abnormality of basophils Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A basophils abnormality. (Human Phenotype Ontology, HP_0001912)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0001912
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Genes

26 genes associated with the abnormality of basophils phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
DOT1L DOT1-like histone H3K79 methyltransferase 0.95642
STAT4 signal transducer and activator of transcription 4 0.944168
MSANTD2 Myb/SANT-like DNA-binding domain containing 2 0.90785
SBF2 SET binding factor 2 0.895167
N4BP2 NEDD4 binding protein 2 0.777194
KATNB1 katanin p80 (WD repeat containing) subunit B 1 0.77499
SLC6A6 solute carrier family 6 (neurotransmitter transporter), member 6 0.771787
LOC339975 uncharacterized LOC339975 0.750909
RARB retinoic acid receptor, beta 0.74676
CDKN2A cyclin-dependent kinase inhibitor 2A 0.721729
ALAD aminolevulinate dehydratase 0.71647
PYCR2 pyrroline-5-carboxylate reductase family, member 2 0.703184
FLJ16171 FLJ16171 protein 0.69768
FRMD6 FERM domain containing 6 0.696021
FGD3 FYVE, RhoGEF and PH domain containing 3 0.694067
CDH13 cadherin 13 0.681396
PTGER3 prostaglandin E receptor 3 (subtype EP3) 0.662854
BTBD9 BTB (POZ) domain containing 9 0.647367
CDKN1A cyclin-dependent kinase inhibitor 1A (p21, Cip1) 0.631765
KLK11 kallikrein-related peptidase 11 0.621094
PDSS2 prenyl (decaprenyl) diphosphate synthase, subunit 2 0.599122
PDE11A phosphodiesterase 11A 0.595599
MAN1A1 mannosidase, alpha, class 1A, member 1 0.594038
PPP2R2C protein phosphatase 2, regulatory subunit B, gamma 0.592349
CAPSL calcyphosine-like 0.588907
MIPOL1 mirror-image polydactyly 1 0.583665