Abnormality Of The Immune System Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An abnormality of the immune system. (Human Phenotype Ontology, HP_0002715)
External Link https://www.disgenet.org/browser/0/1/0/C4021753
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Genes

33 genes associated with the disease Abnormality Of The Immune System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ABCC8 ATP-binding cassette, sub-family C (CFTR/MRP), member 8
ATP6AP1 ATPase, H+ transporting, lysosomal accessory protein 1
C5ORF42 chromosome 5 open reading frame 42
CD244 CD244 molecule, natural killer cell receptor 2B4
CEP126 centrosomal protein 126kDa
CHAT choline O-acetyltransferase
CHRNE cholinergic receptor, nicotinic, epsilon (muscle)
CIITA class II, major histocompatibility complex, transactivator
COLQ collagen-like tail subunit (single strand of homotrimer) of asymmetric acetylcholinesterase
DOK7 docking protein 7
GCK glucokinase (hexokinase 4)
GFPT1 glutamine--fructose-6-phosphate transaminase 1
GH1 growth hormone 1
GIF gastric intrinsic factor (vitamin B synthesis)
GJB2 gap junction protein, beta 2, 26kDa
IKZF1 IKAROS family zinc finger 1 (Ikaros)
IL10 interleukin 10
INS insulin
KCNJ11 potassium channel, inwardly rectifying subfamily J, member 11
MPO myeloperoxidase
MPV17 MpV17 mitochondrial inner membrane protein
MPZ myelin protein zero
NFKBIL1 nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor-like 1
PADI4 peptidyl arginine deiminase, type IV
PDX1 pancreatic and duodenal homeobox 1
PIK3R1 phosphoinositide-3-kinase, regulatory subunit 1 (alpha)
PMP22 peripheral myelin protein 22
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
RAI1 retinoic acid induced 1
SLC22A4 solute carrier family 22 (organic cation/zwitterion transporter), member 4
SLC35A2 solute carrier family 35 (UDP-galactose transporter), member A2
TLR2 toll-like receptor 2
TTC37 tetratricopeptide repeat domain 37