PMS2P5 (Homo sapiens)

{
    "@context": "/terms/",
    "@id": "/genes/ENSG00000123965/",
    "@type": [
        "Gene",
        "Item"
    ],
    "audit": {},
    "creation_timestamp": "2023-04-19T23:56:01.282303+00:00",
    "dbxrefs": [
        "ENTREZ:5383",
        "HGNC:9130"
    ],
    "geneid": "ENSG00000123965",
    "geneid_with_version": "ENSG00000123965.13",
    "locations": [
        {
            "assembly": "GRCh38",
            "chromosome": "chr7",
            "end": 74897835,
            "start": 74894116
        }
    ],
    "name": "PMS1 homolog 2, mismatch repair system component pseudogene 5",
    "release_timestamp": "2024-08-29T21:07:10.809594+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": "PMS2P5 - ENSG00000123965 (Homo sapiens)",
    "symbol": "PMS2P5",
    "synonyms": [
        "PMS2L5",
        "PMS7",
        "postmeiotic segregation increased 2 pseudogene 5",
        "postmeiotic segregation increased 2-like 5"
    ],
    "taxa": "Homo sapiens",
    "title": "PMS2P5 (Homo sapiens)",
    "transcriptome_annotation": "GENCODE 43",
    "uuid": "af7c0c1e-bfde-4887-9abc-af2970636e57",
    "version_number": "13"
}