DisGeNET - a database of gene-disease associations

Source: MGD

Disease: Congenital myopathy (disorder) ×

Gene: B4GAT1 ×

Results per page

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:	11041
Gene Symbol:	B4GAT1

B4GAT1

CUI:	C0270960
Disease:	Congenital myopathy (disorder)

Congenital myopathy (disorder)

0.200

Biomarker

MGD

Dystroglycan organizes axon guidance cue localization and axonal pathfinding.

2012