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AR and infertility are reported together in 2 articles.

Gene

AR

HGNC
HGNC:644
61articles
61mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
Phenotype

Infertility

199articles
199mentions
12co-reported genes shown
Most co-reported genes (articles)

Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.

Publications

2 records shown · first 60

Familial novel androgen receptor gene variant associated with bilateral cryptorchidism and severe male infertility: A case report.

PMID 41142184 | PMCID PMC12549779 | DOI 10.1016/j.eucr.2025.103235 · Urology case reports · 2025 · 3 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneAR“Variants in the androgen receptor (AR) gene cause androgen insensitivity syndrome (AIS), ranging from complete (CAIS) to partial (PAIS) and mild (MAIS) forms.”0.98hgnc_dict_v1
phenotypeinfertility“Familial novel androgen receptor gene variant associated with bilateral cryptorchidism and severe male infertility: A case report.”0.98phenotype_alias_lexicon_v2
variantp.Tyr364His“Whole-genome sequencing revealed a novel AR missense variant (p.Tyr364His) in the N-terminal domain, predicted to cause partial receptor dysfunction.”0.95hgvs_regex_v1
TypeEntitySource evidenceConfidenceExtractor
geneAR“CAG trinucleotide repeats are coded for the polyglutamine tract in the N-terminal of the androgen receptor (AR) gene which varies in normal individuals from 6 to 36 residues.”0.98hgnc_dict_v1
phenotypeinfertility“The results showed a significant association between the length of the AR-CAG repeats and men's infertility (p = .001).”0.98phenotype_alias_lexicon_v2