STX1A (Homo sapiens)

{
    "@context": "/terms/",
    "@id": "/genes/ENSG00000106089/",
    "@type": [
        "Gene",
        "Item"
    ],
    "audit": {},
    "creation_timestamp": "2023-04-19T23:55:55.624582+00:00",
    "dbxrefs": [
        "HGNC:11433",
        "ENTREZ:6804"
    ],
    "geneid": "ENSG00000106089",
    "geneid_with_version": "ENSG00000106089.12",
    "locations": [
        {
            "assembly": "GRCh38",
            "chromosome": "chr7",
            "end": 73719672,
            "start": 73699206
        }
    ],
    "name": "syntaxin 1A",
    "release_timestamp": "2024-08-30T19:13:35.987121+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": "STX1A - ENSG00000106089 (Homo sapiens)",
    "symbol": "STX1A",
    "synonyms": [
        "HPC-1",
        "STX1",
        "neuron-specific antigen HPC-1",
        "SYN1A",
        "P35-1",
        "syntaxin-1A",
        "syntaxin 1A (brain)"
    ],
    "taxa": "Homo sapiens",
    "title": "STX1A (Homo sapiens)",
    "transcriptome_annotation": "GENCODE 43",
    "uuid": "892a75c0-3d4b-4e24-bff4-03422934246b",
    "version_number": "12"
}