Gene + body-part link
What it can look like
104 supporting sources
confidence 97%
novelty 75%
The gene HNF1B shows up in 64 stories together with how the body makes babies
We read 64 stories that talk about both the gene HNF1B and how the body makes babies. That does not prove one causes the other, but they keep showing up together.
How this was derived
This is about what shows up together in the articles. It is not proof that one thing causes the other.
Generated 2026-11-13, last changed
today. Dedup key assoc:HNF1B:mullerian_gu.
The engine re-checks this insight on every analysis run; if more sources agree, its corroboration and confidence go up and it reappears as “new”.
Evidence (4 quotes)
The Genetic Landscape of Müllerian Duct Anomalies: A Comprehensive Review
peer_reviewed
· published 2025-01-01
· live page
…no. 3 (2015): 769-774.e2. 33. Philibert P., Biason‐Lauber A., Gueorguieva I., et al., "Molecular Analysis of WNT4 Gene in Four Adolescent Girls With Mullerian Duct Abnormality and Hyperandrogenism (Atypical Mayer‐Rokitansky‐Küster‐Hauser Syndrome)," Fertility and Sterility 95, no. 8 (2011): 2683-2686. 34. C…
Unraveling the Genetic Mysteries of Müllerian Anomalies: Research Approaches and Clinical Significance
peer_reviewed
· published 2026-01-01
· live page
ABSTRACT Müllerian anomalies are a collection of heterogeneous anatomical disorders of the female genital tract that present with complex clinical features of which sev…
Building a human pluripotent stem cell-based gonadal niche: improving in vitro systems with in vivo insights
peer_reviewed
· published 2025-01-01
· live page
…ML, Massin N, Martinerie L, Picard JY, Rey R, Lombès M et al. Lack of androgen receptor expression in Sertoli cells accounts for the absence of anti-Mullerian hormone repression during early human testis development. J Clin Endocrinol Metab 2009;94:1818-1825. Boulet AM, Capecchi MR. Signaling by FGF4 and FG…
Mayer–Rokitansky–Küster–Hauser syndrome with inguinal hernia, left renal fusion, and malrotation: a rare case
peer_reviewed
· published 2025-01-01
· live page
…ser (MRKH) syndrome refers to a syndrome of genital malformation with normal development of female external genitalia but abnormal development of the Müllerian duct, 1 characterized by congenital dysplasia of the uterus and upper part of the vagina (2/3), but normal development of secondary sexual characteri…