decreased circulating estrogen level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduction in the blood concentration of any substance that causes development of the female reproductive organs and secondary sexual characteristics (Mammalian Phenotype Ontology, MP_0003371)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003371
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Genes

23 gene mutations causing the decreased circulating estrogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCA1 ATP-binding cassette, sub-family A (ABC1), member 1
CLOCK clock circadian regulator
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
DDR2 discoidin domain receptor tyrosine kinase 2
DRD2 dopamine receptor D2
ESR1 estrogen receptor 1
FSHR follicle stimulating hormone receptor
GHR growth hormone receptor
GNRHR gonadotropin-releasing hormone receptor
INHBA inhibin, beta A
IRS2 insulin receptor substrate 2
KISS1 KiSS-1 metastasis-suppressor
KISS1R KISS1 receptor
LHB luteinizing hormone beta polypeptide
LHCGR luteinizing hormone/choriogonadotropin receptor
LHX9 LIM homeobox 9
NCOA3 nuclear receptor coactivator 3
PRL prolactin
PRLR prolactin receptor
SAFB scaffold attachment factor B
SGPL1 sphingosine-1-phosphate lyase 1
TIPARP TCDD-inducible poly(ADP-ribose) polymerase
VPS54 vacuolar protein sorting 54 homolog (S. cerevisiae)