Genopathy
Gene-Disorder Association · Article
Gene
DEPDC5
DEP Domain Containing 5, GATOR1 Subcomplex Subunit
Disorder
Epilepsy, Familial Focal, With Variable Foci 1
First reported 2013
Supporting publications 37
Key publication · gene–disorder Mutations in DEPDC5 cause familial focal epilepsy with variable foci.Nature genetics · 2013
Key publication · disorder Autosomal dominant nocturnal frontal lobe epilepsy. A distinctive clinical disorder.Brain : a journal of neurology · 1995
Manually curated
Association Review

In brief

The association between DEPDC5 (DEP Domain Containing 5, GATOR1 Subcomplex Subunit) and Epilepsy, Familial Focal, With Variable Foci 1 is well established and manually curated, with its 5 contributing sources — 4 of them expert-curated — recording a known molecular basis, pathogenic variants, and a causative germline mutation.

Sources 5
Clinical variants 1,997
Symptoms 49
Compounds 0
Trials 0
Publications 37
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

5 sources

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

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03
DEPDC5

The gene

1 source summary

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

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04
Epilepsy, Familial Focal, With Variable Foci 1

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

30 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

1,997 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

37 publications

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

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09
Provenance

References & sources

16 references

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

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