Genopathy
Gene-Disorder Association · Article
Gene
ALG14
ALG14 UDP-N-Acetylglucosaminyltransferase Subunit
Disorder
Myopathy, Epilepsy, And Progressive Cerebral Atrophy
First reported 2017
Supporting publications 1
Key publication · gene–disorder Early and lethal neurodegeneration with myasthenic and myopathic features: A new ALG14-CDG.Neurology · 2017
Key publication · disorder Late infantile neuroaxonal dystrophy. An unusual case with predominantly myoclonic-epileptic symptomatology.Rivista di patologia nervosa e mentale · 1981
Manually curated
Association Review

In brief

The association between ALG14 (ALG14 UDP-N-Acetylglucosaminyltransferase Subunit) and Myopathy, Epilepsy, And Progressive Cerebral Atrophy is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, likely-pathogenic variants, and causative variation.

Sources 4
Clinical variants 19
Symptoms 46
Compounds 0
Trials 0
Publications 1
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
ALG14

The gene

1 source summary

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

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04
Myopathy, Epilepsy, And Progressive Cerebral Atrophy

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

23 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

19 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

1 publication

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

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09
Provenance

References & sources

7 references

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

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