GNRHR

gonadotropin releasing hormone receptor

Tier: Cilia-Associated Genes

Ensembl:
ENSG00000109163
OMIM:
138850
Synonyms:
GRHR, LHRHR

Ciliogenesis screen results (1 screens)

  • 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

No ciliary localization reported (cilia-associated gene).

References: PMID:36138264

Functional category

  • Motile cilium & axoneme

Function

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