Genopathy
Gene-Disorder Association · Article
Gene
DAG1
Dystroglycan 1
Disorder
Muscular Dystrophy
First reported 1995
Supporting publications 11
Key publication · gene–disorder A severe muscular dystrophy patient with an internally deleted very short (110 kD) dystrophin: presence of the binding site for dystrophin-associated glycoprotein (DAG) may not be enough for physiological function of dystrophin.Neuromuscular disorders : NMD · 1995
Key publication · disorder Myocardial lesions in progressive muscular dystrophy.A.M.A. archives of pathology · 1950
Manually curated
Association Review

In brief

The association between DAG1 (Dystroglycan 1) and Muscular Dystrophy is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 5
Compounds 0
Trials 0
Publications 11
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

Request access
02
Provenance

Evidence and sources

1 source

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

Request access
03
DAG1

The gene

1 source summary

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

Request access
04
Muscular Dystrophy

The disorder

9 database identifiers

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

Request access
05
Literature

Reading

11 publications

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

Request access
06
Provenance

References & sources

11 references

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

Request access