abnormality of macrophages Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of macrophages. (Human Phenotype Ontology, HP_0004311)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004311
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Genes

19 genes associated with the abnormality of macrophages phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CD27 CD27 molecule
CYBA cytochrome b-245, alpha polypeptide
CYBB cytochrome b-245, beta polypeptide
GLB1 galactosidase, beta 1
IGHV4-34 immunoglobulin heavy variable 4-34
LIPA lipase A, lysosomal acid, cholesterol esterase
NCF1 neutrophil cytosolic factor 1
NCF2 neutrophil cytosolic factor 2
NEU1 sialidase 1 (lysosomal sialidase)
NOD2 nucleotide-binding oligomerization domain containing 2
NPC1 Niemann-Pick disease, type C1
NPC2 Niemann-Pick disease, type C2
PRF1 perforin 1 (pore forming protein)
SLC7A7 solute carrier family 7 (amino acid transporter light chain, y+L system), member 7
SMPD1 sphingomyelin phosphodiesterase 1, acid lysosomal
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