Deafness_IsolatedAndComplex
Gene: MIR96
2 families in single paper. expression studiesCreated: 31 Dec 2019, 1:45 a.m. | Last Modified: 31 Dec 2019, 1:45 a.m.
Panel Version: 0.81
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Autosomal dominant hearing loss
Publications
Tag non-coding gene tag was added to gene: MIR96.
Gene: mir96 has been classified as Amber List (Moderate Evidence).
Phenotypes for gene: MIR96 were changed from Autosomal dominant hearing loss to Deafness, autosomal dominant 50, MIM# 613074
Gene: mir96 has been classified as Amber List (Moderate Evidence).
Phenotypes for gene: MIR96 were changed from to Autosomal dominant hearing loss
Publications for gene: MIR96 were set to
Mode of inheritance for gene: MIR96 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Gene: mir96 has been classified as Amber List (Moderate Evidence).
gene: MIR96 was added gene: MIR96 was added to Deafness_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Deafness Flagship Mode of inheritance for gene: MIR96 was set to Unknown