Genopathy
Gene-Disorder Association · Article
Gene
SAMD12
Sterile Alpha Motif Domain Containing 12
Disorder
Epilepsy, Familial Adult Myoclonic, 1
First reported 2018
Supporting publications 4
Key publication · gene–disorder Intronic pentanucleotide TTTCA repeat insertion in the SAMD12 gene causes familial cortical myoclonic tremor with epilepsy type 1.Brain : a journal of neurology · 2018
Key publication · disorder Recurrence risks in families of children with symmetrical spasticity.Developmental medicine and child neurology · 1977
Manually curated
Association Review

In brief

The association between SAMD12 (Sterile Alpha Motif Domain Containing 12) and Epilepsy, Familial Adult Myoclonic, 1 is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording a known molecular basis and pathogenic variants.

Sources 3
Clinical variants 3
Symptoms 16
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
SAMD12

The gene

1 source summary

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

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04
Epilepsy, Familial Adult Myoclonic, 1

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

9 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

3 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

4 publications

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

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09
Provenance

References & sources

9 references

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

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