MYO7A Chromosome 11
Myosin VIIA
Upload your DNA to see your personal genotypes for variants in MYO7A.
What This Gene Does
This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
"A-kinase anchoring proteins|Myosin heavy chains, class VII|FERM domain containing"
Locus Type
gene with protein product
Location
11q13.5
Ensembl
ENSG00000137474
Associated Conditions (40)
Autosomal recessive nonsyndromic hearing loss 2
Usher syndrome type 1
Usher syndrome type 1B
Usher syndrome
Autosomal dominant nonsyndromic hearing loss 11
MYO7A-related disorder
Inborn genetic diseases
Hearing impairment
Retinal dystrophy
Deafness
Hearing loss
autosomal recessive
See cases
Optic atrophy
Retinitis pigmentosa
Pendred syndrome
Meniere disease
Cone-rod dystrophy
Nonsyndromic genetic hearing loss
Auditory neuropathy
+20 more conditions
Key Variants
RS1029122324
Conflicting classifications of pathogenicity
Health Risk
RS111033219
Conflicting classifications of pathogenicity
Autosomal recessive nonsyndromic hearing loss 2, Usher syndrome type 1, Usher syndrome type 1B
Health Risk
RS111033221
Conflicting classifications of pathogenicity
Autosomal dominant nonsyndromic hearing loss 11, Usher syndrome type 1, Autosomal recessive nonsyndromic hearing loss 2
Health Risk
RS111033227
Conflicting classifications of pathogenicity
Usher syndrome type 1, Autosomal recessive nonsyndromic hearing loss 2, Autosomal dominant nonsyndromic hearing loss 11
Health Risk
RS111033228
Conflicting classifications of pathogenicity
Autosomal dominant nonsyndromic hearing loss 11, Usher syndrome type 1, Autosomal recessive nonsyndromic hearing loss 2
Health Risk
RS111033229
Conflicting classifications of pathogenicity
Usher syndrome type 1, Autosomal recessive nonsyndromic hearing loss 2, Autosomal dominant nonsyndromic hearing loss 11
Health Risk
RS111033230
Conflicting classifications of pathogenicity
Autosomal recessive nonsyndromic hearing loss 2, Autosomal dominant nonsyndromic hearing loss 11, Usher syndrome type 1
Health Risk
RS111033252
Conflicting classifications of pathogenicity
Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2, Usher syndrome type 1
Health Risk
RS111033287
Conflicting classifications of pathogenicity
Usher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2
Health Risk
RS111033416
Conflicting classifications of pathogenicity
Autosomal recessive nonsyndromic hearing loss 2, Usher syndrome type 1, Usher syndrome type 1B
Health Risk
RS111033504
Conflicting classifications of pathogenicity
Usher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2
Health Risk
RS111033507
Conflicting classifications of pathogenicity
Usher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2
Health Risk
All Variants (982)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS530520654 | Health Risk | Pathogenic/Likely pathogenic | Autosomal recessive nonsyndromic hearing loss 2, Autosomal recessive nonsyndromic hearing loss 2 |
| RS530700420 | Health Risk | Pathogenic/Likely pathogenic | Usher syndrome type 1, Usher syndrome type 1 |
| RS548172627 | Health Risk | Pathogenic/Likely pathogenic | Autosomal recessive nonsyndromic hearing loss 2, Usher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11 |
| RS746667217 | Health Risk | Pathogenic/Likely pathogenic | Deafness, Hearing loss, autosomal recessive |
| RS747656448 | Health Risk | Pathogenic/Likely pathogenic | Autosomal recessive nonsyndromic hearing loss 2, Usher syndrome, Autosomal dominant nonsyndromic hearing loss 11 |
| RS750358148 | Health Risk | Pathogenic/Likely pathogenic | Usher syndrome, Autosomal recessive nonsyndromic hearing loss 2, Hearing loss |
