Genopathy
Gene-Disorder Association · Article
Gene
DNM1
Dynamin 1
Disorder
Developmental And Epileptic Encephalopathy 31a
First reported 2022
Supporting publications 21
Key publication · gene–disorder Loss-of-function variants in DNM1 cause a specific form of developmental and epileptic encephalopathy only in biallelic state.Journal of medical genetics · 2022
Key publication · disorder Genetic and developmental influences on susceptibility to epilepsy: evidence from twins.Paediatric and perinatal epidemiology · 1992
Manually curated
Association Review

In brief

The association between DNM1 (Dynamin 1) and Developmental And Epileptic Encephalopathy 31a is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic and likely-pathogenic variants, and causative variation.

Sources 4
Clinical variants 735
Symptoms 32
Compounds 0
Trials 0
Publications 21
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
DNM1

The gene

2 source summaries

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

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04
Developmental And Epileptic Encephalopathy 31a

The disorder

7 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

735 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

21 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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