abnormal natural killer cell physiology Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A functional anomaly of the natural killer cell. (Human Phenotype Ontology, HP_0012177)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012177
Similar Terms
Downloads & Tools


4 genes associated with the abnormal natural killer cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
SH2D1A SH2 domain containing 1A
STXBP2 syntaxin binding protein 2
UNC13D unc-13 homolog D (C. elegans)
WIPF1 WAS/WASL interacting protein family, member 1