splicing factor, arginine/serine-rich 2, interacting protein",
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        "protein_names_uniprotkb": "Platelet-activating factor acetylhydrolase; 3.1.1.47",
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        "disease": "obstructive sleep apnea (Disease Ontology:DOID:0050848); glomerulosclerosis (Disease Ontology:DOID:0050851); stroke (Disease Ontology:DOID:0051061); metabolic dysfunction-associated steatotic liver disease (Disease Ontology:DOID:0080208); nephrotic syndrome type 2 (Disease Ontology:DOID:0080379); nephrotic syndrome (Disease Ontology:DOID:1184); hemolytic-uremic syndrome (Disease Ontology:DOID:12554); carotid stenosis (Disease Ontology:DOID:13001); dementia (Disease Ontology:DOID:1307); atherosclerosis (Disease Ontology:DOID:1936); multiple sclerosis (Disease Ontology:DOID:2377); asthma (Disease Ontology:DOID:2841); glomerulonephritis (Disease Ontology:DOID:2921); IgA glomerulonephritis (Disease Ontology:DOID:2986); coronary artery disease (Disease Ontology:DOID:3393); carotid artery disease (Disease Ontology:DOID:3407); cerebral infarction (Disease Ontology:DOID:3526); proteinuria (Disease Ontology:DOID:576); myocardial infarction (Disease Ontology:DOID:5844); congestive heart failure (Disease Ontology:DOID:6000); rheumatoid arthritis (Disease Ontology:DOID:7148); abdominal aortic aneurysm (Disease Ontology:DOID:7693); end stage renal disease (Disease Ontology:DOID:783); type 2 diabetes mellitus (Disease Ontology:DOID:9352)",
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        "go_biological_process": "GO:0009395 phospholipid catabolic process;GO:0034638 phosphatidylcholine catabolic process;GO:0034440 lipid oxidation;GO:0034441 plasma lipoprotein particle oxidation;GO:0090026 positive regulation of monocyte chemotaxis",
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        "protein_names_refseq": "DNA-binding protein RFX6-like; DNA-binding protein RFX6; regulatory factor X domain containing 1",
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        "protein_names_uniprotkb": "Polycomb group RING finger protein 5; RING finger protein 159",
        "protein_names_refseq": "polycomb group RING finger protein 5 isoform 2; polycomb group RING finger protein 5",
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        "pathway": " (R-RNO-8939243)",
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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. Within the PRC1-like complex, regulates RNF2 ubiquitin ligase activity. Plays a redundant role with PCGF3 as part of a PRC1-like complex that mediates monoubiquitination of histone H2A 'Lys-119' on the X chromosome and is required for normal silencing of one copy of the X chromosome in XX females., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0140862 histone H2AK119 ubiquitin ligase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005813 centrosome;GO:0031519 PcG protein complex;GO:0035102 PRC1 complex",
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        "length": 216,
        "protein_name": "Ferritin",
        "gene_name": "LOC120099305",
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        "gene_names_uniprotkb": "LOC120099305; Fth1l1",
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        "protein_names_uniprotkb": "Ferritin",
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        "function": "Stores iron in a soluble, non-toxic, readily available form. Important for iron homeostasis. Iron is taken up in the ferrous form and deposited as ferric hydroxides after oxidation., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0008198 ferrous iron binding;GO:0004322 ferroxidase activity;GO:0008199 ferric iron binding",
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        "protein_names_uniprotkb": "LINE-1 retrotransposable element ORF1 protein; LINE retrotransposable element 1; LINE1 retrotransposable element 1",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6GKV9-1",
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        "length": 320,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or5d45",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Or5d45",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "",
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        "go_cellular_component": "GO:0005886 plasma membrane",
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        "protein_name": "Cystatin domain-containing protein",
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        "gene_names_refseq": "Csta3",
        "protein_names_uniprotkb": "Cystatin domain-containing protein",
        "protein_names_refseq": "stefin-1-like",
        "tax_id": 10116,
        "disease": "peeling skin syndrome 4 (Disease Ontology:DOID:0070523)",
        "pathway": " (rno:100911790);  (rno:689230);  (R-RNO-6809371)",
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        "function": "This is an intracellular thiol proteinase inhibitor., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0004869 cysteine-type endopeptidase inhibitor activity",
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    },
    {
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        "protein_name": "Ig-like domain-containing protein",
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        "record_id": "A0A8I6GM23-1",
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    },
    {
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        "refseq_name": "tetratricopeptide repeat protein 12 isoform X1",
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        "gene_names_refseq": "Ttc12",
        "protein_names_uniprotkb": "Tetratricopeptide repeat protein 12",
        "protein_names_refseq": "tetratricopeptide repeat protein 12 isoform X1",
        "tax_id": 10116,
        "disease": "alcohol dependence (Disease Ontology:DOID:0050741); nicotine dependence (Disease Ontology:DOID:0050742); primary ciliary dyskinesia 45 (Disease Ontology:DOID:0111857); acute lymphoblastic leukemia (Disease Ontology:DOID:9952); drug dependence (Disease Ontology:DOID:9974); heroin dependence (Disease Ontology:DOID:9976)",
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        "function": "Cytoplasmic protein that plays a role in the proper assembly of dynein arm complexes in motile cilia in both respiratory cells and sperm flagella., [UniProtKB, UniProtKB]",
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        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "A0A8J8XQI9-1",
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        "length": 603,
        "protein_name": "Carboxylic ester hydrolase",
        "gene_name": "Bche",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Bche",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Carboxylic ester hydrolase; 3.1.1.-",
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        "tax_id": 10116,
        "disease": "primary progressive multiple sclerosis (Disease Ontology:DOID:0050784); stroke (Disease Ontology:DOID:0051061); trypanosomiasis (Disease Ontology:DOID:10113); Alzheimer's disease (Disease Ontology:DOID:10652); hypertension (Disease Ontology:DOID:10763); amnestic disorder (Disease Ontology:DOID:10914); familial hyperlipidemia (Disease Ontology:DOID:1168); Huntington's disease (Disease Ontology:DOID:12858); dementia (Disease Ontology:DOID:1307); epilepsy (Disease Ontology:DOID:1826); leptospirosis (Disease Ontology:DOID:2297); coronary artery disease (Disease Ontology:DOID:3393); coronary restenosis (Disease Ontology:DOID:4247); schizophrenia (Disease Ontology:DOID:5419); dystonia (Disease Ontology:DOID:543); inherited metabolic disorder (Disease Ontology:DOID:655); hyperhomocysteinemia (Disease Ontology:DOID:9279); type 2 diabetes mellitus (Disease Ontology:DOID:9352); bacterial meningitis (Disease Ontology:DOID:9470); cannabis abuse (Disease Ontology:DOID:9505); type 1 diabetes mellitus (Disease Ontology:DOID:9744); heroin dependence (Disease Ontology:DOID:9976)",
        "pathway": " (R-RNO-422085);  (R-RNO-9749641)",
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        "function": "Esterase with broad substrate specificity. Contributes to the inactivation of the neurotransmitter acetylcholine. Can degrade neurotoxic organophosphate esters., [UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005783 endoplasmic reticulum;GO:0016020 membrane;GO:0043025 neuronal cell body;GO:0097386 glial cell projection",
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        "uniprot_canonical_ac": "A0A8L2QJF1-1",
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        "length": 179,
        "protein_name": "Fas apoptotic inhibitory molecule 1",
        "gene_name": "Faiml",
        "organism": "Rat",
        "refseq_name": "Fas apoptotic inhibitory molecule like",
        "refseq_ac": "NP_001417324",
        "gene_names_uniprotkb": "Faiml; LOC684466",
        "gene_names_refseq": "Faiml",
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        "protein_names_refseq": "Fas apoptotic inhibitory molecule like; fas apoptotic inhibitory molecule 1",
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        "go_cellular_component": "GO:0005737 cytoplasm",
        "go_biological_process": "GO:0043066 negative regulation of apoptotic process;GO:0006915 apoptotic process;GO:0009966 regulation of signal transduction",
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        "hit_score": 0.1,
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    },
    {
        "uniprot_canonical_ac": "A0A8L2QN85-1",
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        "length": 51,
        "protein_name": "Ribosomal protein L39 like 3",
        "gene_name": "Rpl39l3",
        "organism": "Rat",
        "refseq_name": "large ribosomal subunit protein eL39-like",
        "refseq_ac": "XP_038961982",
        "gene_names_uniprotkb": "Rpl39l3; LOC103695152",
        "gene_names_refseq": "Rpl39l3",
        "protein_names_uniprotkb": "Ribosomal protein L39 like 3",
        "protein_names_refseq": "large ribosomal subunit protein eL39-like",
        "tax_id": 10116,
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        "go_molecular_function": "GO:0003735 structural constituent of ribosome",
        "go_cellular_component": "GO:0022625 cytosolic large ribosomal subunit",
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        "record_id": "A0A8L2QN85-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "B6ZGR5-1",
        "uniprot_id": "B6ZGR5_RAT",
        "mass": 35242.0,
        "length": 317,
        "protein_name": "Melanocyte-stimulating hormone receptor",
        "gene_name": "Mc1r",
        "organism": "Rat",
        "refseq_name": "melanocyte-stimulating hormone receptor",
        "refseq_ac": "NP_001388020",
        "gene_names_uniprotkb": "Mc1r",
        "gene_names_refseq": "Mc1r",
        "protein_names_uniprotkb": "Melanocyte-stimulating hormone receptor; MSH-R; Melanocortin receptor 1",
        "protein_names_refseq": "alpha melanocyte stimulating hormone receptor; melanocyte-stimulating hormone receptor",
        "tax_id": 10116,
        "disease": "oculocutaneous albinism type II (Disease Ontology:DOID:0070096); pigmentation disease (Disease Ontology:DOID:10123); major depressive disorder (Disease Ontology:DOID:1470); melanoma (Disease Ontology:DOID:1909); familial melanoma (Disease Ontology:DOID:6846)",
        "pathway": " (rno:102552838);  (R-RNO-375276)",
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        "publication_count": 5,
        "publication_id_list": "30356069;31486022;36446431;37490042;38185389",
        "class_list": "",
        "function": "Activation of Melanocortin 1 Receptor Attenuates Early Brain Injury in a Rat Model of Subarachnoid Hemorrhage viathe Suppression of Neuroinflammation through AMPK/TBK1/NF-kappaB Pathway in Rats., [RefSeq, PubMed]; Activation of the melanocortin-1 receptor attenuates neuronal apoptosis after traumatic brain injury by upregulating Merlin expression., [RefSeq, PubMed]; Found that glomerular MC1R expression was increased in nephrotic syndrome, both in humans and in a rat model. Publication Status: Online-Only, [RefSeq, PubMed]; G protein-coupled receptor that binds melanocyte-stimulating hormones (alpha, beta, and gamma-MSH) and adrenocorticotropic hormone/ACTH, which are peptide products of the POMC precursor protein. Upon activation, MC1R couples with the G(s) protein, stimulating adenylate cyclase and activating the cAMP-dependent signaling pathway. This activation promotes melanogenesis, resulting in the production of eumelanin (black/brown) and pheomelanin (red/yellow) in melanocytes. MC1R interacts with G protein-coupled receptor opsin 3/OPN3, which couples to G(i) proteins and inhibits the alpha-MSH-induced cAMP response, thereby reducing melanin synthesis. Binding to Agouti/ASP precludes alpha-MSH-induced signaling, thereby downregulating melanogenesis. Additionally, interaction with MGRN1 displaces the G(s) protein, further suppressing MC1R signaling., [UniProtKB, UniProtKB, UniProtKB]; Melanocortin 1 receptor regulates cholesterol and bile acid metabolism in the liver. Publication Status: Online-Only, [RefSeq, PubMed]; Negative Modulation of B Cell Activation by Melanocortin 1 Receptor Signaling Protects against Membranous Nephropathy., [RefSeq, PubMed]",
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        "secondary_ac_list": "A6IZY1",
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        "go_molecular_function": "GO:0031625 ubiquitin protein ligase binding;GO:0042562 hormone binding;GO:0004977 melanocortin receptor activity;GO:0004978 corticotropin receptor activity;GO:0004980 melanocyte-stimulating hormone receptor activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005886 plasma membrane",
        "go_biological_process": "GO:0007189 adenylate cyclase-activating G protein-coupled receptor signaling pathway;GO:0035556 intracellular signal transduction;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0019233 sensory perception of pain;GO:0032720 negative regulation of tumor necrosis factor production",
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        "record_id": "B6ZGR5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7EKF1-1",
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        "length": 713,
        "protein_name": "Bardet-Biedl syndrome 10",
        "gene_name": "Bbs10",
        "organism": "Rat",
        "refseq_name": "Bardet-Biedl syndrome 10 protein",
        "refseq_ac": "NP_001102756",
        "gene_names_uniprotkb": "Bbs10",
        "gene_names_refseq": "Bbs10; RGD1560748",
        "protein_names_uniprotkb": "Bardet-Biedl syndrome 10",
        "protein_names_refseq": "Bardet-Biedl syndrome 10 protein",
        "tax_id": 10116,
        "disease": "Bardet-Biedl syndrome 10 (Disease Ontology:DOID:0110132); Bardet-Biedl syndrome (Disease Ontology:DOID:1935)",
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        "go_molecular_function": "GO:0005524 ATP binding;GO:0061629 RNA polymerase II-specific DNA-binding transcription factor binding",
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        "go_biological_process": "GO:0019228 neuronal action potential;GO:0043524 negative regulation of neuron apoptotic process;GO:0006974 DNA damage response;GO:0007601 visual perception;GO:0045494 photoreceptor cell maintenance",
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    {
        "uniprot_canonical_ac": "F7EV63-1",
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        "protein_name": "Polycomb group RING finger protein 3",
        "gene_name": "Pcgf3",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Pcgf3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Polycomb group RING finger protein 3; RING finger protein 3A",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "class_list": "",
        "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. Within the PRC1-like complex, regulates RNF2 ubiquitin ligase activity. Plays a redundant role with PCGF5 as part of a PRC1-like complex that mediates monoubiquitination of histone H2A 'Lys-119' on the X chromosome and is required for normal silencing of one copy of the X chromosome in XX females., [UniProtKB, UniProtKB]",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0140862 histone H2AK119 ubiquitin ligase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0031519 PcG protein complex;GO:0035102 PRC1 complex;GO:0000805 X chromosome",
        "go_biological_process": "GO:0060816 random inactivation of X chromosome;GO:0006357 regulation of transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F7EV63-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7F0L5-1",
        "uniprot_id": "F7F0L5_RAT",
        "mass": 220071.0,
        "length": 1924,
        "protein_name": "Myosin-7B",
        "gene_name": "Myh7b",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Myh7b",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Myosin-7B; Myosin cardiac muscle beta chain; Myosin heavy chain 7B, cardiac muscle beta isoform",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "distal arthrogryposis (Disease Ontology:DOID:0050646); cardiomyopathy (Disease Ontology:DOID:0050700); familial hypertrophic cardiomyopathy (Disease Ontology:DOID:0080326); congenital myopathy 6 (Disease Ontology:DOID:0080719); dilated cardiomyopathy 1S (Disease Ontology:DOID:0110454); autosomal dominant hyaline body myopathy (Disease Ontology:DOID:0111269); distal arthrogryposis type 1 (Disease Ontology:DOID:0111596); distal arthrogryposis type 2B3 (Disease Ontology:DOID:0111602); distal arthrogryposis type 2A (Disease Ontology:DOID:0111605); distal myopathy (Disease Ontology:DOID:11720); hypertrophic cardiomyopathy (Disease Ontology:DOID:11984); dilated cardiomyopathy (Disease Ontology:DOID:12930); myotonia congenita (Disease Ontology:DOID:2106); inclusion body myositis (Disease Ontology:DOID:3429); restrictive cardiomyopathy (Disease Ontology:DOID:397); myopathy (Disease Ontology:DOID:423)",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Involved in muscle contraction., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Muscle contraction., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "go_molecular_function": "GO:0005524 ATP binding;GO:0051015 actin filament binding;GO:0000146 microfilament motor activity;GO:0003779 actin binding;GO:0003774 cytoskeletal motor activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0032982 myosin filament;GO:0097512 cardiac myofibril;GO:0016460 myosin II complex;GO:0016459 myosin complex",
        "go_biological_process": "GO:0051480 regulation of cytosolic calcium ion concentration;GO:0086004 regulation of cardiac muscle cell contraction;GO:0050848 regulation of calcium-mediated signaling;GO:1905289 regulation of CAMKK-AMPK signaling cascade",
        "synthesized_glycan_count": 0,
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        "record_id": "F7F0L5-1",
        "record_type": "protein"
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    {
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        "length": 248,
        "protein_name": "Granzyme F",
        "gene_name": "Gzmf",
        "organism": "Rat",
        "refseq_name": "granzyme H precursor",
        "refseq_ac": "NP_703196",
        "gene_names_uniprotkb": "Gzmf",
        "gene_names_refseq": "Gzmf; Gzmg; Rnkp7",
        "protein_names_uniprotkb": "Granzyme F",
        "protein_names_refseq": "granzyme G-like; granzyme G; granzyme H precursor; granzyme H; natural killer cell protease 7",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:266704);  (R-RNO-2022377);  (R-RNO-381426)",
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        "go_molecular_function": "GO:0004252 serine-type endopeptidase activity",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0044194 cytolytic granule",
        "go_biological_process": "GO:0006508 proteolysis;GO:0051604 protein maturation",
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        "hit_score": 0.2,
        "record_id": "F7FBB5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7FET5-1",
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        "length": 325,
        "protein_name": "Docking protein 4",
        "gene_name": "Dok4",
        "organism": "Rat",
        "refseq_name": "docking protein 4",
        "refseq_ac": "NP_001101908",
        "gene_names_uniprotkb": "Dok4",
        "gene_names_refseq": "Dok4",
        "protein_names_uniprotkb": "Docking protein 4",
        "protein_names_refseq": "docking protein 4",
        "tax_id": 10116,
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        "pathway": " (rno:361364);  (R-RNO-8853659)",
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        "publication_id_list": "21264944",
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        "function": "Dok4 is a novel player in Schwann cell-axon interaction and is required at early stages of myelination; it also aids Schwann cell migration and proliferation., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0035591 signaling adaptor activity",
        "go_cellular_component": "GO:0005739 mitochondrion",
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        "hit_score": 0.2,
        "record_id": "F7FET5-1",
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    },
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        "mass": 34562.0,
        "length": 305,
        "protein_name": "Vomeronasal type-1 receptor",
        "gene_name": "Vom1r113",
        "organism": "Rat",
        "refseq_name": "vomeronasal type-1 receptor 4-like",
        "refseq_ac": "XP_038956665",
        "gene_names_uniprotkb": "Vom1r113",
        "gene_names_refseq": "Vom1r113",
        "protein_names_uniprotkb": "Vomeronasal type-1 receptor",
        "protein_names_refseq": "vomeronasal type-1 receptor 4-like",
        "tax_id": 10116,
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        "pathway": " (rno:108348146)",
        "pathway_count": 1,
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        "function": "Putative pheromone receptor implicated in the regulation of social as well as reproductive behavior., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005550 pheromone binding;GO:0016503 pheromone receptor activity",
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        "hit_score": 0.1,
        "record_id": "F7FLY1-1",
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    },
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        "length": 111,
        "protein_name": "Small integral membrane protein 11",
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        "gene_names_uniprotkb": "Smim11",
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        "protein_names_uniprotkb": "Small integral membrane protein 11",
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        "gene_names_uniprotkb": "LOC120102398; LOC120102396; Senp17; Senp18",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ubiquitin-like protease family profile domain-containing protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "go_molecular_function": "GO:0016929 deSUMOylase activity;GO:0008233 peptidase activity",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0006508 proteolysis;GO:0043066 negative regulation of apoptotic process;GO:0016926 protein desumoylation;GO:0080090 regulation of primary metabolic process;GO:0060255 regulation of macromolecule metabolic process",
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        "record_id": "M0RCW3-1",
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    },
    {
        "uniprot_canonical_ac": "Q04105-1",
        "uniprot_id": "Q04105_RAT",
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        "length": 164,
        "protein_name": "Acidic proline-rich protein PRP25-like; Proline-rich protein 15",
        "gene_name": "Prp15",
        "organism": "Rat",
        "refseq_name": "proline-rich protein 15 precursor",
        "refseq_ac": "NP_036764",
        "gene_names_uniprotkb": "Prp15; LOC120093139",
        "gene_names_refseq": "Prp15; Prpb; Prp; RATRP13; Rp13",
        "protein_names_uniprotkb": "Acidic proline-rich protein PRP25-like; Proline-rich protein 15",
        "protein_names_refseq": "Proline-rich protein salivary; proline-rich protein 15 precursor; proline-rich protein, salivary",
        "tax_id": 10116,
        "disease": "Lafora disease 1 (Disease Ontology:DOID:0070660); Lafora disease (Disease Ontology:DOID:3534); progressive myoclonus epilepsy (Disease Ontology:DOID:891)",
        "pathway": " (rno:24687)",
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        "secondary_ac_list": "F1LV68;F7F912",
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        "go_cellular_component": "GO:0005576 extracellular region",
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    {
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        "length": 271,
        "protein_name": "Hematopoietically-expressed homeobox protein HHEX",
        "gene_name": "Hhex",
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        "refseq_name": "hematopoietically-expressed homeobox protein HHEX",
        "refseq_ac": "NP_077361",
        "gene_names_uniprotkb": "Hhex",
        "gene_names_refseq": "Hex; Hhex",
        "protein_names_uniprotkb": "Hematopoietically-expressed homeobox protein HHEX; Hematopoietically-expressed homeobox protein hhex; Homeobox protein PRH; Proline-rich homeodomain protein",
        "protein_names_refseq": "hematopoietically-expressed homeobox protein HHEX",
        "tax_id": 10116,
        "disease": "candidiasis (Disease Ontology:DOID:1508); type 2 diabetes mellitus (Disease Ontology:DOID:9352)",
        "pathway": " (rno:79237)",
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        "publication_id_list": "26306672;28927755",
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        "function": "Recognizes the DNA sequence 5'-ATTAA-3'. Transcriptional repressor. Activator of WNT-mediated transcription in conjunction with CTNNB1. Establishes anterior identity at two levels; acts early to enhance canonical WNT-signaling by repressing expression of TLE4, and acts later to inhibit NODAL-signaling by directly targeting NODAL. Inhibits EIF4E-mediated mRNA nuclear export. May play a role in hematopoietic differentiation., [UniProtKB, UniProtKB]; These findings suggest a role for HHEX in restricting axon growth in the developing central nervous system., [RefSeq, PubMed]; Vascular smooth muscle protein kinase CK2 inhibition suppresses neointima formation via a proline-rich homeodomain-dependent mechanism., [RefSeq, PubMed]",
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        "secondary_ac_list": "F7F7Q9",
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        "go_molecular_function": "GO:0008301 DNA binding, bending;GO:0003682 chromatin binding;GO:0003700 DNA-binding transcription factor activity;GO:0042803 protein homodimerization activity;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0032993 protein-DNA complex",
        "go_biological_process": "GO:0030878 thyroid gland development;GO:0002573 myeloid leukocyte differentiation;GO:0060431 primary lung bud formation;GO:0061010 gallbladder development;GO:0061011 hepatic duct development",
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    {
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        "length": 841,
        "protein_name": "Zinc finger RNA binding protein 2",
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        "gene_names_uniprotkb": "Zfr2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger RNA binding protein 2",
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0008270 zinc ion binding;GO:0003725 double-stranded RNA binding;GO:0003727 single-stranded RNA binding",
        "go_cellular_component": "GO:0005634 nucleus",
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        "record_id": "A0A8I5Y1D0-1",
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        "uniprot_canonical_ac": "A0A8I5Y218-1",
        "uniprot_id": "A0A8I5Y218_RAT",
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        "length": 521,
        "protein_name": "RING-type E3 ubiquitin-protein ligase PPIL2",
        "gene_name": "LOC134479414",
        "organism": "Rat",
        "refseq_name": "RING-type E3 ubiquitin-protein ligase PPIL2-like",
        "refseq_ac": "XP_063118844",
        "gene_names_uniprotkb": "LOC134479414",
        "gene_names_refseq": "LOC134479414",
        "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": "RING-type E3 ubiquitin-protein ligase PPIL2-like",
        "tax_id": 10116,
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        "pathway": " (rno:134479414)",
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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]",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0061630 ubiquitin protein ligase activity;GO:0003755 peptidyl-prolyl cis-trans isomerase activity",
        "go_cellular_component": "GO:0071013 catalytic step 2 spliceosome",
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        "record_id": "A0A8I5Y218-1",
        "record_type": "protein"
    },
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        "uniprot_canonical_ac": "A0A8I5Y7P6-1",
        "uniprot_id": "A0A8I5Y7P6_RAT",
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        "length": 79,
        "protein_name": "Dolichyl-diphosphooligosaccharide-protein glycosyltransferase subunit TMEM258",
        "gene_name": "Tmem258l3",
        "organism": "Rat",
        "refseq_name": "",
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        "gene_names_uniprotkb": "Tmem258l3; LOC690138",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Dolichyl-diphosphooligosaccharide-protein glycosyltransferase subunit TMEM258; 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]",
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    },
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        "protein_name": "DLG associated protein 5 like 2",
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        "protein_names_uniprotkb": "DLG associated protein 5 like 2",
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    },
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        "length": 107,
        "protein_name": "NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 3",
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        "refseq_name": "NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 3 isoform X1",
        "refseq_ac": "XP_063123013",
        "gene_names_uniprotkb": "Ndufb3",
        "gene_names_refseq": "Ndufb3",
        "protein_names_uniprotkb": "NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 3; Complex I-B12; NADH-ubiquinone oxidoreductase B12 subunit",
        "protein_names_refseq": "NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 3 isoform X1",
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        "disease": "nuclear type mitochondrial complex I deficiency 25 (Disease Ontology:DOID:0112067); Alzheimer's disease (Disease Ontology:DOID:10652)",
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        "function": "Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone., [UniProtKB, UniProtKB]",
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        "protein_name": "Spermine synthase",
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        "refseq_name": "spermine synthase-like",
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        "gene_names_uniprotkb": "Smsl1; AABR07021734.1; RGD1559938",
        "gene_names_refseq": "Smsl1",
        "protein_names_uniprotkb": "Spermine synthase; 2.5.1.22; Spermidine aminopropyltransferase",
        "protein_names_refseq": "spermine synthase-like",
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        "disease": "syndromic X-linked intellectual disability Snyder type (Disease Ontology:DOID:0060802); anxiety disorder (Disease Ontology:DOID:2030)",
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        "length": 166,
