NSUN5P2 (Homo sapiens)

{
    "@context": "/terms/",
    "@id": "/genes/ENSG00000290831/",
    "@type": [
        "Gene",
        "Item"
    ],
    "audit": {},
    "creation_timestamp": "2023-04-19T23:55:48.323445+00:00",
    "dbxrefs": [
        "HGNC:16609"
    ],
    "geneid": "ENSG00000290831",
    "geneid_with_version": "ENSG00000290831.1",
    "locations": [
        {
            "assembly": "GRCh38",
            "chromosome": "chr7",
            "end": 72954790,
            "start": 72947581
        }
    ],
    "release_timestamp": "2024-08-28T19:29:02.375469+00:00",
    "schema_version": "9",
    "status": "released",
    "study_sets": [
        "Williams Syndrome - Park"
    ],
    "submitted_by": {
        "@id": "/users/98fb23d3-0d79-4c3d-981d-01539e6589f1/",
        "title": "Idan Gabdank"
    },
    "summary": "NSUN5P2 - ENSG00000290831 (Homo sapiens)",
    "symbol": "NSUN5P2",
    "taxa": "Homo sapiens",
    "title": "NSUN5P2 (Homo sapiens)",
    "transcriptome_annotation": "GENCODE 43",
    "uuid": "afb38b22-48b6-4479-998f-7005d38486fe",
    "version_number": "1"
}