increased luteinizing hormone level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description higher than normal levels of LH (Mammalian Phenotype Ontology, MP_0005133)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005133
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Genes

24 gene mutations causing the increased 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
NUPR1 nuclear protein, transcriptional regulator, 1
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