Hemophagocytic Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C3887558
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Genes

23 genes associated with the disease Hemophagocytic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ALK anaplastic lymphoma receptor tyrosine kinase
AP3B1 adaptor-related protein complex 3, beta 1 subunit
APCS amyloid P component, serum
ASRGL1 asparaginase like 1
ATF5 activating transcription factor 5
BCL3 B-cell CLL/lymphoma 3
FGL1 fibrinogen-like 1
HAVCR2 hepatitis A virus cellular receptor 2
HPS1 Hermansky-Pudlak syndrome 1
IFNG interferon, gamma
IL10 interleukin 10
IL18 interleukin 18
IL2 interleukin 2
ITK IL2-inducible T-cell kinase
LYST lysosomal trafficking regulator
MIP major intrinsic protein of lens fiber
NCAM1 neural cell adhesion molecule 1
P2RX7 purinergic receptor P2X, ligand gated ion channel, 7
PDLIM7 PDZ and LIM domain 7 (enigma)
RAB27A RAB27A, member RAS oncogene family
SH2D1A SH2 domain containing 1A
TLR9 toll-like receptor 9
TNF tumor necrosis factor