increased circulating luteinizing hormone level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description higher than the normal levels in the bloodstream of LH, the hormone that regulates steroid production by the interstitial cells of the testis and the ovary (Mammalian Phenotype Ontology, MP_0001751)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001751
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Genes

23 gene mutations causing the increased circulating luteinizing hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADRA1B adrenoceptor alpha 1B
AFP alpha-fetoprotein
AR androgen receptor
BGLAP bone gamma-carboxyglutamate (gla) protein
CHST8 carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 8
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
DHH desert hedgehog
ESR1 estrogen receptor 1
ESR2 estrogen receptor 2 (ER beta)
FOXO3 forkhead box O3
FSHB follicle stimulating hormone, beta polypeptide
FSHR follicle stimulating hormone receptor
GABBR1 gamma-aminobutyric acid (GABA) B receptor, 1
GDF9 growth differentiation factor 9
GNRH1 gonadotropin-releasing hormone 1 (luteinizing-releasing hormone)
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
LHCGR luteinizing hormone/choriogonadotropin receptor
MRC1 mannose receptor, C type 1
NOS1 nitric oxide synthase 1 (neuronal)
NPC1 Niemann-Pick disease, type C1
PCYT1B phosphate cytidylyltransferase 1, choline, beta
PTGS2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor