ALG8, ALG8 alpha-1,3-glucosyltransferase, 79053

N. diseases: 64; N. variants: 8
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Congenital disorder of glycosylation type 1H
0.740 Biomarker disease GENOMICS_ENGLAND Nonimmune hydrops fetalis and congenital disorders of glycosylation: A systematic literature review. 31420886 2020
Congenital disorder of glycosylation type 1H
0.740 Biomarker disease GENOMICS_ENGLAND Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes. 27604308 2016
Congenital disorder of glycosylation type 1H
0.740 Biomarker disease BEFREE ALG8-CDG (= CDG-Ih) is one of the less frequently reported types of CDG, maybe due to its severe multi-organ involvement with coagulation disturbances, edema, massive gastrointestinal protein loosing enteropathy, cataracts, and often early death. 26066342 2015
Congenital disorder of glycosylation type 1H
0.740 GeneticVariation disease BEFREE Severe ALG8-CDG (CDG-Ih) associated with homozygosity for two novel missense mutations detected by exome sequencing of candidate genes. 22306853 2012
Congenital disorder of glycosylation type 1H
0.740 Biomarker disease GENOMICS_ENGLAND One of them, ALG8 deficiency (CDG Ih), leads to protein N-glycosylation defects caused by malfunction of glucosyltransferase 2 (Dol-P-Glc:Glc1-Man(9)-GlcNAc(2)-P-P-Dol glucosyltransferase) resulting in inefficient addition of the second glucose residue onto lipid-linked oligosaccharides. 19688606 2009
Congenital disorder of glycosylation type 1H
0.740 Biomarker disease BEFREE One of them, ALG8 deficiency (CDG Ih), leads to protein N-glycosylation defects caused by malfunction of glucosyltransferase 2 (Dol-P-Glc:Glc1-Man(9)-GlcNAc(2)-P-P-Dol glucosyltransferase) resulting in inefficient addition of the second glucose residue onto lipid-linked oligosaccharides. 19688606 2009
Congenital disorder of glycosylation type 1H
0.740 GeneticVariation disease BEFREE Novel ALG8 mutations expand the clinical spectrum of congenital disorder of glycosylation type Ih. 19648040 2009
Congenital disorder of glycosylation type 1H
0.740 GeneticVariation disease UNIPROT Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency). 15235028 2004
Congenital disorder of glycosylation type 1H
0.740 Biomarker disease GENOMICS_ENGLAND Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency). 15235028 2004
Congenital disorder of glycosylation type 1H
0.740 CausalMutation disease CLINVAR
Congenital disorder of glycosylation type 1H
0.740 GeneticVariation disease CLINVAR
Congenital disorder of glycosylation type 1H
0.740 Biomarker disease CTD_human
CUI: C0158683
Disease: Polycystic liver disease
Polycystic liver disease
0.310 Biomarker disease BEFREE These mutations, together with the newly identified ones in SEC61B and Alpha-1,3-Glucosyltransferase (ALG8), can be found in ∼50% of patients with isolated polycystic liver disease. 30652979 2019
CUI: C0158683
Disease: Polycystic liver disease
Polycystic liver disease
0.310 Biomarker disease GENOMICS_ENGLAND Prevalence Estimates of Polycystic Kidney and Liver Disease by Population Sequencing. 30135240 2018
CUI: C1691228
Disease: Cystic Kidney Diseases
Cystic Kidney Diseases
0.300 Biomarker group GENOMICS_ENGLAND Prevalence Estimates of Polycystic Kidney and Liver Disease by Population Sequencing. 30135240 2018
CUI: C4551631
Disease: Cystic liver disease
Cystic liver disease
0.300 Biomarker disease GENOMICS_ENGLAND Prevalence Estimates of Polycystic Kidney and Liver Disease by Population Sequencing. 30135240 2018
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.300 Biomarker disease PSYGENET Among the cognate genes, six including ALG8, DGKE, GNA12, KLF11, LRPAP1, and MMAB are related to multiple genetic diseases such as depressive disorder and Type-II diabetes. 22348086 2012
POLYCYSTIC LIVER DISEASE 3 WITH OR WITHOUT KIDNEY CYSTS
0.300 Biomarker disease GENOMICS_ENGLAND Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency). 15235028 2004
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
0.100 Biomarker phenotype HPO
CUI: C0002871
Disease: Anemia
Anemia
0.100 Biomarker disease HPO
CUI: C0003578
Disease: Apnea
Apnea
0.100 CausalMutation phenotype CLINVAR
CUI: C0003962
Disease: Ascites
Ascites
0.100 Biomarker phenotype HPO
CUI: C0008370
Disease: Cholestasis
Cholestasis
0.100 Biomarker disease HPO
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot
0.100 Biomarker disease HPO
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism
0.100 Biomarker disease HPO