The MYO6 gene homepage

This database is one of the ”Retinal and hearing impairment genetic variant databases”.
General information
Gene symbol MYO6
Gene name myosin VI
Chromosome 6
Chromosomal band q14.1
Imprinted Unknown
Genomic reference NG_009934.1
Transcript reference NM_004999.3
Exon/intron information NM_004999.3 exon/intron table
Associated with diseases DFN, DFNA1, DFNA22, DFNB37
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) David Baux
Total number of public variants reported 230
Unique public DNA variants reported 137
Individuals with public variants 310
Hidden variants 9
Download all this gene's data Download all data
Notes The database is curated by the Montpellier Usher group.
You can directly access the MYO6 database using:
If you wish to perform particular analyses, please do not hesitate to contact us. We hope that you will find these databases useful!
This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created May 03, 2013
Date last updated January 11, 2023
Version MYO6:230111

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_004999.3.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL
External URL Deafness Gene Mutation Database
CCMHC Molecular Genetics Laboratory Mutation Database
Deafness Variation Database
HGNC 7605
Entrez Gene 4646
PubMed articles MYO6
OMIM - Gene 600970
OMIM - Diseases DFNA1 (deafness, autosomal dominant, type 1)
DFNA22 (deafness, autosomal dominant, type 22 (DFNA-22))
DFNB37 (deafness, autosomal recessive, type 37 (DFNB-37))
GeneCards MYO6
GeneTests MYO6
Orphanet MYO6

Active transcripts




NCBI ID     

NCBI Protein ID     

00014181 6 myosin VI NM_004999.3 NP_004990.3 230

Copyright & disclaimer
The contents of this LOVD database are the intellectual property of the respective submitter(s) and curator(s) of the individual records. Individual data entries may indicate which data license applies to that specific record. When no license is listed, no permissions are granted. Any unauthorized use, copying, storage, or distribution of this material without written permission from the curator(s) will lead to copyright infringement with possible ensuing litigation. Copyright © 2013-2023. All Rights Reserved. For further details, refer to Directive 96/9/EC of the European Parliament and the Council of March 11 (1996) on the legal protection of databases.

We have used all reasonable efforts to ensure that the information displayed on these pages and contained in the databases is of high quality. We make no warranty, express or implied, as to its accuracy or that the information is fit for a particular purpose, and will not be held responsible for any consequences arising from any inaccuracies or omissions. Individuals, organizations, and companies that use this database do so on the understanding that no liability whatsoever, either direct or indirect, shall rest upon the data submitter(s), curator(s), or any of their employees or agents for the effects of any product, process, or method that may be produced or adopted by any part, notwithstanding that the formulation of such product, process or method may be based upon information here provided.