human spermatogenic defect Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description disease cluster belonging to disease group reproduction (Genetic Association Database)
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Genes

9 genes associated with the disease human spermatogenic defect in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
COMT catechol-O-methyltransferase
CYP17A1 cytochrome P450, family 17, subfamily A, polypeptide 1
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
CYP1A1 cytochrome P450, family 1, subfamily A, polypeptide 1
CYP1B1 cytochrome P450, family 1, subfamily B, polypeptide 1
ESR1 estrogen receptor 1
ESR2 estrogen receptor 2 (ER beta)
HSD17B2 hydroxysteroid (17-beta) dehydrogenase 2
SHBG sex hormone-binding globulin