        "protein_name": "Myeloid-derived growth factor",
        "gene_name": "Mydgf",
        "organism": "Rat",
        "refseq_name": "myeloid-derived growth factor precursor",
        "refseq_ac": "NP_001386289",
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        "gene_names_refseq": "Mydgf",
        "protein_names_uniprotkb": "Myeloid-derived growth factor",
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        "protein_name": "Similar to human chromosome 5 open reading frame 58",
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        "protein_names_uniprotkb": "Similar to human chromosome 5 open reading frame 58",
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        "protein_name": "Ig-like domain-containing protein",
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        "protein_names_refseq": "interferon regulatory factor 2-binding protein 2",
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        "pathway": " (rno:299121);  (R-RNO-2132295);  (R-RNO-3371497);  (R-RNO-6798695);  (R-RNO-6807878);  (R-RNO-6811436)",
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        "protein_names_uniprotkb": "Protein regulator of cytokinesis 1",
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        "protein_names_uniprotkb": "Parkin coregulated",
        "protein_names_refseq": "Park2 co-regulated; parkin co-regulated gene protein; parkin coregulated gene protein",
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        "go_molecular_function": "GO:0003779 actin binding;GO:0051087 protein-folding chaperone binding;GO:0001664 G protein-coupled receptor binding;GO:0031072 heat shock protein binding;GO:0031625 ubiquitin protein ligase binding",
        "go_cellular_component": "GO:0097229 sperm end piece;GO:0005829 cytosol;GO:0005929 cilium;GO:0036126 sperm flagellum;GO:0043005 neuron projection",
        "go_biological_process": "GO:0030317 flagellated sperm motility;GO:0007286 spermatid development;GO:0008104 intracellular protein localization",
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        "protein_name": "Solute carrier family 2 member 9",
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        "refseq_name": "solute carrier family 2, facilitated glucose transporter member 9 isoform X1",
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        "gene_names_refseq": "Slc2a9",
        "protein_names_uniprotkb": "Solute carrier family 2 member 9",
        "protein_names_refseq": "solute carrier family 2, facilitated glucose transporter member 9 isoform X1",
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        "disease": "abdominal obesity-metabolic syndrome (Disease Ontology:DOID:0060611); hyperuricemia (Disease Ontology:DOID:1920)",
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        "pathway": " (rno:315084);  (R-RNO-111457);  (R-RNO-111458);  (R-RNO-111461);  (R-RNO-448706);  (R-RNO-5620971);  (R-RNO-5686938);  (R-RNO-6798695)",
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        "protein_names_uniprotkb": "T-complex protein 1 subunit eta; CCT-eta; TCP-1-eta",
        "protein_names_refseq": "T-complex protein 1 subunit eta; chaperonin containing Tcp1, subunit 7 (eta); chaperonin subunit 7 (eta)",
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        "gene_names_refseq": "",
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        "pathway": " (rno:362271);  (R-RNO-2029482);  (R-RNO-4420097);  (R-RNO-8849471);  (R-RNO-9013408)",
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        "function": "Involved in cytoskeletal rearrangements required for phagocytosis of apoptotic cells and cell motility. Acts in association with DOCK1 and CRK. Was initially proposed to be required in complex with DOCK1 to activate Rac Rho small GTPases. May enhance the guanine nucleotide exchange factor (GEF) activity of DOCK1., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0017124 SH3 domain binding;GO:0030971 receptor tyrosine kinase binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0016020 membrane;GO:0005829 cytosol",
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        "refseq_name": "striatin-interacting protein 2",
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        "protein_names_uniprotkb": "Striatin interacting protein 2",
        "protein_names_refseq": "striatin-interacting protein 2",
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        "refseq_name": "BCL2/adenovirus E1B 19 kDa protein-interacting protein 2 isoform 2",
        "refseq_ac": "NP_001423391",
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        "protein_names_uniprotkb": "BCL2 interacting protein 2",
        "protein_names_refseq": "BCL2/adenovirus E1B 19 kDa protein-interacting protein 2 isoform 2; BCL2/adenovirus E1B 19 kDa protein-interacting protein 2; BCL2/adenovirus E1B 19kDa-interacting protein 1, NIP2; BCL2/adenovirus E1B interacting protein 2; Bcl-2 and E1B 19 kDa interacting protein",
        "tax_id": 10116,
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        "go_biological_process": "GO:0051057 positive regulation of small GTPase mediated signal transduction;GO:0043410 positive regulation of MAPK cascade;GO:0045666 positive regulation of neuron differentiation;GO:0006915 apoptotic process;GO:0051146 striated muscle cell differentiation",
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    {
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        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein; Centaurin-beta; Cnt-b",
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        "go_molecular_function": "GO:0005096 GTPase activator activity;GO:0008270 zinc ion binding",
        "go_cellular_component": "GO:0010008 endosome membrane;GO:0030426 growth cone",
        "go_biological_process": "GO:0001764 neuron migration;GO:0010975 regulation of neuron projection development",
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        "length": 968,
        "protein_name": "F-actin cross-linking protein",
        "gene_name": "Actn2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Actn2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "F-actin cross-linking protein",
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        "tax_id": 10116,
        "disease": "arrhythmogenic right ventricular cardiomyopathy (Disease Ontology:DOID:0050431); congenital myopathy 8 (Disease Ontology:DOID:0081342); dilated cardiomyopathy 1AA (Disease Ontology:DOID:0110428); focal segmental glomerulosclerosis 1 (Disease Ontology:DOID:0111128)",
        "pathway": " (R-RNO-114608);  (R-RNO-390522);  (R-RNO-438066);  (R-RNO-5673001)",
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        "go_molecular_function": "GO:0003779 actin binding;GO:0005509 calcium ion binding;GO:0051015 actin filament binding;GO:0003713 transcription coactivator activity;GO:0005546 phosphatidylinositol-4,5-bisphosphate binding",
        "go_cellular_component": "GO:0005829 cytosol;GO:0015629 actin cytoskeleton;GO:0005886 plasma membrane;GO:0030054 cell junction;GO:0030018 Z disc",
        "go_biological_process": "GO:0030036 actin cytoskeleton organization;GO:0055001 muscle cell development;GO:0042391 regulation of membrane potential;GO:0072659 protein localization to plasma membrane;GO:0043268 positive regulation of potassium ion transport",
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        "length": 720,
        "protein_name": "Transmembrane protein 62",
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        "gene_names_uniprotkb": "Tmem62",
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        "protein_names_uniprotkb": "Transmembrane protein 62",
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        "go_molecular_function": "GO:0016787 hydrolase activity",
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    },
    {
        "uniprot_canonical_ac": "A0A8I6GGN2-1",
        "uniprot_id": "A0A8I6GGN2_RAT",
        "mass": 112991.0,
        "length": 1037,
        "protein_name": "Integrin alpha-IIb",
        "gene_name": "Itga2b",
        "organism": "Rat",
        "refseq_name": "integrin alpha-IIb precursor",
        "refseq_ac": "NP_001413964",
        "gene_names_uniprotkb": "Itga2b",
        "gene_names_refseq": "Itga2b",
        "protein_names_uniprotkb": "Integrin alpha-IIb; GPalpha IIb; Platelet membrane glycoprotein IIb",
        "protein_names_refseq": "integrin alpha 2b (Cd41b); integrin alpha-IIb precursor; integrin alpha-IIb; integrin, alpha 2B",
        "tax_id": 10116,
        "disease": "stroke (Disease Ontology:DOID:0051061); von Willebrand's disease 1 (Disease Ontology:DOID:0060573); platelet-type bleeding disorder 16 (Disease Ontology:DOID:0060691); intellectual disability (Disease Ontology:DOID:1059); thrombocytopenia (Disease Ontology:DOID:1588); Glanzmann's thrombasthenia (Disease Ontology:DOID:2219); severe acute respiratory syndrome (Disease Ontology:DOID:2945)",
        "pathway": " (rno:685269);  (R-RNO-114608);  (R-RNO-216083);  (R-RNO-3000178);  (R-RNO-354192);  (R-RNO-354194);  (R-RNO-372708);  (R-RNO-445144);  (R-RNO-5674135);  (R-RNO-9769733)",
        "pathway_count": 10,
        "publication_count": 3,
        "publication_id_list": "23082158;28097150;30359790",
        "class_list": "",
        "function": "Integrin alpha-IIb/beta-3 (ITGA2B:ITGB3) is a receptor for fibronectin, fibrinogen, plasminogen, prothrombin, thrombospondin and vitronectin. It recognizes the sequence R-G-D in a wide array of ligands. It recognizes the sequence H-H-L-G-G-G-A-K-Q-A-G-D-V in fibrinogen gamma chain. Following activation integrin alpha-IIb/beta-3 brings about platelet/platelet interaction through binding of soluble fibrinogen. This step leads to rapid platelet aggregation which physically plugs ruptured endothelial cell surface. Integrin ITGA2B:ITGB3 is also the receptor of erythrocyte-specific ICAM4 ligand involved in heterotypic cell-cell adhesion between erythrocytes and activated platelets., [UniProtKB, UniProtKB, UniProtKB]; PI3K/Akt signaling is utilized by alphaIIb-mediated outside-in signaling to activate platelets., [RefSeq, PubMed]; TNF-alpha decreases calcium internal mobilization and calcium influx in platelets. TNF-alpha significantly reduced (Tyr 416)-c-Src and (Tyr773)-beta3 subunit of integrin alphaIIbbeta3 phosphorylation., [RefSeq, PubMed]; Taken together, our results reveal that ND-1 is a novel antagonist of alphaIIb3 with strong antithrombotic effect and lower bleeding risk., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0046872 metal ion binding;GO:0060090 molecular adaptor activity;GO:0042802 identical protein binding;GO:0050840 extracellular matrix binding;GO:0038023 signaling receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0008305 integrin complex;GO:0005925 focal adhesion;GO:0009986 cell surface;GO:0070062 extracellular exosome",
        "go_biological_process": "GO:0007155 cell adhesion;GO:0007229 integrin-mediated signaling pathway;GO:0001525 angiogenesis;GO:0007160 cell-matrix adhesion;GO:0033631 cell-cell adhesion mediated by integrin",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "A0A8I6GGN2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6GH32-1",
        "uniprot_id": "A0A8I6GH32_RAT",
        "mass": 57054.0,
        "length": 510,
        "protein_name": "acid phosphatase",
        "gene_name": "Acp4",
        "organism": "Rat",
        "refseq_name": "testicular acid phosphatase isoform 1",
        "refseq_ac": "NP_001388455",
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        "protein_names_uniprotkb": "acid phosphatase; 3.1.3.2",
        "protein_names_refseq": "acid phosphatase, testicular; testicular acid phosphatase isoform 1; testicular acid phosphatase",
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        "protein_names_uniprotkb": "Zinc finger protein 236",
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        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "protein_name": "Small G protein signaling modulator 1",
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        "go_molecular_function": "GO:0004672 protein kinase activity;GO:0005524 ATP binding;GO:0004674 protein serine/threonine kinase activity",
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    },
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        "protein_name": "Inner nuclear membrane protein Man1",
        "gene_name": "Lemd3",
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        "refseq_name": "inner nuclear membrane protein Man1",
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        "gene_names_refseq": "Lemd3; RGD1561001",
        "protein_names_uniprotkb": "Inner nuclear membrane protein Man1; LEM domain-containing protein 3",
        "protein_names_refseq": "inner nuclear membrane protein Man1",
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        "disease": "arteriovenous malformations of the brain (Disease Ontology:DOID:0060688); cataract 46 juvenile-onset (Disease Ontology:DOID:0110243); Buschke-Ollendorff syndrome (Disease Ontology:DOID:0111536); Emery-Dreifuss muscular dystrophy (Disease Ontology:DOID:11726)",
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        "function": "Can function as a specific repressor of TGF-beta, activin, and BMP signaling through its interaction with the R-SMAD proteins. Antagonizes TGF-beta-induced cell proliferation arrest., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003677 DNA binding;GO:0031490 chromatin DNA binding;GO:0003676 nucleic acid binding",
        "go_cellular_component": "GO:0005637 nuclear inner membrane;GO:0005635 nuclear envelope;GO:0016020 membrane;GO:0031965 nuclear membrane",
        "go_biological_process": "GO:0002044 blood vessel endothelial cell migration involved in intussusceptive angiogenesis;GO:0001525 angiogenesis;GO:0030514 negative regulation of BMP signaling pathway;GO:1903053 regulation of extracellular matrix organization;GO:0032926 negative regulation of activin receptor signaling pathway",
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        "record_type": "protein"
    },
    {
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        "length": 486,
        "protein_name": "ArfGAP with FG repeats 2",
        "gene_name": "Agfg2",
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        "gene_names_uniprotkb": "Agfg2",
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        "protein_names_uniprotkb": "ArfGAP with FG repeats 2",
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        "go_molecular_function": "GO:0005096 GTPase activator activity;GO:0008270 zinc ion binding",
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    {
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        "length": 693,
        "protein_name": "Signal recognition particle subunit SRP68",
        "gene_name": "Srp68",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Srp68",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Signal recognition particle subunit SRP68; Signal recognition particle 68 kDa protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "severe congenital neutropenia (Disease Ontology:DOID:0050590)",
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        "function": "Component of the signal recognition particle (SRP) complex, a ribonucleoprotein complex that mediates the cotranslational targeting of secretory and membrane proteins to the endoplasmic reticulum (ER). The SRP complex interacts with the signal sequence in nascent secretory and membrane proteins and directs them to the membrane of the ER. The SRP complex targets the ribosome-nascent chain complex to the SRP receptor (SR), which is anchored in the ER, where SR compaction and GTPase rearrangement drive cotranslational protein translocation into the ER. Binds the signal recognition particle RNA (7SL RNA), SRP72 binds to this complex subsequently. The SRP complex possibly participates in the elongation arrest function., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0005047 signal recognition particle binding;GO:0030942 endoplasmic reticulum signal peptide binding;GO:0008312 7S RNA binding;GO:0019904 protein domain specific binding;GO:0043022 ribosome binding",
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        "gene_names_uniprotkb": "Mrpl39",
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        "protein_names_uniprotkb": "Large ribosomal subunit protein mL39; 39S ribosomal protein L39, mitochondrial",
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        "tax_id": 10116,
        "disease": "combined oxidative phosphorylation deficiency (Disease Ontology:DOID:0060286)",
        "pathway": " (rno:684304);  (R-RNO-5389840);  (R-RNO-5419276);  (R-RNO-9937383)",
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        "go_molecular_function": "GO:0000166 nucleotide binding",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005840 ribosome;GO:1990904 ribonucleoprotein complex;GO:0005762 mitochondrial large ribosomal subunit",
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    },
    {
        "uniprot_canonical_ac": "A0A8I6AEI1-1",
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        "length": 706,
        "protein_name": "HPS1, biogenesis of lysosomal organelles complex 3 subunit 1",
        "gene_name": "Hps1",
        "organism": "Rat",
        "refseq_name": "BLOC-3 complex member HPS1",
        "refseq_ac": "NP_001420708",
        "gene_names_uniprotkb": "Hps1",
        "gene_names_refseq": "Hps1; Hps",
        "protein_names_uniprotkb": "HPS1, biogenesis of lysosomal organelles complex 3 subunit 1",
        "protein_names_refseq": "BLOC-3 complex member HPS1; Hermansky-Pudlak syndrome 1 homolog",
        "tax_id": 10116,
        "disease": "oculocutaneous albinism (Disease Ontology:DOID:0050632); Hermansky-Pudlak syndrome 1 (Disease Ontology:DOID:0060539); platelet storage pool deficiency (Disease Ontology:DOID:2223); proteinuria (Disease Ontology:DOID:576)",
        "pathway": " (R-RNO-8876198)",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0046983 protein dimerization activity;GO:0005085 guanyl-nucleotide exchange factor activity",
        "go_cellular_component": "GO:0031085 BLOC-3 complex;GO:0005737 cytoplasm;GO:0031410 cytoplasmic vesicle",
        "go_biological_process": "GO:1903232 melanosome assembly;GO:0003016 respiratory system process;GO:0006629 lipid metabolic process;GO:0006954 inflammatory response;GO:0007283 spermatogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6AEI1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6G4I5-1",
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        "length": 625,
        "protein_name": "G-rich sequence factor 1",
        "gene_name": "Grsf1",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Grsf1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "G-rich sequence factor 1",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
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        "pathway_count": 0,
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        "publication_id_list": "",
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        "function": "Regulator of post-transcriptional mitochondrial gene expression, required for assembly of the mitochondrial ribosome and for recruitment of mRNA and lncRNA. Binds RNAs containing the 14 base G-rich element. Preferentially binds RNAs transcribed from three contiguous genes on the light strand of mtDNA, the ND6 mRNA, and the long non-coding RNAs for MT-CYB and MT-ND5, each of which contains multiple consensus binding sequences. Involved in the degradosome-mediated decay of non-coding mitochondrial transcripts (MT-ncRNA) and tRNA-like molecules. Acts by unwinding G-quadruplex RNA structures in MT-ncRNA, thus facilitating their degradation by the degradosome. G-quadruplexes (G4) are non-canonical 4 stranded structures formed by transcripts from the light strand of mtDNA., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003723 RNA binding;GO:0003729 mRNA binding",
        "go_cellular_component": "GO:0005759 mitochondrial matrix;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005739 mitochondrion;GO:0042645 mitochondrial nucleoid",
        "go_biological_process": "GO:0006397 mRNA processing;GO:0008033 tRNA processing;GO:0009952 anterior/posterior pattern specification;GO:0016331 morphogenesis of embryonic epithelium;GO:0043484 regulation of RNA splicing",
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    },
    {
        "uniprot_canonical_ac": "A0A8I6ALH8-1",
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        "length": 891,
        "protein_name": "TBC domain-containing protein kinase-like protein",
        "gene_name": "Tbck",
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        "protein_names_uniprotkb": "TBC domain-containing protein kinase-like protein",
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        "tax_id": 10116,
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        "function": "Component of the FERRY complex (Five-subunit Endosomal Rab5 and RNA/ribosome intermediary). The FERRY complex directly interacts with mRNAs and RAB5A, and functions as a RAB5A effector involved in the localization and the distribution of specific mRNAs most likely by mediating their endosomal transport. The complex recruits mRNAs and ribosomes to early endosomes through direct mRNA-interaction. Also involved in the modulation of mTOR signaling and expression of mTOR complex components. Involved in the control of actin-cytoskeleton organization., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0004672 protein kinase activity;GO:0005096 GTPase activator activity;GO:0005524 ATP binding",
        "go_cellular_component": "GO:0005769 early endosome;GO:0005819 spindle;GO:0030496 midbody;GO:0005737 cytoplasm;GO:0072686 mitotic spindle",
        "go_biological_process": "GO:0008283 cell population proliferation;GO:0030036 actin cytoskeleton organization;GO:0032006 regulation of TOR signaling",
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        "hit_score": 0.2,
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        "protein_name": "Eva-1 homolog A, regulator of programmed cell death",
        "gene_name": "Eva1a",
        "organism": "Rat",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Eva1a",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Eva-1 homolog A, regulator of programmed cell death",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "go_molecular_function": "",
        "go_cellular_component": "GO:0016020 membrane",
        "go_biological_process": "GO:0007507 heart development;GO:0006915 apoptotic process;GO:0030324 lung development;GO:0006914 autophagy;GO:0009791 post-embryonic development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6GHW1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6ADM6-1",
        "uniprot_id": "A0A8I6ADM6_RAT",
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        "length": 352,
        "protein_name": "Protein Wnt",
        "gene_name": "Wnt3a",
        "organism": "Rat",
        "refseq_name": "protein Wnt-3a precursor",
        "refseq_ac": "NP_001401278",
        "gene_names_uniprotkb": "Wnt3a",
        "gene_names_refseq": "Wnt3a",
        "protein_names_uniprotkb": "Protein Wnt",
        "protein_names_refseq": "protein Wnt-3a precursor; protein Wnt-3a; wingless-related MMTV integration site 3A; wingless-type MMTV integration site family, member 3A",
        "tax_id": 10116,
        "disease": "traumatic brain injury (Disease Ontology:DOID:0081292); hypothyroidism (Disease Ontology:DOID:1459)",
        "pathway": " (rno:303181)",
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        "publication_id_list": "33236141;33243628;34399774;36633501;37858855",
        "class_list": "",
        "function": "Ligand for members of the frizzled family of seven transmembrane receptors., [UniProtKB, UniProtKB, UniProtKB]; Morphological neurite changes induced by porcupine inhibition are rescued by Wnt ligands. Publication Status: Online-Only, [RefSeq, PubMed]; Wnt-3a improves functional recovery after spinal cord injury by regulating the inflammatory and apoptotic response in rats via wnt/beta-catenin signaling pathway., [RefSeq, PubMed]; Wnt3a promotes odonto/osteogenic differentiation in vitro and tertiary dentin formation in a rat model., [RefSeq, PubMed]; Wnt3a upregulation is involved in TGFbeta1-induced cardiac hypertrophy., [RefSeq, PubMed]; YAP and Wnt3a independently promote AECIIs proliferation and differentiation by increasing nuclear betacatenin expression in experimental bronchopulmonary dysplasia., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "secondary_ac_list": "",
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        "go_molecular_function": "GO:0005102 signaling receptor binding;GO:0003713 transcription coactivator activity;GO:0005109 frizzled binding;GO:0019904 protein domain specific binding;GO:0042802 identical protein binding",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0098978 glutamatergic synapse;GO:0005615 extracellular space;GO:0009986 cell surface;GO:0045202 synapse",
        "go_biological_process": "GO:0010557 positive regulation of macromolecule biosynthetic process;GO:0060070 canonical Wnt signaling pathway;GO:0010468 regulation of gene expression;GO:0048513 animal organ development;GO:2000347 positive regulation of hepatocyte proliferation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.6,
        "record_id": "A0A8I6ADM6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6AI89-1",
        "uniprot_id": "A0A8I6AI89_RAT",
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        "length": 796,
        "protein_name": "Vacuolar protein sorting-associated protein 35",
        "gene_name": "Vps35",
        "organism": "Rat",
        "refseq_name": "vacuolar protein sorting-associated protein 35",
        "refseq_ac": "NP_001099188",
        "gene_names_uniprotkb": "Vps35",
        "gene_names_refseq": "Mem3; Vps35",
        "protein_names_uniprotkb": "Vacuolar protein sorting-associated protein 35",
        "protein_names_refseq": "Maternal embryonic message 3; vacuolar protein sorting 35 homolog; vacuolar protein sorting-associated protein 35",
        "tax_id": 10116,
        "disease": "Parkinson's disease 17 (Disease Ontology:DOID:0060897); brain cancer (Disease Ontology:DOID:1319); Parkinson's disease (Disease Ontology:DOID:14330)",
        "pathway": " (rno:25479);  (R-RNO-3238698)",
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        "publication_count": 3,
        "publication_id_list": "22673903;37542299;37830626",
        "class_list": "",
        "function": "Plays a role in vesicular protein sorting., [UniProtKB, UniProtKB, UniProtKB]; Unveiling Neuroprotection and Regeneration Mechanisms in Optic Nerve Injury: Insight from Neural Progenitor Cell Therapy with Focus on Vps35 and Syntaxin12. Publication Status: Online-Only, [RefSeq, PubMed]; VPS35 and alpha-Synuclein fail to interact to modulate neurodegeneration in rodent models of Parkinson's disease. Publication Status: Online-Only, [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0031748 D1 dopamine receptor binding",
        "go_cellular_component": "GO:0030906 retromer, cargo-selective complex;GO:0005829 cytosol;GO:0005770 late endosome;GO:0030904 retromer complex;GO:0098978 glutamatergic synapse",
        "go_biological_process": "GO:0006886 intracellular protein transport;GO:0042147 retrograde transport, endosome to Golgi;GO:0050882 voluntary musculoskeletal movement;GO:0098887 neurotransmitter receptor transport, endosome to postsynaptic membrane;GO:2000331 regulation of terminal button organization",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "A0A8I6AI89-1",
        "record_type": "protein"
    },
    {
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        "protein_names_refseq": "heat shock factor protein 5; heat shock transcription factor 5 isoform 1; heat shock transcription factor family member 5",
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        "protein_names_refseq": "ankyrin repeat domain containing 11; ankyrin repeat domain-containing protein 11",
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        "protein_names_uniprotkb": "BCL2 interacting protein 3 like",
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        "disease": "metabolic dysfunction-associated steatohepatitis (Disease Ontology:DOID:0080547); gestational diabetes (Disease Ontology:DOID:11714); middle cerebral artery infarction (Disease Ontology:DOID:3525); pancreatitis (Disease Ontology:DOID:4989)",
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        "protein_names_uniprotkb": "Testis expressed 30",
        "protein_names_refseq": "testis-expressed protein 30; testis-expressed sequence 30 protein",
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        "protein_names_uniprotkb": "Hes-related family bHLH transcription factor with YRPW motif 1",
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        "go_molecular_function": "GO:0003700 DNA-binding transcription factor activity;GO:0042802 identical protein binding;GO:0046983 protein dimerization activity;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding",
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        "length": 127,
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        "refseq_ac": "",
        "gene_names_uniprotkb": "ENSRNOG00000070302",
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        "protein_names_uniprotkb": "Keratin-associated protein",
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        "refseq_ac": "NP_001385955",
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        "length": 136,
        "protein_name": "Histone H3",
        "gene_name": "H3f3bl2",
        "organism": "Rat",
        "refseq_name": "histone H3.3A-like",
        "refseq_ac": "XP_017445789",
        "gene_names_uniprotkb": "H3f3bl2; LOC108349691",
        "gene_names_refseq": "H3f3bl2",
        "protein_names_uniprotkb": "Histone H3",
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        "go_molecular_function": "GO:0046982 protein heterodimerization activity;GO:0031492 nucleosomal DNA binding;GO:0030527 structural constituent of chromatin",
        "go_cellular_component": "GO:0005634 nucleus;GO:0000776 kinetochore;GO:0000786 nucleosome",
        "go_biological_process": "GO:0051382 kinetochore assembly;GO:0007080 mitotic metaphase chromosome alignment;GO:0031507 heterochromatin formation",
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        "record_id": "A0A8I6A289-1",
        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "A0A8I6A2C1-1",
        "uniprot_id": "A0A8I6A2C1_RAT",
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        "length": 76,
        "protein_name": "Small nuclear ribonucleoprotein G",
        "gene_name": "LOC120100604",
        "organism": "Rat",
        "refseq_name": "small nuclear ribonucleoprotein G-like",
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        "gene_names_uniprotkb": "LOC120100604",
        "gene_names_refseq": "LOC120100604",
        "protein_names_uniprotkb": "Small nuclear ribonucleoprotein G; snRNP-G",
        "protein_names_refseq": "small nuclear ribonucleoprotein G-like",
        "tax_id": 10116,
        "disease": "nasopharynx carcinoma (Disease Ontology:DOID:9261)",
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        "function": "Plays role in pre-mRNA splicing as core component of the SMN-Sm complex that mediates spliceosomal snRNP assembly and as component of the spliceosomal U1, U2, U4 and U5 small nuclear ribonucleoproteins (snRNPs), the building blocks of the spliceosome. Component of both the pre-catalytic spliceosome B complex and activated spliceosome C complexes. Is also a component of the minor U12 spliceosome. As part of the U7 snRNP it is involved in histone 3'-end processing., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0003723 RNA binding",
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        "uniprot_canonical_ac": "A0A8I6A2H6-1",
