abnormal nk t cell physiology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any functional anomaly of the distinct lineage of T cells expressing natural killer cell markers and having T cell receptors characterized by the usage of a restricted repertoire of variable region gene segments (Mammalian Phenotype Ontology, MP_0008042)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008042
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Genes

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

Symbol Name
AIRE autoimmune regulator
CCR5 chemokine (C-C motif) receptor 5 (gene/pseudogene)
CD1D CD1d molecule
CLNK cytokine-dependent hematopoietic cell linker
CXCR2 chemokine (C-X-C motif) receptor 2
FCER1G Fc fragment of IgE, high affinity I, receptor for; gamma polypeptide
GIMAP1-GIMAP5 GIMAP1-GIMAP5 readthrough
HCST hematopoietic cell signal transducer
MYD88 myeloid differentiation primary response 88
SH2D1A SH2 domain containing 1A
TICAM1 toll-like receptor adaptor molecule 1
TLR3 toll-like receptor 3
TLR9 toll-like receptor 9
TYROBP TYRO protein tyrosine kinase binding protein