Genopathy
Gene-Disorder Association · Article
Gene
SLC26A4-AS1
SLC26A4 Antisense RNA 1
Disorder
Pendred Syndrome
First reported 2001
Supporting publications 30
Key publication · gene–disorder Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations.Human mutation · 2001
Key publication · disorder A study of a family of goitrous cretins.The Journal of clinical endocrinology and metabolism · 1950
Manually curated
Association Review

In brief

The association between SLC26A4-AS1 (SLC26A4 Antisense RNA 1) and Pendred Syndrome is well established and manually curated, drawing on a single expert-curated source, which records pathogenic and likely-pathogenic variants.

Sources 1
Clinical variants 32
Symptoms 26
Compounds 0
Trials 0
Publications 30
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
SLC26A4-AS1

The gene

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

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04
Pendred Syndrome

The disorder

13 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

20 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

32 clinical variants

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

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07
Literature

Reading

30 publications

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

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08
Provenance

References & sources

13 references

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

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