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        "length": 523,
        "protein_name": "Calcium uptake protein 3, mitochondrial",
        "gene_name": "Micu3",
        "organism": "Rat",
        "refseq_name": "calcium uptake protein 3, mitochondrial isoform 1",
        "refseq_ac": "NP_001423513",
        "gene_names_uniprotkb": "Micu3",
        "gene_names_refseq": "Efha2; Micu3",
        "protein_names_uniprotkb": "Calcium uptake protein 3, mitochondrial",
        "protein_names_refseq": "EF hand domain family, member A2; EF-hand domain-containing family member A2; calcium uptake protein 3, mitochondrial isoform 1; calcium uptake protein 3, mitochondrial; mitochondrial calcium uptake family, member 3; mitochondrial uptake family, member 3",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:364601);  (R-RNO-8949215);  (R-RNO-8949664)",
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        "publication_id_list": "31862210;36549422",
        "class_list": "",
        "function": "Downregulation of mitochondrial calcium uptake family 3 attenuates secondary brain injury after intracerebral hemorrhage in rats., [RefSeq, PubMed]; Tissue-specific calcium sensor of the mitochondrial calcium uniporter (MCU) channel, which specifically regulates MCU channel activity in the central nervous system and skeletal muscle (PubMed:31862210). Senses calcium level via its EF-hand domains: compared to MICU1 and MICU2, MICU3 has a higher affinity for calcium (PubMed:31862210). MICU1 and MICU3 form a disulfide-linked heterodimer that stimulates and inhibits MCU activity, depending on the concentration of calcium (PubMed:31862210). At low calcium levels, MICU1 occludes the pore of the MCU channel, preventing mitochondrial calcium uptake (PubMed:31862210). At higher calcium levels, calcium-binding to MICU1 and MICU3 induces a conformational change that weakens MCU-MICU1 interactions and moves the MICU1-MICU3 heterodimer away from the pore, allowing calcium permeation through the MCU channel (PubMed:31862210). The high calcium affinity of MICU3 lowers the calcium threshold necessary for calcium permeation through the MCU channel (PubMed:31862210). The MICU1-MICU3 heterodimer promotes flexibility of neurotransmission in neuronal cells by enhancing mitochondrial calcium uptake in presynapses (PubMed:31862210). It is also required to increase mitochondrial calcium uptake in skeletal muscle cells, thereby increasing ATP production (By similarity)., [UniProtKB, UniProtKB, PubMed]",
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    },
    {
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        "uniprot_id": "FIGL2_RAT",
        "mass": 66314.0,
        "length": 648,
        "protein_name": "Fidgetin-like protein 2",
        "gene_name": "Fignl2",
        "organism": "Rat",
        "refseq_name": "fidgetin-like protein 2",
        "refseq_ac": "NP_001388812",
        "gene_names_uniprotkb": "Fignl2",
        "gene_names_refseq": "AABR07058914.1; Fignl2; RGD1566321",
        "protein_names_uniprotkb": "Fidgetin-like protein 2; 3.6.4.-",
        "protein_names_refseq": "fidgetin-like protein 2; putative fidgetin-like protein 2-like",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:102555469)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "33872220",
        "class_list": "",
        "function": "Microtubule-severing enzyme that negatively regulates cell migration and wound healing (By similarity). In migrating cells, targets dynamic microtubules (MTs) at the leading edge and severs them, thereby suppressing motility (By similarity). Microtubule severing releases ARHGEF2 which activates RHOA, which in turn regulates focal ahesion turnover via focal adhesion kinase, as opposed to F-actin polymerization, to suppress cell motility (By similarity). Negative regulator of axon regeneration that suppresses axonal growth by selectively severing dynamic MTs in the distal axon shaft and growth cone (PubMed:33872220). Contributes to proper cell branching during endothelial and neuronal development (By similarity)., [UniProtKB, PubMed, UniProtKB, UniProtKB]",
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        "ec_number_list": "5.6.2.3;3.6.4.13;3.6.4.12;2.7.11.1;3.6.1.5;3.6.4.10;3.6.4.-;2.3.2.27;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:0008568 microtubule severing ATPase activity;GO:0005524 ATP binding;GO:0016887 ATP hydrolysis activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005938 cell cortex;GO:0031252 cell leading edge",
        "go_biological_process": "GO:1903690 negative regulation of wound healing, spreading of epidermal cells;GO:0051013 microtubule severing;GO:0030336 negative regulation of cell migration;GO:0001763 morphogenesis of a branching structure;GO:0048681 negative regulation of axon regeneration",
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    },
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        "length": 875,
        "protein_name": "GRB2-associated and regulator of MAPK1",
        "gene_name": "Garem1",
        "organism": "Rat",
        "refseq_name": "GRB2-associated and regulator of MAPK protein 1",
        "refseq_ac": "NP_001414178",
        "gene_names_uniprotkb": "Garem1",
        "gene_names_refseq": "Garem1; Garem; RGD1562080",
        "protein_names_uniprotkb": "GRB2-associated and regulator of MAPK1",
        "protein_names_refseq": "GRB2 associated regulator of MAPK1, member 1; GRB2 associated, regulator of MAPK1; GRB2-associated and regulator of MAPK protein 1; GRB2-associated and regulator of MAPK protein-like",
        "tax_id": 10116,
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        "publication_id_list": "24003223",
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        "function": "Acts as an adapter protein that plays a role in intracellular signaling cascades triggered either by the cell surface activated epidermal growth factor receptor and/or cytoplasmic protein tyrosine kinases. Promotes activation of the MAPK/ERK signaling pathway. Plays a role in the regulation of cell proliferation., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Data indicate that a subtype of GAREM, GAREM2, is specifically expressed in the mouse, rat, and human brain., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0070064 proline-rich region binding",
        "go_cellular_component": "",
        "go_biological_process": "GO:0008284 positive regulation of cell population proliferation;GO:0070374 positive regulation of ERK1 and ERK2 cascade;GO:0035264 multicellular organism growth;GO:0007173 epidermal growth factor receptor signaling pathway;GO:0071364 cellular response to epidermal growth factor stimulus",
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    },
    {
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        "length": 189,
        "protein_name": "small monomeric GTPase",
        "gene_name": "Hrasl1",
        "organism": "Rat",
        "refseq_name": "HRas proto-oncogene, GTPase like 1",
        "refseq_ac": "NP_001395928",
        "gene_names_uniprotkb": "Hrasl1; LOC367858",
        "gene_names_refseq": "AABR07039356.1; Hrasl1",
        "protein_names_uniprotkb": "small monomeric GTPase; 3.6.5.2",
        "protein_names_refseq": "GTPase HRas; HRas proto-oncogene, GTPase like 1",
        "tax_id": 10116,
        "disease": "Costello syndrome (Disease Ontology:DOID:0050469); cardiomyopathy (Disease Ontology:DOID:0050700); Noonan syndrome 3 (Disease Ontology:DOID:0060581); RASopathy (Disease Ontology:DOID:0080690); epidermal nevus (Disease Ontology:DOID:0111162); large congenital melanocytic nevus (Disease Ontology:DOID:0111359); linear nevus sebaceous syndrome (Disease Ontology:DOID:0111530); intestinal cancer (Disease Ontology:DOID:10155); prostate cancer (Disease Ontology:DOID:10283); Alzheimer's disease (Disease Ontology:DOID:10652); obsessive-compulsive disorder (Disease Ontology:DOID:10933); urinary bladder cancer (Disease Ontology:DOID:11054); heart disease (Disease Ontology:DOID:114); hypertrophic cardiomyopathy (Disease Ontology:DOID:11984); leukemia (Disease Ontology:DOID:1240); autistic disorder (Disease Ontology:DOID:12849); cancer (Disease Ontology:DOID:162); squamous cell carcinoma (Disease Ontology:DOID:1749); autoimmune hepatitis (Disease Ontology:DOID:2048); kidney cancer (Disease Ontology:DOID:263); transitional cell carcinoma (Disease Ontology:DOID:2671); endometrial carcinoma (Disease Ontology:DOID:2871); carcinoma (Disease Ontology:DOID:305); glioblastoma (Disease Ontology:DOID:3068); malignant astrocytoma (Disease Ontology:DOID:3069); high grade glioma (Disease Ontology:DOID:3070); skin benign neoplasm (Disease Ontology:DOID:3165); papillary thyroid carcinoma (Disease Ontology:DOID:3969); cervical cancer (Disease Ontology:DOID:4362); seminoma (Disease Ontology:DOID:4440); liver cirrhosis (Disease Ontology:DOID:5082); phobic disorder (Disease Ontology:DOID:591); hepatocellular carcinoma (Disease Ontology:DOID:684); colorectal cancer (Disease Ontology:DOID:9256)",
        "pathway": " (rno:367858)",
        "pathway_count": 1,
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        "ec_number_list": "3.6.5.2;3.6.1.1;3.6.5.-;3.6.5.3;2.3.2.27;2.7.11.1;3.6.5.5;3.6.1.5;3.6.1.-;3.6.5.4",
        "go_molecular_function": "GO:0003924 GTPase activity;GO:0005525 GTP binding;GO:0003925 G protein activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
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        "length": 808,
        "protein_name": "Enhancer of polycomb homolog",
        "gene_name": "Epc2l1",
        "organism": "Rat",
        "refseq_name": "enhancer of polycomb homolog 2 (Drosophila)-like 1",
        "refseq_ac": "NP_001395698",
        "gene_names_uniprotkb": "Epc2l1; AC142154.1",
        "gene_names_refseq": "Epc2l1; RGD1561337",
        "protein_names_uniprotkb": "Enhancer of polycomb homolog",
        "protein_names_refseq": "enhancer of polycomb homolog 2 (Drosophila)-like 1; enhancer of polycomb homolog 2-like",
        "tax_id": 10116,
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        "pathway": " (rno:499105)",
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        "go_molecular_function": "GO:0030674 protein-macromolecule adaptor activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0035267 NuA4 histone acetyltransferase complex;GO:0032777 piccolo histone acetyltransferase complex",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0006325 chromatin organization",
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        "length": 103,
        "protein_name": "Ig-like domain-containing protein",
        "gene_name": "ENSRNOG00000062682",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "ENSRNOG00000062682",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ig-like domain-containing protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-173623);  (R-RNO-198933);  (R-RNO-202733);  (R-RNO-2029481);  (R-RNO-2029482);  (R-RNO-2029485);  (R-RNO-2168880);  (R-RNO-2454202);  (R-RNO-2730905);  (R-RNO-2871796);  (R-RNO-2871809);  (R-RNO-2871837);  (R-RNO-5690714);  (R-RNO-977606);  (R-RNO-983695)",
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003823 antigen binding",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0019814 immunoglobulin complex",
        "go_biological_process": "GO:0016064 immunoglobulin mediated immune response",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6AKK2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6AKW7-1",
        "uniprot_id": "A0A8I6AKW7_RAT",
        "mass": 45022.0,
        "length": 407,
        "protein_name": "Protein arginine methyltransferase NDUFAF7",
        "gene_name": "AABR07025743.1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "AABR07025743.1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Protein arginine methyltransferase NDUFAF7; 2.1.1.320",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
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        "publication_id_list": "",
        "class_list": "",
        "function": "Arginine methyltransferase involved in the assembly or stability of mitochondrial NADH:ubiquinone oxidoreductase complex (complex I). Acts by mediating symmetric dimethylation of 'Arg-118' of NDUFS2 after it assembles into the complex I, stabilizing the early intermediate complex., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "biomarker_type": "",
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        "ec_number_list": "2.1.1.320",
        "go_molecular_function": "GO:0035243 protein-arginine omega-N symmetric methyltransferase activity",
        "go_cellular_component": "GO:0005739 mitochondrion",
        "go_biological_process": "GO:0032981 mitochondrial respiratory chain complex I assembly;GO:0032259 methylation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
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        "record_type": "protein"
    },
    {
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        "ec_number_list": "",
        "go_molecular_function": "GO:0046914 transition metal ion binding;GO:0005509 calcium ion binding",
        "go_cellular_component": "GO:0001533 cornified envelope;GO:0036457 keratohyalin granule",
        "go_biological_process": "GO:0061436 establishment of skin barrier",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6AT81-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6AU44-1",
        "uniprot_id": "A0A8I6AU44_RAT",
        "mass": 9012.0,
        "length": 79,
        "protein_name": "Dolichyl-diphosphooligosaccharide-protein glycosyltransferase subunit TMEM258",
        "gene_name": "Tmem258l5",
        "organism": "Rat",
        "refseq_name": "transmembrane protein 258-like",
        "refseq_ac": "XP_038959242",
        "gene_names_uniprotkb": "Tmem258l5; LOC100363048",
        "gene_names_refseq": "Tmem258l5",
        "protein_names_uniprotkb": "Dolichyl-diphosphooligosaccharide-protein glycosyltransferase subunit TMEM258; Transmembrane protein 258",
        "protein_names_refseq": "transmembrane protein 258-like",
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        "pathway": " (rno:100363048)",
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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]",
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        "go_molecular_function": "GO:0062062 oligosaccharyltransferase complex binding",
        "go_cellular_component": "GO:0005789 endoplasmic reticulum membrane;GO:0008250 oligosaccharyltransferase complex",
        "go_biological_process": "GO:0006487 protein N-linked glycosylation;GO:0034976 response to endoplasmic reticulum stress",
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        "hit_score": 0.1,
        "record_id": "A0A8I6AU44-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6AUS6-1",
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        "protein_name": "Purkinje cell protein 4-like 1",
        "gene_name": "Pcp4l1",
        "organism": "Rat",
        "refseq_name": "Purkinje cell protein 4-like protein 1 isoform X2",
        "refseq_ac": "XP_063128675",
        "gene_names_uniprotkb": "Pcp4l1",
        "gene_names_refseq": "Pcp4l1",
        "protein_names_uniprotkb": "Purkinje cell protein 4-like 1",
        "protein_names_refseq": "Purkinje cell protein 4-like protein 1 isoform X2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:685448)",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6AW68-1",
        "uniprot_id": "A0A8I6AW68_RAT",
        "mass": 31038.0,
        "length": 269,
        "protein_name": "Prolactin family 7, subfamily a, member 1 like, pseudogene",
        "gene_name": "Prl7a1l-ps1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Prl7a1l-ps1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Prolactin family 7, subfamily a, member 1 like, pseudogene",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "alcohol dependence (Disease Ontology:DOID:0050741); withdrawal disorder (Disease Ontology:DOID:0060001); impulse control disorder (Disease Ontology:DOID:10937); depressive disorder (Disease Ontology:DOID:1596); severe acute respiratory syndrome (Disease Ontology:DOID:2945); carotid artery disease (Disease Ontology:DOID:3407); prolactinoma (Disease Ontology:DOID:5394); hepatocellular carcinoma (Disease Ontology:DOID:684); cocaine abuse (Disease Ontology:DOID:809); obesity (Disease Ontology:DOID:9970); cocaine dependence (Disease Ontology:DOID:9975); hypoglycemia (Disease Ontology:DOID:9993)",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0005148 prolactin receptor binding;GO:0046872 metal ion binding;GO:0005179 hormone activity",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005576 extracellular region",
        "go_biological_process": "GO:0007166 cell surface receptor signaling pathway;GO:0031667 response to nutrient levels;GO:0007565 female pregnancy;GO:0046427 positive regulation of receptor signaling pathway via JAK-STAT;GO:0030879 mammary gland development",
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        "hit_score": 0.1,
        "record_id": "A0A8I6AW68-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6AWT3-1",
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        "length": 212,
        "protein_name": "Histone H2A",
        "gene_name": "ENSRNOG00000062927",
        "organism": "Rat",
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        "gene_names_uniprotkb": "ENSRNOG00000062927",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Histone H2A",
        "protein_names_refseq": "",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0046982 protein heterodimerization activity;GO:0030527 structural constituent of chromatin",
        "go_cellular_component": "GO:0005634 nucleus;GO:0000786 nucleosome",
        "go_biological_process": "GO:0031507 heterochromatin formation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6AWT3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6AWV7-1",
        "uniprot_id": "A0A8I6AWV7_RAT",
        "mass": 87968.0,
        "length": 755,
        "protein_name": "Zinc finger protein 808 like 1",
        "gene_name": "Zfp808l1",
        "organism": "Rat",
        "refseq_name": "zinc finger protein 431-like",
        "refseq_ac": "XP_038964868",
        "gene_names_uniprotkb": "Zfp808l1; LOC102547920",
        "gene_names_refseq": "Zfp808l1",
        "protein_names_uniprotkb": "Zinc finger protein 808 like 1",
        "protein_names_refseq": "zinc finger protein 431-like",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:102547920)",
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        "go_molecular_function": "GO:0008270 zinc ion binding",
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        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006355 regulation of DNA-templated transcription",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6AWV7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6B3N3-1",
        "uniprot_id": "A0A8I6B3N3_RAT",
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        "length": 118,
        "protein_name": "V-type proton ATPase subunit G",
        "gene_name": "Atp6v1g1",
        "organism": "Rat",
        "refseq_name": "V-type proton ATPase subunit G 1",
        "refseq_ac": "NP_001100130",
        "gene_names_uniprotkb": "Atp6v1g1",
        "gene_names_refseq": "Atp6v1g1",
        "protein_names_uniprotkb": "V-type proton ATPase subunit G",
        "protein_names_refseq": "ATPase, H transporting, lysosomal V1 subunit G1; ATPase, H+ transporting, V1 subunit G; V-type proton ATPase subunit G 1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:298103);  (R-RNO-1222556);  (R-RNO-77387);  (R-RNO-917977);  (R-RNO-9639288);  (R-RNO-983712)",
        "pathway_count": 6,
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        "publication_id_list": "",
        "class_list": "",
        "function": "Subunit of the V1 complex of vacuolar(H+)-ATPase (V-ATPase), a multisubunit enzyme composed of a peripheral complex (V1) that hydrolyzes ATP and a membrane integral complex (V0) that translocates protons. V-ATPase is responsible for acidifying and maintaining the pH of intracellular compartments and in some cell types, is targeted to the plasma membrane, where it is responsible for acidifying the extracellular environment., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0051117 ATPase binding;GO:0046961 proton-transporting ATPase activity, rotational mechanism",
        "go_cellular_component": "GO:0033180 proton-transporting V-type ATPase, V1 domain;GO:0033176 proton-transporting V-type ATPase complex;GO:0098850 extrinsic component of synaptic vesicle membrane;GO:0005829 cytosol;GO:0005886 plasma membrane",
        "go_biological_process": "GO:0006879 intracellular iron ion homeostasis;GO:0036295 cellular response to increased oxygen levels;GO:0097401 synaptic vesicle lumen acidification",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6B3N3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6G2S6-1",
        "uniprot_id": "A0A8I6G2S6_RAT",
        "mass": 35202.0,
        "length": 313,
        "protein_name": "rRNA adenine N(6)-methyltransferase",
        "gene_name": "Dimt1",
        "organism": "Rat",
        "refseq_name": "probable dimethyladenosine transferase",
        "refseq_ac": "NP_001099878",
        "gene_names_uniprotkb": "Dimt1",
        "gene_names_refseq": "Dimt1l; Dimt1; RGD1311752",
        "protein_names_uniprotkb": "rRNA adenine N(6)-methyltransferase; 2.1.1.-",
        "protein_names_refseq": "DIM1 dimethyladenosine transferase 1 homolog; DIM1 dimethyladenosine transferase 1-like; DIMT1 rRNA methyltransferase and ribosome maturation factor; probable dimethyladenosine transferase",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
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        "publication_id_list": "",
        "class_list": "",
        "function": "Specifically dimethylates two adjacent adenosines in the loop of a conserved hairpin near the 3'-end of 18S rRNA in the 40S particle. Involved in the pre-rRNA processing steps leading to small-subunit rRNA production independently of its RNA-modifying catalytic activity. 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]",
        "predicted_glycosites": 0,
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        "gene_names_uniprotkb": "Plekha7",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Pleckstrin homology domain containing A7",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "glomerulosclerosis (Disease Ontology:DOID:0050851); hypertension (Disease Ontology:DOID:10763)",
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        "function": "Required for zonula adherens biogenesis and maintenance. Acts via its interaction with CAMSAP3, which anchors microtubules at their minus-ends to zonula adherens, leading to the recruitment of KIFC3 kinesin to the junctional site. Mediates docking of ADAM10 to zonula adherens through a PDZD11-dependent interaction with the ADAM10-binding protein TSPAN33., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_biological_process": "GO:0042311 vasodilation;GO:0046931 pore complex assembly;GO:0044331 cell-cell adhesion mediated by cadherin;GO:0045218 zonula adherens maintenance;GO:0090136 epithelial cell-cell adhesion",
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        "protein_name": "BPTF-associated chromatin complex component 1",
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        "gene_names_uniprotkb": "Bacc1; Rnasek; Bacc1; C10h17orf49; RGD1308134",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "BPTF-associated chromatin complex component 1; BPTF-associated protein of 18 kDa",
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        "pathway": " (rno:287453)",
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        "publication_id_list": "22673903;32165585;38900912",
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        "function": "Component of chromatin complexes such as the MLL1/MLL and NURF complexes., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_biological_process": "GO:0006898 receptor-mediated endocytosis;GO:0048388 endosomal lumen acidification;GO:0019065 receptor-mediated endocytosis of virus by host cell;GO:1902600 proton transmembrane transport;GO:0006325 chromatin organization",
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        "go_biological_process": "GO:0007010 cytoskeleton organization;GO:0006366 transcription by RNA polymerase II;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0030032 lamellipodium assembly;GO:0060271 cilium assembly",
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        "protein_name": "Nuclear receptor-binding protein",
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        "gene_names_refseq": "Nrbp1; Nrbp",
        "protein_names_uniprotkb": "Nuclear receptor-binding protein",
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        "go_molecular_function": "GO:0004672 protein kinase activity;GO:0005524 ATP binding;GO:0042802 identical protein binding;GO:0042803 protein homodimerization activity",
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        "go_biological_process": "GO:0035556 intracellular signal transduction;GO:0006888 endoplasmic reticulum to Golgi vesicle-mediated transport;GO:0001701 in utero embryonic development;GO:0030855 epithelial cell differentiation;GO:0050673 epithelial cell proliferation",
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    {
        "uniprot_canonical_ac": "A0A8I5ZPP7-1",
        "uniprot_id": "A0A8I5ZPP7_RAT",
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        "length": 3203,
        "protein_name": "Laminin subunit alpha-2",
        "gene_name": "Lama2",
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        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Lama2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Laminin subunit alpha-2; Laminin M chain; Laminin-12 subunit alpha; Laminin-2 subunit alpha; Laminin-4 subunit alpha; Merosin heavy chain",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "autosomal recessive limb-girdle muscular dystrophy type 23 (Disease Ontology:DOID:0061132); congenital merosin-deficient muscular dystrophy 1A (Disease Ontology:DOID:0110636); myopia (Disease Ontology:DOID:11830); renovascular hypertension (Disease Ontology:DOID:1591); muscular dystrophy (Disease Ontology:DOID:9884)",
        "pathway": " (rno:309368)",
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        "class_list": "",
        "function": "Binding to cells via a high affinity receptor, laminin is thought to mediate the attachment, migration and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 2,
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        "go_molecular_function": "GO:0005102 signaling receptor binding;GO:0005201 extracellular matrix structural constituent",
        "go_cellular_component": "GO:0031594 neuromuscular junction;GO:0043197 dendritic spine;GO:0043083 synaptic cleft;GO:0042383 sarcolemma;GO:0005604 basement membrane",
        "go_biological_process": "GO:0032224 positive regulation of synaptic transmission, cholinergic;GO:0007155 cell adhesion;GO:0030155 regulation of cell adhesion;GO:0009887 animal organ morphogenesis;GO:0030334 regulation of cell migration",
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    },
    {
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        "length": 6900,
        "protein_name": "Nesprin-2",
        "gene_name": "Syne2",
        "organism": "Rat",
        "refseq_name": "nesprin-2 isoform X5",
        "refseq_ac": "XP_038969191",
        "gene_names_uniprotkb": "Syne2",
        "gene_names_refseq": "AABR07064873.1; RGD1305248; Syne2",
        "protein_names_uniprotkb": "Nesprin-2; KASH domain-containing protein 2; Nuclear envelope spectrin repeat protein 2; Nucleus and actin connecting element protein; Synaptic nuclear envelope protein 2",
        "protein_names_refseq": "nesprin-2 isoform X5",
        "tax_id": 10116,
        "disease": "autosomal dominant Emery-Dreifuss muscular dystrophy 5 (Disease Ontology:DOID:0070250); cryptorchidism (Disease Ontology:DOID:11383); Emery-Dreifuss muscular dystrophy (Disease Ontology:DOID:11726)",
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        "go_molecular_function": "GO:0003779 actin binding;GO:0019894 kinesin binding;GO:0140444 cytoskeleton-nuclear membrane anchor activity",
        "go_cellular_component": "GO:0005640 nuclear outer membrane;GO:0005654 nucleoplasm;GO:0005739 mitochondrion;GO:0005856 cytoskeleton;GO:0005886 plasma membrane",
        "go_biological_process": "GO:1902017 regulation of cilium assembly;GO:0051642 centrosome localization;GO:0007097 nuclear migration;GO:0021817 nucleokinesis involved in cell motility in cerebral cortex radial glia guided migration;GO:0031022 nuclear migration along microfilament",
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    {
        "uniprot_canonical_ac": "A0A8I5ZTX5-1",
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        "length": 885,
        "protein_name": "Phosphodiesterase",
        "gene_name": "Pde8b",
        "organism": "Rat",
        "refseq_name": "high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8B isoform 1",
        "refseq_ac": "NP_954889",
        "gene_names_uniprotkb": "Pde8b",
        "gene_names_refseq": "Pde8b; RNPDE8B",
        "protein_names_uniprotkb": "Phosphodiesterase; 3.1.4.-",
        "protein_names_refseq": "cAMP-specific cyclic nucleotide phosphodiesterase PDE8; high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8B isoform 1; high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8B",
        "tax_id": 10116,
        "disease": "primary pigmented nodular adrenocortical disease 3 (Disease Ontology:DOID:0070548)",
        "pathway": " (R-RNO-418555)",
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        "publication_id_list": "17991719",
        "class_list": "",
        "function": "Hydrolyzes the second messenger cAMP, which is a key regulator of many important physiological processes. May be involved in specific signaling in the thyroid gland., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; PDE8B, an 3-isobutyl-1-methylxanthine-insensitive cAMP-specific phosphodiesterase, could prove a novel target for enhanced insulin response, [RefSeq, PubMed]",
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        "refseq_name": "vacuolar protein sorting-associated protein 4B",
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        "publication_id_list": "22673903;24077878",
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        "go_biological_process": "GO:0015031 protein transport;GO:0051301 cell division;GO:0016197 endosomal transport;GO:0007033 vacuole organization;GO:0090611 ubiquitin-independent protein catabolic process via the multivesicular body sorting pathway",
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        "protein_names_uniprotkb": "Pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial",
        "protein_names_refseq": "pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial",
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        "function": "Decreases the sensitivity of PDP1 to magnesium ions, and this inhibition is reversed by the polyamine spermine., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "protein_name": "Muscleblind-like protein 1",
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        "refseq_name": "muscleblind-like protein 1 isoform 1",
        "refseq_ac": "NP_001178495",
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        "gene_names_refseq": "Mbnl1; Mbnl",
        "protein_names_uniprotkb": "Muscleblind-like protein 1",
        "protein_names_refseq": "muscleblind-like 1; muscleblind-like protein 1 isoform 1; muscleblind-like protein 1",
        "tax_id": 10116,
        "disease": "myotonic dystrophy type 2 (Disease Ontology:DOID:0050759); myotonic dystrophy type 1 (Disease Ontology:DOID:11722); dilated cardiomyopathy (Disease Ontology:DOID:12930); myotonic disease (Disease Ontology:DOID:450); schizophrenia (Disease Ontology:DOID:5419)",
