Galactorrhea Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Spontaneous flow of milk from the breast, unassociated with childbirth or nursing. (Human Phenotype Ontology, HP_0100829)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D005687
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Genes

10 genes/proteins associated with the disease Galactorrhea from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
PRL prolactin 2.88009
DRD2 dopamine receptor D2 1.85046
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6 1.63473
HTR2C 5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled 1.61782
KCNH2 potassium channel, voltage gated eag related subfamily H, member 2 1.54839
CYP3A4 cytochrome P450, family 3, subfamily A, polypeptide 4 1.45777
DRD1 dopamine receptor D1 1.36677
SLC22A2 solute carrier family 22 (organic cation transporter), member 2 1.20097
BDNF brain-derived neurotrophic factor 1.06479
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1 1.052