GTR Home > Genes

FSHR follicle stimulating hormone receptor

Gene ID: 2492, updated on 30-Sep-2018
Also known as: LGR1; ODG1; FSHR1; FSHRO

Summary

The protein encoded by this gene belongs to family 1 of G-protein coupled receptors. It is the receptor for follicle stimulating hormone and functions in gonad development. Mutations in this gene cause ovarian dysgenesis type 1, and also ovarian hyperstimulation syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]

Associated conditions

See all available tests in GTR for this gene

DescriptionTests
Dizygotic twins
MedGen: C0220761OMIM: 276400GeneReviews: Not available
See labs
Ovarian dysgenesis 1
MedGen: C0949595OMIM: 233300GeneReviews: Not available
See labs
Ovarian hyperstimulation syndrome
MedGen: C0085083OMIM: 608115GeneReviews: Not available
See labs

Genomic context

Location:
2p16.3
Sequence:
Chromosome: 2; NC_000002.12 (48953161..49154527, complement)
Total number of exons:
14

Links

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.

Support Center