Monogenic hearing loss
Gene: MSRB3New review confirms gene status and mode of inheritance; no changes required.Created: 1 Jun 2018, 2:56 p.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
#613718:Deafness, autosomal recessive 74[Deafness, neurosensorySevere to profound deafness]
Comment when marking as ready: Expert review and OMIM confirmedCreated: 29 Jan 2016, 3:52 p.m.
Publications for MSRB3 were set to PMID:14699060; 15249228; 19650862; 21185009; 24191262
Mode of inheritance for MSRB3 was changed to BIALLELIC, autosomal or pseudoautosomal
This gene has been classified as Green List (High Evidence).
MSRB3 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: UKGTN,Emory Genetics Laboratory,Radboud University Medical Center, Nijmegen,Expert
MSRB3 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: UKGTN,Emory Genetics Laboratory,Radboud University Medical Center, Nijmegen,Expert
MSRB3 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: UKGTN,Emory Genetics Laboratory,Radboud University Medical Center, Nijmegen,Expert
MSRB3 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: UKGTN,Emory Genetics Laboratory,Radboud University Medical Center, Nijmegen,Expert