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Molecular Mechanisms and Clinical Phenotypes of Missense Variants. | LitMetric

Molecular Mechanisms and Clinical Phenotypes of Missense Variants.

Biology (Basel)

Precision Medicine Center, Academy of Medical Science, Zhengzhou University, Zhengzhou 450052, China.

Published: March 2023

AI Article Synopsis

Article Abstract

The gene is the most common gene responsible for hearing loss (HL) worldwide, and missense variants are the most abundant type. pathogenic missense variants cause nonsyndromic HL (autosomal recessive and dominant) and syndromic HL combined with skin diseases. However, the mechanism by which these different missense variants cause the different phenotypes is unknown. Over 2/3 of the missense variants have yet to be functionally studied and are currently classified as variants of uncertain significance (VUS). Based on these functionally determined missense variants, we reviewed the clinical phenotypes and investigated the molecular mechanisms that affected hemichannel and gap junction functions, including connexin biosynthesis, trafficking, oligomerization into connexons, permeability, and interactions between other coexpressed connexins. We predict that all possible missense variants will be described in the future by deep mutational scanning technology and optimizing computational models. Therefore, the mechanisms by which different missense variants cause different phenotypes will be fully elucidated.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10135792PMC
http://dx.doi.org/10.3390/biology12040505DOI Listing

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