Source: LHGDN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2683
Gene Symbol: B4GALT1
B4GALT1
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus 		0.110 Biomarker LHGDN Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId. 11901181

2002
Entrez Id: 2683
Gene Symbol: B4GALT1
B4GALT1
CUI: C0026848
Disease: Myopathy
Myopathy 		0.110 Biomarker LHGDN Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId. 11901181

2002
Entrez Id: 2683
Gene Symbol: B4GALT1
B4GALT1
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.030 AlteredExpression LHGDN Identification of beta-1,4-galactosyltransferase I as a target gene of HBx-induced cell cycle progression of hepatoma cell. 18929424

2008
Entrez Id: 2683
Gene Symbol: B4GALT1
B4GALT1
CUI: C0019158
Disease: Hepatitis
Hepatitis 		0.010 AlteredExpression LHGDN Identification of beta-1,4-galactosyltransferase I as a target gene of HBx-induced cell cycle progression of hepatoma cell. 18929424

2008
Entrez Id: 2683
Gene Symbol: B4GALT1
B4GALT1
CUI: C0024121
Disease: Lung Neoplasms
Lung Neoplasms 		0.010 AlteredExpression LHGDN Elevated beta1,4-galactosyltransferase I in highly metastatic human lung cancer cells. Identification of E1AF as important transcription activator. 15611127

2005