ENSG00000136238

GPTKB entity

Statements (82)
Predicate Object
gptkbp:instanceOf Ensembl gene ID
gptkbp:associatedWith gptkb:cancer
gptkb:hypoparathyroidism
gptkb:HDR_syndrome
deafness
renal dysplasia
gptkbp:encodes gptkb:GATA3
gptkbp:Entrez_Gene_ID 2625
gptkbp:gene gptkb:GATA3
gptkbp:geneType protein-coding
gptkbp:GO_term gptkb:nucleus
regulation of transcription, DNA-templated
DNA-binding transcription factor activity
zinc ion binding
gptkbp:hasRefSeqID NM_002051
gptkbp:hasTranscript ENST00000375416
ENST00000457361
ENST00000457362
ENST00000457363
ENST00000457364
ENST00000457365
ENST00000457366
ENST00000457367
ENST00000457368
ENST00000457369
ENST00000457370
ENST00000457371
ENST00000457372
ENST00000457373
ENST00000457374
ENST00000457375
ENST00000457376
ENST00000457377
ENST00000457378
ENST00000457379
ENST00000457380
ENST00000457381
ENST00000457382
ENST00000457383
ENST00000457384
ENST00000457385
ENST00000457386
ENST00000457387
ENST00000457388
ENST00000457389
ENST00000457390
ENST00000457391
ENST00000457392
ENST00000457393
ENST00000457394
ENST00000457395
ENST00000457396
ENST00000457397
ENST00000457398
ENST00000457399
ENST00000457400
ENST00000457401
ENST00000457402
ENST00000457403
ENST00000457404
ENST00000457405
ENST00000457406
ENST00000457407
ENST00000457408
ENST00000457409
ENST00000457410
ENST00000457411
ENST00000457412
ENST00000457413
ENST00000457414
ENST00000457415
gptkbp:HGNC_ID gptkb:HGNC:4172
https://www.w3.org/2000/01/rdf-schema#label ENSG00000136238
gptkbp:locatedOnChromosome gptkb:chromosome_10
gptkbp:OMIM 131320
gptkbp:organism gptkb:Homo_sapiens
gptkbp:startPoint 80924136
80962709
gptkbp:strand plus
gptkbp:UniProtID gptkb:P23771
gptkbp:bfsParent gptkb:Rac1
gptkbp:bfsLayer 7