Deafness_Isolated
Gene: MYO15A

MYO15A (myosin XVA)
EnsemblGeneIds (GRCh38): ENSG00000091536
EnsemblGeneIds (GRCh37): ENSG00000091536
OMIM: 602666, Gene2Phenotype
MYO15A is in 5 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Green List (high evidence)

Multiple families and supportive mouse models, DEFINITIVE by ClinGen.
Created: 30 Sep 2020, 11:47 p.m. | Last Modified: 30 Sep 2020, 11:47 p.m.

Panel Version: 0.508

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Deafness, autosomal recessive 3, MIM# 600316

Publications

Created: 30 Sep 2020, 11:47 p.m.
Last Modified: 30 Sep 2020, 11:47 p.m.
Panel version: Imported from Deafness_IsolatedAndComplex panel version 0.508

Details

Mode of Inheritance

BIALLELIC, autosomal or pseudoautosomal

Sources

Expert Review Green
Victorian Clinical Genetics Services
Melbourne Genomics Health Alliance Deafness Flagship
Melbourne Genomics Health Alliance Deafness Flagship
Victorian Clinical Genetics Services

Phenotypes

Deafness, autosomal recessive 3, MIM# 600316

OMIM

602666

Clinvar variants

Variants in MYO15A

Penetrance

None

Publications

Panels with this gene