decreased luteinizing hormone level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description lower than normal concentration of LH (Mammalian Phenotype Ontology, MP_0005132)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005132
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Genes

26 gene mutations causing the decreased luteinizing hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CGA glycoprotein hormones, alpha polypeptide
CLOCK clock circadian regulator
CRTC1 CREB regulated transcription coactivator 1
EGR1 early growth response 1
FOXN1 forkhead box N1
GHR growth hormone receptor
GNRH1 gonadotropin-releasing hormone 1 (luteinizing-releasing hormone)
GNRHR gonadotropin-releasing hormone receptor
INSM1 insulinoma-associated 1
IRS2 insulin receptor substrate 2
KISS1 KiSS-1 metastasis-suppressor
KISS1R KISS1 receptor
LATS1 large tumor suppressor kinase 1
LHCGR luteinizing hormone/choriogonadotropin receptor
LHX3 LIM homeobox 3
NPEPPS aminopeptidase puromycin sensitive
NR1H3 nuclear receptor subfamily 1, group H, member 3
NUPR1 nuclear protein, transcriptional regulator, 1
OTX2 orthodenticle homeobox 2
PGR progesterone receptor
PITX2 paired-like homeodomain 2
PRL prolactin
PROP1 PROP paired-like homeobox 1
SIRT1 sirtuin 1
SOD1 superoxide dismutase 1, soluble
SOX2 SRY (sex determining region Y)-box 2