Pervasive mislocalization of pathogenic coding variants underlying human disorders.

ABSTRACT: Widespread sequencing has yielded thousands of missense variants predicted or confirmed as disease causing. This creates a new bottleneck: determining the functional impact of each variant-typically a painstaking, customized process undertaken one or a few genes and variants at a time. Here, we established a high-throughput imaging platform to assay the impact of coding variation on protein localization, evaluating 3,448 missense variants of over 1,000 genes and phenotypes. We discovered that mislocalization is a common consequence of coding variation, affecting about one-sixth of all pathogenic missense variants, all cellular compartments, and recessive and dominant disorders alike. Mislocalization is primarily driven by effects on protein stability and membrane insertion rather than disr

SUBMITTER: Lacoste J 

PROVIDER: S-EPMC11568917 | biostudies-literature | 2024 Nov

REPOSITORIES: biostudies-literature