Genopathy
Gene-Disorder Association · Article
Gene
MYO7A
Myosin VIIA
Disorder
Usher Syndrome Type 1b
First reported 1992
Supporting publications 8
Key publication · disorder Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11.Genomics · 1992
Association Review

In brief

The association between MYO7A (Myosin VIIA) and Usher Syndrome Type 1b is supported by expert-curated evidence, drawing on a single expert-curated source, which records pathogenic variants.

Sources 1
Clinical variants 559
Symptoms 0
Compounds 0
Trials 0
Publications 8
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

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02
Provenance

Evidence and sources

1 source

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

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03
MYO7A

The gene

1 source summary

A gene summary alongside the source descriptions it was distilled from.

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04
Usher Syndrome Type 1b

The disorder

4 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

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05
ClinVar and variant evidence

Genetic basis

559 clinical variants

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

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06
Literature

Reading

8 publications

Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.

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07
Provenance

References & sources

10 references

Every source and publication cited across this dossier, as one numbered reference list.

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