Genopathy
Gene-Disorder Association · Article
Gene
MT-TE
Mitochondrially Encoded TRNA-Glu (GAA/G)
Disorder
Mitochondrial Myopathy With Reversible Cytochrome C Oxidase Deficiency
First reported 2009
Supporting publications 3
Key publication · gene–disorder Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy.Brain : a journal of neurology · 2009
Key publication · disorder A novel gly290asp mitochondrial cytochrome b mutation linked to a complex III deficiency in progressive exercise intolerance.Molecular and cellular probes · 1996
Manually curated
Association Review

In brief

The association between MT-TE (Mitochondrially Encoded TRNA-Glu (GAA/G)) and Mitochondrial Myopathy With Reversible Cytochrome C Oxidase Deficiency is well established and manually curated, with its 2 contributing sources — 2 of them expert-curated — recording pathogenic variants and a causative germline mutation.

Sources 2
Clinical variants 3
Symptoms 26
Compounds 0
Trials 0
Publications 3
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

2 sources

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

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03
MT-TE

The gene

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

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04
Mitochondrial Myopathy With Reversible Cytochrome C Oxidase Deficiency

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

24 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

3 publications

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

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09
Provenance

References & sources

8 references

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

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