Genopathy
Gene-Disorder Association · Article
Gene
LOC130067862
ATAC-STARR-Seq Lymphoblastoid Silent Region 13986
Disorder
Mitochondrial Neurogastrointestinal Encephalomyopathy
First reported 1999
Supporting publications 15
Key publication · gene–disorder Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder.Science (New York, N.Y.) · 1999
Key publication · disorder Myo-, neuro-, gastrointestinal encephalopathy (MNGIE syndrome) due to partial deficiency of cytochrome-c-oxidase. A new mitochondrial multisystem disorder.Acta neuropathologica · 1987
Manually curated
Association Review

In brief

The association between LOC130067862 (ATAC-STARR-Seq Lymphoblastoid Silent Region 13986) and Mitochondrial Neurogastrointestinal Encephalomyopathy is well established and manually curated, drawing on a single expert-curated source, which records likely-pathogenic variants.

Sources 1
Clinical variants 82
Symptoms 50
Compounds 0
Trials 0
Publications 15
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

1 source

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

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03
LOC130067862

The gene

1 source summary

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

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04
Mitochondrial Neurogastrointestinal Encephalomyopathy

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

48 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

82 clinical variants

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

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07
Literature

Reading

15 publications

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

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08
Provenance

References & sources

14 references

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

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