hormone disturbance Gene Set

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

19 genes associated with the disease hormone disturbance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
CALCR calcitonin receptor
CASR calcium-sensing receptor
COMT catechol-O-methyltransferase
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
CYP17A1 cytochrome P450, family 17, subfamily A, polypeptide 1
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
CYP1B1 cytochrome P450, family 1, subfamily B, polypeptide 1
DBH dopamine beta-hydroxylase (dopamine beta-monooxygenase)
DIO2 deiodinase, iodothyronine, type II
DRD4 dopamine receptor D4
ESR1 estrogen receptor 1
ESR2 estrogen receptor 2 (ER beta)
HSD17B2 hydroxysteroid (17-beta) dehydrogenase 2
HTR2C 5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled
HTR3A 5-hydroxytryptamine (serotonin) receptor 3A, ionotropic
PGR progesterone receptor
SHBG sex hormone-binding globulin
THRB thyroid hormone receptor, beta
TSHR thyroid stimulating hormone receptor