Monogenic hearing loss
Gene: RDXNew review confirms gene status and mode of inheritance; no changes required.Created: 1 Jun 2018, 2:45 p.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Comment when marking as ready: Expert review and OMIM confirmedCreated: 29 Jan 2016, 4:17 p.m.
Publications for RDX were set to PMID:12068294; 14758359; 14983055; 15314067; 17226784; 19215054; 8486357
This gene has been classified as Green List (High Evidence).
Model of inheritance for gene RDX was changed to BIALLELIC, autosomal or pseudoautosomal
RDX was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Illumina TruGenome Clinical Sequencing Services,UKGTN,Emory Genetics Laboratory,Radboud University Medical Center, Nijmegen,Expert
Model of inheritance for gene RDX was changed to BIALLELIC, autosomal or pseudoautosomal
RDX was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Illumina TruGenome Clinical Sequencing Services,UKGTN,Emory Genetics Laboratory,Radboud University Medical Center, Nijmegen,Expert
Model of inheritance for gene RDX was changed to BIALLELIC, autosomal or pseudoautosomal
RDX was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Illumina TruGenome Clinical Sequencing Services,UKGTN,Emory Genetics Laboratory,Radboud University Medical Center, Nijmegen,Expert
Model of inheritance for gene RDX was changed to BIALLELIC, autosomal or pseudoautosomal
RDX was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Illumina TruGenome Clinical Sequencing Services,UKGTN,Emory Genetics Laboratory,Radboud University Medical Center, Nijmegen,Expert
RDX was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Illumina TruGenome Clinical Sequencing Services,UKGTN,Emory Genetics Laboratory,Radboud University Medical Center, Nijmegen,Expert