Genopathy
Gene-Disorder Association · Article
Gene
TARID
TCF21 Antisense RNA Inducing Promoter Demethylation
Disorder
Deafness, Autosomal Dominant 10
First reported 1996
Supporting publications 5
Key publication · disorder A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6.Human molecular genetics · 1996
Association Review

In brief

The association between TARID (TCF21 Antisense RNA Inducing Promoter Demethylation) and Deafness, Autosomal Dominant 10 is supported by expert-curated evidence, drawing on a single expert-curated source, which records likely-pathogenic variants.

Sources 1
Clinical variants 81
Symptoms 2
Compounds 0
Trials 0
Publications 5
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

1 source

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

Request access
03
TARID

The gene

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

Request access
04
Deafness, Autosomal Dominant 10

The disorder

8 database identifiers

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

Request access
05
Phenotype

Clinical features

1 clinical feature

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

81 clinical variants

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

Request access
07
Literature

Reading

5 publications

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

Request access
08
Provenance

References & sources

8 references

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

Request access