PMS2P9 (Homo sapiens)

{
    "@context": "/terms/",
    "@id": "/genes/ENSG00000233448/",
    "@type": [
        "Gene",
        "Item"
    ],
    "audit": {},
    "creation_timestamp": "2023-04-19T23:56:14.867000+00:00",
    "dbxrefs": [
        "ENTREZ:100132832",
        "HGNC:9135"
    ],
    "geneid": "ENSG00000233448",
    "geneid_with_version": "ENSG00000233448.2",
    "locations": [
        {
            "assembly": "GRCh38",
            "chromosome": "chr7",
            "end": 77043776,
            "start": 77039944
        }
    ],
    "name": "PMS1 homolog 2, mismatch repair system component pseudogene 9",
    "release_timestamp": "2024-08-30T06:45:07.929932+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": "PMS2P9 - ENSG00000233448 (Homo sapiens)",
    "symbol": "PMS2P9",
    "synonyms": [
        "PMS2LP1",
        "PMS2L17",
        "PMS2 postmeiotic segregation increased 2 pseudogene",
        "postmeiotic segregation increased 2-like 17",
        "postmeiotic segregation increased 2-like pseudogene 1",
        "postmeiotic segregation increased 2 pseudogene 9",
        "PMSR5"
    ],
    "taxa": "Homo sapiens",
    "title": "PMS2P9 (Homo sapiens)",
    "transcriptome_annotation": "GENCODE 43",
    "uuid": "8d99eb3f-26a7-4bc2-83ec-e5dae7caf3b8",
    "version_number": "2"
}