abnormality of macrophages Gene Set
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
|