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        "go_molecular_function": "GO:0001069 regulatory region RNA binding;GO:0003723 RNA binding;GO:0008270 zinc ion binding;GO:0003725 double-stranded RNA binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0010494 cytoplasmic stress granule",
        "go_biological_process": "GO:0001701 in utero embryonic development;GO:0007399 nervous system development;GO:0030326 embryonic limb morphogenesis;GO:0008380 RNA splicing;GO:0043484 regulation of RNA splicing",
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        "length": 780,
        "protein_name": "ADP-ribosylation factor like GTPase 9",
        "gene_name": "Arl9",
        "organism": "Rat",
        "refseq_name": "ADP-ribosylation factor-like protein 9 isoform X1",
        "refseq_ac": "XP_017454588",
        "gene_names_uniprotkb": "Arl9",
        "gene_names_refseq": "Arl9",
        "protein_names_uniprotkb": "ADP-ribosylation factor like GTPase 9",
        "protein_names_refseq": "ADP-ribosylation factor-like protein 9 isoform X1",
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        "pathway": " (rno:289565)",
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        "length": 1845,
        "protein_name": "Coiled coil domain containing 88A",
        "gene_name": "Ccdc88a",
        "organism": "Rat",
        "refseq_name": "girdin isoform X2",
        "refseq_ac": "XP_038948821",
        "gene_names_uniprotkb": "Ccdc88a",
        "gene_names_refseq": "Ape; Ccdc88a; GIV; Hkrp1; RGD1306694",
        "protein_names_uniprotkb": "Coiled coil domain containing 88A",
        "protein_names_refseq": "girdin isoform X2",
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        "pathway": " (rno:305605);  (R-RNO-9696264);  (R-RNO-9696273)",
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        "go_molecular_function": "GO:0003779 actin binding;GO:0005158 insulin receptor binding;GO:0008017 microtubule binding;GO:0042803 protein homodimerization activity;GO:0005080 protein kinase C binding",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005794 Golgi apparatus;GO:0005813 centrosome;GO:0005829 cytosol;GO:0005886 plasma membrane",
        "go_biological_process": "GO:0016477 cell migration;GO:0032956 regulation of actin cytoskeleton organization;GO:0042127 regulation of cell population proliferation;GO:0051897 positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction;GO:0061024 membrane organization",
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        "protein_name": "Developmental pluripotency associated 1, pseudogene 1",
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        "protein_names_uniprotkb": "Developmental pluripotency associated 1, pseudogene 1",
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        "length": 354,
        "protein_name": "Killer cell lectin-like receptor subfamily A, member 22",
        "gene_name": "ENSRNOG00000062693; Klra22",
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        "gene_names_uniprotkb": "ENSRNOG00000062693; Klra22",
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        "disease": "fetal alcohol spectrum disorder (Disease Ontology:DOID:0050696); alcohol dependence (Disease Ontology:DOID:0050741); nicotine dependence (Disease Ontology:DOID:0050742); Parkinsonism (Disease Ontology:DOID:0080855); traumatic brain injury (Disease Ontology:DOID:0081292); migraine with aura (Disease Ontology:DOID:10024); Alzheimer's disease (Disease Ontology:DOID:10652); hypertension (Disease Ontology:DOID:10763); Gilles de la Tourette syndrome (Disease Ontology:DOID:11119); hyperprolactinemia (Disease Ontology:DOID:12700); dementia (Disease Ontology:DOID:1307); Parkinson's disease (Disease Ontology:DOID:14330); alcohol use disorder (Disease Ontology:DOID:1574); depressive disorder (Disease Ontology:DOID:1596); drug psychosis (Disease Ontology:DOID:1742); anxiety disorder (Disease Ontology:DOID:2030); brain ischemia (Disease Ontology:DOID:2316); alcohol-induced mental disorder (Disease Ontology:DOID:251); opiate dependence (Disease Ontology:DOID:2559); morphine dependence (Disease Ontology:DOID:2560); toxic encephalopathy (Disease Ontology:DOID:3602); primary hyperaldosteronism (Disease Ontology:DOID:446); movement disease (Disease Ontology:DOID:480); schizophrenia (Disease Ontology:DOID:5419); ovarian hyperstimulation syndrome (Disease Ontology:DOID:5425); end stage renal disease (Disease Ontology:DOID:783); type 2 diabetes mellitus (Disease Ontology:DOID:9352); obesity (Disease Ontology:DOID:9970); cocaine dependence (Disease Ontology:DOID:9975); heroin dependence (Disease Ontology:DOID:9976)",
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        "protein_name": "Ataxin 2",
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        "protein_names_refseq": "THO complex subunit 7 homolog isoform X1",
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        "protein_names_uniprotkb": "Microfibril associated protein 5",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific",
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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": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "3.1.3.-;3.1.3.95;3.1.3.36;3.1.3.64",
        "go_molecular_function": "GO:0043812 phosphatidylinositol-4-phosphate phosphatase activity;GO:0034596 phosphatidylinositol phosphate 4-phosphatase activity;GO:0042803 protein homodimerization activity;GO:0034595 phosphatidylinositol phosphate 5-phosphatase activity;GO:0052833 inositol monophosphate 4-phosphatase activity",
        "go_cellular_component": "GO:0005769 early endosome;GO:0045334 clathrin-coated endocytic vesicle;GO:0005737 cytoplasm;GO:0005905 clathrin-coated pit;GO:0030424 axon",
        "go_biological_process": "GO:0051896 regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction;GO:0046627 negative regulation of insulin receptor signaling pathway;GO:0051898 negative regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction;GO:0046856 phosphatidylinositol dephosphorylation;GO:2001135 regulation of endocytic recycling",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A8I5ZLP4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A096MKD1-1",
        "uniprot_id": "A0A096MKD1_RAT",
        "mass": 27850.0,
        "length": 244,
        "protein_name": "EEF1A lysine methyltransferase 1",
        "gene_name": "Eef1akmt1",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Eef1akmt1; EEF1AKMT1; N6AMT2; N6amt2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "EEF1A lysine methyltransferase 1; 2.1.1.-; N(6)-adenine-specific DNA methyltransferase 2; Protein-lysine N-methyltransferase N6AMT2",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-8876725)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Protein-lysine methyltransferase that selectively catalyzes the trimethylation of EEF1A at 'Lys-79'., [UniProtKB, HAMAP, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
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        "reported_phosphosites": 0,
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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": "2.1.1.-;2.1.1.359;2.1.1.372;3.6.5.-",
        "go_molecular_function": "GO:0003676 nucleic acid binding;GO:0016279 protein-lysine N-methyltransferase activity;GO:0008168 methyltransferase activity",
        "go_cellular_component": "GO:0005737 cytoplasm",
        "go_biological_process": "GO:0032259 methylation;GO:0018022 peptidyl-lysine methylation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A096MKD1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZLE8-1",
        "uniprot_id": "A0A8I5ZLE8_RAT",
        "mass": 81465.0,
        "length": 713,
        "protein_name": "Choline transporter-like protein",
        "gene_name": "Slc44a5",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Slc44a5",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Choline transporter-like protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:365962);  (R-RNO-1483191);  (R-RNO-9958517)",
        "pathway_count": 3,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Choline transporter., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; Choline/H+ antiporter., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "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_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 0,
        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0022857 transmembrane transporter activity;GO:0015297 antiporter activity;GO:0015220 choline transmembrane transporter activity",
        "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane",
        "go_biological_process": "GO:0055085 transmembrane transport;GO:0015871 choline transport;GO:0015695 organic cation transport",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I5ZLE8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6A0B6-1",
        "uniprot_id": "A0A8I6A0B6_RAT",
        "mass": 82122.0,
        "length": 781,
        "protein_name": "Sp3 transcription factor",
        "gene_name": "Sp3",
        "organism": "Rat",
        "refseq_name": "transcription factor Sp3",
        "refseq_ac": "NP_001414334",
        "gene_names_uniprotkb": "Sp3",
        "gene_names_refseq": "Sp3",
        "protein_names_uniprotkb": "Sp3 transcription factor",
        "protein_names_refseq": "trans-acting transcription factor 3; transcription factor Sp3",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-3232118)",
        "pathway_count": 1,
        "publication_count": 8,
        "publication_id_list": "11870074;12297531;12584202;20884886;21289081;23093703;25476526;30110572",
        "class_list": "",
        "function": "Results provide new insight into the regulatory mechanisms of Pdgfra transcription in Leydig cells, which includes a role for the transcription factors SP1 and SP3. Publication Status: Online-Only, [RefSeq, PubMed]; Sp1 and Sp3 transcription factors mediate leptin-induced collagen alpha1(I) gene expression in primary culture of male rat hepatic stellate cells, [RefSeq, PubMed]; Sp1, Sp3, and Egr1 transcription factors play a critical role in Dmrt1 regulation in the testis, [RefSeq, PubMed]; Sp3 as a downstream effector of a Ras/p42/44(MAPK) signaling pathway which increases CTP:phosphocholine cytidylyltransferase alpha gene transcription, [RefSeq, PubMed]; Studies suggest that Sp transcription factors may be involved in transcription of the histone H1t gene and the GC-box and the TE1 subelement are required for activation of the H1t promoter, [RefSeq, PubMed]; Superoxide activates renal Sp3 via lysine acetylation increasing renin activity, AT1R function, and blood pressure in rats., [RefSeq, PubMed]; The role of Sp3 in apoptosis was assessed via gene silencing and glutamine administration., [RefSeq, PubMed]; These results suggest that XT-1 expression is refractory to the disease process and to inhibition by inflammatory cytokines and that signaling through AP-1, Sp1, and Sp3 is important in the maintenance of XT-1 levels in NP cells., [RefSeq, PubMed]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0061629 RNA polymerase II-specific DNA-binding transcription factor binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0017053 transcription repressor complex;GO:0032993 protein-DNA complex;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0045892 negative regulation of DNA-templated transcription;GO:0030219 megakaryocyte differentiation;GO:0001779 natural killer cell differentiation;GO:0030851 granulocyte differentiation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.9,
        "record_id": "A0A8I6A0B6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6AE50-1",
        "uniprot_id": "A0A8I6AE50_RAT",
        "mass": 124673.0,
        "length": 1134,
        "protein_name": "Anillin",
        "gene_name": "Anln",
        "organism": "Rat",
        "refseq_name": "anillin isoform X1",
        "refseq_ac": "XP_038938195",
        "gene_names_uniprotkb": "Anln; RGD1561367",
        "gene_names_refseq": "Anln; RGD1561367",
        "protein_names_uniprotkb": "Anillin",
        "protein_names_refseq": "anillin isoform X1",
        "tax_id": 10116,
        "disease": "focal segmental glomerulosclerosis 8 (Disease Ontology:DOID:0111133)",
        "pathway": " (R-RNO-8980692);  (R-RNO-9013026);  (R-RNO-9013106)",
        "pathway_count": 3,
        "publication_count": 1,
        "publication_id_list": "16641100",
        "class_list": "",
        "function": "Required for cytokinesis. Essential for the structural integrity of the cleavage furrow and for completion of cleavage furrow ingression. Plays a role in bleb assembly during metaphase and anaphase of mitosis. May play a significant role in podocyte cell migration., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
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        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003779 actin binding",
        "go_cellular_component": "GO:0032059 bleb;GO:0005654 nucleoplasm;GO:0005938 cell cortex;GO:0015629 actin cytoskeleton;GO:0030496 midbody",
        "go_biological_process": "GO:0000281 mitotic cytokinesis;GO:0002244 hematopoietic progenitor cell differentiation;GO:0090521 podocyte cell migration;GO:1904172 positive regulation of bleb assembly;GO:0000915 actomyosin contractile ring assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A8I6AE50-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZQP3-1",
        "uniprot_id": "A0A8I5ZQP3_RAT",
        "mass": 133545.0,
        "length": 1188,
        "protein_name": "Phospholipid-transporting ATPase",
        "gene_name": "Atp8a2",
        "organism": "Rat",
        "refseq_name": "phospholipid-transporting ATPase IB isoform X3",
        "refseq_ac": "XP_003751540",
        "gene_names_uniprotkb": "Atp8a2; LOC691889",
        "gene_names_refseq": "Atp8a2",
        "protein_names_uniprotkb": "Phospholipid-transporting ATPase; 7.6.2.1",
        "protein_names_refseq": "phospholipid-transporting ATPase IB isoform X3",
        "tax_id": 10116,
        "disease": "cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome (Disease Ontology:DOID:0050997); cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 4 (Disease Ontology:DOID:0070559)",
        "pathway": " (rno:691889)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "",
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        "mined_s_glycosites": 0,
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        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
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        "total_n_glycosites": 0,
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        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "glyco_site_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "7.6.2.1;7.6.2.2",
        "go_molecular_function": "GO:0000287 magnesium ion binding;GO:0005524 ATP binding;GO:0016887 ATP hydrolysis activity;GO:0090556 phosphatidylserine floppase activity;GO:0015247 aminophospholipid flippase activity",
        "go_cellular_component": "GO:0005794 Golgi apparatus;GO:0005886 plasma membrane;GO:0016020 membrane;GO:0005768 endosome;GO:1990531 phospholipid-translocating ATPase complex",
        "go_biological_process": "GO:0031175 neuron projection development;GO:0061092 positive regulation of phospholipid translocation;GO:0007409 axonogenesis;GO:0010976 positive regulation of neuron projection development;GO:0042472 inner ear morphogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A8I5ZQP3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6ADP6-1",
        "uniprot_id": "A0A8I6ADP6_RAT",
        "mass": 54366.0,
        "length": 485,
        "protein_name": "Phosphatidylinositol N-acetylglucosaminyltransferase subunit A",
        "gene_name": "Piga",
        "organism": "Rat",
        "refseq_name": "phosphatidylinositol N-acetylglucosaminyltransferase subunit A isoform 1",
        "refseq_ac": "NP_001387965",
        "gene_names_uniprotkb": "Piga",
        "gene_names_refseq": "Piga",
        "protein_names_uniprotkb": "Phosphatidylinositol N-acetylglucosaminyltransferase subunit A; 2.4.1.198; GlcNAc-PI synthesis protein; Phosphatidylinositol-glycan biosynthesis class A protein",
        "protein_names_refseq": "N-acetylglucosaminyl-phosphatidylinositol biosynthetic protein; phosphatidylinositol N-acetylglucosaminyltransferase subunit A isoform 1; phosphatidylinositol N-acetylglucosaminyltransferase subunit A; phosphatidylinositol glycan, class A",
        "tax_id": 10116,
        "disease": "paroxysmal nocturnal hemoglobinuria (Disease Ontology:DOID:0060284); autosomal recessive congenital ichthyosis 4B (Disease Ontology:DOID:0060713); multiple congenital anomalies-hypotonia-seizures syndrome 2 (Disease Ontology:DOID:0080139)",
        "pathway": " (R-RNO-162710)",
        "pathway_count": 1,
        "publication_count": 5,
        "publication_id_list": "22923490;24449360;24574022;25868128;33198937",
        "class_list": "",
        "function": "Catalytic subunit of the glycosylphosphatidylinositol-N-acetylglucosaminyltransferase (GPI-GnT) complex that catalyzes the transfer of N-acetylglucosamine from UDP-N-acetylglucosamine to phosphatidylinositol and participates in the first step of GPI biosynthesis., [UniProtKB, UniProtKB]; Data demonstrate the value of integrating Pig-a mutation and micronucleus endpoints into in vivo toxicology studies., [RefSeq, PubMed]; Data suggest the use of both sexes for phosphatidylinositolglycan class A protein Pig-a gene mutation studies., [RefSeq, PubMed]; Molecular analysis of GPI-anchor biosynthesis pathway genes in rat strains used for the Pig-a gene mutation assay., [RefSeq, PubMed]; Pig-a gene mutation is associated with micronucleated reticulocyte induction., [RefSeq, PubMed]; Pig-a mutation is associated with diethylnitrosamine genotoxicity., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
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        "total_n_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 3,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "2.4.1.198",
        "go_molecular_function": "GO:0017176 phosphatidylinositol N-acetylglucosaminyltransferase activity",
        "go_cellular_component": "GO:0000506 glycosylphosphatidylinositol-N-acetylglucosaminyltransferase (GPI-GnT) complex;GO:0016020 membrane;GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0006506 GPI anchor biosynthetic process;GO:1990830 cellular response to leukemia inhibitory factor",
        "synthesized_glycan_count": 0,
        "hit_score": 0.6,
        "record_id": "A0A8I6ADP6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZY40-1",
        "uniprot_id": "A0A8I5ZY40_RAT",
        "mass": 73774.0,
        "length": 662,
        "protein_name": "A-kinase anchor protein 10, mitochondrial",
        "gene_name": "Akap10",
        "organism": "Rat",
        "refseq_name": "A-kinase anchor protein 10, mitochondrial",
        "refseq_ac": "NP_001108078",
        "gene_names_uniprotkb": "Akap10",
        "gene_names_refseq": "Akap10; D-akap2",
        "protein_names_uniprotkb": "A-kinase anchor protein 10, mitochondrial; Dual specificity A kinase-anchoring protein 2; Protein kinase A-anchoring protein 10",
        "protein_names_refseq": "A kinase (PRKA) anchor protein 10; A-kinase anchor protein 10, mitochondrial; Dual specific A kinase anchoring protein 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:360540);  (R-RNO-983231)",
        "pathway_count": 2,
        "publication_count": 2,
        "publication_id_list": "17081990;22673903",
        "class_list": "",
        "function": "Differentially targeted protein that binds to type I and II regulatory subunits of protein kinase A and anchors them to the mitochondria or the plasma membrane. Although the physiological relevance between PKA and AKAPS with mitochondria is not fully understood, one idea is that BAD, a proapoptotic member, is phosphorylated and inactivated by mitochondria-anchored PKA. It cannot be excluded too that it may facilitate PKA as well as G protein signal transduction, by acting as an adapter for assembling multiprotein complexes. With its RGS domain, it could lead to the interaction to G-alpha proteins, providing a link between the signaling machinery and the downstream kinase., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]; The crystal structure of the helical motif from D-AKAP2 (Akap10), a dual-specific AKAP, bound to the RIIalpha D/D domain from Prkar2a, was analysed., [RefSeq, PubMed]",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0051018 protein kinase A binding",
        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0032991 protein-containing complex",
        "go_biological_process": "GO:0008104 intracellular protein localization",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZLS0-1",
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        "length": 520,
        "protein_name": "Vascular endothelial zinc finger 1",
        "gene_name": "Vezf1",
        "organism": "Rat",
        "refseq_name": "vascular endothelial zinc finger 1",
        "refseq_ac": "NP_001291284",
        "gene_names_uniprotkb": "Vezf1",
        "gene_names_refseq": "Vezf1",
        "protein_names_uniprotkb": "Vascular endothelial zinc finger 1",
        "protein_names_refseq": "vascular endothelial zinc finger 1",
        "tax_id": 10116,
        "disease": "dilated cardiomyopathy (Disease Ontology:DOID:12930)",
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        "publication_id_list": "18683930;22673903",
        "class_list": "",
        "function": "Transcriptional regulator. Acts as a transcriptional activator that binds to purine-rich GAGA sites found in the promoter of many genes including insulin I and II and islet amyloid polypeptide., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific;GO:0001228 DNA-binding transcription activator activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0001525 angiogenesis;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0045603 positive regulation of endothelial cell differentiation",
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    },
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        "uniprot_canonical_ac": "A0A8I6A197-1",
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        "protein_name": "Syntrophin, gamma 2",
        "gene_name": "Sntg2",
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        "refseq_name": "gamma-2-syntrophin isoform 1",
        "refseq_ac": "NP_001401843",
        "gene_names_uniprotkb": "Sntg2",
        "gene_names_refseq": "Sntg2",
        "protein_names_uniprotkb": "Syntrophin, gamma 2",
        "protein_names_refseq": "gamma-2-syntrophin isoform 1; gamma-2-syntrophin",
        "tax_id": 10116,
        "disease": "Duchenne muscular dystrophy (Disease Ontology:DOID:11723)",
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        "protein_names_uniprotkb": "Pleckstrin homology domain containing B2",
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        "go_molecular_function": "GO:0005547 phosphatidylinositol-3,4,5-trisphosphate binding",
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    {
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        "length": 797,
        "protein_name": "Plakophilin-3",
        "gene_name": "Pkp3",
        "organism": "Rat",
        "refseq_name": "plakophilin-3 isoform 2",
        "refseq_ac": "NP_001402747",
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        "go_molecular_function": "GO:0003723 RNA binding;GO:0019899 enzyme binding;GO:0045296 cadherin binding;GO:0050839 cell adhesion molecule binding;GO:0045294 alpha-catenin binding",
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        "go_biological_process": "GO:0022409 positive regulation of cell-cell adhesion;GO:0002718 regulation of cytokine production involved in immune response;GO:0030036 actin cytoskeleton organization;GO:0002159 desmosome assembly;GO:0010669 epithelial structure maintenance",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZZR0-1",
        "uniprot_id": "A0A8I5ZZR0_RAT",
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        "length": 961,
        "protein_name": "RIKEN cDNA 4933427D14 gene like",
        "gene_name": "4933427D14Rikl",
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        "refseq_name": "protein moonraker",
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        "gene_names_uniprotkb": "4933427D14Rikl; RGD1304728",
        "gene_names_refseq": "4933427D14Rikl; RGD1304728",
        "protein_names_uniprotkb": "RIKEN cDNA 4933427D14 gene like",
        "protein_names_refseq": "protein moonraker",
        "tax_id": 10116,
        "disease": "asphyxiating thoracic dystrophy (Disease Ontology:DOID:0050592); Joubert syndrome (Disease Ontology:DOID:0050777); orofaciodigital syndrome (Disease Ontology:DOID:4501)",
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        "go_cellular_component": "GO:0005813 centrosome;GO:0005815 microtubule organizing center;GO:0034451 centriolar satellite",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6AAR8-1",
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        "length": 274,
        "protein_name": "Mitochondrial S-adenosylmethionine carrier protein",
        "gene_name": "Slc25a26",
        "organism": "Rat",
        "refseq_name": "mitochondrial S-adenosylmethionine carrier protein",
        "refseq_ac": "NP_001382534",
        "gene_names_uniprotkb": "Slc25a26",
        "gene_names_refseq": "Slc25a26",
        "protein_names_uniprotkb": "Mitochondrial S-adenosylmethionine carrier protein; Solute carrier family 25 member 26",
        "protein_names_refseq": "S-adenosylmethionine mitochondrial carrier protein; mitochondrial S-adenosylmethionine carrier protein; solute carrier family 25 (S-adenosylmethionine carrier), member 26; solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 26",
        "tax_id": 10116,
        "disease": "combined oxidative phosphorylation deficiency 28 (Disease Ontology:DOID:0111470)",
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        "function": "Mitochondrial S-adenosyl-L-methionine/S-adenosyl-L-homocysteine antiporter. Mediates the exchange of cytosolic S-adenosyl-L-methionine, the predominant methyl-group donor for macromolecule methylation processes, for mitochondrial S-adenosylhomocysteine(SAH), a by-product of methylation reactions., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "go_molecular_function": "GO:0000095 S-adenosyl-L-methionine transmembrane transporter activity;GO:0180003 S-adenosyl-L-methionine:S-adenosyl-L-homocysteine antiporter activity",
        "go_cellular_component": "GO:0016020 membrane;GO:0005739 mitochondrion;GO:0005743 mitochondrial inner membrane",
        "go_biological_process": "GO:0015805 S-adenosyl-L-methionine transport;GO:0043414 macromolecule methylation;GO:1990543 mitochondrial S-adenosyl-L-methionine transmembrane transport",
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        "length": 709,
        "protein_name": "RAN binding protein 9",
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        "refseq_name": "ran-binding protein 9",
        "refseq_ac": "NP_001414343",
        "gene_names_uniprotkb": "Ranbp9",
        "gene_names_refseq": "RGD1561940; RanBPM; Ranbp9",
        "protein_names_uniprotkb": "RAN binding protein 9",
        "protein_names_refseq": "ran-binding protein 9; ran-binding protein M",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-373760);  (R-RNO-5673001);  (R-RNO-8851805);  (R-RNO-9861718)",
        "pathway_count": 4,
        "publication_count": 2,
        "publication_id_list": "22673903;32622424",
        "class_list": "",
        "function": "MicroRNA-26a-5p alleviates neuronal apoptosis and brain injury in intracerebral hemorrhage by targeting RAN binding protein 9., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0019899 enzyme binding;GO:0030674 protein-macromolecule adaptor activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005829 cytosol;GO:0016604 nuclear body",
        "go_biological_process": "GO:1902993 positive regulation of amyloid precursor protein catabolic process;GO:0007010 cytoskeleton organization;GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process;GO:0070373 negative regulation of ERK1 and ERK2 cascade",
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        "hit_score": 0.3,
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZU78-1",
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        "length": 902,
        "protein_name": "leucine--tRNA ligase",
        "gene_name": "Lars2",
        "organism": "Rat",
        "refseq_name": "leucine--tRNA ligase, mitochondrial",
        "refseq_ac": "NP_001400771",
        "gene_names_uniprotkb": "Lars2",
        "gene_names_refseq": "Lars2",
        "protein_names_uniprotkb": "leucine--tRNA ligase; 6.1.1.4; Leucyl-tRNA synthetase",
        "protein_names_refseq": "leucine--tRNA ligase, mitochondrial; probable leucine--tRNA ligase, mitochondrial; probable leucyl-tRNA synthetase, mitochondrial",
        "tax_id": 10116,
        "disease": "Perrault syndrome (Disease Ontology:DOID:0050857); mitochondrial metabolism disease (Disease Ontology:DOID:700)",
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        "ec_number_list": "6.1.1.4",
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        "go_cellular_component": "GO:0005739 mitochondrion",
        "go_biological_process": "GO:0006429 leucyl-tRNA aminoacylation;GO:0032543 mitochondrial translation",
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        "hit_score": 0.1,
        "record_id": "A0A8I5ZU78-1",
        "record_type": "protein"
    },
    {
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        "length": 1125,
        "protein_name": "Ubiquitin carboxyl-terminal hydrolase 25",
        "gene_name": "Usp25",
        "organism": "Rat",
        "refseq_name": "ubiquitin carboxyl-terminal hydrolase 25 isoform X1",
        "refseq_ac": "XP_063126672",
        "gene_names_uniprotkb": "Usp25",
        "gene_names_refseq": "Usp25",
        "protein_names_uniprotkb": "Ubiquitin carboxyl-terminal hydrolase 25; 3.4.19.12; Deubiquitinating enzyme 25; Ubiquitin thioesterase 25; Ubiquitin-specific-processing protease 25",
        "protein_names_refseq": "ubiquitin carboxyl-terminal hydrolase 25 isoform X1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:304150);  (R-RNO-5689880)",
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        "function": "The muscle-specific isoform (USP25m) may have a role in the regulation of muscular differentiation and function., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "ec_number_list": "3.4.19.12;3.6.4.13",
        "go_molecular_function": "GO:0004843 cysteine-type deubiquitinase activity;GO:0051117 ATPase binding;GO:0031625 ubiquitin protein ligase binding;GO:0032183 SUMO binding;GO:0101005 deubiquitinase activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005783 endoplasmic reticulum;GO:0005829 cytosol",
        "go_biological_process": "GO:0006508 proteolysis;GO:0016579 protein deubiquitination;GO:0016071 mRNA metabolic process;GO:0006955 immune response;GO:0006979 response to oxidative stress",
        "synthesized_glycan_count": 0,
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        "record_type": "protein"
    },
    {
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        "length": 372,
        "protein_name": "Tribbles homolog 1",
        "gene_name": "Trib1",
        "organism": "Rat",
        "refseq_name": "tribbles homolog 1",
        "refseq_ac": "NP_076475",
        "gene_names_uniprotkb": "Trib1",
        "gene_names_refseq": "Gig2; Trib1",
        "protein_names_uniprotkb": "Tribbles homolog 1",
        "protein_names_refseq": "G-protein-coupled receptor induced protein GIG2; tribbles homolog 1",
        "tax_id": 10116,
        "disease": "glucose metabolism disease (Disease Ontology:DOID:4194)",
