Gene: B3GLCT ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 145173
Gene Symbol: B3GLCT
B3GLCT 		0.110 GeneticVariation disease BEFREE Peters plus syndrome (MIM #261540 PTRPLS), characterized by defects in eye development, prominent forehead, hypertelorism, short stature, and brachydactyly, is caused by mutations in the β3-glucosyltransferase (B3GLCT) gene. 31600785 2019
Entrez Id: 145173
Gene Symbol: B3GLCT
B3GLCT 		0.110 Biomarker disease HPO