Genopathy
Gene-Disorder Association · Article
Gene
MIEF2
Mitochondrial Elongation Factor 2
Disorder
Combined Oxidative Phosphorylation Deficiency 49
First reported 2018
Supporting publications 1
Key publication · gene–disorder A novel mechanism causing imbalance of mitochondrial fusion and fission in human myopathies.Human molecular genetics · 2018
Key publication · disorder Familial dystonia and visual failure with striatal CT lucencies.Journal of neurology, neurosurgery, and psychiatry · 1986
Manually curated
Association Review

In brief

The association between MIEF2 (Mitochondrial Elongation Factor 2) and Combined Oxidative Phosphorylation Deficiency 49 is well established and manually curated, with its 2 contributing sources — 2 of them expert-curated — recording a known molecular basis and pathogenic variants.

Sources 2
Clinical variants 1
Symptoms 22
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.

Request access
02
Provenance

Evidence and sources

2 sources

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

Request access
03
MIEF2

The gene

1 source summary

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

Request access
04
Combined Oxidative Phosphorylation Deficiency 49

The disorder

7 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

Request access
05
Phenotype

Clinical features

12 clinical features

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

Request access
06
ClinVar and variant evidence

Genetic basis

1 clinical variant

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

Request access
07
Mechanism overlap

Shared mechanisms

Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.

Request access
08
Literature

Reading

1 publication

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

Request access
09
Provenance

References & sources

5 references

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

Request access