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        "go_molecular_function": "GO:0055106 ubiquitin-protein transferase regulator activity;GO:0004672 protein kinase activity;GO:0005524 ATP binding;GO:0019901 protein kinase binding;GO:0031434 mitogen-activated protein kinase kinase binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0045645 positive regulation of eosinophil differentiation;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0032496 response to lipopolysaccharide;GO:0014912 negative regulation of smooth muscle cell migration;GO:0048662 negative regulation of smooth muscle cell proliferation",
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        "record_id": "A0A8I6A5Q0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6A600-1",
        "uniprot_id": "A0A8I6A600_RAT",
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        "length": 260,
        "protein_name": "DnaJ homolog subfamily C member 4",
        "gene_name": "Dnajc4",
        "organism": "Rat",
        "refseq_name": "dnaJ homolog subfamily C member 4 isoform 1",
        "refseq_ac": "NP_001426941",
        "gene_names_uniprotkb": "Dnajc4",
        "gene_names_refseq": "Dnajc4",
        "protein_names_uniprotkb": "DnaJ homolog subfamily C member 4",
        "protein_names_refseq": "DnaJ (Hsp40) homolog, subfamily C, member 4; dnaJ homolog subfamily C member 4 isoform 1; dnaJ homolog subfamily C member 4",
        "tax_id": 10116,
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        "go_cellular_component": "GO:0016020 membrane",
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        "record_id": "A0A8I6A600-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZVY5-1",
        "uniprot_id": "A0A8I5ZVY5_RAT",
        "mass": 114967.0,
        "length": 1016,
        "protein_name": "Pre-mRNA-processing factor 40 homolog A",
        "gene_name": "Prpf40a",
        "organism": "Rat",
        "refseq_name": "pre-mRNA-processing factor 40 homolog A isoform X1",
        "refseq_ac": "XP_008759932",
        "gene_names_uniprotkb": "Prpf40a",
        "gene_names_refseq": "Fnbp3; Prpf40a",
        "protein_names_uniprotkb": "Pre-mRNA-processing factor 40 homolog A; Formin-binding protein 11; Formin-binding protein 3",
        "protein_names_refseq": "pre-mRNA-processing factor 40 homolog A isoform X1",
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        "function": "Binds to WASL/N-WASP and suppresses its translocation from the nucleus to the cytoplasm, thereby inhibiting its cytoplasmic function. Plays a role in the regulation of cell morphology and cytoskeletal organization. Required in the control of cell shape and migration. May play a role in cytokinesis. May be involved in pre-mRNA splicing., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003723 RNA binding;GO:0070064 proline-rich region binding",
        "go_cellular_component": "GO:0016607 nuclear speck;GO:0016363 nuclear matrix;GO:0005685 U1 snRNP;GO:0071004 U2-type prespliceosome;GO:0005634 nucleus",
        "go_biological_process": "GO:0045292 mRNA cis splicing, via spliceosome;GO:0000398 mRNA splicing, via spliceosome",
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        "record_id": "A0A8I5ZVY5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZKF8-1",
        "uniprot_id": "A0A8I5ZKF8_RAT",
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        "length": 721,
        "protein_name": "Similar to human chromosome 10 open reading frame 90",
        "gene_name": "C1h10orf90",
        "organism": "Rat",
        "refseq_name": "(E2-independent) E3 ubiquitin-conjugating enzyme FATS isoform X1",
        "refseq_ac": "XP_038962623",
        "gene_names_uniprotkb": "C1h10orf90; LOC100302465",
        "gene_names_refseq": "C1h10orf90",
        "protein_names_uniprotkb": "Similar to human chromosome 10 open reading frame 90",
        "protein_names_refseq": "(E2-independent) E3 ubiquitin-conjugating enzyme FATS isoform X1",
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        "pathway": " (rno:100302465)",
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        "go_molecular_function": "GO:0061630 ubiquitin protein ligase activity;GO:0042826 histone deacetylase binding",
        "go_cellular_component": "GO:0005813 centrosome;GO:0005829 cytosol;GO:0005814 centriole;GO:0005737 cytoplasm;GO:0015629 actin cytoskeleton",
        "go_biological_process": "GO:0046599 regulation of centriole replication;GO:0006974 DNA damage response;GO:0050821 protein stabilization;GO:0010212 response to ionizing radiation;GO:0030308 negative regulation of cell growth",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6A273-1",
        "uniprot_id": "A0A8I6A273_RAT",
        "mass": 76542.0,
        "length": 662,
        "protein_name": "Zinc finger protein 182",
        "gene_name": "Zfp182",
        "organism": "Rat",
        "refseq_name": "",
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        "gene_names_uniprotkb": "Zfp182; LOC100911831",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger protein 182; Zinc finger protein 21",
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        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB, UniProtKB]; May have a role during differentiation processes., [UniProtKB, UniProtKB]",
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003677 DNA binding;GO:0008270 zinc ion binding;GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific",
        "go_cellular_component": "GO:0031981 nuclear lumen;GO:0005634 nucleus",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006351 DNA-templated transcription;GO:0009891 positive regulation of biosynthetic process;GO:0006357 regulation of transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
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    },
    {
        "uniprot_canonical_ac": "A0A8I6A596-1",
        "uniprot_id": "A0A8I6A596_RAT",
        "mass": 88335.0,
        "length": 766,
        "protein_name": "Mitotic spindle assembly checkpoint protein MAD1",
        "gene_name": "Mad1l1",
        "organism": "Rat",
        "refseq_name": "mitotic spindle assembly checkpoint protein MAD1 isoform X1",
        "refseq_ac": "XP_063127720",
        "gene_names_uniprotkb": "Mad1l1",
        "gene_names_refseq": "Mad1l1",
        "protein_names_uniprotkb": "Mitotic spindle assembly checkpoint protein MAD1; Mitotic arrest deficient 1-like protein 1",
        "protein_names_refseq": "mitotic spindle assembly checkpoint protein MAD1 isoform X1",
        "tax_id": 10116,
        "disease": "lymphoma (Disease Ontology:DOID:0060058); mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition (Disease Ontology:DOID:0060982); prostate cancer (Disease Ontology:DOID:10283); microcephaly (Disease Ontology:DOID:10907)",
        "pathway": " (rno:680006);  (R-RNO-141430);  (R-RNO-141444);  (R-RNO-2467813);  (R-RNO-2500257);  (R-RNO-5663220);  (R-RNO-68877);  (R-RNO-9648025)",
        "pathway_count": 8,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Component of the spindle-assembly checkpoint that prevents the onset of anaphase until all chromosomes are properly aligned at the metaphase plate. Forms a heterotetrameric complex with the closed conformation form of MAD2L1 (C-MAD2) at unattached kinetochores during prometaphase, recruits an open conformation of MAD2L1 (O-MAD2) and promotes the conversion of O-MAD2 to C-MAD2, which ensures mitotic checkpoint signaling., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "ec_number_list": "",
        "go_molecular_function": "GO:0043515 kinetochore binding",
        "go_cellular_component": "GO:0044615 nuclear pore nuclear basket;GO:0000922 spindle pole;GO:0005634 nucleus;GO:0005635 nuclear envelope;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0051315 attachment of mitotic spindle microtubules to kinetochore;GO:1902426 deactivation of mitotic spindle assembly checkpoint;GO:0090235 regulation of metaphase plate congression;GO:0051301 cell division;GO:0042130 negative regulation of T cell proliferation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6A596-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6A6Z0-1",
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        "length": 544,
        "protein_name": "Tubby-like protein",
        "gene_name": "Tulp1",
        "organism": "Rat",
        "refseq_name": "tubby-related protein 1 isoform 1",
        "refseq_ac": "NP_001401996",
        "gene_names_uniprotkb": "Tulp1",
        "gene_names_refseq": "Tulp1",
        "protein_names_uniprotkb": "Tubby-like protein",
        "protein_names_refseq": "tubby like protein 1; tubby-related protein 1 isoform 1; tubby-related protein 1",
        "tax_id": 10116,
        "disease": "Leber congenital amaurosis 15 (Disease Ontology:DOID:0110189); retinitis pigmentosa 14 (Disease Ontology:DOID:0110381); retinitis pigmentosa (Disease Ontology:DOID:10584); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (rno:309900)",
        "pathway_count": 1,
        "publication_count": 1,
        "publication_id_list": "26427465",
        "class_list": "",
        "function": "Data suggest that photoreceptors-specific protein Tulp1 is involved in the trafficking of proteins from the inner segment (IS) to the outer segment (OS) and the continuous membrane remodeling and vesicle cycling at the synaptic terminal., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0005546 phosphatidylinositol-4,5-bisphosphate binding;GO:0051015 actin filament binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005576 extracellular region;GO:0005829 cytosol;GO:0005886 plasma membrane;GO:0005929 cilium",
        "go_biological_process": "GO:0016358 dendrite development;GO:0045494 photoreceptor cell maintenance;GO:0060041 retina development in camera-type eye;GO:0001895 retina homeostasis;GO:0050766 positive regulation of phagocytosis",
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        "record_type": "protein"
    },
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        "length": 497,
        "protein_name": "Annexin",
        "gene_name": "Anxa7",
        "organism": "Rat",
        "refseq_name": "annexin A7 isoform X1",
        "refseq_ac": "XP_006251686",
        "gene_names_uniprotkb": "Anxa7",
        "gene_names_refseq": "Anxa7",
        "protein_names_uniprotkb": "Annexin",
        "protein_names_refseq": "annexin A7 isoform X1",
        "tax_id": 10116,
        "disease": "non-Hodgkin lymphoma (Disease Ontology:DOID:0060060); amyotrophic lateral sclerosis type 23 (Disease Ontology:DOID:0080225); prostate cancer (Disease Ontology:DOID:10283); breast cancer (Disease Ontology:DOID:1612); colon adenocarcinoma (Disease Ontology:DOID:234); ovarian cancer (Disease Ontology:DOID:2394); skin cancer (Disease Ontology:DOID:4159)",
        "pathway": " (rno:155423)",
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        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Calcium/phospholipid-binding protein which promotes membrane fusion and is involved in exocytosis., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
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        "go_molecular_function": "GO:0005509 calcium ion binding;GO:0005544 calcium-dependent phospholipid binding;GO:0001786 phosphatidylserine binding;GO:0005178 integrin binding;GO:0048306 calcium-dependent protein binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005886 plasma membrane;GO:0012506 vesicle membrane;GO:0005635 nuclear envelope",
        "go_biological_process": "GO:0007207 phospholipase C-activating G protein-coupled acetylcholine receptor signaling pathway;GO:0008283 cell population proliferation;GO:0010629 negative regulation of gene expression;GO:0030855 epithelial cell differentiation;GO:0051592 response to calcium ion",
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        "record_id": "F7F6D1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6ATX5-1",
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        "length": 373,
        "protein_name": "StAR-related lipid transfer protein 7, mitochondrial",
        "gene_name": "Stard7",
        "organism": "Rat",
        "refseq_name": "stAR-related lipid transfer protein 7, mitochondrial",
        "refseq_ac": "NP_001386207",
        "gene_names_uniprotkb": "Stard7",
        "gene_names_refseq": "Stard7",
        "protein_names_uniprotkb": "StAR-related lipid transfer protein 7, mitochondrial; START domain-containing protein 7",
        "protein_names_refseq": "START domain containing 7; StAR-related lipid transfer (START) domain containing 7; stAR-related lipid transfer protein 7, mitochondrial",
        "tax_id": 10116,
        "disease": "familial adult myoclonic epilepsy 2 (Disease Ontology:DOID:0111692)",
        "pathway": " (rno:296128);  (R-RNO-1483191);  (R-RNO-2142789)",
        "pathway_count": 3,
        "publication_count": 1,
        "publication_id_list": "20042613",
        "class_list": "",
        "function": "May play a protective role in mucosal tissues by preventing exaggerated allergic responses., [UniProtKB, UniProtKB, UniProtKB]; These results suggest that StarD7 facilitates the delivery of phosphatidylcholine to mitochondria in non-vesicular system., [RefSeq, PubMed]",
        "predicted_glycosites": 0,
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        "ec_number_list": "",
        "go_molecular_function": "GO:0008289 lipid binding;GO:0120019 phosphatidylcholine transfer activity;GO:0140104 molecular carrier activity",
        "go_cellular_component": "GO:0005829 cytosol;GO:0005576 extracellular region;GO:0005737 cytoplasm;GO:0005741 mitochondrial outer membrane;GO:0005758 mitochondrial intermembrane space",
        "go_biological_process": "GO:0006869 lipid transport;GO:0043457 regulation of cellular respiration;GO:0006954 inflammatory response;GO:0061436 establishment of skin barrier;GO:0001773 myeloid dendritic cell activation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A8I6ATX5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5XVA3-1",
        "uniprot_id": "A0A8I5XVA3_RAT",
        "mass": 143946.0,
        "length": 1298,
        "protein_name": "Tenascin-N",
        "gene_name": "Tnn",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Tnn",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Tenascin-N; Tenascin-W",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:304913);  (R-RNO-3000178)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Extracellular matrix protein that seems to be a ligand for ITGA8:ITGB1, ITGAV:ITGB1 and ITGA4:ITGB1. Involved in neurite outgrowth and cell migration in hippocampal explants. During endochondral bone formation, inhibits proliferation and differentiation of proteoblasts mediated by canonical WNT signaling. In tumors, stimulates angiogenesis by elongation, migration and sprouting of endothelial cells. Expressed in most mammary tumors, may facilitate tumorigenesis by supporting the migratory behavior of breast cancer cells., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005178 integrin binding;GO:0042802 identical protein binding",
        "go_cellular_component": "GO:0009986 cell surface;GO:0043025 neuronal cell body;GO:1990026 hippocampal mossy fiber expansion;GO:0097442 CA3 pyramidal cell dendrite;GO:0090733 tenascin complex",
        "go_biological_process": "GO:1903672 positive regulation of sprouting angiogenesis;GO:1903010 regulation of bone development;GO:0010976 positive regulation of neuron projection development;GO:0030155 regulation of cell adhesion;GO:0001764 neuron migration",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I5XVA3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZPZ4-1",
        "uniprot_id": "A0A8I5ZPZ4_RAT",
        "mass": 99090.0,
        "length": 861,
        "protein_name": "Cytosolic carboxypeptidase 2",
        "gene_name": "Agbl2",
        "organism": "Rat",
        "refseq_name": "cytosolic carboxypeptidase 2 isoform X1",
        "refseq_ac": "XP_038962721",
        "gene_names_uniprotkb": "Agbl2",
        "gene_names_refseq": "Agbl2",
        "protein_names_uniprotkb": "Cytosolic carboxypeptidase 2; ATP/GTP-binding protein-like 2; Protein deglutamylase CCP2",
        "protein_names_refseq": "cytosolic carboxypeptidase 2 isoform X1",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 1,
        "publication_id_list": "22673903",
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "3.4.17.24;3.4.17.-",
        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0004181 metallocarboxypeptidase activity;GO:0015631 tubulin binding",
        "go_cellular_component": "GO:0005829 cytosol;GO:0005814 centriole;GO:0005737 cytoplasm;GO:0015630 microtubule cytoskeleton;GO:0036064 ciliary basal body",
        "go_biological_process": "GO:0006508 proteolysis;GO:0035610 protein side chain deglutamylation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A8I5ZPZ4-1",
        "record_type": "protein"
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    {
        "uniprot_canonical_ac": "A0A8I5ZUV5-1",
        "uniprot_id": "A0A8I5ZUV5_RAT",
        "mass": 116387.0,
        "length": 1022,
        "protein_name": "FERM domain containing 4B",
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        "protein_name": "Prostate transmembrane protein, androgen induced 1",
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        "refseq_name": "protein TMEPAI isoform 1",
        "refseq_ac": "NP_001400513",
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        "gene_names_refseq": "Pmepa1; Tmepai",
        "protein_names_uniprotkb": "Prostate transmembrane protein, androgen induced 1",
        "protein_names_refseq": "protein TMEPAI isoform 1; transmembrane prostate androgen-induced protein; transmembrane, prostate androgen induced RNA",
        "tax_id": 10116,
        "disease": "prostate cancer (Disease Ontology:DOID:10283); breast cancer (Disease Ontology:DOID:1612); rectal benign neoplasm (Disease Ontology:DOID:1984); gastric adenocarcinoma (Disease Ontology:DOID:3717); renal cell carcinoma (Disease Ontology:DOID:4450)",
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        "go_molecular_function": "GO:0050699 WW domain binding;GO:0070412 R-SMAD binding;GO:0140311 protein sequestering activity",
        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0031901 early endosome membrane;GO:0010008 endosome membrane",
        "go_biological_process": "GO:0030512 negative regulation of transforming growth factor beta receptor signaling pathway;GO:0060392 negative regulation of SMAD protein signal transduction",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "A0A8I5ZNU8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "M0RBE4-1",
        "uniprot_id": "M0RBE4_RAT",
        "mass": 22074.0,
        "length": 197,
        "protein_name": "Proteasome maturation protein",
        "gene_name": "Pomp",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Pomp",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Proteasome maturation protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "proteosome-associated autoinflammatory syndrome 2 (Disease Ontology:DOID:0060914)",
        "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,
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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": "",
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        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0016607 nuclear speck",
        "go_biological_process": "GO:0043248 proteasome assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "M0RBE4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7EXE9-1",
        "uniprot_id": "F7EXE9_RAT",
        "mass": 21172.0,
        "length": 199,
        "protein_name": "Similar to human chromosome 1 open reading frame 53",
        "gene_name": "C13h1orf53",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "C13h1orf53; RGD1566099",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Similar to human chromosome 1 open reading frame 53",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "mined_glycosites": 0,
        "mined_n_glycosites": 0,
        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
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        "reported_fully_resolved_glycans": 0,
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        "reported_mutagensis": 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_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F7EXE9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7F0E5-1",
        "uniprot_id": "F7F0E5_RAT",
        "mass": 144857.0,
        "length": 1270,
        "protein_name": "Protein flightless-1 homolog",
        "gene_name": "Flii",
        "organism": "Rat",
        "refseq_name": "protein flightless-1 homolog isoform 1",
        "refseq_ac": "NP_001008280",
        "gene_names_uniprotkb": "Flii",
        "gene_names_refseq": "Fliih; Flii",
        "protein_names_uniprotkb": "Protein flightless-1 homolog",
        "protein_names_refseq": "flightless I actin binding protein; protein flightless-1 homolog isoform 1; protein flightless-1 homolog",
        "tax_id": 10116,
        "disease": "dilated cardiomyopathy (Disease Ontology:DOID:12930); obesity (Disease Ontology:DOID:9970)",
        "pathway": " (rno:287375)",
        "pathway_count": 1,
        "publication_count": 2,
        "publication_id_list": "21191408;21400204",
        "class_list": "",
        "function": "Decreased expression of Flightless I in early-gestation fetal wounds improves healing., [RefSeq, PubMed]; Flii appears to have a positive role in the regeneration of hair follicles, contrary to its negative influence on wound healing in skin, [RefSeq, PubMed]; Is a regulator of actin polymerization, required for proper myofibril organization and regulation of the length of sarcomeric thin filaments. It also plays a role in the assembly of cardiomyocyte cell adhesion complexes. Regulates cytoskeletal rearrangements involved in cytokinesis and cell migration, by inhibiting Rac1-dependent paxillin phosphorylation. May play a role as coactivator in transcriptional activation by hormone-activated nuclear receptors (NR) and acts in cooperation with NCOA2 and CARM1. Involved in estrogen hormone signaling., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "reported_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "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:0003779 actin binding;GO:0005546 phosphatidylinositol-4,5-bisphosphate binding;GO:0051015 actin filament binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005829 cytosol;GO:0005903 brush border;GO:0015629 actin cytoskeleton",
        "go_biological_process": "GO:0051016 barbed-end actin filament capping;GO:0008154 actin polymerization or depolymerization;GO:0045214 sarcomere organization;GO:0051014 actin filament severing;GO:0030239 myofibril assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "F7F0E5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7F6Z7-1",
        "uniprot_id": "F7F6Z7_RAT",
        "mass": 56589.0,
        "length": 499,
        "protein_name": "DNA-directed DNA/RNA polymerase mu",
        "gene_name": "Polm",
        "organism": "Rat",
        "refseq_name": "DNA-directed DNA/RNA polymerase mu isoform X3",
        "refseq_ac": "XP_006251275",
        "gene_names_uniprotkb": "Polm",
        "gene_names_refseq": "Polm",
        "protein_names_uniprotkb": "DNA-directed DNA/RNA polymerase mu; 2.7.7.7",
        "protein_names_refseq": "DNA-directed DNA/RNA polymerase mu isoform X3",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-5693571)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Gap-filling polymerase involved in repair of DNA double-strand breaks by non-homologous end joining (NHEJ). Participates in immunoglobulin (Ig) light chain gene rearrangement in V(D)J recombination., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
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        "reported_c_glycosites_with_glycan": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "2.7.7.7;2.7.7.102;2.7.11.1;6.5.1.1;2.7.7.49;3.6.4.12;2.7.7.31;4.2.99.18;5.6.2.4;3.1.11.-;4.2.99.-;3.1.-.-",
        "go_molecular_function": "GO:0003887 DNA-directed DNA polymerase activity;GO:0003677 DNA binding;GO:0046872 metal ion binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm",
        "go_biological_process": "GO:0006303 double-strand break repair via nonhomologous end joining;GO:0030183 B cell differentiation;GO:0016446 somatic hypermutation of immunoglobulin genes",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F7F6Z7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7F8T0-1",
        "uniprot_id": "F7F8T0_RAT",
        "mass": 37386.0,
        "length": 330,
        "protein_name": "Exostosin-like 2",
        "gene_name": "Extl2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Extl2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Exostosin-like 2; 2.4.1.223; Alpha-1,4-N-acetylhexosaminyltransferase EXTL2; Alpha-GalNAcT EXTL2; EXT-related protein 2; Glucuronyl-galactosyl-proteoglycan 4-alpha-N-acetylglucosaminyltransferase",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-2022928)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Glycosyltransferase required for the biosynthesis of heparan-sulfate and responsible for the alternating addition of beta-1-4-linked glucuronic acid (GlcA) and alpha-1-4-linked N-acetylglucosamine (GlcNAc) units to nascent heparan sulfate chains., [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,
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        "reported_c_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "total_reported_s_glycosites": 0,
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        "reported_phosphosites": 0,
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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "2.4.1.223",
        "go_molecular_function": "GO:0030145 manganese ion binding;GO:0005539 glycosaminoglycan binding;GO:0047237 glucuronylgalactosylproteoglycan 4-beta-N-acetylgalactosaminyltransferase activity;GO:0001888 glucuronyl-galactosyl-proteoglycan 4-alpha-N-acetylglucosaminyltransferase activity;GO:0035248 alpha-1,4-N-acetylgalactosaminyltransferase activity",
        "go_cellular_component": "GO:0005783 endoplasmic reticulum;GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0006044 N-acetylglucosamine metabolic process;GO:0019276 UDP-N-acetylgalactosamine metabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F7F8T0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7FFC6-1",
        "uniprot_id": "F7FFC6_RAT",
        "mass": 64685.0,
        "length": 580,
        "protein_name": "mRNA m(6)A methyltransferase",
        "gene_name": "Mettl3",
        "organism": "Rat",
        "refseq_name": "N6-adenosine-methyltransferase catalytic subunit",
        "refseq_ac": "NP_001019965",
        "gene_names_uniprotkb": "Mettl3",
        "gene_names_refseq": "Mettl3",
        "protein_names_uniprotkb": "mRNA m(6)A methyltransferase; 2.1.1.348",
        "protein_names_refseq": "N6-adenosine-methyltransferase 70 kDa subunit; N6-adenosine-methyltransferase catalytic subunit; methyltransferase-like 3",
        "tax_id": 10116,
        "disease": "infertility (Disease Ontology:DOID:5223)",
        "pathway": " (rno:361035);  (R-RNO-72203)",
        "pathway_count": 2,
        "publication_count": 6,
        "publication_id_list": "22673903;38462207;39075530;39129231;39357736;39407279",
        "class_list": "",
        "function": "METTL3 mediated ferroptosis in chondrocytes and promoted pain in KOA via HMGB1 m6A modification., [RefSeq, PubMed]; METTL3 mediates m6A modification of lncRNA CRNDE to promote ATG10 expression and improve brain ischemia/reperfusion injury through YTHDC1. Publication Status: Online-Only, [RefSeq, PubMed]; METTL3 promotes trophoblast ferroptosis in preeclampsia by stabilizing the ACSL4 m[6]A modification., [RefSeq, PubMed]; Methyltransferase METTL3 regulates neuropathic pain through m6A methylation modification of SOCS1., [RefSeq, PubMed]; MiR-340-3p-modified bone marrow mesenchymal stem cell-derived exosomes inhibit ferroptosis through METTL3-mediated m[6]A modification of HMOX1 to promote recovery of injured rat uterus. Erratum:[Stem Cell Res Ther. 2024 Oct 10;15(1):357. doi: 10.1186/s13287-024-03985-w. PMID: 39390524] Publication Status: Online-Only, [RefSeq, PubMed]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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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,
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        "total_reported_n_glycosites": 0,
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        "total_reported_s_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "2.7.7.6;2.1.1.348;1.13.11.27",
        "go_molecular_function": "GO:0001734 mRNA m(6)A methyltransferase activity;GO:0003729 mRNA binding;GO:0046982 protein heterodimerization activity;GO:1990931 mRNA N6-methyladenosine dioxygenase activity;GO:0008173 RNA methyltransferase activity",
        "go_cellular_component": "GO:0036396 RNA N6-methyladenosine methyltransferase complex;GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005829 cytosol;GO:0016607 nuclear speck",
        "go_biological_process": "GO:0021861 forebrain radial glial cell differentiation;GO:1903679 positive regulation of cap-independent translational initiation;GO:0006397 mRNA processing;GO:0007283 spermatogenesis;GO:0016556 mRNA modification",
        "synthesized_glycan_count": 0,
        "hit_score": 0.7,
        "record_id": "F7FFC6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7FLB7-1",
        "uniprot_id": "F7FLB7_RAT",
        "mass": 65047.0,
        "length": 606,
        "protein_name": "Annexin",
        "gene_name": "Anxa11",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Anxa11",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Annexin",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "amyotrophic lateral sclerosis type 23 (Disease Ontology:DOID:0080225); inclusion body myopathy and brain white matter abnormalities (Disease Ontology:DOID:0081121)",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "reported_n_glycosites_with_glycan": 0,
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        "total_reported_n_glycosites": 0,
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        "biomarker_type": "",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0048306 calcium-dependent protein binding;GO:0005509 calcium ion binding;GO:0005544 calcium-dependent phospholipid binding;GO:0008429 phosphatidylethanolamine binding;GO:0044548 S100 protein binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005635 nuclear envelope;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005819 spindle",
        "go_biological_process": "GO:0051592 response to calcium ion;GO:0006909 phagocytosis;GO:0032506 cytokinetic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F7FLB7-1",
        "record_type": "protein"
    },
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        "uniprot_id": "A0A0G2JVS5_RAT",
        "mass": 26512.0,
        "length": 234,
        "protein_name": "StAR-related lipid transfer domain containing 6",
        "gene_name": "Stard6",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Stard6",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "StAR-related lipid transfer domain containing 6",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-196108)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "May be involved in the intracellular transport of sterols or other lipids. May bind cholesterol or other sterols., [UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "ec_number_list": "",
        "go_molecular_function": "GO:0008289 lipid binding",
        "go_cellular_component": "",
        "go_biological_process": "GO:0006869 lipid transport",
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        "hit_score": 0.1,
        "record_id": "A0A0G2JVS5-1",
        "record_type": "protein"
    },
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        "uniprot_canonical_ac": "F7FPK8-1",
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        "length": 358,
        "protein_name": "Lectin, mannose-binding 2",
