Genopathy
Gene-Disorder Association · Article
Gene
BSND
Barttin CLCNK Type Accessory Subunit Beta
Disorder
Bartter Disease Type 4a
First reported 2001
Supporting publications 14
Key publication · gene–disorder Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure.Nature genetics · 2001
Key publication · disorder Linkage of infantile Bartter syndrome with sensorineural deafness to chromosome 1p.American journal of human genetics · 1998
Manually curated
Association Review

In brief

The association between BSND (Barttin CLCNK Type Accessory Subunit Beta) and Bartter Disease Type 4a is well established and manually curated, with its 2 contributing sources — 1 of them expert-curated — recording likely-pathogenic variants.

Sources 2
Clinical variants 79
Symptoms 1
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

2 sources

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

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03
BSND

The gene

1 source summary

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

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04
Bartter Disease Type 4a

The disorder

3 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

79 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

14 publications

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

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07
Provenance

References & sources

12 references

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

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