Back to search

Article

Comprehensively Testing the Function of Missense Variation in the <i>STK11</i> Tumour Suppressor

2025-07-18

Abstract excerpt

The tumor suppressor gene STK11 encoding Serine/Threonine Kinase 11 (STK11) is associated with Peutz-Jeghers Syndrome (PJS), a heritable gastrointestinal disease that increases lifetime cancer risk, and with somatic variation that contributes to ∼30% of lung and 20% of cervical cancers. Although identifying pathogenic variants is clinically actionable, over 94% of STK11 missense variants that have been observed...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
68af2102-91f0-5278-bfe6-81556c8c8c7b
DOI
10.1101/2025.07.14.664734
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Comprehensively Testing the Function of Missense Variation in the <i>STK11</i> Tumour SuppressorDOI 10.1101/2025.07.14.664734
Select a neighboring publication to make it the new centre.