BCL7B (Homo sapiens)

{
    "@context": "/terms/",
    "@id": "/genes/ENSG00000106635/",
    "@type": [
        "Gene",
        "Item"
    ],
    "audit": {},
    "creation_timestamp": "2023-04-19T23:55:54.321928+00:00",
    "dbxrefs": [
        "HGNC:1005",
        "ENTREZ:9275"
    ],
    "geneid": "ENSG00000106635",
    "geneid_with_version": "ENSG00000106635.8",
    "locations": [
        {
            "assembly": "GRCh38",
            "chromosome": "chr7",
            "end": 73557690,
            "start": 73536356
        }
    ],
    "name": "BAF chromatin remodeling complex subunit BCL7B",
    "release_timestamp": "2024-08-28T18:10:30.476758+00:00",
    "schema_version": "9",
    "status": "released",
    "study_sets": [
        "Williams Syndrome - Shendure",
        "Williams Syndrome - Park"
    ],
    "submitted_by": {
        "@id": "/users/98fb23d3-0d79-4c3d-981d-01539e6589f1/",
        "title": "Idan Gabdank"
    },
    "summary": "BCL7B - ENSG00000106635 (Homo sapiens)",
    "symbol": "BCL7B",
    "synonyms": [
        "B-cell CLL/lymphoma 7B",
        "SMARCJ2",
        "BCL7B, BAF complex component",
        "B-cell CLL/lymphoma 7 protein family member B",
        "BCL tumor suppressor 7B"
    ],
    "taxa": "Homo sapiens",
    "title": "BCL7B (Homo sapiens)",
    "transcriptome_annotation": "GENCODE 43",
    "uuid": "c6836b11-b9e1-4442-bbc3-d9ce7dba9c9c",
    "version_number": "8"
}