Genopathy
Gene-Disorder Association · Article
Gene
TUBB4A
Tubulin Beta 4A Class IVa
Disorder
Dystonia
Manually curated
Association Review

In brief

The association between TUBB4A (Tubulin Beta 4A Class IVa) and Dystonia is reported, with clinical genetic testing available.

Sources 1
Clinical variants 1
Symptoms 19
Compounds 0
Trials 0
Publications 0
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
TUBB4A

The gene

1 source summary

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

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04
Dystonia

The disorder

12 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

1 clinical variant

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

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06
Provenance

References & sources

4 references

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

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