abnormal t-helper 1 cell number Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the number of the subset of the type of T-helper cell whose cytokine production favors cellular immune responses and delayed type hypersensitivity (Mammalian Phenotype Ontology, MP_0008085)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008085
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Genes

14 gene mutations causing the abnormal t-helper 1 cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
B2M beta-2-microglobulin
CD274 CD274 molecule
IL9R interleukin 9 receptor
ITGB2 integrin, beta 2 (complement component 3 receptor 3 and 4 subunit)
LGALS9B lectin, galactoside-binding, soluble, 9B
NLRP3 NLR family, pyrin domain containing 3
PDCD1 programmed cell death 1
REG3G regenerating islet-derived 3 gamma
TAP1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)
TBX21 T-box 21
TGFB1 transforming growth factor, beta 1
TNFSF12 tumor necrosis factor (ligand) superfamily, member 12
UNC93B1 unc-93 homolog B1 (C. elegans)
VTCN1 V-set domain containing T cell activation inhibitor 1