        "gene_name": "Lman2",
        "organism": "Rat",
        "refseq_name": "vesicular integral-membrane protein VIP36 precursor",
        "refseq_ac": "NP_001108496",
        "gene_names_uniprotkb": "Lman2",
        "gene_names_refseq": "Lman2; Vip36",
        "protein_names_uniprotkb": "Lectin, mannose-binding 2",
        "protein_names_refseq": "Vesicular integral-membrane protein 36; vesicular integral-membrane protein VIP36 precursor; vesicular integral-membrane protein VIP36",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:290994);  (R-RNO-204005);  (R-RNO-5694530)",
        "pathway_count": 3,
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        "publication_id_list": "12951436",
        "class_list": "",
        "function": "Results suggest that actin filaments are involved in glycoprotein transport between the endoplasmic reticulum and cis-Golgi cisterna by using vesicular integral membrane protein-36 (VIP36)., [RefSeq, PubMed]",
        "predicted_glycosites": 1,
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        "secondary_ac_list": "",
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        "go_molecular_function": "GO:0031072 heat shock protein binding;GO:0030246 carbohydrate binding;GO:0005537 D-mannose binding",
        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005615 extracellular space;GO:0005794 Golgi apparatus;GO:0005886 plasma membrane;GO:0009986 cell surface",
        "go_biological_process": "GO:0006888 endoplasmic reticulum to Golgi vesicle-mediated transport;GO:0050766 positive regulation of phagocytosis;GO:0006890 retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum",
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        "hit_score": 0.2,
        "record_id": "F7FPK8-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "M0R3L8-1",
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        "length": 515,
        "protein_name": "Glucosylceramidase",
        "gene_name": "Gba1",
        "organism": "Rat",
        "refseq_name": "lysosomal acid glucosylceramidase precursor",
        "refseq_ac": "NP_001121111",
        "gene_names_uniprotkb": "Gba1; Gba",
        "gene_names_refseq": "Gba1; Gba",
        "protein_names_uniprotkb": "Glucosylceramidase; 3.2.1.45",
        "protein_names_refseq": "glucocerebrosidase; glucosidase, beta, acid; lysosomal acid glucosylceramidase precursor; lysosomal acid glucosylceramidase",
        "tax_id": 10116,
        "disease": "Netherton syndrome (Disease Ontology:DOID:0050474); late onset Parkinson's disease (Disease Ontology:DOID:0060892); Parkinsonism (Disease Ontology:DOID:0080855); Gaucher's disease type I (Disease Ontology:DOID:0110957); Gaucher's disease type II (Disease Ontology:DOID:0110958); Gaucher's disease type III (Disease Ontology:DOID:0110959); Gaucher's disease perinatal lethal (Disease Ontology:DOID:0110960); Gaucher's disease type IIIC (Disease Ontology:DOID:0112250); Lewy body dementia (Disease Ontology:DOID:12217); Parkinson's disease (Disease Ontology:DOID:14330); Gaucher's disease (Disease Ontology:DOID:1926); psoriasis (Disease Ontology:DOID:8893)",
        "pathway": " (rno:684536);  (R-RNO-9840310)",
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        "class_list": "",
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        "ec_number_list": "3.2.1.45;3.2.1.21;3.2.1.46;2.4.1.-;3.2.1.-",
        "go_molecular_function": "GO:0004348 glucosylceramidase activity;GO:0005124 scavenger receptor binding;GO:0008422 beta-glucosidase activity;GO:0005102 signaling receptor binding;GO:0016787 hydrolase activity",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0005783 endoplasmic reticulum;GO:0005794 Golgi apparatus;GO:0005764 lysosome;GO:0005765 lysosomal membrane",
        "go_biological_process": "GO:0098773 skin epidermis development;GO:0006680 glucosylceramide catabolic process;GO:0008203 cholesterol metabolic process;GO:0042391 regulation of membrane potential;GO:0046513 ceramide biosynthetic process",
        "synthesized_glycan_count": 0,
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        "record_id": "M0R3L8-1",
        "record_type": "protein"
    },
    {
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        "length": 328,
        "protein_name": "Serine protease 21",
        "gene_name": "Prss21",
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        "refseq_name": "serine protease 21 precursor",
        "refseq_ac": "NP_852142",
        "gene_names_uniprotkb": "Prss21",
        "gene_names_refseq": "Esp-1; Prss21; Resp-1",
        "protein_names_uniprotkb": "Serine protease 21",
        "protein_names_refseq": "eosinophil serine protease-1; protease, serine, 21; serine protease 21 precursor; testisin",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:353251);  (R-RNO-163125)",
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        "publication_id_list": "12630572",
        "class_list": "",
        "function": "A role in species-specific proteolytic events during spermatogenesis and fertilization GeneRIF: Esp-1/Testisin plays a role in species-specific proteolytic events during spermatogenesis and fertilization., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0004252 serine-type endopeptidase activity;GO:0008236 serine-type peptidase activity",
        "go_cellular_component": "GO:0005615 extracellular space;GO:0016020 membrane",
        "go_biological_process": "GO:0006508 proteolysis;GO:0007283 spermatogenesis",
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        "record_id": "M0R778-1",
        "record_type": "protein"
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        "length": 315,
        "protein_name": "Olfactory receptor family 10 subfamily AK member 7E",
        "gene_name": "Or10ak7e",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr868",
        "refseq_ac": "NP_001000821",
        "gene_names_uniprotkb": "Or10ak7e",
        "gene_names_refseq": "Olr868; Or10ak7e",
        "protein_names_uniprotkb": "Olfactory receptor family 10 subfamily AK member 7E",
        "protein_names_refseq": "olfactory receptor 868; olfactory receptor Olr868; olfactory receptor gene Olr868",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:405110)",
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0050911 detection of chemical stimulus involved in sensory perception of smell",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I5Y173-1",
        "record_type": "protein"
    },
    {
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        "length": 308,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or8w1b",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr567",
        "refseq_ac": "NP_001000326",
        "gene_names_uniprotkb": "Or8w1b",
        "gene_names_refseq": "Olr567; Or8w1b",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 567; olfactory receptor Olr567; olfactory receptor gene Olr567",
        "tax_id": 10116,
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        "pathway": " (rno:295806)",
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        "function": "Odorant receptor., [UniProtKB, UniProtKB]; Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding",
        "go_cellular_component": "GO:0005886 plasma membrane",
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        "record_id": "A0A8I6A2Y5-1",
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    {
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        "uniprot_id": "A0A8I6A426_RAT",
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        "length": 307,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or5b114",
        "organism": "Rat",
        "refseq_name": "",
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        "gene_names_uniprotkb": "Or5b114",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Olfactory receptor",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding",
        "go_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0007186 G protein-coupled receptor signaling pathway;GO:0007608 sensory perception of smell",
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        "record_id": "A0A8I6A426-1",
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    {
        "uniprot_canonical_ac": "A0A8I6A6L9-1",
        "uniprot_id": "A0A8I6A6L9_RAT",
        "mass": 15991.0,
        "length": 140,
        "protein_name": "Immunoglobulin V-set domain-containing protein",
        "gene_name": "ENSRNOG00000069261",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "ENSRNOG00000069261",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Immunoglobulin V-set domain-containing protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "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_cellular_component": "GO:0005886 plasma membrane",
        "go_biological_process": "GO:0007166 cell surface receptor signaling pathway;GO:0002250 adaptive immune response",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6A6L9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6AEX4-1",
        "uniprot_id": "A0A8I6AEX4_RAT",
        "mass": 32891.0,
        "length": 291,
        "protein_name": "Lys-63-specific deubiquitinase",
        "gene_name": "Brcc3dc",
        "organism": "Rat",
        "refseq_name": "BRCA1/BRCA2-containing complex, subunit 3, domain containing",
        "refseq_ac": "NP_001395993",
        "gene_names_uniprotkb": "Brcc3dc; LOC103692848",
        "gene_names_refseq": "Brcc3dc",
        "protein_names_uniprotkb": "Lys-63-specific deubiquitinase; 3.4.19.-",
        "protein_names_refseq": "BRCA1/BRCA2-containing complex, subunit 3, domain containing; lys-63-specific deubiquitinase BRCC36-like",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:103692848)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Metalloprotease that specifically cleaves 'Lys-63'-linked polyubiquitin chains. Component of the BRCA1-A complex, a complex that specifically recognizes 'Lys-63'-linked ubiquitinated histones H2A and H2AX at DNA lesions sites, leading to target the brca1-bard1 heterodimer to sites of DNA damage at double-strand breaks (DSBs). Catalytic subunit of the BRISC complex, a multiprotein complex that specifically cleaves 'Lys-63'-linked ubiquitin in various substrates. Mediates the specific 'Lys-63'-specific deubiquitination associated with the COP9 signalosome complex (CSN), via the interaction of the BRISC complex with the CSN complex. The BRISC complex is required for normal mitotic spindle assembly and microtubule attachment to kinetochores via its role in deubiquitinating NUMA1., [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,
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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:0008237 metallopeptidase activity;GO:0031593 polyubiquitin modification-dependent protein binding;GO:0046872 metal ion binding;GO:0004843 cysteine-type deubiquitinase activity;GO:0140492 metal-dependent deubiquitinase activity",
        "go_cellular_component": "GO:0000922 spindle pole;GO:0005737 cytoplasm;GO:0070552 BRISC complex;GO:0070531 BRCA1-A complex",
        "go_biological_process": "GO:0006508 proteolysis;GO:0051301 cell division;GO:0070536 protein K63-linked deubiquitination;GO:0006302 double-strand break repair;GO:0010212 response to ionizing radiation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6AEX4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6AFP5-1",
        "uniprot_id": "A0A8I6AFP5_RAT",
        "mass": 23113.0,
        "length": 207,
        "protein_name": "Transcription initiation factor TFIID subunit 11",
        "gene_name": "Taf11l1",
        "organism": "Rat",
        "refseq_name": "transcription initiation factor TFIID subunit 11-like",
        "refseq_ac": "XP_038943305",
        "gene_names_uniprotkb": "Taf11l1; RGD1562272",
        "gene_names_refseq": "Taf11l1",
        "protein_names_uniprotkb": "Transcription initiation factor TFIID subunit 11; TFIID subunit p30-beta; Transcription initiation factor TFIID 28 kDa subunit",
        "protein_names_refseq": "transcription initiation factor TFIID subunit 11-like",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:303433)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "The TFIID basal transcription factor complex plays a major role in the initiation of RNA polymerase II (Pol II)-dependent transcription. TFIID recognizes and binds promoters with or without a TATA box via its subunit TBP, a TATA-box-binding protein, and promotes assembly of the pre-initiation complex (PIC). The TFIID complex consists of TBP and TBP-associated factors (TAFs), including TAF1, TAF2, TAF3, TAF4, TAF5, TAF6, TAF7, TAF8, TAF9, TAF10, TAF11, TAF12 and TAF13. TAF11, together with TAF13 and TBP, play key roles during promoter binding by the TFIID and TFIIA transcription factor complexes., [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,
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        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "glyco_site_count": 1,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0046982 protein heterodimerization activity",
        "go_cellular_component": "GO:0005669 transcription factor TFIID complex",
        "go_biological_process": "GO:0051123 RNA polymerase II preinitiation complex assembly",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6AFP5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6AGM4-1",
        "uniprot_id": "A0A8I6AGM4_RAT",
        "mass": 32328.0,
        "length": 308,
        "protein_name": "Proline rich 18",
        "gene_name": "Prr18",
        "organism": "Rat",
        "refseq_name": "proline-rich protein 18",
        "refseq_ac": "NP_001101934",
        "gene_names_uniprotkb": "Prr18",
        "gene_names_refseq": "Prr18; RGD1564079",
        "protein_names_uniprotkb": "Proline rich 18",
        "protein_names_refseq": "proline rich region 18-like; proline rich region 18; proline-rich protein 18",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:361481)",
        "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,
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        "mined_glycosites": 0,
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        "mined_o_glycosites": 0,
        "mined_c_glycosites": 0,
        "mined_s_glycosites": 0,
        "reported_n_glycosites": 0,
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        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
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        "go_molecular_function": "",
        "go_cellular_component": "",
        "go_biological_process": "",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6AGM4-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6AN69-1",
        "uniprot_id": "A0A8I6AN69_RAT",
        "mass": 40879.0,
        "length": 367,
        "protein_name": "Protein Wnt",
        "gene_name": "Wnt3",
        "organism": "Rat",
        "refseq_name": "proto-oncogene Wnt-3 isoform X1",
        "refseq_ac": "XP_017452517",
        "gene_names_uniprotkb": "Wnt3",
        "gene_names_refseq": "INT4; Wnt3",
        "protein_names_uniprotkb": "Protein Wnt",
        "protein_names_refseq": "proto-oncogene Wnt-3 isoform X1",
        "tax_id": 10116,
        "disease": "tetraamelia syndrome 1 (Disease Ontology:DOID:0112192); pulmonary emphysema (Disease Ontology:DOID:9675)",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Ligand for members of the frizzled family of seven transmembrane receptors., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "predicted_c_glycosites": 0,
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        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
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        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
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        "reported_snv": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 2,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005109 frizzled binding;GO:0019904 protein domain specific binding;GO:0048018 receptor ligand activity",
        "go_cellular_component": "GO:0005576 extracellular region;GO:0031012 extracellular matrix",
        "go_biological_process": "GO:0060323 head morphogenesis;GO:0010628 positive regulation of gene expression;GO:0000902 cell morphogenesis;GO:0001558 regulation of cell growth;GO:0009952 anterior/posterior pattern specification",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6AN69-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6AVM2-1",
        "uniprot_id": "A0A8I6AVM2_RAT",
        "mass": 15396.0,
        "length": 137,
        "protein_name": "Ig-like domain-containing protein",
        "gene_name": "ENSRNOG00000063931",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "ENSRNOG00000063931",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ig-like domain-containing protein",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "reported_phosphosites": 0,
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        "reported_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_cellular_component": "GO:0042101 T cell receptor complex",
        "go_biological_process": "GO:0002250 adaptive immune response",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6AVM2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6AWW2-1",
        "uniprot_id": "A0A8I6AWW2_RAT",
        "mass": 13515.0,
        "length": 121,
        "protein_name": "40S ribosomal protein S12",
        "gene_name": "Rps12l2",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Rps12l2",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "40S ribosomal protein S12",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:100360558)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Part of the small subunit (SSU) processome, first precursor of the small eukaryotic ribosomal subunit. During the assembly of the SSU processome in the nucleolus, many ribosome biogenesis factors, an RNA chaperone and ribosomal proteins associate with the nascent pre-rRNA and work in concert to generate RNA folding, modifications, rearrangements and cleavage as well as targeted degradation of pre-ribosomal RNA by the RNA exosome. Subunit of the 40S ribosomal complex., [UniProtKB, UniProtKB]",
        "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,
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        "reported_n_glycosites": 0,
        "reported_o_glycosites": 0,
        "reported_c_glycosites": 0,
        "reported_s_glycosites": 0,
        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
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        "total_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": 0,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0003735 structural constituent of ribosome",
        "go_cellular_component": "GO:0022627 cytosolic small ribosomal subunit",
        "go_biological_process": "GO:1990145 maintenance of translational fidelity;GO:0042274 ribosomal small subunit biogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6AWW2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6B2Z0-1",
        "uniprot_id": "A0A8I6B2Z0_RAT",
        "mass": 10254.0,
        "length": 95,
        "protein_name": "Late cornified envelope 7A",
        "gene_name": "Lce7a",
        "organism": "Rat",
        "refseq_name": "late cornified envelope 7A",
        "refseq_ac": "NP_001420276",
        "gene_names_uniprotkb": "Lce7a",
        "gene_names_refseq": "Lce7a",
        "protein_names_uniprotkb": "Late cornified envelope 7A",
        "protein_names_refseq": "late cornified envelope 7A; late cornified envelope protein 7A",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:134485746)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
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        "reported_n_glycosites": 0,
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        "gene_names_uniprotkb": "ENSRNOG00000064486; Hrnr",
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        "protein_names_uniprotkb": "EF-hand domain-containing protein",
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        "go_molecular_function": "GO:0046914 transition metal ion binding;GO:0005509 calcium ion binding",
        "go_cellular_component": "GO:0001533 cornified envelope;GO:0036457 keratohyalin granule",
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    },
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        "length": 467,
        "protein_name": "Zinc finger protein 431-like",
        "gene_name": "LOC120095871",
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        "refseq_name": "zinc finger protein 431-like isoform X1",
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        "gene_names_uniprotkb": "LOC120095871",
        "gene_names_refseq": "LOC120095871",
        "protein_names_uniprotkb": "Zinc finger protein 431-like",
        "protein_names_refseq": "zinc finger protein 431-like isoform X1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:120095871);  (R-RNO-212436);  (R-RNO-9843940)",
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        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding;GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific",
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        "protein_name": "Mitochondrial adenyl nucleotide antiporter SLC25A24",
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        "refseq_ac": "NP_001121016",
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        "protein_names_uniprotkb": "Mitochondrial adenyl nucleotide antiporter SLC25A24; Small calcium-binding mitochondrial carrier protein 1; Solute carrier family 25 member 24",
        "protein_names_refseq": "calcium-binding mitochondrial carrier protein SCaMC-1; solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 24",
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        "pathway": " (rno:310791)",
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        "function": "Electroneutral antiporter that mediates the transport of adenyl nucleotides through the inner mitochondrial membrane. Originally identified as an ATP-magnesium/inorganic phosphate antiporter, it also acts as a broad specificity adenyl nucleotide antiporter. By regulating the mitochondrial matrix adenyl nucleotide pool, could adapt to changing cellular energetic demands and indirectly regulate adenyl nucleotide-dependent metabolic pathways. In vitro, a low activity is also observed with guanyl and pyrimidine nucleotides. May play a role in protecting cells against oxidative stress-induced cell death, by buffering calcium levels in the mitochondrial matrix through the formation of calcium-phosphate precipitates., [UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005739 mitochondrion;GO:0005743 mitochondrial inner membrane;GO:0016020 membrane",
        "go_biological_process": "GO:0006839 mitochondrial transport;GO:0071277 cellular response to calcium ion;GO:0034599 cellular response to oxidative stress;GO:0015866 ADP transport;GO:0015867 ATP transport",
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        "protein_name": "Lymphotoxin beta receptor",
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        "protein_names_uniprotkb": "Lymphotoxin beta receptor",
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        "go_molecular_function": "GO:0042802 identical protein binding;GO:0031625 ubiquitin protein ligase binding",
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        "go_biological_process": "GO:0006955 immune response;GO:0046330 positive regulation of JNK cascade;GO:0043123 positive regulation of canonical NF-kappaB signal transduction;GO:2001238 positive regulation of extrinsic apoptotic signaling pathway;GO:0071260 cellular response to mechanical stimulus",
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        "protein_name": "Ganglioside GM2 activator",
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        "gene_names_uniprotkb": "Gm2a",
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        "disease": "GM2 gangliosidosis (Disease Ontology:DOID:3321); GM2 gangliosidosis, AB variant (Disease Ontology:DOID:4795)",
        "pathway": " (rno:282838);  (R-RNO-6798695);  (R-RNO-9840310)",
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        "go_molecular_function": "GO:0008047 enzyme activator activity;GO:0005319 lipid transporter activity;GO:0008289 lipid binding;GO:0016004 phospholipase activator activity;GO:0004563 beta-N-acetylhexosaminidase activity",
        "go_cellular_component": "GO:0016020 membrane;GO:0016323 basolateral plasma membrane;GO:0016324 apical plasma membrane;GO:0009898 cytoplasmic side of plasma membrane",
        "go_biological_process": "GO:0006689 ganglioside catabolic process;GO:0006869 lipid transport;GO:0007611 learning or memory;GO:0050885 neuromuscular process controlling balance;GO:0050877 nervous system process",
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        "protein_name": "Ribosomal protein L32 like 2",
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        "refseq_name": "large ribosomal subunit protein eL32-like",
        "refseq_ac": "XP_038956309",
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        "gene_names_refseq": "Rpl32l2",
        "protein_names_uniprotkb": "Ribosomal protein L32 like 2",
        "protein_names_refseq": "large ribosomal subunit protein eL32-like",
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        "go_molecular_function": "GO:0003735 structural constituent of ribosome",
        "go_cellular_component": "GO:0022625 cytosolic large ribosomal subunit",
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    {
        "uniprot_canonical_ac": "A0A8I5Y9B8-1",
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        "length": 103,
        "protein_name": "Transcription initiation factor IIA subunit 2",
        "gene_name": "ENSRNOG00000064241",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "ENSRNOG00000064241",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Transcription initiation factor IIA subunit 2",
        "protein_names_refseq": "",
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        "function": "TFIIA is a component of the transcription machinery of RNA polymerase II and plays an important role in transcriptional activation. TFIIA in a complex with TBP mediates transcriptional activity., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0017025 TBP-class protein binding;GO:0016251 RNA polymerase II general transcription initiation factor activity",
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    {
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        "protein_name": "Olfactory receptor",
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        "protein_name": "Ig-like domain-containing protein",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "ENSRNOG00000069940",
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        "protein_names_uniprotkb": "Ig-like domain-containing protein",
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        "tax_id": 10116,
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        "pathway": " (R-RNO-173623);  (R-RNO-198933);  (R-RNO-202733);  (R-RNO-2029481);  (R-RNO-2029482);  (R-RNO-2029485);  (R-RNO-2168880);  (R-RNO-2454202);  (R-RNO-2730905);  (R-RNO-2871796);  (R-RNO-2871809);  (R-RNO-2871837);  (R-RNO-5690714);  (R-RNO-977606);  (R-RNO-983695)",
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        "go_molecular_function": "GO:0003823 antigen binding",
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        "go_biological_process": "GO:0016064 immunoglobulin mediated immune response",
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    {
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        "protein_name": "ATP synthase peripheral stalk subunit F6, mitochondrial",
        "gene_name": "ENSRNOG00000066253",
        "organism": "Rat",
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        "gene_names_uniprotkb": "ENSRNOG00000066253; Atp5j",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "ATP synthase peripheral stalk subunit F6, mitochondrial; ATPase subunit F6",
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        "function": "Mitochondrial membrane ATP synthase (F(1)F(0) ATP synthase or Complex V) produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain., [UniProtKB, UniProtKB]; Subunit F6, of the mitochondrial membrane ATP synthase complex (F(1)F(0) ATP synthase or Complex V) that produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. ATP synthase complex consist of a soluble F(1) head domain - the catalytic core - and a membrane F(1) domain - the membrane proton channel. These two domains are linked by a central stalk rotating inside the F(1) region and a stationary peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation. In vivo, can only synthesize ATP although its ATP hydrolase activity can be activated artificially in vitro. Part of the complex F(0) domain. Part of the complex F(0) domain and the peripheric stalk, which acts as a stator to hold the catalytic alpha(3)beta(3) subcomplex and subunit a/ATP6 static relative to the rotary elements., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0015078 proton transmembrane transporter activity",
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        "length": 312,
        "protein_name": "Olfactory receptor",
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        "refseq_name": "olfactory receptor Olr402",
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        "gene_names_uniprotkb": "Or1j14",
        "gene_names_refseq": "Olr402; Or1j14",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 402; olfactory receptor Olr402; olfactory receptor gene Olr402",
        "tax_id": 10116,
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "gene_names_uniprotkb": "Dnajb6-ps10",
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        "tax_id": 10116,
        "disease": "autosomal dominant limb-girdle muscular dystrophy type 1 (Disease Ontology:DOID:0110305)",
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    {
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        "protein_names_uniprotkb": "Cytochrome c oxidase subunit 8; Cytochrome c oxidase polypeptide VIII",
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        "go_cellular_component": "GO:0005743 mitochondrial inner membrane;GO:0045277 respiratory chain complex IV",
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        "protein_name": "Zinc finger protein 619",
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        "protein_names_refseq": "zinc finger protein 619; zinc finger protein 709; zinc finger protein 850-like; zinc finger protein 91",
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        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB]",
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        "protein_name": "Vomeronasal type-1 receptor",
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        "gene_names_uniprotkb": "Vom1r66",
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        "protein_names_uniprotkb": "Vomeronasal type-1 receptor",
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        "go_molecular_function": "GO:0005550 pheromone binding;GO:0016503 pheromone receptor activity",
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        "protein_name": "IQ motif and ankyrin repeat containing 1",
        "gene_name": "Iqank1",
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        "refseq_ac": "NP_001419532",
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        "gene_names_refseq": "Iqank1; RGD1563870",
        "protein_names_uniprotkb": "IQ motif and ankyrin repeat containing 1",
        "protein_names_refseq": "IQ motif and ankyrin repeat containing 1 isoform 1; IQ motif and ankyrin repeat domain-containing protein 1; putative IQ motif and ankyrin repeat domain-containing protein LOC642574 homolog",
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    {
