Rare germline disorders implicate long non-coding RNAs disrupted by chromosomal structural rearrangements.

ABSTRACT: In recent years, there has been increased focus on exploring the role the non-protein-coding genome plays in Mendelian disorders. One class of particular interest is long non-coding RNAs (lncRNAs), which has recently been implicated in the regulation of diverse molecular processes. However, because lncRNAs do not encode protein, there is uncertainty regarding what constitutes a pathogenic lncRNA variant, and thus annotating such elements is challenging. The Developmental Genome Anatomy Project (DGAP) and similar projects recruit individuals with apparently balanced chromosomal abnormalities (BCAs) that disrupt or dysregulate genes in order to annotate the human genome. We hypothesized that rearrangements disrupting lncRNAs could be the underlying genetic etiology for the phenotypes of a su

SUBMITTER: Andersen RE 

PROVIDER: S-EPMC11213069 | biostudies-literature | 2024 Jun

REPOSITORIES: biostudies-literature