Statements (22)
Predicate | Object |
---|---|
gptkbp:instanceOf |
gptkb:gene
|
gptkbp:alsoKnownAs |
gptkb:NKX2-5
gptkb:CSX |
gptkbp:associatedWith |
gptkb:atrial_septal_defect
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 |
transcription factor
|
gptkbp:HGNC_ID |
7837
|
https://www.w3.org/2000/01/rdf-schema#label |
NKX2-5 cardiac homeobox
|
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
|