ATP7B (Homo sapiens)

{
    "@context": "/terms/",
    "@id": "/genes/ENSG00000123191/",
    "@type": [
        "Gene",
        "Item"
    ],
    "audit": {},
    "collections": [
        "ACMG73"
    ],
    "creation_timestamp": "2023-04-20T00:35:33.911094+00:00",
    "dbxrefs": [
        "HGNC:870",
        "ENTREZ:540"
    ],
    "geneid": "ENSG00000123191",
    "geneid_with_version": "ENSG00000123191.16",
    "locations": [
        {
            "assembly": "GRCh38",
            "chromosome": "chr13",
            "end": 52012125,
            "start": 51930436
        }
    ],
    "name": "ATPase copper transporting beta",
    "release_timestamp": "2024-08-29T19:25:05.939536+00:00",
    "schema_version": "9",
    "status": "released",
    "submitted_by": {
        "@id": "/users/98fb23d3-0d79-4c3d-981d-01539e6589f1/",
        "title": "Idan Gabdank"
    },
    "summary": "ATP7B - ENSG00000123191 (Homo sapiens)",
    "symbol": "ATP7B",
    "synonyms": [
        "WC1",
        "ATPase, Cu++ transporting, beta polypeptide",
        "WND",
        "copper pump 2",
        "Wilson disease-associated protein",
        "WD",
        "copper-transporting ATPase 2",
        "PWD",
        "ATPase, Cu(2+)- transporting, beta polypeptide",
        "copper-transporting protein ATP7B"
    ],
    "taxa": "Homo sapiens",
    "title": "ATP7B (Homo sapiens)",
    "transcriptome_annotation": "GENCODE 43",
    "uuid": "d014a5f2-6b53-42e2-9557-d550af0c4fab",
    "version_number": "16"
}