abnormality of t cells Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of T cells. (Human Phenotype Ontology, HP_0002843)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002843
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Genes

36 genes associated with the abnormality of t cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACP5 acid phosphatase 5, tartrate resistant
AK2 adenylate kinase 2
ATM ATM serine/threonine kinase
CASP10 caspase 10, apoptosis-related cysteine peptidase
CASP8 caspase 8, apoptosis-related cysteine peptidase
CD247 CD247 molecule
CD40LG CD40 ligand
CD8A CD8a molecule
CIITA class II, major histocompatibility complex, transactivator
COG6 component of oligomeric golgi complex 6
DNMT3B DNA (cytosine-5-)-methyltransferase 3 beta
EPG5 ectopic P-granules autophagy protein 5 homolog (C. elegans)
FAS Fas cell surface death receptor
FASLG Fas ligand (TNF superfamily, member 6)
ICOS inducible T-cell co-stimulator
IL2RA interleukin 2 receptor, alpha
IL2RG interleukin 2 receptor, gamma
IL7R interleukin 7 receptor
JAK3 Janus kinase 3
MAGT1 magnesium transporter 1
NBN nibrin
PNP purine nucleoside phosphorylase
PTPRC protein tyrosine phosphatase, receptor type, C
RAB27A RAB27A, member RAS oncogene family
RAG1 recombination activating gene 1
RAG2 recombination activating gene 2
RFX5 regulatory factor X, 5 (influences HLA class II expression)
RFXANK regulatory factor X-associated ankyrin-containing protein
RFXAP regulatory factor X-associated protein
SLC39A4 solute carrier family 39 (zinc transporter), member 4
SMARCAL1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
TBX1 T-box 1
TNFRSF13B tumor necrosis factor receptor superfamily, member 13B
UMPS uridine monophosphate synthetase
WAS Wiskott-Aldrich syndrome
WIPF1 WAS/WASL interacting protein family, member 1