Genopathy
Gene-Disorder Association · Article
Gene
COX6B1
Cytochrome C Oxidase Subunit 6B1
Disorder
Mitochondrial Complex Iv Deficiency, Nuclear Type 1
First reported 2008
Supporting publications 2
Key publication · gene–disorder Severe infantile encephalomyopathy caused by a mutation in COX6B1, a nucleus-encoded subunit of cytochrome c oxidase.American journal of human genetics · 2008
Key publication · disorder Letter: A metabolic myopathy associated with chronic lactic acidemia, growth failure, and nerve deafness.The Journal of pediatrics · 1975
Manually curated
Association Review

In brief

The association between COX6B1 (Cytochrome C Oxidase Subunit 6B1) and Mitochondrial Complex Iv Deficiency, Nuclear Type 1 is well established and manually curated, with its 2 contributing sources — 1 of them expert-curated — recording likely-pathogenic variants.

Sources 2
Clinical variants 11
Symptoms 77
Compounds 0
Trials 0
Publications 2
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
COX6B1

The gene

1 source summary

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

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04
Mitochondrial Complex Iv Deficiency, Nuclear Type 1

The disorder

19 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

55 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

11 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

2 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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