Genopathy
Gene-Disorder Association · Article
Gene
ATP6V0A4
ATPase H+ Transporting V0 Subunit A4
Disorder
Renal Tubular Acidosis, Distal, 3, With Or Without Sensorineural Hearing Loss
First reported 2000
Supporting publications 14
Key publication · gene–disorder Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing.Nature genetics · 2000
Key publication · disorder SOME OBSERVATIONS OF RENAL TUBULAR ACIDOSIS--A FAMILY STUDY.South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde · 1964
Manually curated
Association Review

In brief

The association between ATP6V0A4 (ATPase H+ Transporting V0 Subunit A4) and Renal Tubular Acidosis, Distal, 3, With Or Without Sensorineural Hearing Loss is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, likely-pathogenic variants, and causative variation.

Sources 4
Clinical variants 204
Symptoms 16
Compounds 0
Trials 0
Publications 14
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
ATP6V0A4

The gene

2 source summaries

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

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04
Renal Tubular Acidosis, Distal, 3, With Or Without Sensorineural Hearing Loss

The disorder

7 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

11 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

204 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

14 publications

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

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09
Provenance

References & sources

15 references

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

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