Ectodermal dysplasia
Gene: PPP1R13L
Multiple individuals reported with variants in this gene. Phenotype consists of cardiac defects and variable ectodermal abnormalities affecting hair, skin and teeth. Given this is a prominent component of the phenotype in some cases and there are a sufficient number of individuals to support this gene-disease association, there is enough evidence to promote PPP1R13L to green status at the next GMS panel update.
Sources: LiteratureCreated: 16 Oct 2023, 4:41 p.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities, OMIM:620519
Publications
Gene: ppp1r13l has been classified as Amber List (Moderate Evidence).
gene: PPP1R13L was added gene: PPP1R13L was added to Ectodermal dysplasia. Sources: Literature Q4_23_promote_green tags were added to gene: PPP1R13L. Mode of inheritance for gene: PPP1R13L was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: PPP1R13L were set to 28069640; 32666529; 35924320 Phenotypes for gene: PPP1R13L were set to Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities, OMIM:620519 Review for gene: PPP1R13L was set to GREEN