Gene: B3GALNT2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 148789
Gene Symbol: B3GALNT2
B3GALNT2 		0.020 GeneticVariation disease BEFREE The dystroglycanopathies are a heterogeneous group of conditions, with mutations in B3GALNT2 described in association with congenital muscular dystrophy. 28303321 2017
Entrez Id: 148789
Gene Symbol: B3GALNT2
B3GALNT2 		0.020 Biomarker disease BEFREE B3GALNT2 is a gene associated with congenital muscular dystrophy with brain malformations. 24084573 2014