abnormality of eosinophils Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An eosinophil abnormality. (Human Phenotype Ontology, HP_0001879)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001879
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Genes

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

Symbol Name
ADA adenosine deaminase
ADAM17 ADAM metallopeptidase domain 17
CAPN3 calpain 3, (p94)
CASP10 caspase 10, apoptosis-related cysteine peptidase
CD247 CD247 molecule
CHD7 chromodomain helicase DNA binding protein 7
DCLRE1C DNA cross-link repair 1C
DOCK8 dedicator of cytokinesis 8
ELANE elastase, neutrophil expressed
FAS Fas cell surface death receptor
FASLG Fas ligand (TNF superfamily, member 6)
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
IL2RG interleukin 2 receptor, gamma
IL7R interleukin 7 receptor
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
LIG4 ligase IV, DNA, ATP-dependent
PDGFRA platelet-derived growth factor receptor, alpha polypeptide
RAG1 recombination activating gene 1
RAG2 recombination activating gene 2
RBM8A RNA binding motif protein 8A
RMRP RNA component of mitochondrial RNA processing endoribonuclease
SLC46A1 solute carrier family 46 (folate transporter), member 1
STAT3 signal transducer and activator of transcription 3 (acute-phase response factor)