Autosomal dominant nanophthalmos and high hyperopia associated with a C-terminal frameshift variant in MYRF.

ABSTRACT: Purpose:Nanophthalmos is a rare subtype of microphthalmia associated with high hyperopia and an increased risk of angle-closure glaucoma. We investigated the genetic cause of nanophthalmos and high hyperopia in an autosomal dominant kindred. Methods:A proband with short axial length, high hyperopia, and dextrocardia was subjected to exome sequencing. Human and rodent gene expression data sets were used to investigate the expression of relevant genes. Results:We identified a segregating heterozygous frameshift variant at the 3' end of the penultimate exon of MYRF. Using Myc-MYRF chromatin immunoprecipitation data from rat oligodendrocytes, MYRF was found to bind immediately upstream of the transcriptional start site of Tmem98, a gene that itself has been implicated in autosomal dominant nan

SUBMITTER: Siggs OM 

PROVIDER: S-EPMC6817736 | biostudies-literature | 2019

REPOSITORIES: biostudies-literature