abnormality of t cell physiology Gene Set
Genes
22 genes associated with the abnormality of t cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
AK2
|
adenylate kinase 2
|
|
CASP10
|
caspase 10, apoptosis-related cysteine peptidase
|
|
CASP8
|
caspase 8, apoptosis-related cysteine peptidase
|
|
CD40LG
|
CD40 ligand
|
|
CIITA
|
class II, major histocompatibility complex, transactivator
|
|
COG6
|
component of oligomeric golgi complex 6
|
|
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
|
|
JAK3
|
Janus kinase 3
|
|
MAGT1
|
magnesium transporter 1
|
|
PNP
|
purine nucleoside phosphorylase
|
|
RAB27A
|
RAB27A, member RAS oncogene family
|
|
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
|
|
TBX1
|
T-box 1
|
|
TNFRSF13B
|
tumor necrosis factor receptor superfamily, member 13B
|
|
UMPS
|
uridine monophosphate synthetase
|
|
WAS
|
Wiskott-Aldrich syndrome
|
