cellulitis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100658
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Genes

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

Symbol Name
AGGF1 angiogenic factor with G patch and FHA domains 1
BLNK B-cell linker
BTK Bruton agammaglobulinemia tyrosine kinase
CD79A CD79a molecule, immunoglobulin-associated alpha
CD79B CD79b molecule, immunoglobulin-associated beta
COL1A1 collagen, type I, alpha 1
CYBA cytochrome b-245, alpha polypeptide
CYBB cytochrome b-245, beta polypeptide
GATA2 GATA binding protein 2
GJC2 gap junction protein, gamma 2, 47kDa
IGHM immunoglobulin heavy constant mu
IGLL1 immunoglobulin lambda-like polypeptide 1
KIF11 kinesin family member 11
LMNA lamin A/C
LRRC8A leucine rich repeat containing 8 family, member A
NCF1 neutrophil cytosolic factor 1
NCF2 neutrophil cytosolic factor 2
PIK3CD phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit delta
PIK3R1 phosphoinositide-3-kinase, regulatory subunit 1 (alpha)
PLCG2 phospholipase C, gamma 2 (phosphatidylinositol-specific)
SHANK3 SH3 and multiple ankyrin repeat domains 3
STAT3 signal transducer and activator of transcription 3 (acute-phase response factor)
TCF3 transcription factor 3
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A