abnormality of natural killer cells Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly of the natural killer cell, which is a lymphocyte that can spontaneously kill a variety of target cells without prior antigenic activation via germline encoded activation receptors and also regulate immune responses via cytokine release and direct contact with other cells. (Human Phenotype Ontology, HP_0012176)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012176
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Genes

5 genes associated with the abnormality of natural killer cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GATA2 GATA binding protein 2
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