Genopathy
Gene-Disorder Association · Article
Gene
POLR3A
RNA Polymerase III Subunit A
Disorder
Wiedemann-Rautenstrauch Syndrome
First reported 2005
Supporting publications 17
Key publication · gene–disorder Follow-up study of Wiedemann-Rautenstrauch syndrome: long-term survival and comparison with Rautenstrauch's patient "G".Birth defects research. Part A, Clinical and molecular teratology · 2005
Key publication · disorder Progeria: a cell culture study and clinical report of familial incidence.European journal of pediatrics · 1977
Manually curated
Association Review

In brief

The association between POLR3A (RNA Polymerase III Subunit A) and Wiedemann-Rautenstrauch Syndrome is well established and manually curated, with its 3 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic and likely-pathogenic variants, and a causative germline mutation.

Sources 3
Clinical variants 40
Symptoms 243
Compounds 0
Trials 0
Publications 17
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

3 sources

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

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03
POLR3A

The gene

1 source summary

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

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04
Wiedemann-Rautenstrauch Syndrome

The disorder

12 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

187 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

40 clinical variants

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

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07
Mechanism overlap

Shared mechanisms

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

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08
Literature

Reading

17 publications

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

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09
Provenance

References & sources

15 references

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

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