Source: GENOMICS_ENGLAND

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7355
Gene Symbol: SLC35A2
SLC35A2
CUI: C3806688
Disease: Solute carrier family 35 member A2 congenital disorder of glycosylation
Solute carrier family 35 member A2 congenital disorder of glycosylation 		0.730 Biomarker GENOMICS_ENGLAND Clinical, neuroradiological, and biochemical features of SLC35A2-CDG patients. 30746764

2019
Entrez Id: 7355
Gene Symbol: SLC35A2
SLC35A2
CUI: C3806688
Disease: Solute carrier family 35 member A2 congenital disorder of glycosylation
Solute carrier family 35 member A2 congenital disorder of glycosylation 		0.730 Biomarker GENOMICS_ENGLAND Mosaicism of the UDP-galactose transporter SLC35A2 causes a congenital disorder of glycosylation. 23561849

2013
Entrez Id: 7355
Gene Symbol: SLC35A2
SLC35A2
CUI: C3806688
Disease: Solute carrier family 35 member A2 congenital disorder of glycosylation
Solute carrier family 35 member A2 congenital disorder of glycosylation 		0.730 Biomarker GENOMICS_ENGLAND Mosaicism of the UDP-galactose transporter SLC35A2 causes a congenital disorder of glycosylation. 23561849

2013
Entrez Id: 7355
Gene Symbol: SLC35A2
SLC35A2
CUI: C0282577
Disease: Congenital Disorders of Glycosylation
Congenital Disorders of Glycosylation 		0.390 Biomarker GENOMICS_ENGLAND

Entrez Id: 7355
Gene Symbol: SLC35A2
SLC35A2
CUI: C0014544
Disease: Epilepsy
Epilepsy 		0.340 Biomarker GENOMICS_ENGLAND Clinical, neuroradiological, and biochemical features of SLC35A2-CDG patients. 30746764

2019
Entrez Id: 7355
Gene Symbol: SLC35A2
SLC35A2
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		0.310 Biomarker GENOMICS_ENGLAND Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes. 27604308

2016
Entrez Id: 7355
Gene Symbol: SLC35A2
SLC35A2
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		0.310 Biomarker GENOMICS_ENGLAND Mosaicism of the UDP-galactose transporter SLC35A2 causes a congenital disorder of glycosylation. 23561849

2013