17q12 Knowledge Basedeletion syndrome · static snapshot
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Gene–trait link Signs & symptoms 11 supporting sources confidence 97% novelty 53%

LHX1 appears alongside tumour risk in 11 sources

Across the collected corpus, the gene LHX1 co-occurs with tumour risk in 11 independent documents (of 66 documents mentioning LHX1 and 133 mentioning tumour risk). Association strength 0.08.

How this was derived

Co-occurrence is an *observation about the literature*, not proof of causation: it says these topics are discussed together in the sources we hold.

Generated 2026-11-14, last changed today. Dedup key assoc:LHX1:cancer. 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)

…some 22. Courtesy of Kristin Andersen, Oslo University Hospital-Radiumhospitalet. In addition to the Philadelphia chromosome, several other important tumor-associated chromosomal abnormalities were identified during the pre-banding period. In 1963, Lele, Penrose and Stallard reported a visible deletion o…
…east. Lymphovascular invasion (LVI) and histologic grade are clinical parameters of high prognostic value in breast cancer and indicate the level of tumor aggressiveness. Many studies have focused on the association of breast cancer subtypes with gene expression and chromosomal profiles, but considerabl…
…e derived is a 58-year-old female diagnosed with moderately differentiated primary lung adenocarcinoma. Immunohistochemistry of the patient's primary tumor showed positive staining for thyroid transcription factor 1 (TTF1) and Napsin A. Pleural effusion was collected from the patient at the Molecular Dia…
…sms by which inherited genetics facilitate cancer initiation might transit through its cooperation with specific somatic events that then dictate the tumor features. Through a germline-somatic tandem leading to steroid biosynthesis, we suggest a paradigm to study cancer initiation. Abstract The biologica…

Supporting documents (38)

DocumentSourcePublishedSeenRelevance
17q12 Recurrent Deletion Syndrome in Childhood pmc 2025-01-01 yesterday 1.00
HNF1β, LHX1, and GGNBP2 deletion contributed to kidney and reproduc... pmc 2024-01-01 yesterday 1.00
Prenatal diagnosis of 17q12 copy number variants in fetuses via chr... 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
De novo HNF1 homeobox B mutation as a cause for chronic, treatment-... pubmed 2018-01-01 yesterday 1.00
Copy number variation and regions of homozygosity analysis in patie... pubmed 2018-01-01 yesterday 1.00
Cross-Cancer Pleiotropic Associations with Lung Cancer Risk in Afri... pubmed 2019-04-01 yesterday 1.00
Extensive germline-somatic interplay contributes to prostate cancer... pubmed 2022-11-28 yesterday 1.00
Autism and duplication of 17q12q21.2 by array-CGH: a case report. pubmed 2023-01-01 yesterday 1.00
Genetics of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: advance... pubmed 2024-01-01 yesterday 1.00
The computational analysis of tumor cell sensitivity to supertarget... pubmed 2026-03-01 yesterday 0.79
HNF1B-MODY (MODY-5): a rare form of diabetes with multisystemic fea... pubmed 2026-01-01 yesterday 1.00
Loss of Hnf1b in differentiated proximal tubule cells uncovers neph... pubmed 2026-08-13 yesterday 1.00
Decreased T helper 1 cell function underlies recurrent sinopulmonar... pmc 2025-01-01 yesterday 1.00
Distinct chromosome abnormality patterns for differential diagnosis... pmc 2025-01-01 yesterday 1.00
Genetic Predisposition in Müllerian Malformations: A Case Report pmc 2025-01-01 yesterday 1.00
Multi- and Transgenerational Histological and Transcriptomic Outcom... pmc 2025-01-01 yesterday 0.97
Comparative Copy Number Variation Profiling of GL01, an Immortalize... pmc 2025-01-01 yesterday 1.00
Case Report: Unraveling complex genomic alterations in a case of ch... pmc 2025-01-01 yesterday 1.00
Germline–Somatic Liaison Dictates Cancer Subtypes via de novo Stero... pmc 2025-01-01 yesterday 1.00
Molecular Landscape of Acute Myeloid Leukemia in Pediatric Patient-... pmc 2025-01-01 yesterday 1.00
Building a human pluripotent stem cell-based gonadal niche: improvi... pmc 2025-01-01 yesterday 0.97
TBX6, LHX1 and copy number variations in the complex genetics of Mü... pubmed 2013-08-16 yesterday 1.00
Lymphovascular invasion and histologic grade are associated with sp... pubmed 2015-03-01 yesterday 1.00
The Genetic Landscape of Müllerian Duct Anomalies: A Comprehensive Review pmc 2025-01-01 yesterday 1.00
Subtype distribution, clinical presentation, and molecular spectrum... pmc 2025-01-01 yesterday 1.00
Clinical and genetic aspects of Mayer-Rokitansky-Küster-Hauser syndrome. pubmed 2018-01-01 yesterday 1.00
Maternal DNA methylation signatures of gestational diabetes across ... pmc 2025-01-01 yesterday 0.76
Chromosome instability region analysis and identification of the dr... pubmed 2023-11-01 yesterday 1.00
A complex microdeletion 17q12 phenotype in a patient with recurrent... pubmed 2012-05-14 yesterday 1.00
Genetic and embryonic transcriptome analyses reveal the molecular a... pmc 2025-01-01 yesterday 1.00
Unraveling the Genetic Mysteries of Müllerian Anomalies: Research A... pmc 2026-01-01 yesterday 1.00
A novel inversion at 17q12 disrupting HNF1B gene in a patient with ... pmc 2026-01-01 yesterday 1.00
Cancer Cytogenetics: Deep Roots, New Branches in the Age of Omics pmc 2026-01-01 yesterday 1.00
BART-spatial unravels biologically significant transcriptional regu... pmc 2026-01-01 yesterday 0.76
A familial case report of 17q12 recurrent deletion syndrome: clinic... pmc 2026-01-01 yesterday 1.00
Precision Medicine in Pediatric Nephrology: From Shared Clinical Ph... pmc 2026-01-01 yesterday 1.00
Molecular characterization of HER2-negative breast cancers reveals ... pubmed 2025-02-01 yesterday 1.00