MYO7A gene homepage


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
General information
Gene symbol MYO7A
Gene name myosin VIIA
Chromosome 11
Chromosomal band q13.5
Imprinted Unknown
Genomic reference NG_009086.1
Transcript reference NM_000260.3
Exon/intron information NM_000260.3 exon/intron table
Associated with diseases DFN, DFNA, DFNA-11, DFNB, DFNB-2, USH, USH-1, USH-1B
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) David Baux
Total number of public variants reported 3645
Unique public DNA variants reported 656
Individuals with public variants 853
Hidden variants 655
Download all this gene's data Download all data
Notes The database is curated by the Montpellier Usher group.
You can directly access the MYO7A database using: www.LOVD.nl/MYO7A
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 February 17, 2010
Date last updated July 23, 2018
Version MYO7A:180723

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_000260.3.
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 https://www.LOVD.nl/MYO7A
External URL Orphanet
KMeyeDB
USMA (Usher Syndrome Missense Analysis
Deafness Variation Database
HGNC 7606
Entrez Gene 4647
PubMed articles MYO7A
OMIM - Gene 276903
OMIM - Diseases DFNA (deafness, nonsyndromic (DFNA, autosomal dominant))
DFNA-11 (deafness, autosomal dominant, type 11 (DFNA-11))
DFNB-2 (deafness, autosomal recessive, type 2 (DFNB-2))
USH-1B (Usher syndrome, type Ib (USH-1B))
HGMD MYO7A
GeneCards MYO7A
GeneTests MYO7A


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00001646 11 transcript variant 1 NM_000260.3 NP_000251.3 3645


Copyright & disclaimer
The contents of this LOVD database are the intellectual property of the respective curator(s). Any unauthorised 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 © 2010-2019. 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 out of any inaccuracies or omissions. Individuals, organisations and companies which use this database do so on the understanding that no liability whatsoever either direct or indirect shall rest upon the 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.