17q12, explained for kidsdeletion syndrome · static snapshot
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Gene + body-part link What it can look like 40 supporting sources confidence 97% novelty 62%

The gene HNF1B shows up in 30 stories together with bones and arms or legs

We read 30 stories that talk about both the gene HNF1B and bones and arms or legs. 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:musculoskeletal. 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)

Abstract Physical activity is widely recognized for its health benefits; however, it also increases the risk of musculoskeletal soft tissue injuries, with muscle-related cases constituting a considerable proportion. These injuries impair well-being, athletic performance, and c…
…bsence of alternative etiology and the already described widely spaced teeth [ 10 , 14 ], tooth agenesis could be a new finding. An additional unique skeletal finding was a duplicated hallux found in P4. Skeletal and extremity anomalies were frequent in the PIGW cohort. Some fetuses presented shortening of…
…ominent supraorbital ridges, wide nasal bridge, cleft ala nasi, microretrognathia, gothic palate, short neck, funnel chest, nipple hypertelorism, and flat feet. A single‐gene duplication of the BDH1 gene, a candidate gene for chromosome 3q29 duplication syndrome (OMIM 611936), was detected in Patient 3.1 (ar…
…ease or kidney failure, consanguinity, and extrarenal findings. Assessment of hearing, vision, hematologic, neurodevelopmental, hepatopancreatic, and skeletal or dysmorphic features may reveal a syndromic diagnosis not apparent from the kidney phenotype alone [ 1 , 2 , 3 ]. Encoding granular observations wi…

Supporting documents (51)

