abnormal circulating estrogen level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description aberration in the blood concentration of any substance that causes development of the female reproductive organs and secondary sexual characteristics (Mammalian Phenotype Ontology, MP_0003369)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003369
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Genes

36 gene mutations causing the abnormal 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
BGLAP bone gamma-carboxyglutamate (gla) protein
CHST10 carbohydrate sulfotransferase 10
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
DRD2 dopamine receptor D2
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
MRC1 mannose receptor, C type 1
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
VPS54 vacuolar protein sorting 54 homolog (S. cerevisiae)