gangrene Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A serious and potentially life-threatening condition that arises when a considerable mass of body tissue dies (necrosis). (Human Phenotype Ontology, HP_0100758)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100758
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Genes

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

Symbol Name
ABCA12 ATP-binding cassette, sub-family A (ABC1), member 12
AGXT alanine-glyoxylate aminotransferase
ALOX12B arachidonate 12-lipoxygenase, 12R type
C4A complement component 4A (Rodgers blood group)
CTLA4 cytotoxic T-lymphocyte-associated protein 4
CYP4F22 cytochrome P450, family 4, subfamily F, polypeptide 22
HLA-B major histocompatibility complex, class I, B
HLA-DPB1 major histocompatibility complex, class II, DP beta 1
IL10 interleukin 10
IL12B interleukin 12B
IL12RB2 interleukin 12 receptor, beta 2
IL23R interleukin 23 receptor
KIF11 kinesin family member 11
KRT1 keratin 1, type II
LIPN lipase, family member N
MEFV Mediterranean fever
MLX MLX, MAX dimerization protein
NIPAL4 NIPA-like domain containing 4
NOD2 nucleotide-binding oligomerization domain containing 2
PROC protein C (inactivator of coagulation factors Va and VIIIa)
PROS1 protein S (alpha)
PRTN3 proteinase 3
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
STAT4 signal transducer and activator of transcription 4
TGM1 transglutaminase 1
TLR4 toll-like receptor 4