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Gene profile

FSHR

HGNC:3969 · SaudiVarKB evidence summary derived from retained literature mentions.

6Gene mentions
6Publications
2Linked variants
3Associated phenotypes

Associated phenotypes

Co-mentioned in FSHR publications
PhenotypeIdentifierArticlesMentions
infertility22
primary ciliary dyskinesia11
recurrent pregnancy loss11

Linked variants

Variants normalized to FSHR
VariantHGVS / rsIDArticlesMentions
A307T11
N680S11

Population context

Reported in the same publications
Country / regionGroupCohortArticles
Not specified801
Not specified8,2651

Supporting publications

6 records
  1. 2025FOLLICLE-STIMULATING HORMONE RECEPTOR MUTATIONS IN SUDANESE WOMEN: A STUDY ON POLYCYSTIC OVARY SYNDROME.Georgian medical newsPubMed ↗
  2. 2025Metformin-Driven Activation of Polymorphic Follicle-Stimulating Hormone Receptors for Polycystic Ovary Syndrome Treatment: A Computational Study.Medical science monitor : international medical journal of experimental and clinical researchPubMed ↗
  3. 2024Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundity.Human reproduction (Oxford, England)PubMed ↗
  4. 2024Laying performance, genetic parameters, and the expression of FSHβ, LHβ, FSHR, and LHR genes in Japanese quails selected for early egg production.Poultry sciencePubMed ↗
  5. 2020A genomics approach to females with infertility and recurrent pregnancy loss.Human geneticsPubMed ↗
  6. 2019Pathophysiological mechanisms of gonadotropins- and steroid hormones-related genes in etiology of polycystic ovary syndrome.Iranian journal of basic medical sciencesPubMed ↗