{
"@context": "/terms/",
"@id": "/genes/ENSG00000099940/",
"@type": [
"Gene",
"Item"
],
"audit": {},
"creation_timestamp": "2023-04-20T01:17:58.954597+00:00",
"dbxrefs": [
"HGNC:11133",
"ENTREZ:9342"
],
"geneid": "ENSG00000099940",
"geneid_with_version": "ENSG00000099940.12",
"locations": [
{
"assembly": "GRCh38",
"chromosome": "chr22",
"end": 20891214,
"start": 20859006
}
],
"name": "synaptosome associated protein 29",
"release_timestamp": "2024-08-30T13:56:31.652028+00:00",
"schema_version": "10",
"status": "released",
"study_sets": [
"DiGeorge Syndrome - Shendure"
],
"submitted_by": {
"@id": "/users/98fb23d3-0d79-4c3d-981d-01539e6589f1/",
"title": "Idan Gabdank"
},
"summary": "SNAP29 - ENSG00000099940 (Homo sapiens)",
"symbol": "SNAP29",
"synonyms": [
"soluble 29 kDa NSF attachment protein",
"SNAP29",
"synaptosome associated protein 29",
"synaptosome associated protein 29kDa",
"synaptosomal-associated protein 29",
"synaptosomal-associated protein, 29kDa",
"cerebral dysgenesis, neuropathy, ichthyosis and keratoderma syndrome",
"synaptosomal-associated protein, 29kD",
"CEDNIK",
"SNAP-29",
"vesicle-membrane fusion protein SNAP-29"
],
"taxa": "Homo sapiens",
"title": "SNAP29 (Homo sapiens)",
"transcriptome_annotation": "GENCODE 43",
"uuid": "f06ff43d-3c45-4147-ae5b-02671dfd50e7",
"version_number": "12"
}