Genopathy
Gene-Disorder Association · Article
Gene
GABRB3
Gamma-Aminobutyric Acid Type A Receptor Subunit Beta3
Disorder
Epilepsy, Childhood Absence 5
First reported 2008
Supporting publications 26
Key publication · gene–disorder Hyperglycosylation and reduced GABA currents of mutated GABRB3 polypeptide in remitting childhood absence epilepsy.American journal of human genetics · 2008
Key publication · disorder Quisqualate receptors in epileptic fowl: the absence of coupling between quisqualate and N-methyl-D-aspartate receptors.European journal of pharmacology · 1990
Manually curated
Association Review

In brief

The association between GABRB3 (Gamma-Aminobutyric Acid Type A Receptor Subunit Beta3) and Epilepsy, Childhood Absence 5 is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, causative variation, and a susceptibility locus.

Sources 4
Clinical variants 508
Symptoms 1
Compounds 0
Trials 0
Publications 26
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

4 sources

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

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03
GABRB3

The gene

2 source summaries

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

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04
Epilepsy, Childhood Absence 5

The disorder

5 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

1 clinical feature

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

508 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

26 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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