Genopathy
Gene-Disorder Association · Article
Gene
POMGNT1
Protein O-Linked Mannose N-Acetylglucosaminyltransferase 1 (Beta 1,2-)
Disorder
Congenital Muscular Dystrophy-Dystroglycanopathy Type A3
First reported 2001
Supporting publications 32
Key publication · disorder Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1.Developmental cell · 2001
Manually curated
Association Review

In brief

The association between POMGNT1 (Protein O-Linked Mannose N-Acetylglucosaminyltransferase 1 (Beta 1,2-)) and Congenital Muscular Dystrophy-Dystroglycanopathy Type A3 is well established and manually curated, drawing on a single expert-curated source, which records pathogenic and likely-pathogenic variants.

Sources 1
Clinical variants 212
Symptoms 0
Compounds 0
Trials 0
Publications 32
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
POMGNT1

The gene

1 source summary

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

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04
Congenital Muscular Dystrophy-Dystroglycanopathy Type A3

The disorder

2 database identifiers

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

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05
ClinVar and variant evidence

Genetic basis

212 clinical variants

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

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06
Literature

Reading

32 publications

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

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07
Provenance

References & sources

10 references

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

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