StorySourcePublishedSeenRelevance
Ten tips for ordering, interpreting, and communicating genetic test... pmc 2026-01-01 yesterday 1.00
17q12 Recurrent Deletion Syndrome in Childhood pmc 2025-01-01 yesterday 1.00
Genetics of CAKUT pmc 2026-01-01 yesterday 1.00
Renal and Extrarenal Phenotypes in Patients With HNF1B Variants and... pmc 2024-01-01 yesterday 1.00
A Korean Family Presenting with Renal Cysts and Maturity-Onset Diab... pmc 2024-01-01 yesterday 1.00
Monogenic Defects of Beta Cell Function: From Clinical Suspicion to... pmc 2024-01-01 yesterday 0.45
HNF1B Transcription Factor: Key Regulator in Renal Physiology and P... pmc 2024-01-01 yesterday 1.00
A Case of Diabetes Mellitus Type MODY5 as a Feature of 17q12 Deleti... pmc 2024-01-01 yesterday 1.00
Copy number variation and regions of homozygosity analysis in patie... pubmed 2018-01-01 yesterday 1.00
School level of children carrying a HNF1B variant or a deletion. pubmed 2020-01-01 yesterday 1.00
The Clinical Characteristics and Gene Mutations of Maturity-Onset D... pubmed 2022-01-01 yesterday 1.00
Identification of Genetic Causes in Mayer-Rokitansky-Küster-Hauser ... pubmed 2022-06-27 yesterday 1.00
Hepatocyte nuclear factor 1B deletion, but not intragenic mutation,... pubmed 2024-01-01 yesterday 1.00
Large Kidney Cysts in HNF1B Nephropathy Mimicking Autosomal Dominan... pubmed 2024-01-01 yesterday 1.00
Etiology and outcomes of fetal renal abnormalities in Southern Chin... pubmed 2025-08-13 yesterday 1.00
HNF1B-MODY (MODY-5): a rare form of diabetes with multisystemic fea... pubmed 2026-01-01 yesterday 1.00
From Exome to Optical Mapping: Resolving a Complex 17q12 Rearrangem... pubmed 2026-10-09 yesterday 1.00
In-Depth Phenotyping of PIGW -Related Disease and Its Role in 17q12... pmc 2024-01-01 yesterday 1.00
Delineation of the Genetic Architecture and Clinical Polymorphism o... pmc 2024-01-01 yesterday 1.00
The genetic etiologies of bilateral renal agenesis pmc 2024-01-01 yesterday 1.00
Identification and functional analysis of a novel SMARCC2 splicing ... pmc 2025-01-01 yesterday 1.00
Multiple-testing corrections in selection scans using identity-by-d... pmc 2025-01-01 yesterday 1.00
Prenatally and postnatally sequential genetic etiology detection in... pmc 2025-01-01 yesterday 1.00
Multi- and Transgenerational Histological and Transcriptomic Outcom... pmc 2025-01-01 yesterday 0.97
Prenatal diagnosis of fetuses with renal abnormalities: a retrospec... pmc 2025-01-01 yesterday 1.00
A Case of Amyotrophic Lateral Sclerosis With Coexisting Maturity-on... pmc 2025-01-01 yesterday 1.00
MODY5 and 17q12 Microdeletion Syndrome: Phenotype Variability, Pren... pmc 2025-01-01 yesterday 1.00
The Genetic Landscape of Müllerian Duct Anomalies: A Comprehensive Review pmc 2025-01-01 yesterday 1.00
Genetic Susceptibility to Sport-Related Muscle Injuries: Insights f... pmc 2025-01-01 yesterday 0.73
Clinical and genetic aspects of Mayer-Rokitansky-Küster-Hauser syndrome. pubmed 2018-01-01 yesterday 1.00
Mayer–Rokitansky–Küster–Hauser syndrome with inguinal hernia, left ... pmc 2025-01-01 yesterday 1.00
From mutation to symptoms: a multi-center study on HNF1B -related n... pmc 2025-01-01 yesterday 1.00
Neurological diagnoses in children potentially fulfilling the crite... pmc 2025-01-01 yesterday 1.00
HNF1B variant without hyperglycaemia as a cause of isolated profoun... pubmed 2023-02-09 yesterday 1.00
The Genetic Landscape and Precision Medicine in Neonatal Diabetes M... pmc 2026-01-01 yesterday 1.00
A complex microdeletion 17q12 phenotype in a patient with recurrent... pubmed 2012-05-14 yesterday 1.00
Case Report: Nephrocalcinosis from pancreatic hypoplasia in HNF1B d... pmc 2026-01-01 yesterday 1.00
Genetic and embryonic transcriptome analyses reveal the molecular a... pmc 2025-01-01 yesterday 1.00
Pediatric Hepatocyte Nuclear Factor 1B ( HNF1B ) Disease: Diabetes ... pmc 2025-01-01 yesterday 1.00
A novel inversion at 17q12 disrupting HNF1B gene in a patient with ... pmc 2026-01-01 yesterday 1.00
Hepatic dysfunction, hyperuricemia, and multiple renal cysts in ado... pmc 2026-01-01 yesterday 1.00
Transient neonatal diabetes mellitus as an early diagnostic clue to... pmc 2026-01-01 yesterday 1.00
Functional validation of a non-canonical HNF1B splice-site variant in MODY5 pmc 2026-01-01 yesterday 1.00
Molecular impact of a novel HNF1B missense variant in childhood-ons... pmc 2026-01-01 yesterday 1.00
HNF1B-MODY in the Norwegian MODY Registry and the Norwegian Childho... pmc 2026-01-01 yesterday 1.00
HNF1B-MODY (MODY-5): a rare form of diabetes with multisystemic fea... pmc 2026-01-01 yesterday 1.00
HNF1B -related disease: developmental origins, molecular mechanisms... pmc 2026-01-01 yesterday 1.00
Clinical Spectrum and Early Renal Functional Variability in a Natio... pmc 2026-01-01 yesterday 1.00
Precision Medicine in Pediatric Nephrology: From Shared Clinical Ph... pmc 2026-01-01 yesterday 1.00
Genetic Insights into Pediatric Polycystic Kidney Disease and Overl... pmc 2026-01-01 yesterday 1.00
PMC12903773 local_files - yesterday 1.00