| RS750647872 | Health Risk | Pathogenic/Likely pathogenic | Usher syndrome type 1B, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2 |
| RS751769391 | Health Risk | Pathogenic/Likely pathogenic | Autosomal recessive nonsyndromic hearing loss 2, Usher syndrome, Hearing loss |
| RS760292207 | Health Risk | Pathogenic/Likely pathogenic | — |
| RS761469964 | Health Risk | Pathogenic/Likely pathogenic | Retinal dystrophy, Usher syndrome type 1B, Usher syndrome type 1 |
| RS770778096 | Health Risk | Pathogenic/Likely pathogenic | Usher syndrome type 1, Usher syndrome type 1 |
| RS776930594 | Health Risk | Pathogenic/Likely pathogenic | Autosomal recessive nonsyndromic hearing loss 2, Usher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11 |
| RS780609120 | Health Risk | Pathogenic/Likely pathogenic | Retinal dystrophy, Usher syndrome type 1B, Retinal dystrophy |
| RS781815916 | Health Risk | Pathogenic/Likely pathogenic | Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2, Usher syndrome type 1 |
| RS781977497 | Health Risk | Pathogenic/Likely pathogenic | Usher syndrome type 1, Autosomal recessive nonsyndromic hearing loss 2, Autosomal dominant nonsyndromic hearing loss 11 |
| RS781988557 | Health Risk | Pathogenic/Likely pathogenic | Rare genetic deafness, Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2 |
| RS781989117 | Health Risk | Pathogenic/Likely pathogenic | Autosomal recessive nonsyndromic hearing loss 2, Hearing loss, autosomal recessive |
| RS782064437 | Health Risk | Pathogenic/Likely pathogenic | Autosomal recessive nonsyndromic hearing loss 2, Usher syndrome type 1, Autosomal recessive nonsyndromic hearing loss 2 |
| RS782166819 | Health Risk | Pathogenic/Likely pathogenic | Usher syndrome, Usher syndrome type 1, Autosomal recessive nonsyndromic hearing loss 2 |
| RS782312060 | Health Risk | Pathogenic/Likely pathogenic | MYO7A-related disorder, MYO7A-related disorder |
| RS782339376 | Health Risk | Pathogenic/Likely pathogenic | Usher syndrome type 1, Usher syndrome type 1 |
| RS782347270 | Health Risk | Pathogenic/Likely pathogenic | Usher syndrome type 1, Autosomal recessive nonsyndromic hearing loss 2, Usher syndrome type 1B |
| RS782468194 | Health Risk | Pathogenic/Likely pathogenic | Autosomal recessive nonsyndromic hearing loss 2, Usher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11 |
| RS782598897 | Health Risk | Pathogenic/Likely pathogenic | — |
| RS782636104 | Health Risk | Pathogenic/Likely pathogenic | MYO7A-related disorder, MYO7A-related disorder |
| RS782639389 | Health Risk | Pathogenic/Likely pathogenic | Retinal dystrophy, Autosomal dominant nonsyndromic hearing loss 11, Usher syndrome type 1 |
| RS782787126 | Health Risk | Pathogenic/Likely pathogenic | Autosomal recessive nonsyndromic hearing loss 2, Usher syndrome type 1, Meniere disease |
| RS797044512 | Health Risk | Pathogenic/Likely pathogenic | Rare genetic deafness, Autosomal dominant nonsyndromic hearing loss 11, Bilateral sensorineural hearing impairment |
| RS797044518 | Health Risk | Pathogenic/Likely pathogenic | Rare genetic deafness, Usher syndrome type 1, Usher syndrome |
| RS866352637 | Health Risk | Pathogenic/Likely pathogenic | Usher syndrome type 1B, Usher syndrome, Usher syndrome type 1B |
| RS878853236 | Health Risk | Pathogenic/Likely pathogenic | Autosomal recessive nonsyndromic hearing loss 2, Usher syndrome type 1, Autosomal dominant nonsyndromic hearing loss 11 |
| RS957394613 | Health Risk | Pathogenic/Likely pathogenic | Usher syndrome, Usher syndrome |