DisGeNET - a database of gene-disease associations

Gene: DPM3 ×

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Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Gene

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	54344
Gene Symbol:	DPM3

DPM3

CUI:	C0686353
Disease:	Muscular Dystrophies, Limb-Girdle

Muscular Dystrophies, Limb-Girdle

0.320

Biomarker

GENOMICS_ENGLAND

Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies.

2009