NSUN5 (Homo sapiens)

{
    "@context": "/terms/",
    "@id": "/genes/ENSG00000130305/",
    "@type": [
        "Gene",
        "Item"
    ],
    "audit": {},
    "creation_timestamp": "2023-04-19T23:55:52.234428+00:00",
    "dbxrefs": [
        "HGNC:16385",
        "ENTREZ:55695"
    ],
    "geneid": "ENSG00000130305",
    "geneid_with_version": "ENSG00000130305.17",
    "locations": [
        {
            "assembly": "GRCh38",
            "chromosome": "chr7",
            "end": 73308826,
            "start": 73302516
        }
    ],
    "name": "NOP2/Sun RNA methyltransferase 5",
    "release_timestamp": "2024-08-30T02:37:27.727733+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": "NSUN5 - ENSG00000130305 (Homo sapiens)",
    "symbol": "NSUN5",
    "synonyms": [
        "probable 28S rRNA (cytosine-C(5))-methyltransferase",
        "NOP2/Sun domain family, member 5A",
        "NSUN5A",
        "NOP2/Sun RNA methyltransferase family member 5",
        "WBSCR20",
        "NOL1-related protein",
        "p120",
        "28S rRNA (cytosine-C(5))-methyltransferase",
        "Williams Beuren syndrome chromosome region 20A",
        "Williams-Beuren syndrome chromosomal region 20A protein",
        "WBSCR20A",
        "NOL1",
        "NOL1R",
        "NOP2/Sun domain family, member 5",
        "Williams-Beuren syndrome critical region protein 20 copy A",
        "NOL1/NOP2/Sun domain family member 5",
        "p120(NOL1)",
        "putative methyltransferase NSUN5"
    ],
    "taxa": "Homo sapiens",
    "title": "NSUN5 (Homo sapiens)",
    "transcriptome_annotation": "GENCODE 43",
    "uuid": "c7939ce7-3a73-4a68-aa8b-0405522c981e",
    "version_number": "17"
}