{
    "uniprot_canonical_ac": "A0A0G2K1F7-1",
    "uniprot_id": [
        {
            "id": "A0A0G2K1F7_RAT",
            "url": "https://www.uniprot.org/uniprot/A0A0G2K1F7_RAT",
            "type": "external"
        }
    ],
    "mass": 395569.0,
    "length": 3512,
    "protein_name": "Myosin XVA",
    "gene_name": "Myo15a",
    "organism": "Rat",
    "refseq_name": "unconventional myosin-XV",
    "refseq_ac": [
        {
            "id": "NP_001414755",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001414755",
            "type": "external"
        }
    ],
    "gene_names_uniprotkb": "Myo15a",
    "gene_names_refseq": "Myo15; RGD1561873; Myo15a",
    "protein_names_uniprotkb": "Myosin XVA",
    "protein_names_refseq": "myosin XV; unconventional myosin-XV-like; unconventional myosin-XV",
    "tax_id": 10116,
    "disease": "autosomal recessive nonsyndromic deafness 3 (Disease Ontology:DOID:0110488); sensorineural hearing loss (Disease Ontology:DOID:10003); blindness (Disease Ontology:DOID:1432)",
    "pathway": "",
    "pathway_count": 0,
    "publication_count": 2,
    "publication_id_list": "14629112;21479269",
    "function": "Mutations in binding domains of myosin XV do not only cause non-syndromic hearing loss but can also lead to syndromic disorders including retinal dysfunction. Publication Status: Online-Only, [RefSeq, PubMed]; Myo15 and Kcnj12 can be regarded as candidate genes for the deafblind phenotype of the LEW-ci2 rat., [RefSeq, PubMed]",
    "predicted_glycosites": 1,
    "predicted_n_glycosites": 0,
    "predicted_o_glycosites": 1,
    "mined_glycosites": 0,
    "mined_n_glycosites": 0,
    "mined_o_glycosites": 0,
    "reported_n_glycosites": 0,
    "reported_o_glycosites": 0,
    "reported_n_glycosites_with_glycan": 0,
    "reported_o_glycosites_with_glycan": 0,
    "total_reported_n_glycosites": 0,
    "total_reported_o_glycosites": 0,
    "total_n_glycosites": 0,
    "total_o_glycosites": 1,
    "reported_fully_resolved_glycans": 0,
    "reported_phosphosites": 0,
    "reported_mutagensis": 0,
    "reported_glycation": 0,
    "reported_snv": 0,
    "reported_interactions": 0,
    "missing_score": 10000,
    "biomarker_type": "",
    "glycan_count": 0,
    "disease_count": 3,
    "glyco_site_count": 1,
    "binding_glycan_count": 0,
    "secondary_ac_list": "",
    "ec_number_list": [],
    "go_molecular_function": "GO:0005524 ATP binding;GO:0051015 actin filament binding;GO:0000146 microfilament motor activity",
    "go_cellular_component": "GO:0005737 cytoplasm;GO:0015629 actin cytoskeleton;GO:0016020 membrane;GO:0032421 stereocilium bundle;GO:0032420 stereocilium",
    "go_biological_process": "GO:0007015 actin filament organization;GO:0007626 locomotory behavior;GO:0042472 inner ear morphogenesis;GO:0007605 sensory perception of sound;GO:0009416 response to light stimulus",
    "synthesized_glycan_count": 0,
    "record_id": "A0A0G2K1F7-1",
    "record_type": "protein",
    "filter_code": "0000000.0000110.001000.0000000000001000.00010.001"
}