abnormality of cytokine secretion Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality in the production or cellular release of a cytokine (i.e., any of the non-antibody proteins made by inflammatory leukocytes and some non-leukocytic cells that affect the behavior of other cells). (Human Phenotype Ontology, HP_0011113)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0011113
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12 genes associated with the abnormality of cytokine secretion phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
PMS1 PMS1 postmeiotic segregation increased 1 (S. cerevisiae) 1.41252
CDYL2 chromodomain protein, Y-like 2 1.37715
TBX1 T-box 1 1.32041
YWHAZ tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta 1.26613
IPO7 importin 7 1.22336
SUPT20H suppressor of Ty 20 homolog (S. cerevisiae) 1.14406
ALG5 ALG5, dolichyl-phosphate beta-glucosyltransferase 1.12851
SLC26A11 solute carrier family 26 (anion exchanger), member 11 1.06304
RNF220 ring finger protein 220 1.02289
CHAT choline O-acetyltransferase 1.01883
SNTG1 syntrophin, gamma 1 1.01499
BACH2 BTB and CNC homology 1, basic leucine zipper transcription factor 2 0.928309