gonadal disease Gene Set

Dataset GWASdb SNP-Disease Associations
Category disease or phenotype associations
Type disease
Description An endocrine system disease that is located_in the gonads. (Human Disease Ontology, DOID_2277)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:2277
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Genes

22 genes associated with the disease gonadal disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1 2.28372
MPDU1 mannose-P-dolichol utilization defect 1 1.96807
SENP3 SUMO1/sentrin/SMT3 specific peptidase 3 1.96531
REEP3 receptor accessory protein 3 1.42467
GYS1 glycogen synthase 1 (muscle) 1.35834
IL1R2 interleukin 1 receptor, type II 1.32087
SYNE3 spectrin repeat containing, nuclear envelope family member 3 1.28906
GLDN gliomedin 1.21996
ADGB androglobin 1.19386
NR6A1 nuclear receptor subfamily 6, group A, member 1 1.14463
MAST4 microtubule associated serine/threonine kinase family member 4 1.12155
CUBN cubilin (intrinsic factor-cobalamin receptor) 1.00407
ARMC9 armadillo repeat containing 9 1.00407
ZFPM1 zinc finger protein, FOG family member 1 0.986376
SLC2A5 solute carrier family 2 (facilitated glucose/fructose transporter), member 5 0.933664
CYP2R1 cytochrome P450, family 2, subfamily R, polypeptide 1 0.914528
UGT1A10 UDP glucuronosyltransferase 1 family, polypeptide A10 0.859982
HTR4 5-hydroxytryptamine (serotonin) receptor 4, G protein-coupled 0.779837
ARHGAP24 Rho GTPase activating protein 24 0.731451
CACNA2D1 calcium channel, voltage-dependent, alpha 2/delta subunit 1 0.670054
UPK1B uroplakin 1B 0.617756
AMPH amphiphysin 0.583982