Genopathy
Gene-Disorder Association · Article
Gene
LOC112840921
BRD4-Independent Group 4 Enhancer GRCh37_chr2:26685720-26686919
Disorder
Nonsyndromic Hearing Loss
First reported 1975
Key publication · disorder Symposium on sensorineural hearing loss in children: early detection and intervention. Genetic factors in deafness of early life.Otolaryngologic clinics of North America · 1975
Manually curated
Association Review

In brief

The association between LOC112840921 (BRD4-Independent Group 4 Enhancer GRCh37_chr2:26685720-26686919) and Nonsyndromic Hearing Loss is a manually-curated gene–disease association, drawing on a single expert-curated source, which records pathogenic variants.

Sources 1
Clinical variants 1
Symptoms 0
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
LOC112840921

The gene

1 source summary

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

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04
Nonsyndromic Hearing Loss

The disorder

1 database identifier

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

2 references

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

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