abnormal memory t cell physiology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any functional anomaly of the set of long-lived T cells differentiated from T cells activated by a specific antigen encountered during a past immune response (Mammalian Phenotype Ontology, MP_0008051)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008051
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Genes

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

Symbol Name
BCL2L1 BCL2-like 1
CD69 CD69 molecule
EBAG9 estrogen receptor binding site associated, antigen, 9
FLT3LG fms-related tyrosine kinase 3 ligand
HLA-E major histocompatibility complex, class I, E
HNRNPLL heterogeneous nuclear ribonucleoprotein L-like
IL21R interleukin 21 receptor
IL23A interleukin 23, alpha subunit p19
SH2D1A SH2 domain containing 1A
TCF7 transcription factor 7 (T-cell specific, HMG-box)
TNFRSF9 tumor necrosis factor receptor superfamily, member 9
ZBTB46 zinc finger and BTB domain containing 46