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WT1 and infertility are reported together in 2 articles.

Gene

WT1

HGNC
HGNC:12796
17articles
17mentions
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

Effect of obesity on fertility parameters in WIO mice model.

PMID 35092652 | DOI 10.17219/acem/145510 · Advances in clinical and experimental medicine : official organ Wroclaw Medical University · 2022 · 5 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneWT1“Real-time polymerase chain reaction (RT-PCR) was performed for SYCP3, VEGFA and WT1 genes.”0.98hgnc_dict_v1
phenotypeinfertility“BACKGROUND: Male infertility is mostly due to low sperm quality, which accounts for about 50% of the causes of infertility.”0.98phenotype_alias_lexicon_v2
geneSYCP3“Real-time polymerase chain reaction (RT-PCR) was performed for SYCP3, VEGFA and WT1 genes.”0.98hgnc_dict_v1
geneVEGFA“Real-time polymerase chain reaction (RT-PCR) was performed for SYCP3, VEGFA and WT1 genes.”0.98hgnc_dict_v1

Autosomal single-gene disorders involved in human infertility.

PMID 30108436 | PMCID PMC6088112 | DOI 10.1016/j.sjbs.2017.12.005 · Saudi journal of biological sciences · 2018 · 11 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneWT1“The genes reviewed are CFTR, SPATA16, AURKC, CATSPER1, GNRHR, MTHFR, SYCP3, SOX9, WT1 and NR5A1 genes.”0.98hgnc_dict_v1
phenotypeinfertility“Autosomal single-gene disorders involved in human infertility.”0.98phenotype_alias_lexicon_v2
geneCFTR“The genes reviewed are CFTR, SPATA16, AURKC, CATSPER1, GNRHR, MTHFR, SYCP3, SOX9, WT1 and NR5A1 genes.”0.98hgnc_dict_v1
geneSPATA16“The genes reviewed are CFTR, SPATA16, AURKC, CATSPER1, GNRHR, MTHFR, SYCP3, SOX9, WT1 and NR5A1 genes.”0.98hgnc_dict_v1