Genopathy
Gene-Disorder Association · Article
Gene
QRICH1
Glutamine Rich 1
Disorder
Ververi-Brady Syndrome
First reported 2021
Supporting publications 4
Key publication · gene–disorder QRICH1 variants in Ververi-Brady syndrome-delineation of the genotypic and phenotypic spectrum.Clinical genetics · 2021
Key publication · disorder Phenotypic spectrum associated with de novo mutations in QRICH1 gene.Clinical genetics · 2018
Manually curated
Association Review

In brief

The association between QRICH1 (Glutamine Rich 1) and Ververi-Brady Syndrome is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording pathogenic and likely-pathogenic variants and a causative germline mutation.

Sources 3
Clinical variants 68
Symptoms 0
Compounds 0
Trials 0
Publications 4
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
QRICH1

The gene

1 source summary

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

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04
Ververi-Brady Syndrome

The disorder

4 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

68 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

4 publications

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

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07
Provenance

References & sources

9 references

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

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