hemophagocytosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Phagocytosis by macrophages of erythrocytes, leukocytes, platelets, and their precursors in bone marrow and other tissues. (Human Phenotype Ontology, HP_0012156)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012156
Similar Terms
Downloads & Tools

Genes

7 genes associated with the hemophagocytosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CD27 CD27 molecule
PRF1 perforin 1 (pore forming protein)
SLC7A7 solute carrier family 7 (amino acid transporter light chain, y+L system), member 7
STX11 syntaxin 11
STXBP2 syntaxin binding protein 2
UNC13D unc-13 homolog D (C. elegans)
XIAP X-linked inhibitor of apoptosis, E3 ubiquitin protein ligase