GNRHR

gonadotropin releasing hormone receptor

Ensembl:
ENSG00000109163
OMIM:
138850
Synonyms:
GRHR, LHRHR

Cilia effects upon perturbation of GNRHR

Ciliogenesis screen results (1 screen)

  • Wheway et al. 2015 (siRNA) [siRNA]: Ciliogenesis Defect (z=-5.19) PMID:26167766

Phenotypes

Human ciliopathy phenotype:
hypogonadotropic hypogonadism; infertility

Ciliopathy associations

  • Kallmann Syndrome

Subcellular localization

Ciliary associated gene

Functional category

  • Motile cilium & axoneme

Function

Mutations in GNRHR cause Kallmann Syndrome (PMID: 36138264).