Statements (44)
| 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:hasRefSeqID |
NM_002051
|
| gptkbp:hasTranscript |
gptkb:ENST00000470094
ENST00000544313 ENST00000545613 ENST00000547413 ENST00000547713 ENST00000548013 ENST00000548313 ENST00000548613 ENST00000548913 ENST00000549213 ENST00000549513 ENST00000549813 ENST00000375416 ENST00000483589 ENST00000496438 ENST00000542124 ENST00000547009 ENST00000550113 ENST00000550413 ENST00000550713 |
| gptkbp:HGNC_ID |
gptkb:HGNC:4172
|
| https://www.w3.org/2000/01/rdf-schema#label |
ENSG00000138795
|
| gptkbp:locatedOnChromosome |
gptkb:chromosome_10
|
| gptkbp:OMIM |
131320
|
| gptkbp:organism |
gptkb:Homo_sapiens
|
| gptkbp:startPoint |
8092512
8108827 |
| gptkbp:strand |
reverse
|
| gptkbp:UniProtID |
gptkb:P23771
|
| gptkbp:bfsParent |
gptkb:PTPRB
gptkb:LEF1 gptkb:LEF |
| gptkbp:bfsLayer |
7
|