abnormal circulating estradiol level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description aberration in the blood concentration of this most potent estrogen (Mammalian Phenotype Ontology, MP_0005183)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005183
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Genes

32 gene mutations causing the abnormal circulating estradiol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCA1 ATP-binding cassette, sub-family A (ABC1), member 1
BGLAP bone gamma-carboxyglutamate (gla) protein
CLOCK clock circadian regulator
CNR1 cannabinoid receptor 1 (brain)
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
DDR2 discoidin domain receptor tyrosine kinase 2
ESR1 estrogen receptor 1
FSHR follicle stimulating hormone receptor
GHR growth hormone receptor
GNRH1 gonadotropin-releasing hormone 1 (luteinizing-releasing hormone)
GNRHR gonadotropin-releasing hormone receptor
GPRC6A G protein-coupled receptor, class C, group 6, member A
INHA inhibin, alpha
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
NCOA1 nuclear receptor coactivator 1
NCOA3 nuclear receptor coactivator 3
NOS2 nitric oxide synthase 2, inducible
NOS3 nitric oxide synthase 3 (endothelial cell)
NR1H3 nuclear receptor subfamily 1, group H, member 3
PRL prolactin
PRLR prolactin receptor
SAFB scaffold attachment factor B
SGPL1 sphingosine-1-phosphate lyase 1
SULT1E1 sulfotransferase family 1E, estrogen-preferring, member 1
TIMP1 TIMP metallopeptidase inhibitor 1
TIPARP TCDD-inducible poly(ADP-ribose) polymerase