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        "protein_name": "Ras-related protein Rab-42",
        "gene_name": "Rab42",
        "organism": "Rat",
        "refseq_name": "ras-related protein Rab-42",
        "refseq_ac": "NP_001386744",
        "gene_names_uniprotkb": "Rab42",
        "gene_names_refseq": "Rab42",
        "protein_names_uniprotkb": "Ras-related protein Rab-42; 3.6.5.2",
        "protein_names_refseq": "putative Ras-related protein Rab-42; ras-related protein Rab-42",
        "tax_id": 10116,
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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. The physiological function of RAB42 remains undefined., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0003924 GTPase activity;GO:0005525 GTP binding;GO:0046872 metal ion binding;GO:0003925 G protein activity",
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        "length": 322,
        "protein_name": "Olfactory receptor",
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        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr1605",
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        "gene_names_refseq": "Olr1605; Or2t35; ratchr15-12385736-12384768_ORF",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 1605; olfactory receptor Olr1605; olfactory receptor gene Olr1605",
        "tax_id": 10116,
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        "go_biological_process": "GO:0006955 immune response;GO:0002250 adaptive immune response",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "AABR07019403.1; Uggt2; AABR07019403.1; Uggt2",
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        "protein_names_uniprotkb": "UDP-glucose:glycoprotein glucosyltransferase 1; UDP--Glc:glycoprotein glucosyltransferase; UDP-glucose ceramide glucosyltransferase-like 1",
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        "ec_number_list": "2.4.1.-",
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        "protein_name": "RBPJ-interacting and tubulin-associated protein 1",
        "gene_name": "Rita1l1",
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        "refseq_name": "RBPJ-interacting and tubulin-associated protein 1-like",
        "refseq_ac": "XP_038956077",
        "gene_names_uniprotkb": "Rita1l1; LOC102546324",
        "gene_names_refseq": "Rita1l1",
        "protein_names_uniprotkb": "RBPJ-interacting and tubulin-associated protein 1; RBPJ-interacting and tubulin-associated protein",
        "protein_names_refseq": "RBPJ-interacting and tubulin-associated protein 1-like",
        "tax_id": 10116,
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        "function": "Tubulin-binding protein that acts as a negative regulator of Notch signaling pathway. Shuttles between the cytoplasm and the nucleus and mediates the nuclear export of RBPJ/RBPSUH, thereby preventing the interaction between RBPJ/RBPSUH and NICD product of Notch proteins (Notch intracellular domain), leading to down-regulate Notch-mediated transcription. May play a role in neurogenesis., [UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0015631 tubulin binding",
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        "go_biological_process": "GO:0007219 Notch signaling pathway;GO:0007399 nervous system development;GO:0051168 nuclear export;GO:0045746 negative regulation of Notch signaling pathway",
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    {
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        "protein_name": "Olfactory receptor",
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        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr1259",
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        "protein_names_refseq": "olfactory receptor 1259; olfactory receptor 8B8-like; olfactory receptor Olr1259; olfactory receptor gene Olr1259",
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        "function": "Odorant receptor., [UniProtKB, UniProtKB]; Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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        "go_molecular_function": "GO:0004930 G protein-coupled receptor activity;GO:0004984 olfactory receptor activity;GO:0005549 odorant binding",
        "go_cellular_component": "GO:0005886 plasma membrane",
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        "length": 594,
        "protein_name": "BBSome complex member BBS1",
        "gene_name": "Bbs1",
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        "refseq_name": "Bardet-Biedl syndrome 1 protein",
        "refseq_ac": "NP_001101039",
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        "gene_names_refseq": "Bbs1",
        "protein_names_uniprotkb": "BBSome complex member BBS1",
        "protein_names_refseq": "Bardet-Biedl syndrome 1 homolog; Bardet-Biedl syndrome 1 protein",
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        "disease": "Bardet-Biedl syndrome 1 (Disease Ontology:DOID:0110123); Bardet-Biedl syndrome (Disease Ontology:DOID:1935); obesity (Disease Ontology:DOID:9970)",
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        "protein_name": "Leupaxin",
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        "protein_name": "Fibroblast activation protein, alpha",
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        "disease": "esophagus squamous cell carcinoma (Disease Ontology:DOID:3748); lung squamous cell carcinoma (Disease Ontology:DOID:3907); lung non-small cell carcinoma (Disease Ontology:DOID:3908)",
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        "function": "In this study, we show for the first time the expression of FAP in activated fibroblasts after MI and its activation by TGFbeta1. Effects of FAP on fibroblast migration and gelatinolytic activity indicate a potential role in cardiac wound healing, [RefSeq, PubMed]",
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        "refseq_name": "zinc finger protein 821",
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        "protein_names_uniprotkb": "Zinc finger protein 821",
        "protein_names_refseq": "zinc finger protein 821",
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        "function": "May be involved in transcriptional regulation., [UniProtKB, UniProtKB]",
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        "protein_name": "Thrombospondin type-1 domain-containing protein 4",
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        "refseq_name": "thrombospondin type 1 domain containing 4 isoform 1 precursor",
        "refseq_ac": "NP_001416176",
        "gene_names_uniprotkb": "Thsd4",
        "gene_names_refseq": "AABR07070307.1; RGD1566296; Thsd4",
        "protein_names_uniprotkb": "Thrombospondin type-1 domain-containing protein 4; A disintegrin and metalloproteinase with thrombospondin motifs-like protein 6",
        "protein_names_refseq": "thrombospondin type 1 domain containing 4 isoform 1 precursor; thrombospondin type-1 domain-containing protein 4; thrombospondin, type I, domain containing 4",
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        "disease": "ectopia lentis with ectopia of pupil (Disease Ontology:DOID:0111648); thoracic aortic aneurysm (Disease Ontology:DOID:14004); craniosynostosis (Disease Ontology:DOID:2340); asthma (Disease Ontology:DOID:2841)",
        "pathway": " (R-RNO-5173214)",
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        "function": "Promotes FBN1 matrix assembly. Attenuates TGFB signaling, possibly by accelerating the sequestration of large latent complexes of TGFB or active TGFB by FBN1 microfibril assembly, thereby negatively regulating the expression of TGFB regulatory targets, such as POSTN., [UniProtKB, UniProtKB, UniProtKB]",
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        "protein_name": "Protein ILRUN",
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        "refseq_name": "protein ILRUN isoform 1",
        "refseq_ac": "NP_001397221",
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        "protein_names_uniprotkb": "Protein ILRUN",
        "protein_names_refseq": "chromosome 6 open reading frame 106-like; protein ILRUN isoform 1; uncharacterized protein C6orf106 homolog",
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        "function": "Negative regulator of innate antiviral response. Blocks IRF3-dependent cytokine production such as IFNA, IFNB and TNF. Interacts with IRF3 and inhibits IRF3 recruitment to type I IFN promoter sequences while also reducing nuclear levels of the coactivators EP300 and CREBBP., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0043130 ubiquitin binding",
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        "go_biological_process": "GO:0045087 innate immune response;GO:1900181 negative regulation of protein localization to nucleus;GO:0016236 macroautophagy;GO:0032720 negative regulation of tumor necrosis factor production;GO:0050687 negative regulation of defense response to virus",
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        "protein_name": "Outer mitochondrial membrane lipid metabolism regulator OPA3",
        "gene_name": "Opa3",
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        "gene_names_uniprotkb": "Opa3",
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        "protein_names_uniprotkb": "Outer mitochondrial membrane lipid metabolism regulator OPA3",
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        "tax_id": 10116,
        "disease": "3-methylglutaconic aciduria type 3 (Disease Ontology:DOID:0110004); optic atrophy 3 (Disease Ontology:DOID:0111433)",
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        "function": "May play some role in mitochondrial processes., [UniProtKB, UniProtKB, UniProtKB]",
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        "go_cellular_component": "GO:0005739 mitochondrion",
        "go_biological_process": "GO:0040008 regulation of growth;GO:0050905 neuromuscular process;GO:0019216 regulation of lipid metabolic process;GO:0007601 visual perception;GO:0045444 fat cell differentiation",
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        "protein_name": "Thioesterase superfamily member 5",
        "gene_name": "Them5",
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        "gene_names_uniprotkb": "Them5",
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        "protein_names_uniprotkb": "Thioesterase superfamily member 5",
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        "go_biological_process": "GO:0006955 immune response;GO:0008284 positive regulation of cell population proliferation;GO:0002260 lymphocyte homeostasis;GO:0030890 positive regulation of B cell proliferation;GO:0048298 positive regulation of isotype switching to IgA isotypes",
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    },
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        "protein_name": "Bromodomain adjacent to zinc finger domain protein 1A",
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        "function": "Odorant receptor., [UniProtKB, UniProtKB, UniProtKB]; Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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    {
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        "length": 739,
        "protein_name": "AP complex subunit beta",
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        "refseq_ac": "NP_001101179",
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        "protein_names_uniprotkb": "AP complex subunit beta",
        "protein_names_refseq": "AP-4 complex subunit beta-1 isoform 1; AP-4 complex subunit beta-1; adaptor-related protein complex 4, beta 1 subunit; adaptor-related protein complex AP-4, beta 1",
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        "disease": "hereditary spastic paraplegia 47 (Disease Ontology:DOID:0110799)",
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        "function": "Component of the adaptor protein complex 4 (AP-4). Adaptor protein complexes are vesicle coat components involved both in vesicle formation and cargo selection. They control the vesicular transport of proteins in different trafficking pathways. AP-4 forms a non clathrin-associated coat on vesicles departing the trans-Golgi network (TGN) and may be involved in the targeting of proteins from the trans-Golgi network (TGN) to the endosomal-lysosomal system. It is also involved in protein sorting to the basolateral membrane in epithelial cells and the proper asymmetric localization of somatodendritic proteins in neurons. AP-4 is involved in the recognition and binding of tyrosine-based sorting signals found in the cytoplasmic part of cargos, but may also recognize other types of sorting signal., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "go_molecular_function": "GO:0030276 clathrin binding",
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        "protein_name": "Vomeronasal 2 receptor, 33",
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        "organism": "Rat",
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        "protein_names_uniprotkb": "Vomeronasal 2 receptor, 33",
        "protein_names_refseq": "vomeronasal 2 receptor, 33 precursor",
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        "length": 464,
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        "protein_names_refseq": "mixed lineage kinase domain-like protein; rCG51567-like",
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        "disease": "",
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        "protein_names_uniprotkb": "histone acetyltransferase; 2.3.1.48",
        "protein_names_refseq": "K(lysine) acetyltransferase 6B; histone acetyltransferase KAT6B; lysine acetyltransferase 6B isoform 1",
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        "disease": "Ohdo syndrome, SBBYS variant (Disease Ontology:DOID:0060290); leiomyoma (Disease Ontology:DOID:127); breast cancer (Disease Ontology:DOID:1612); bipolar disorder (Disease Ontology:DOID:3312); Noonan syndrome (Disease Ontology:DOID:3490)",
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        "protein_name": "Calmodulin-binding transcription activator 1",
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        "gene_names_refseq": "Camta1",
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        "protein_names_refseq": "calmodulin-binding transcription activator 1 isoform 1",
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        "function": "Cell-cell communications between the stem cells and adjacent cardiomyocytes induce Ca(2+) signals that activate a myocardial gene program in the stem cells via a novel and early Ca(2+)-dependent intermediate, up-regulation of CAMTA1., [RefSeq, PubMed]; These results indicate that Camta1 is required not only for expression of the miR-212/miR-132 cluster but at multiple levels for regulating beta cell insulin content and secretion., [RefSeq, PubMed]; Transcriptional activator., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
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        "protein_name": "Threonine aldolase 1",
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        "refseq_name": "threonine aldolase 1",
        "refseq_ac": "NP_001417204",
        "gene_names_uniprotkb": "Tha1; LOC688286",
        "gene_names_refseq": "Tha1",
        "protein_names_uniprotkb": "Threonine aldolase 1",
        "protein_names_refseq": "probable low-specificity L-threonine aldolase 1; probable low-specificity L-threonine aldolase 2; threonine aldolase 1",
        "tax_id": 10116,
        "disease": "",
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        "pathway_count": 0,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0008732 L-allo-threonine aldolase activity;GO:0016829 lyase activity",
        "go_cellular_component": "GO:0005829 cytosol",
        "go_biological_process": "GO:0006545 glycine biosynthetic process;GO:0006567 L-threonine catabolic process;GO:0006520 amino acid metabolic process;GO:0044283 small molecule biosynthetic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6GL69-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6AU85-1",
        "uniprot_id": "A0A8I6AU85_RAT",
        "mass": 57475.0,
        "length": 527,
        "protein_name": "Thymocyte selection-associated high mobility group box",
        "gene_name": "Tox",
        "organism": "Rat",
        "refseq_name": "thymocyte selection-associated high mobility group box protein TOX isoform X1",
        "refseq_ac": "XP_063143968",
        "gene_names_uniprotkb": "Tox",
        "gene_names_refseq": "Tox",
        "protein_names_uniprotkb": "Thymocyte selection-associated high mobility group box",
        "protein_names_refseq": "thymocyte selection-associated high mobility group box protein TOX isoform X1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:362481)",
        "pathway_count": 1,
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        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 2,
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        "missing_score": 10000,
        "biomarker_type": "",
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        "ec_number_list": "",
        "go_molecular_function": "GO:0031490 chromatin DNA binding;GO:0003677 DNA binding",
        "go_cellular_component": "GO:0005634 nucleus",
        "go_biological_process": "GO:0001779 natural killer cell differentiation;GO:0002362 CD4-positive, CD25-positive, alpha-beta regulatory T cell lineage commitment;GO:1902232 regulation of positive thymic T cell selection;GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6AU85-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A096MK19-1",
        "uniprot_id": "A0A096MK19_RAT",
        "mass": 48447.0,
        "length": 421,
        "protein_name": "m7GpppN-mRNA hydrolase",
        "gene_name": "Dcp2",
        "organism": "Rat",
        "refseq_name": "m7GpppN-mRNA hydrolase",
        "refseq_ac": "NP_001163940",
        "gene_names_uniprotkb": "Dcp2",
        "gene_names_refseq": "Dcp2; RGD1562909",
        "protein_names_uniprotkb": "m7GpppN-mRNA hydrolase; 3.6.1.62; mRNA-decapping enzyme 2",
        "protein_names_refseq": "DCP2 decapping enzyme homolog; m7GpppN-mRNA hydrolase-like; m7GpppN-mRNA hydrolase; mRNA-decapping enzyme 2-like; mRNA-decapping enzyme 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:291604);  (R-RNO-430039);  (R-RNO-450385);  (R-RNO-450513);  (R-RNO-450604)",
        "pathway_count": 5,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Decapping metalloenzyme that catalyzes the cleavage of the cap structure on mRNAs. Removes the 7-methyl guanine cap structure from mRNA molecules, yielding a 5'-phosphorylated mRNA fragment and 7m-GDP. Necessary for the degradation of mRNAs, both in normal mRNA turnover and in nonsense-mediated mRNA decay. Plays a role in replication-dependent histone mRNA degradation. Has higher activity towards mRNAs that lack a poly(A) tail. Has no activity towards a cap structure lacking an RNA moiety. The presence of a N(6)-methyladenosine methylation at the second transcribed position of mRNAs (N(6),2'-O-dimethyladenosine cap; m6A(m)) provides resistance to DCP2-mediated decapping. Blocks autophagy in nutrient-rich conditions by repressing the expression of ATG-related genes through degradation of their transcripts., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "3.6.1.62;3.6.4.13;3.1.13.-;3.6.1.64;3.6.1.59;3.6.1.52;3.6.1.10;3.6.1.61",
        "go_molecular_function": "GO:0003723 RNA binding;GO:0016787 hydrolase activity;GO:0030145 manganese ion binding;GO:0140933 5'-(N(7)-methylguanosine 5'-triphospho)-[mRNA] hydrolase activity;GO:0004534 5'-3' RNA exonuclease activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0000932 P-body;GO:0036464 cytoplasmic ribonucleoprotein granule;GO:0016442 RISC complex",
        "go_biological_process": "GO:0000290 deadenylation-dependent decapping of nuclear-transcribed mRNA;GO:0000184 nuclear-transcribed mRNA catabolic process, nonsense-mediated decay;GO:0043488 regulation of mRNA stability;GO:0032211 negative regulation of telomere maintenance via telomerase;GO:0006402 mRNA catabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A096MK19-1",
        "record_type": "protein"
    },
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        "uniprot_canonical_ac": "F7EY43-1",
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        "protein_name": "Zinc finger AN1-type containing 4",
        "gene_name": "Zfand4",
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        "refseq_ac": "",
        "gene_names_uniprotkb": "Zfand4",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger AN1-type containing 4",
        "protein_names_refseq": "",
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        "pathway": " (rno:286998)",
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        "record_id": "F7EY43-1",
        "record_type": "protein"
    },
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        "uniprot_canonical_ac": "F7EUW3-1",
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        "length": 708,
        "protein_name": "C2CD2-like",
        "gene_name": "C2cd2l",
        "organism": "Rat",
        "refseq_name": "phospholipid transfer protein C2CD2L isoform 1",
        "refseq_ac": "NP_001420153",
        "gene_names_uniprotkb": "C2cd2l",
        "gene_names_refseq": "C2cd2l; Tmem24",
        "protein_names_uniprotkb": "C2CD2-like",
        "protein_names_refseq": "C2 calcium-dependent domain containing 2-like; C2 domain-containing protein 2-like; phospholipid transfer protein C2CD2L isoform 1; phospholipid transfer protein C2CD2L; transmembrane protein 24",
        "tax_id": 10116,
        "disease": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0035091 phosphatidylinositol binding;GO:0008526 phosphatidylinositol transfer activity;GO:0043559 insulin binding",
        "go_cellular_component": "GO:0098592 cytoplasmic side of apical plasma membrane;GO:0005886 plasma membrane;GO:0016020 membrane;GO:0032541 cortical endoplasmic reticulum;GO:0140268 endoplasmic reticulum-plasma membrane contact site",
        "go_biological_process": "GO:0035774 positive regulation of insulin secretion involved in cellular response to glucose stimulus",
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        "hit_score": 0.2,
        "record_id": "F7EUW3-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6G4T5-1",
        "uniprot_id": "A0A8I6G4T5_RAT",
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        "length": 312,
        "protein_name": "Ribokinase",
        "gene_name": "Rbks",
        "organism": "Rat",
        "refseq_name": "ribokinase isoform X7",
        "refseq_ac": "XP_038968398",
        "gene_names_uniprotkb": "Rbks; RBKS",
        "gene_names_refseq": "Rbks",
        "protein_names_uniprotkb": "Ribokinase; 2.7.1.15; RK",
        "protein_names_refseq": "ribokinase isoform X7",
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        "disease": "",
        "pathway": " (rno:362706);  (R-RNO-71336)",
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        "publication_id_list": "",
        "class_list": "",
        "function": "Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5-phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway., [UniProtKB, HAMAP, UniProtKB]",
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        "ec_number_list": "2.7.1.15",
        "go_molecular_function": "GO:0005524 ATP binding;GO:0046872 metal ion binding;GO:0004747 ribokinase activity;GO:0042802 identical protein binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0019303 D-ribose catabolic process;GO:0006098 pentose-phosphate shunt",
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        "hit_score": 0.1,
        "record_id": "A0A8I6G4T5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I5ZWA1-1",
        "uniprot_id": "A0A8I5ZWA1_RAT",
        "mass": 45672.0,
        "length": 418,
        "protein_name": "Zinc finger protein 362",
        "gene_name": "Zfp362",
        "organism": "Rat",
        "refseq_name": "zinc finger protein 362 isoform a",
        "refseq_ac": "NP_001178541",
        "gene_names_uniprotkb": "Zfp362",
        "gene_names_refseq": "RGD1306498; Zfp362",
        "protein_names_uniprotkb": "Zinc finger protein 362",
        "protein_names_refseq": "zinc finger protein 362 isoform a",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:297879)",
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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_biological_process": "GO:0006351 DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "A0A8I5ZWA1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6GJS0-1",
        "uniprot_id": "A0A8I6GJS0_RAT",
        "mass": 20490.0,
        "length": 178,
        "protein_name": "Dynein light chain Tctex-type family member 5",
        "gene_name": "Dynlt5",
        "organism": "Rat",
        "refseq_name": "dynein light chain Tctex-type 5 isoform X1",
        "refseq_ac": "XP_006238521",
        "gene_names_uniprotkb": "Dynlt5; Tctex1d1",
        "gene_names_refseq": "Dynlt5; RGD1311932; Tctex1d1",
        "protein_names_uniprotkb": "Dynein light chain Tctex-type family member 5",
        "protein_names_refseq": "dynein light chain Tctex-type 5 isoform X1",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:362553);  (R-RNO-5620924)",
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        "protein_names_refseq": "myb-related protein A isoform 1; myb-related protein A; myeloblastosis oncogene-like 1",
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        "protein_name": "ADAM metallopeptidase domain 12",
        "gene_name": "Adam12",
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        "refseq_name": "disintegrin and metalloproteinase domain-containing protein 12 precursor",
        "refseq_ac": "NP_001414222",
        "gene_names_uniprotkb": "Adam12",
        "gene_names_refseq": "Adam12",
        "protein_names_uniprotkb": "ADAM metallopeptidase domain 12",
        "protein_names_refseq": "a disintegrin and metallopeptidase domain 12 (meltrin alpha); disintegrin and metalloproteinase domain-containing protein 12 precursor; disintegrin and metalloproteinase domain-containing protein 12; meltrin alpha",
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        "reported_n_glycosites_with_glycan": 0,
        "reported_o_glycosites_with_glycan": 0,
        "reported_c_glycosites_with_glycan": 0,
        "reported_s_glycosites_with_glycan": 0,
        "total_reported_n_glycosites": 0,
        "total_reported_o_glycosites": 0,
        "total_reported_c_glycosites": 0,
        "total_reported_s_glycosites": 0,
        "total_n_glycosites": 0,
        "total_o_glycosites": 0,
        "total_c_glycosites": 0,
        "total_s_glycosites": 0,
        "reported_fully_resolved_glycans": 0,
        "reported_phosphosites": 0,
        "reported_mutagensis": 0,
        "reported_glycation": 0,
        "reported_snv": 0,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 1,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004222 metalloendopeptidase activity;GO:0046872 metal ion binding;GO:0017124 SH3 domain binding",
        "go_cellular_component": "GO:0016020 membrane;GO:0005886 plasma membrane",
        "go_biological_process": "GO:0006508 proteolysis;GO:0045766 positive regulation of angiogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.4,
        "record_id": "A0A8I6AGQ6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7FF81-1",
        "uniprot_id": "F7FF81_RAT",
        "mass": 17326.0,
        "length": 154,
        "protein_name": "Prefoldin subunit 5",
        "gene_name": "Pfdn5",
        "organism": "Rat",
        "refseq_name": "prefoldin subunit 5",
        "refseq_ac": "NP_001100264",
        "gene_names_uniprotkb": "Pfdn5",
        "gene_names_refseq": "Pfdn5",
        "protein_names_uniprotkb": "Prefoldin subunit 5",
        "protein_names_refseq": "prefoldin 5; prefoldin subunit 5",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:300257)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Binds specifically to cytosolic chaperonin (c-CPN) and transfers target proteins to it. Binds to nascent polypeptide chain and promotes folding in an environment in which there are many competing pathways for nonnative proteins. Represses the transcriptional activity of MYC., [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:0051082 unfolded protein binding;GO:0001540 amyloid-beta binding",
        "go_cellular_component": "GO:0016272 prefoldin complex;GO:0005737 cytoplasm;GO:0005829 cytosol",
        "go_biological_process": "GO:0006457 protein folding;GO:0090090 negative regulation of canonical Wnt signaling pathway;GO:0045892 negative regulation of DNA-templated transcription;GO:0060041 retina development in camera-type eye;GO:1905907 negative regulation of amyloid fibril formation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F7FF81-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6A2Z6-1",
        "uniprot_id": "A0A8I6A2Z6_RAT",
        "mass": 61051.0,
        "length": 543,
        "protein_name": "tRNA (guanine(6)-N(2))-methyltransferase THUMP3",
        "gene_name": "Thumpd3",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Thumpd3",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "tRNA (guanine(6)-N(2))-methyltransferase THUMP3; 2.1.1.256; THUMP domain-containing protein 3; tRNA(Trp) (guanine(7)-N(2))-methyltransferase THUMP3",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:500288)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Catalytic subunit of the THUMPD3-TRM112 methyltransferase complex, that specifically mediates the S-adenosyl-L-methionine-dependent N(2)-methylation of guanosine nucleotide at position 6 (m2G6) in tRNAs. This is one of the major tRNA (guanine-N(2))-methyltransferases. Also catalyzes the S-adenosyl-L-methionine-dependent N(2)-methylation of guanosine nucleotide at position 7 of tRNA(Trp)., [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": "2.1.1.256",
        "go_molecular_function": "GO:0003723 RNA binding;GO:0008173 RNA methyltransferase activity;GO:0016423 tRNA (guanine) methyltransferase activity;GO:0160117 tRNA (guanine(6)-N2)-methyltransferase activity;GO:0160118 tRNA (guanine(7)-N2)-methyltransferase activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0043527 tRNA methyltransferase complex;GO:0005730 nucleolus;GO:0005829 cytosol",
        "go_biological_process": "GO:0008033 tRNA processing;GO:0032259 methylation;GO:0030488 tRNA methylation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6A2Z6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6AGB5-1",
        "uniprot_id": "A0A8I6AGB5_RAT",
        "mass": 65902.0,
        "length": 565,
        "protein_name": "RIKEN cDNA 2010315B03 gene like",
        "gene_name": "2010315B03Rikl",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "2010315B03Rikl; LOC102553278",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "RIKEN cDNA 2010315B03 gene like",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:102553278)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "May be involved in transcriptional regulation., [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,
        "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: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_biological_process": "GO:0006351 DNA-templated transcription;GO:0006355 regulation of DNA-templated transcription;GO:0006357 regulation of transcription by RNA polymerase II",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6AGB5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7EMK2-1",
        "uniprot_id": "F7EMK2_RAT",
        "mass": 46461.0,
        "length": 410,
        "protein_name": "UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase",
        "gene_name": "Dpagt1",
        "organism": "Rat",
        "refseq_name": "UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase",
        "refseq_ac": "NP_955420",
        "gene_names_uniprotkb": "Dpagt1",
