abnormal t-helper 2 cell number Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the number of the type of T-helper cell whose cytokine production promotes defense against extracellular parasites and humoral immune responses typical of allergy (Mammalian Phenotype Ontology, MP_0008089)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008089
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Genes

16 gene mutations causing the abnormal t-helper 2 cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APOE apolipoprotein E
CHI3L1 chitinase 3-like 1 (cartilage glycoprotein-39)
EBI3 Epstein-Barr virus induced 3
IL13 interleukin 13
IL13RA1 interleukin 13 receptor, alpha 1
IL4R interleukin 4 receptor
IRF1 interferon regulatory factor 1
LAT linker for activation of T cells
MIR155 microRNA 155
MMP9 matrix metallopeptidase 9
NDFIP1 Nedd4 family interacting protein 1
NFATC2IP nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 2 interacting protein
POLB polymerase (DNA directed), beta
PTPN13 protein tyrosine phosphatase, non-receptor type 13 (APO-1/CD95 (Fas)-associated phosphatase)
STAT6 signal transducer and activator of transcription 6, interleukin-4 induced
TBX21 T-box 21