Genopathy
Gene-Disorder Association · Article
Gene
NDUFB11
NADH:Ubiquinone Oxidoreductase Subunit B11
Disorder
Linear Skin Defects With Multiple Congenital Anomalies 3
First reported 2015
Supporting publications 6
Key publication · gene–disorder Mutations in NDUFB11, encoding a complex I component of the mitochondrial respiratory chain, cause microphthalmia with linear skin defects syndrome.American journal of human genetics · 2015
Key publication · disorder Lyonization and the lines of Blaschko.Human genetics · 1985
Manually curated
Association Review

In brief

The association between NDUFB11 (NADH:Ubiquinone Oxidoreductase Subunit B11) and Linear Skin Defects With Multiple Congenital Anomalies 3 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 7
Symptoms 37
Compounds 0
Trials 0
Publications 6
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
NDUFB11

The gene

1 source summary

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

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04
Linear Skin Defects With Multiple Congenital Anomalies 3

The disorder

8 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

22 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

7 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

6 publications

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

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09
Provenance

References & sources

11 references

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

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