        "gene_names_refseq": "Dpagt1; H2afx",
        "protein_names_uniprotkb": "UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase; 2.7.8.15; GlcNAc-1-P transferase; N-acetylglucosamine-1-phosphate transferase",
        "protein_names_refseq": "UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase; dolichyl-phosphate (UDP-N-acetylglucosamine) N-acetylglucosaminephosphotransferase 1 (GlcNAc-1-P transferase); dolichyl-phosphate (UDP-N-acetylglucosamine) acetylglucosaminephosphotransferase 1 (GlcNAc-1-P transferase)",
        "tax_id": 10116,
        "disease": "congenital disorder of glycosylation Ij (Disease Ontology:DOID:0080562); congenital myasthenic syndrome 13 (Disease Ontology:DOID:0110676)",
        "pathway": " (rno:300668);  (R-RNO-446193)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase that operates in the biosynthetic pathway of dolichol-linked oligosaccharides, the glycan precursors employed in protein asparagine (N)-glycosylation. The assembly of dolichol-linked oligosaccharides begins on the cytosolic side of the endoplasmic reticulum membrane and finishes in its lumen. The sequential addition of sugars to dolichol pyrophosphate produces dolichol-linked oligosaccharides containing fourteen sugars, including two GlcNAcs, nine mannoses and three glucoses. Once assembled, the oligosaccharide is transferred from the lipid to nascent proteins by oligosaccharyltransferases. Catalyzes the initial step of dolichol-linked oligosaccharide biosynthesis, transferring GlcNAc-1-P from cytosolic UDP-GlcNAc onto the carrier lipid dolichyl phosphate (P-dolichol), yielding GlcNAc-P-P-dolichol embedded in the cytoplasmic leaflet of the endoplasmic reticulum membrane., [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": 2,
        "glyco_site_count": 0,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "2.7.8.15",
        "go_molecular_function": "GO:0046872 metal ion binding;GO:0016757 glycosyltransferase activity;GO:0003975 UDP-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase activity;GO:0003976 UDP-N-acetylglucosamine-lysosomal-enzyme N-acetylglucosaminephosphotransferase activity",
        "go_cellular_component": "GO:0005789 endoplasmic reticulum membrane;GO:0005794 Golgi apparatus;GO:0016020 membrane",
        "go_biological_process": "GO:0006488 dolichol-linked oligosaccharide biosynthetic process;GO:0006487 protein N-linked glycosylation",
        "synthesized_glycan_count": 15150,
        "hit_score": 0.1,
        "record_id": "F7EMK2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6AHL9-1",
        "uniprot_id": "A0A8I6AHL9_RAT",
        "mass": 358357.0,
        "length": 3316,
        "protein_name": "Collagen alpha-3(VI) chain",
        "gene_name": "Col6a3",
        "organism": "Rat",
        "refseq_name": "collagen alpha-3(VI) chain precursor",
        "refseq_ac": "NP_001414426",
        "gene_names_uniprotkb": "Col6a3",
        "gene_names_refseq": "Col6a3",
        "protein_names_uniprotkb": "Collagen alpha-3(VI) chain",
        "protein_names_refseq": "collagen alpha-3(VI) chain precursor; collagen alpha-3(VI) chain; collagen, type VI, alpha 3; procollagen, type VI, alpha 3",
        "tax_id": 10116,
        "disease": "congenital muscular dystrophy (Disease Ontology:DOID:0050557); Ullrich congenital muscular dystrophy (Disease Ontology:DOID:0050558); Ullrich congenital muscular dystrophy 1C (Disease Ontology:DOID:0060943); Bethlem myopathy 1C (Disease Ontology:DOID:0061200); dystonia 27 (Disease Ontology:DOID:0090050); stomach cancer (Disease Ontology:DOID:10534); primary open angle glaucoma (Disease Ontology:DOID:1070); hypertension (Disease Ontology:DOID:10763); urinary bladder cancer (Disease Ontology:DOID:11054); proliferative diabetic retinopathy (Disease Ontology:DOID:13207); uterine fibroid (Disease Ontology:DOID:13223); thoracic aortic aneurysm (Disease Ontology:DOID:14004); communication disorder (Disease Ontology:DOID:2033); colon cancer (Disease Ontology:DOID:219); myocardial infarction (Disease Ontology:DOID:5844); chronic kidney disease (Disease Ontology:DOID:784); ulcerative colitis (Disease Ontology:DOID:8577); Crohn's disease (Disease Ontology:DOID:8778); muscular dystrophy (Disease Ontology:DOID:9884)",
        "pathway": " (rno:367313);  (R-RNO-1650814)",
        "pathway_count": 2,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Collagen VI acts as a cell-binding protein., [UniProtKB, UniProtKB, UniProtKB]",
        "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": 1,
        "reported_interactions": 0,
        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
        "disease_count": 19,
        "glyco_site_count": 2,
        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0004867 serine-type endopeptidase inhibitor activity",
        "go_cellular_component": "GO:0031012 extracellular matrix;GO:0005615 extracellular space;GO:0042383 sarcolemma;GO:0005581 collagen trimer;GO:0005589 collagen type VI trimer",
        "go_biological_process": "GO:0007155 cell adhesion;GO:0051402 neuron apoptotic process;GO:0009411 response to UV;GO:0009749 response to glucose;GO:0043491 phosphatidylinositol 3-kinase/protein kinase B signal transduction",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8I6AHL9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6A915-1",
        "uniprot_id": "A0A8I6A915_RAT",
        "mass": 35381.0,
        "length": 312,
        "protein_name": "Olfactory receptor",
        "gene_name": "Or6z7",
        "organism": "Rat",
        "refseq_name": "olfactory receptor Olr6",
        "refseq_ac": "NP_001000539",
        "gene_names_uniprotkb": "Or6z7",
        "gene_names_refseq": "Olr6; Or6z7",
        "protein_names_uniprotkb": "Olfactory receptor",
        "protein_names_refseq": "olfactory receptor 6; olfactory receptor Olr6; olfactory receptor gene Olr6",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:365175)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
        "predicted_glycosites": 0,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 0,
        "predicted_c_glycosites": 0,
        "predicted_s_glycosites": 0,
        "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: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": "A0A8I6A915-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8I6GCI5-1",
        "uniprot_id": "A0A8I6GCI5_RAT",
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        "protein_name": "Maestro heat-like repeat family member 3",
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        "refseq_name": "uncharacterized protein LOC498236",
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        "gene_names_uniprotkb": "Mroh3; LOC498236",
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        "protein_names_refseq": "LRRGT00186; uncharacterized protein LOC498236",
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        "pathway": " (rno:498236)",
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    },
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        "length": 214,
        "protein_name": "Isochorismatase domain containing 2A",
        "gene_name": "Isoc2a",
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        "gene_names_uniprotkb": "Isoc2a",
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        "protein_names_uniprotkb": "Isochorismatase domain containing 2A",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8J8XDG1-1",
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        "length": 664,
        "protein_name": "E3 ubiquitin-protein ligase CHFR",
        "gene_name": "Chfr",
        "organism": "Rat",
        "refseq_name": "E3 ubiquitin-protein ligase CHFR isoform 1",
        "refseq_ac": "NP_001424199",
        "gene_names_uniprotkb": "Chfr",
        "gene_names_refseq": "Chfr",
        "protein_names_uniprotkb": "E3 ubiquitin-protein ligase CHFR; 2.3.2.27; Checkpoint with forkhead and RING finger domains protein; RING-type E3 ubiquitin transferase CHFR",
        "protein_names_refseq": "E3 ubiquitin-protein ligase CHFR isoform 1; E3 ubiquitin-protein ligase CHFR; checkpoint with forkhead and ring finger domains, E3 ubiquitin protein ligase",
        "tax_id": 10116,
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        "publication_id_list": "22673903;25578860",
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        "function": "E3 ubiquitin-protein ligase that functions in the antephase checkpoint by actively delaying passage into mitosis in response to microtubule poisons. Acts in early prophase before chromosome condensation, when the centrosome move apart from each other along the periphery of the nucleus. Probably involved in signaling the presence of mitotic stress caused by microtubule poisons by mediating the 'Lys-48'-linked ubiquitination of target proteins, leading to their degradation by the proteasome. Promotes the ubiquitination and subsequent degradation of AURKA and PLK1. Probably acts as a tumor suppressor, possibly by mediating the polyubiquitination of HDAC1, leading to its degradation. May also promote the formation of 'Lys-63'-linked polyubiquitin chains and functions with the specific ubiquitin-conjugating UBC13-MMS2 (UBE2N-UBE2V2) heterodimer. Substrates that are polyubiquitinated at 'Lys-63' are usually not targeted for degradation, but are rather involved in signaling cellular stress., [UniProtKB, UniProtKB, UniProtKB, UniProtKB]; These results show that Chfr and Grb14 collaborate in a negative feedback loop controlling insulin-stimulated cell division., [RefSeq, PubMed]",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0061630 ubiquitin protein ligase activity;GO:0000166 nucleotide binding;GO:0004842 ubiquitin-protein transferase activity",
        "go_cellular_component": "GO:0016605 PML body;GO:0005634 nucleus",
        "go_biological_process": "GO:0000278 mitotic cell cycle;GO:0051301 cell division;GO:0016567 protein ubiquitination;GO:0031398 positive regulation of protein ubiquitination;GO:0000209 protein polyubiquitination",
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        "record_type": "protein"
    },
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        "length": 400,
        "protein_name": "G protein pathway suppressor 2",
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        "refseq_name": "G protein pathway suppressor 2 isoform X1",
        "refseq_ac": "XP_006246845",
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        "protein_names_uniprotkb": "G protein pathway suppressor 2",
        "protein_names_refseq": "G protein pathway suppressor 2 isoform X1",
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        "pathway": " (R-RNO-3214815);  (R-RNO-9029569);  (R-RNO-9841922)",
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        "go_molecular_function": "GO:0003713 transcription coactivator activity;GO:0003714 transcription corepressor activity;GO:0003712 transcription coregulator activity;GO:0030332 cyclin binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0005737 cytoplasm;GO:0005739 mitochondrion;GO:0005829 cytosol",
        "go_biological_process": "GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0006357 regulation of transcription by RNA polymerase II;GO:0010875 positive regulation of cholesterol efflux;GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0019216 regulation of lipid metabolic process",
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        "length": 233,
        "protein_name": "Secreted and transmembrane 1A",
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        "organism": "Rat",
        "refseq_name": "secreted and transmembrane 1 isoform X1",
        "refseq_ac": "XP_006247947",
        "gene_names_uniprotkb": "Sectm1a",
        "gene_names_refseq": "Sectm1a; Sectm1",
        "protein_names_uniprotkb": "Secreted and transmembrane 1A",
        "protein_names_refseq": "secreted and transmembrane 1 isoform X1",
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        "go_molecular_function": "GO:0005125 cytokine activity",
        "go_cellular_component": "GO:0016020 membrane",
        "go_biological_process": "GO:0006955 immune response",
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        "hit_score": 0.1,
        "record_id": "A0A8I6AEM6-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7F0L0-1",
        "uniprot_id": "F7F0L0_RAT",
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        "length": 591,
        "protein_name": "CTP synthase",
        "gene_name": "Ctps1",
        "organism": "Rat",
        "refseq_name": "CTP synthase 1",
        "refseq_ac": "NP_001128345",
        "gene_names_uniprotkb": "Ctps1",
        "gene_names_refseq": "Ctps1; Ctps",
        "protein_names_uniprotkb": "CTP synthase; 6.3.4.2; UTP--ammonia ligase",
        "protein_names_refseq": "CTP synthase 1; cytidine 5'-triphosphate synthase",
        "tax_id": 10116,
        "disease": "biliary tract benign neoplasm (Disease Ontology:DOID:0050625); immunodeficiency 24 (Disease Ontology:DOID:0111938)",
        "pathway": " (rno:313560);  (R-RNO-499943)",
        "pathway_count": 2,
        "publication_count": 2,
        "publication_id_list": "22673903;24008161",
        "class_list": "",
        "function": "CTPS1 inhibition selectively blocks smooth muscle cell proliferation without disturbing or even promoting re-endothelialization for effective vascular repair after injury., [RefSeq, PubMed]; Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen., [UniProtKB, UniProtKB, UniProtKB, UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "6.3.4.2",
        "go_molecular_function": "GO:0005524 ATP binding;GO:0003883 CTP synthase activity;GO:0042802 identical protein binding;GO:0160260 protein asparagine deamidase activity;GO:0160264 histone H1N76/N77 asparagine deamidase activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0097268 cytoophidium;GO:0005634 nucleus;GO:0000785 chromatin",
        "go_biological_process": "GO:0044210 'de novo' CTP biosynthetic process;GO:0006241 CTP biosynthetic process;GO:0019856 pyrimidine nucleobase biosynthetic process;GO:1902340 negative regulation of chromosome condensation;GO:0042100 B cell proliferation",
        "synthesized_glycan_count": 0,
        "hit_score": 0.3,
        "record_id": "F7F0L0-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8J8YPE2-1",
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        "length": 500,
        "protein_name": "Polycomb protein EED",
        "gene_name": "Eed",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Eed",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Polycomb protein EED; Polycomb protein eed",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "transient cerebral ischemia (Disease Ontology:DOID:224)",
        "pathway": " (R-RNO-212300);  (R-RNO-2559580);  (R-RNO-3214841);  (R-RNO-8943724);  (R-RNO-8953750);  (R-RNO-9764725);  (R-RNO-9909649)",
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        "go_molecular_function": "GO:0003682 chromatin binding;GO:0008047 enzyme activator activity;GO:0042802 identical protein binding;GO:1990841 promoter-specific chromatin binding;GO:0001222 transcription corepressor binding",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0035098 ESC/E(Z) complex;GO:0005677 chromatin silencing complex;GO:0045120 pronucleus",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0000122 negative regulation of transcription by RNA polymerase II;GO:0021510 spinal cord development;GO:1990830 cellular response to leukemia inhibitory factor;GO:0071514 genomic imprinting",
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        "record_id": "A0A8J8YPE2-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7FGW7-1",
        "uniprot_id": "F7FGW7_RAT",
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        "length": 215,
        "protein_name": "NADH dehydrogenase [ubiquinone] iron-sulfur protein 8, mitochondrial",
        "gene_name": "Ndufs8",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Ndufs8",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "NADH dehydrogenase [ubiquinone] iron-sulfur protein 8, mitochondrial; 7.1.1.2; Complex I-23kD; NADH-ubiquinone oxidoreductase 23 kDa subunit",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "nuclear type mitochondrial complex I deficiency 2 (Disease Ontology:DOID:0112083); Leigh disease (Disease Ontology:DOID:3652); mitochondrial metabolism disease (Disease Ontology:DOID:700)",
        "pathway": " (R-RNO-611105);  (R-RNO-6799198)",
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        "protein_name": "Vomeronasal type-1 receptor",
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        "gene_names_refseq": "Olr623",
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        "protein_names_uniprotkb": "Aspartate aminotransferase, mitochondrial; 2.6.1.1; 2.6.1.7; Fatty acid-binding protein; Glutamate oxaloacetate transaminase 2; Kynurenine aminotransferase 4; Kynurenine aminotransferase IV; Kynurenine--oxoglutarate transaminase 4; Kynurenine--oxoglutarate transaminase IV; Plasma membrane-associated fatty acid-binding protein",
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        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8J8XFR5-1",
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        "length": 622,
        "protein_name": "Polypeptide N-acetylgalactosaminyltransferase",
        "gene_name": "Galnt18",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Galnt18",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Polypeptide N-acetylgalactosaminyltransferase; 2.4.1.-; Protein-UDP acetylgalactosaminyltransferase",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-913709)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
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        "missing_score": 10000,
        "biomarker_type": "",
        "glycan_count": 0,
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        "secondary_ac_list": "",
        "ec_number_list": "2.4.1.-;2.4.1.41",
        "go_molecular_function": "GO:0046872 metal ion binding;GO:0030246 carbohydrate binding;GO:0004653 polypeptide N-acetylgalactosaminyltransferase activity",
        "go_cellular_component": "GO:0000139 Golgi membrane;GO:0005794 Golgi apparatus",
        "go_biological_process": "GO:0006493 protein O-linked glycosylation;GO:0016266 protein O-linked glycosylation via N-acetyl-galactosamine",
        "synthesized_glycan_count": 7434,
        "hit_score": 0.1,
        "record_id": "A0A8J8XFR5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8J8XIM5-1",
        "uniprot_id": "A0A8J8XIM5_RAT",
        "mass": 39714.0,
        "length": 372,
        "protein_name": "Glyoxylate reductase/hydroxypyruvate reductase",
        "gene_name": "Grhpr",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Grhpr",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Glyoxylate reductase/hydroxypyruvate reductase",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "primary hyperoxaluria type 2 (Disease Ontology:DOID:0111671); primary hyperoxaluria (Disease Ontology:DOID:2977)",
        "pathway": " (R-RNO-389661)",
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        "class_list": "",
        "function": "",
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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:0008465 hydroxypyruvate reductase (NADH) activity;GO:0016618 hydroxypyruvate reductase [NAD(P)H] activity;GO:0030267 glyoxylate reductase (NADPH) activity;GO:0042803 protein homodimerization activity;GO:0051287 NAD binding",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005829 cytosol;GO:1902494 catalytic complex",
        "go_biological_process": "GO:0043648 dicarboxylic acid metabolic process;GO:0046487 glyoxylate metabolic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8J8XIM5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8J8Y4G1-1",
        "uniprot_id": "A0A8J8Y4G1_RAT",
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        "length": 498,
        "protein_name": "BTB domain containing 35, family member 28",
        "gene_name": "Btbd35f28",
        "organism": "Rat",
        "refseq_name": "germ cell-less protein-like 2",
        "refseq_ac": "XP_038956315",
        "gene_names_uniprotkb": "Btbd35f28; LOC120099275",
        "gene_names_refseq": "Btbd35f28",
        "protein_names_uniprotkb": "BTB domain containing 35, family member 28",
        "protein_names_refseq": "germ cell-less protein-like 2",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (rno:120099275)",
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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_cellular_component": "",
        "go_biological_process": "GO:0007281 germ cell development",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8J8Y4G1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "A0A8J8YBF1-1",
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        "length": 465,
        "protein_name": "Zinc transporter 6",
        "gene_name": "Slc30a6",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Slc30a6",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc transporter 6; Solute carrier family 30 member 6",
        "protein_names_refseq": "",
        "tax_id": 10116,
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        "class_list": "",
        "function": "Has probably no intrinsic transporter activity but together with SLC30A5 forms a functional zinc ion:proton antiporter heterodimer, mediating zinc entry into the lumen of organelles along the secretory pathway. As part of that zinc ion:proton antiporter, contributes to zinc ion homeostasis within the early secretory pathway and regulates the activation and folding of enzymes like alkaline phosphatases and enzymes involved in phosphatidylinositol glycan anchor biosynthesis., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
        "predicted_n_glycosites": 0,
        "predicted_o_glycosites": 1,
        "predicted_c_glycosites": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:0005385 zinc ion transmembrane transporter activity",
        "go_cellular_component": "GO:0005737 cytoplasm;GO:0005794 Golgi apparatus;GO:0005829 cytosol;GO:0032588 trans-Golgi network membrane;GO:0016324 apical plasma membrane",
        "go_biological_process": "GO:0006829 zinc ion transport;GO:0006895 Golgi to endosome transport;GO:0071579 regulation of zinc ion transport;GO:1904257 zinc ion import into Golgi lumen",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "A0A8J8YBF1-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "B4F7D7-1",
        "uniprot_id": "B4F7D7_RAT",
        "mass": 54934.0,
        "length": 487,
        "protein_name": "Ethanolaminephosphotransferase 1",
        "gene_name": "Selenoi",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Selenoi; Ept1",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Ethanolaminephosphotransferase 1; 2.7.8.1; Selenoprotein I",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "hereditary spastic paraplegia 81 (Disease Ontology:DOID:0112349)",
        "pathway": " (R-RNO-1483213)",
        "pathway_count": 1,
        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "Ethanolaminephosphotransferase that catalyzes the transfer of phosphoethanolamine (PE) from CDP-ethanolamine to lipid acceptors, the final step in the synthesis of PE via the 'Kennedy' pathway. PE is the second most abundant phospholipid of membranes in mammals and is involved in various membrane-related cellular processes. The enzyme is critical for the synthesis of several PE species and also catalyzes the synthesis of plasmanyl-PE, a lipid required for proper myelination and neurodevelopment, from 1-alkyl-2-acylglycerol., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 0,
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        "biomarker_type": "",
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        "secondary_ac_list": "A0A0G2JUD4",
        "ec_number_list": "2.7.8.1;2.7.8.2;2.7.8.22",
        "go_molecular_function": "GO:0004307 ethanolaminephosphotransferase activity",
        "go_cellular_component": "GO:0005794 Golgi apparatus;GO:0005789 endoplasmic reticulum membrane",
        "go_biological_process": "GO:0008611 ether lipid biosynthetic process;GO:0042552 myelination;GO:0006646 phosphatidylethanolamine biosynthetic process",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "B4F7D7-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7EKZ5-1",
        "uniprot_id": "F7EKZ5_RAT",
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        "length": 664,
        "protein_name": "CXXC-type zinc finger protein 1",
        "gene_name": "Cxxc1",
        "organism": "Rat",
        "refseq_name": "CXXC-type zinc finger protein 1 isoform X3",
        "refseq_ac": "XP_006254979",
        "gene_names_uniprotkb": "Cxxc1",
        "gene_names_refseq": "Cxxc1",
        "protein_names_uniprotkb": "CXXC-type zinc finger protein 1; CpG-binding protein; PHD finger and CXXC domain-containing protein 1",
        "protein_names_refseq": "CXXC-type zinc finger protein 1 isoform X3",
        "tax_id": 10116,
        "disease": "",
        "pathway": " (R-RNO-9772755)",
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        "publication_count": 0,
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        "class_list": "",
        "function": "Transcriptional activator that exhibits a unique DNA binding specificity for CpG unmethylated motifs with a preference for CpGG., [UniProtKB, UniProtKB]",
        "predicted_glycosites": 1,
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        "secondary_ac_list": "",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0000987 cis-regulatory region sequence-specific DNA binding;GO:0045322 unmethylated CpG binding;GO:0140002 histone H3K4me3 reader activity",
        "go_cellular_component": "GO:0005634 nucleus;GO:0005654 nucleoplasm;GO:0016607 nuclear speck;GO:0016363 nuclear matrix;GO:0035097 histone methyltransferase complex",
        "go_biological_process": "GO:0006351 DNA-templated transcription;GO:0006355 regulation of DNA-templated transcription;GO:0045893 positive regulation of DNA-templated transcription",
        "synthesized_glycan_count": 0,
        "hit_score": 0.1,
        "record_id": "F7EKZ5-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "F7FMG9-1",
        "uniprot_id": "F7FMG9_RAT",
        "mass": 24602.0,
        "length": 224,
        "protein_name": "Zinc finger protein 593",
        "gene_name": "Zfp593",
        "organism": "Rat",
        "refseq_name": "",
        "refseq_ac": "",
        "gene_names_uniprotkb": "Zfp593",
        "gene_names_refseq": "",
        "protein_names_uniprotkb": "Zinc finger protein 593; Zinc finger protein T86",
        "protein_names_refseq": "",
        "tax_id": 10116,
        "disease": "",
        "pathway": "",
        "pathway_count": 0,
        "publication_count": 1,
        "publication_id_list": "22673903",
        "class_list": "",
        "function": "Involved in pre-60S ribosomal particles maturation by promoting the nuclear export of the 60S ribosome. Negatively modulates the DNA binding activity of Oct-2 and therefore its transcriptional regulatory activity., [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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        "binding_glycan_count": 0,
        "secondary_ac_list": "",
        "ec_number_list": "",
        "go_molecular_function": "GO:1990275 preribosome binding;GO:0008270 zinc ion binding;GO:0003676 nucleic acid binding",
        "go_cellular_component": "GO:0005654 nucleoplasm;GO:0005730 nucleolus;GO:0005737 cytoplasm",
        "go_biological_process": "GO:0045944 positive regulation of transcription by RNA polymerase II;GO:0042254 ribosome biogenesis",
        "synthesized_glycan_count": 0,
        "hit_score": 0.2,
        "record_id": "F7FMG9-1",
        "record_type": "protein"
    },
    {
        "uniprot_canonical_ac": "Q5GAM3-1",
        "uniprot_id": "Q5GAM3_RAT",
        "mass": 17685.0,
        "length": 156,
        "protein_name": "Eosinophil-associated, ribonuclease A family, member 1 like 1",
        "gene_name": "Ear1l1",
        "organism": "Rat",
        "refseq_name": "ribonuclease 16-like precursor",
        "refseq_ac": "NP_001395897",
        "gene_names_uniprotkb": "Ear1l1; LOC100361814",
        "gene_names_refseq": "Ear1l1; R16; Raf2",
        "protein_names_uniprotkb": "Eosinophil-associated, ribonuclease A family, member 1 like 1",
        "protein_names_refseq": "ribonuclease 16-like precursor; ribonuclease 16-like; ribonuclease 16; ribonuclease A f2",
        "tax_id": 10116,
        "disease": "idiopathic pulmonary fibrosis (Disease Ontology:DOID:0050156)",
        "pathway": " (rno:100361814);  (R-RNO-6798695)",
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        "publication_count": 0,
        "publication_id_list": "",
        "class_list": "",
        "function": "",
        "predicted_glycosites": 0,
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        "function": "Because rat-OBP3 exhibits typical odorant-binding characteristics, the results not only provide fundamental information on the kinetics of odorant mass transfer induced by the presence of OBPs in the olfactory mucus layer but also support the possibility that vertebrate OBPs may facilitate the accumulation of odorants in the olfactory epithelium, [RefSeq, PubMed]; Down-regulation of alpha-2u globulin in renal mitochondria of STZ-induced diabetic rats., [RefSeq, PubMed]; Obp3 binding energetics are modulated by two desolvation processes with quite different thermodynamic signatures, [RefSeq, PubMed]; T. gondii infection enhances hepatic production and urinary excretion of alpha2u-globulins in rats; alpha2u-globulins are sufficient to recapitulate male sexual attractiveness akin to effects of the infection, [RefSeq, PubMed]",
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        "disease": "hereditary ataxia (Disease Ontology:DOID:0050951); autosomal dominant sensory ataxia 1 (Disease Ontology:DOID:0111170); hereditary spastic paraplegia 85 (Disease Ontology:DOID:0112345); hereditary spastic paraplegia (Disease Ontology:DOID:2476)",
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        "go_molecular_function": "GO:0008270 zinc ion binding;GO:0061630 ubiquitin protein ligase activity",
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        "go_biological_process": "GO:0016567 protein ubiquitination;GO:0045087 innate immune response;GO:0009266 response to temperature stimulus;GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process;GO:0007628 adult walking behavior",
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        "protein_name": "GDP-D-glucose phosphorylase 1",
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        "protein_names_uniprotkb": "GDP-D-glucose phosphorylase 1; 2.7.7.78",
        "protein_names_refseq": "GDP-D-glucose phosphorylase 1 isoform 1",
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    {
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        "protein_name": "Olfactory receptor family 2 subfamily AG member 2B",
        "gene_name": "Or2ag2b",
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        "gene_names_uniprotkb": "Or2ag2b",
        "gene_names_refseq": "Olr210; Or2ag2b",
        "protein_names_uniprotkb": "Olfactory receptor family 2 subfamily AG member 2B",
        "protein_names_refseq": "olfactory receptor 210; olfactory receptor Olr210; olfactory receptor gene Olr210",
        "tax_id": 10116,
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        "function": "Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]., [RefSeq]",
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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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        "protein_name": "Olfactory receptor",
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        "gene_names_refseq": "Olr633; Or4c31",
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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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