Statements (22)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:gene
|
| gptkbp:alsoKnownAs |
gptkb:NKX2-5
gptkb:CSX |
| gptkbp:associatedWith |
gptkb:atrial_septal_defect
gptkb:congenital_heart_disease cardiac conduction defects |
| gptkbp:encodes |
NK2 homeobox 5
|
| gptkbp:Entrez_Gene_ID |
1482
|
| gptkbp:expressedIn |
heart
|
| gptkbp:foundIn |
gptkb:Homo_sapiens
|
| gptkbp:function |
gptkb:transcription_factor
|
| gptkbp:HGNC_ID |
7837
|
| gptkbp:locatedOnChromosome |
gptkb:chromosome_5
|
| gptkbp:mutationAssociatedWith |
congenital heart malformations
|
| gptkbp:OMIM |
600584
|
| gptkbp:orthologInMouse |
gptkb:Nkx2-5
|
| gptkbp:proteinFamily |
homeobox protein
|
| gptkbp:regulates |
cardiac development
|
| gptkbp:UniProtID |
O95096
|
| gptkbp:bfsParent |
gptkb:NKX2-5
|
| gptkbp:bfsLayer |
7
|
| http://www.w3.org/2000/01/rdf-schema#label |
NKX2-5 cardiac homeobox
|