{
    "uniprot_canonical_ac": "A0A0B4KH86-1",
    "uniprot_id": [
        {
            "id": "A0A0B4KH86_DROME",
            "url": "https://www.uniprot.org/uniprot/A0A0B4KH86_DROME",
            "type": "external"
        }
    ],
    "mass": 71724.0,
    "length": 652,
    "protein_name": "Inwardly rectifying potassium channel 1, isoform F; Inwardly rectifying potassium channel 1, isoform G",
    "gene_name": "Irk1",
    "organism": "Fruit fly",
    "refseq_name": "inwardly rectifying potassium channel 1, isoform F",
    "refseq_ac": [
        {
            "id": "NP_001262861",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001262861",
            "type": "external"
        }
    ],
    "gene_names_uniprotkb": "Irk1; CG13836; CG44159; CG6747; DIR; Dir; Dm_3R:100326; Dm_3R:100349; Dmel\\CG44159; Dmel_CG44159; Ir-RB; Ir; Kir1; dIRK; dKirI; irk1; ir",
    "gene_names_refseq": "CG13836; CG44159; CG6747; Dir; DIR; dIRK; dKirI; Dmel\\CG44159; Dm_3R:100326; Dm_3R:100349; ir; Ir; irk1; Kir1; Irk1",
    "protein_names_uniprotkb": "Inwardly rectifying potassium channel 1, isoform F; Inwardly rectifying potassium channel 1, isoform G",
    "protein_names_refseq": "CG44159-PF; Irk1-PF; drosophila inward rectifier; inwardly rectifying potassium channel; inwardly rectifying potassium channel 1, isoform F",
    "tax_id": 7227,
    "disease": "Andersen-Tawil syndrome (Disease Ontology:DOID:0050434); familial atrial fibrillation (Disease Ontology:DOID:0050650); metabolic acidosis (Disease Ontology:DOID:0050758); short QT syndrome (Disease Ontology:DOID:0050793); atrial fibrillation (Disease Ontology:DOID:0060224); hypertrichotic osteochondrodysplasia Cantu type (Disease Ontology:DOID:0060569); permanent neonatal diabetes mellitus (Disease Ontology:DOID:0060639); familial hyperinsulinemic hypoglycemia 2 (Disease Ontology:DOID:0070218); Parkinsonism (Disease Ontology:DOID:0080855); long QT syndrome 13 (Disease Ontology:DOID:0110654); maturity-onset diabetes of the young type 13 (Disease Ontology:DOID:0111110); familial periodic paralysis (Disease Ontology:DOID:1029); hypertension (Disease Ontology:DOID:10763); sciatic neuropathy (Disease Ontology:DOID:11446); prediabetes syndrome (Disease Ontology:DOID:11716); Leber congenital amaurosis (Disease Ontology:DOID:14791); alcohol use disorder (Disease Ontology:DOID:1574); status epilepticus (Disease Ontology:DOID:1824); epilepsy (Disease Ontology:DOID:1826); hyperinsulinism (Disease Ontology:DOID:2018); coronary artery disease (Disease Ontology:DOID:3393); primary hyperaldosteronism (Disease Ontology:DOID:446); hypokalemia (Disease Ontology:DOID:4500); diabetes mellitus (Disease Ontology:DOID:9351); type 2 diabetes mellitus (Disease Ontology:DOID:9352); heroin dependence (Disease Ontology:DOID:9976)",
    "pathway": " (dme:Dmel_CG44159);  (R-DME-1296025);  (R-DME-1296041);  (R-DME-1296053);  (R-DME-1296067);  (R-DME-382556);  (R-DME-422356);  (R-DME-5576886);  (R-DME-5578775);  (R-DME-997272)",
    "pathway_count": 10,
    "publication_count": 12,
    "publication_id_list": "10731132;11964404;12537568;12537572;12537573;12537574;16110336;17569856;17569867;25589440;26109356;26109357",
    "function": "",
    "predicted_glycosites": 0,
    "predicted_n_glycosites": 0,
    "predicted_o_glycosites": 0,
    "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": 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": 26,
    "glyco_site_count": 0,
    "binding_glycan_count": 0,
    "secondary_ac_list": "",
    "ec_number_list": [],
    "go_molecular_function": "GO:0005242 inward rectifier potassium channel activity",
    "go_cellular_component": "GO:0005886 plasma membrane;GO:0016020 membrane;GO:0034702 monoatomic ion channel complex",
    "go_biological_process": "GO:0042391 regulation of membrane potential;GO:0006813 potassium ion transport;GO:0045475 locomotor rhythm;GO:0034765 regulation of monoatomic ion transmembrane transport;GO:1990573 potassium ion import across plasma membrane",
    "synthesized_glycan_count": 0,
    "record_id": "A0A0B4KH86-1",
    "record_type": "protein",
    "filter_code": "0000000.0000111.100000.0000100000000000.00000.000"
}