Genopathy
Gene-Disorder Association · Article
Gene
VWA3B
Von Willebrand Factor A Domain Containing 3B
Disorder
Spinocerebellar Ataxia, Autosomal Recessive 22
First reported 2016
Supporting publications 1
Key publication · gene–disorder A homozygous mutation of VWA3B causes cerebellar ataxia with intellectual disability.Journal of neurology, neurosurgery, and psychiatry · 2016
Key publication · disorder Diabetes mellitus in ataxia-telangiectasia, Fanconi anemia, xeroderma pigmentosum, common variable immune deficiency, and severe combined immune deficiency families.Diabetes · 1986
Manually curated
Association Review

In brief

The association between VWA3B (Von Willebrand Factor A Domain Containing 3B) and Spinocerebellar Ataxia, Autosomal Recessive 22 is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic and likely-pathogenic variants, and causative variation.

Sources 4
Clinical variants 12
Symptoms 18
Compounds 0
Trials 0
Publications 1
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

4 sources

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

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03
VWA3B

The gene

1 source summary

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

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04
Spinocerebellar Ataxia, Autosomal Recessive 22

The disorder

8 database identifiers

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

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05
Phenotype

Clinical features

13 clinical features

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

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06
ClinVar and variant evidence

Genetic basis

12 clinical variants

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

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07
Mechanism overlap

Shared mechanisms

Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.

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08
Literature

Reading

1 publication

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

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09
Provenance

References & sources

7 references

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

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