SLC7A4 (Homo sapiens)

released
1{
2    "@context": "/terms/",
3    "@id": "/genes/ENSG00000099960/",
4    "@type": [
5        "Gene",
6        "Item"
7    ],
8    "audit": {},
9    "creation_timestamp": "2023-04-20T01:18:00.978324+00:00",
10    "dbxrefs": [
11        "HGNC:11062",
12        "ENTREZ:6545"
13    ],
14    "geneid": "ENSG00000099960",
15    "geneid_with_version": "ENSG00000099960.13",
16    "locations": [
17        {
18            "assembly": "GRCh38",
19            "chromosome": "chr22",
20            "end": 21032840,
21            "start": 21028717
22        }
23    ],
24    "name": "solute carrier family 7 member 4",
25    "release_timestamp": "2024-08-30T14:35:05.611378+00:00",
26    "schema_version": "10",
27    "status": "released",
28    "study_sets": [
29        "DiGeorge Syndrome - Shendure"
30    ],
31    "submitted_by": {
32        "@id": "/users/98fb23d3-0d79-4c3d-981d-01539e6589f1/",
33        "title": "Idan Gabdank"
34    },
35    "summary": "SLC7A4 - ENSG00000099960 (Homo sapiens)",
36    "symbol": "SLC7A4",
37    "synonyms": [
38        "VH",
39        "CAT-4",
40        "SLC7A4",
41        "solute carrier family 7 (cationic amino acid transporter, y+ system), member 4",
42        "Ig heavy chain variable region",
43        "solute carrier family 7 member 4",
44        "cationic amino acid transporter 4",
45        "CAT4",
46        "HCAT3",
47        "solute carrier family 7 (orphan transporter), member 4",
48        "VH 3 family"
49    ],
50    "taxa": "Homo sapiens",
51    "title": "SLC7A4 (Homo sapiens)",
52    "transcriptome_annotation": "GENCODE 43",
53    "uuid": "6cda64a4-55d8-4964-9a9d-1f9920791c63",
54    "version_number": "13"
55}