Statements (68)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
Ensembl gene ID
|
| gptkbp:associatedWith |
gptkb:cancer
gptkb:hypoparathyroidism,_sensorineural_deafness,_and_renal_dysplasia_syndrome |
| gptkbp:encodes |
gptkb:GATA3
|
| gptkbp:Entrez_Gene_ID |
2625
|
| gptkbp:gene |
gptkb:GATA3
|
| gptkbp:geneType |
protein-coding
|
| gptkbp:hasTranscript |
ENST00000375416
ENST00000423634 ENST00000423635 ENST00000423636 ENST00000423637 ENST00000423638 ENST00000423639 ENST00000423640 ENST00000423641 ENST00000423642 ENST00000423643 ENST00000423644 ENST00000423645 ENST00000423646 ENST00000423647 ENST00000423648 ENST00000423649 ENST00000423650 ENST00000423651 ENST00000423652 ENST00000423653 ENST00000423654 ENST00000423655 ENST00000423656 ENST00000423657 ENST00000423658 ENST00000423659 ENST00000423660 ENST00000423661 ENST00000423662 ENST00000423663 ENST00000423664 ENST00000423665 ENST00000423666 ENST00000423667 ENST00000423668 ENST00000423669 ENST00000423670 ENST00000423671 ENST00000423672 ENST00000423673 ENST00000423674 ENST00000423675 ENST00000423676 ENST00000423677 ENST00000423678 ENST00000423679 ENST00000423680 ENST00000423681 ENST00000423682 |
| gptkbp:HGNC_ID |
HGNC:4171
|
| https://www.w3.org/2000/01/rdf-schema#label |
ENSG00000068024
|
| gptkbp:locatedOnChromosome |
gptkb:chromosome_10
|
| gptkbp:OMIM |
131320
|
| gptkbp:organism |
gptkb:Homo_sapiens
|
| gptkbp:startPoint |
8108827
8092511 |
| gptkbp:strand |
plus
|
| gptkbp:UniProtID |
gptkb:P23771
|
| gptkbp:bfsParent |
gptkb:HDAC4
|
| gptkbp:bfsLayer |
8
|