KMT2D (Homo sapiens)

{
    "@context": "/terms/",
    "@id": "/genes/ENSG00000167548/",
    "@type": [
        "Gene",
        "Item"
    ],
    "audit": {},
    "collections": [
        "StanfordFCC"
    ],
    "creation_timestamp": "2023-04-20T00:28:54.045277+00:00",
    "dbxrefs": [
        "ENTREZ:8085",
        "HGNC:7133"
    ],
    "geneid": "ENSG00000167548",
    "geneid_with_version": "ENSG00000167548.18",
    "locations": [
        {
            "assembly": "GRCh38",
            "chromosome": "chr12",
            "end": 49060794,
            "start": 49018975
        }
    ],
    "name": "lysine methyltransferase 2D",
    "release_timestamp": "2024-08-30T01:33:08.876051+00:00",
    "schema_version": "9",
    "status": "released",
    "study_sets": [
        "Cardiac - Engreitz"
    ],
    "submitted_by": {
        "@id": "/users/98fb23d3-0d79-4c3d-981d-01539e6589f1/",
        "title": "Idan Gabdank"
    },
    "summary": "KMT2D - ENSG00000167548 (Homo sapiens)",
    "symbol": "KMT2D",
    "synonyms": [
        "AAD10",
        "lysine (K)-specific methyltransferase 2D",
        "lysine N-methyltransferase 2D",
        "histone-lysine N-methyltransferase MLL2",
        "MLL4",
        "KABUK1",
        "BCAHH",
        "ALL1-related protein",
        "MLL2",
        "histone-lysine N-methyltransferase 2D",
        "CAGL114",
        "TNRC21",
        "Kabuki make-up syndrome",
        "KMS",
        "ALR",
        "myeloid/lymphoid or mixed-lineage leukemia 2",
        "trinucleotide repeat containing 21"
    ],
    "taxa": "Homo sapiens",
    "title": "KMT2D (Homo sapiens)",
    "transcriptome_annotation": "GENCODE 43",
    "uuid": "31b36be8-e8b8-4a9d-add4-e04e79af02c2",
    "version_number": "18"
}