Genopathy
Gene-Disorder Association · Article
Gene
ATP6V1B2
ATPase H+ Transporting V1 Subunit B2
Disorder
Autosomal Dominant Deafness - Onychodystrophy Syndrome
First reported 2017
Supporting publications 4
Key publication · gene–disorder Dominant deafness-onychodystrophy syndrome caused by an ATP6V1B2 mutation.Clinical case reports · 2017
Key publication · disorder Report of a further family with dominant deafness-onychodystrophy (DDOD) syndrome.American journal of medical genetics. Part A · 2011
Manually curated
Association Review

In brief

The association between ATP6V1B2 (ATPase H+ Transporting V1 Subunit B2) and Autosomal Dominant Deafness - Onychodystrophy Syndrome is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording likely-pathogenic variants and a causative germline mutation.

Sources 3
Clinical variants 12
Symptoms 20
Compounds 0
Trials 0
Publications 4
01
At a glance

Association overview

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

Request access
02
Provenance

Evidence and sources

3 sources

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

Request access
03
ATP6V1B2

The gene

2 source summaries

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

Request access
04
Autosomal Dominant Deafness - Onychodystrophy Syndrome

The disorder

7 database identifiers

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

Request access
05
Phenotype

Clinical features

20 clinical features

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

Request access
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.

Request access
07
Mechanism overlap

Shared mechanisms

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

Request access
08
Literature

Reading

4 publications

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

Request access
09
Provenance

References & sources

11 references

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

Request access