elevated follicle stimulating hormone Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An elevated concentration of follicle-stimulating hormone in the blood. (Human Phenotype Ontology, HP_0008232)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0008232
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Genes

21 genes associated with the elevated follicle stimulating hormone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1 2.23321
MPDU1 mannose-P-dolichol utilization defect 1 1.9103
SENP3 SUMO1/sentrin/SMT3 specific peptidase 3 1.90598
GYS1 glycogen synthase 1 (muscle) 1.18704
IL1R2 interleukin 1 receptor, type II 1.15743
SYNE3 spectrin repeat containing, nuclear envelope family member 3 1.12851
GLDN gliomedin 1.0674
ADGB androglobin 1.04365
NR6A1 nuclear receptor subfamily 6, group A, member 1 1.00059
MAST4 microtubule associated serine/threonine kinase family member 4 0.981095
CUBN cubilin (intrinsic factor-cobalamin receptor) 0.882984
ARMC9 armadillo repeat containing 9 0.882984
ZFPM1 zinc finger protein, FOG family member 1 0.868241
SLC2A5 solute carrier family 2 (facilitated glucose/fructose transporter), member 5 0.82221
CYP2R1 cytochrome P450, family 2, subfamily R, polypeptide 1 0.804323
UGT1A10 UDP glucuronosyltransferase 1 family, polypeptide A10 0.753299
HTR4 5-hydroxytryptamine (serotonin) receptor 4, G protein-coupled 0.67722
ARHGAP24 Rho GTPase activating protein 24 0.630689
CACNA2D1 calcium channel, voltage-dependent, alpha 2/delta subunit 1 0.57412
UPK1B uroplakin 1B 0.52446
AMPH amphiphysin 0.496801