DisGeNET - a database of gene-disease associations

GSS, glutathione synthetase, 2937

N. diseases: 73; N. variants: 20

Source: ALL

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Variant

Gene

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs121909307

Entrez Id:	2937
Gene Symbol:	GSS

GSS

CUI:	C0398746
Disease:

Gluthathione synthetase deficiency

0.700

CausalMutation

CLINVAR

Genotype, enzyme activity, glutathione level, and clinical phenotype in patients with glutathione synthetase deficiency.

15717202

2005

dbSNP:

rs121909307

Entrez Id:	2937
Gene Symbol:	GSS

GSS

CUI:	C0398746
Disease:

Gluthathione synthetase deficiency

0.700

CausalMutation

CLINVAR

Mutations in the glutathione synthetase gene cause 5-oxoprolinuria.

8896573

1996

dbSNP:

rs121909307

Entrez Id:	2937
Gene Symbol:	GSS

GSS

CUI:	C0398746
Disease:

Gluthathione synthetase deficiency

0.700

CausalMutation

CLINVAR

Five Chinese patients with 5-oxoprolinuria due to glutathione synthetase and 5-oxoprolinase deficiencies.

25851806

2015

dbSNP:

rs121909307

Entrez Id:	2937
Gene Symbol:	GSS

GSS

CUI:	C0398746
Disease:

Gluthathione synthetase deficiency

0.700

CausalMutation

CLINVAR

Acetaminophen-induced hepatotoxicity in a glutathione synthetase-deficient patient.

17479648

2007

dbSNP:

rs1555889738

Entrez Id:	2937;57644
Gene Symbol:	GSS;MYH7B

GSS;MYH7B

CUI:	C0398746
Disease:

Gluthathione synthetase deficiency

0.700

CausalMutation

CLINVAR

Genotype, enzyme activity, glutathione level, and clinical phenotype in patients with glutathione synthetase deficiency.

15717202

2005

dbSNP:

rs1555889738

Entrez Id:	2937;57644
Gene Symbol:	GSS;MYH7B

GSS;MYH7B

CUI:	C0398746
Disease:

Gluthathione synthetase deficiency

0.700

CausalMutation

CLINVAR

Diagnostics in patients with glutathione synthetase deficiency but without mutations in the exons of the GSS gene.

14635114

2003

dbSNP:

rs2273684

Entrez Id:	2937
Gene Symbol:	GSS

GSS

CUI:	C0017654
Disease:

Glomerular Filtration Rate

0.700

GeneticVariation

GWASCAT

A catalog of genetic loci associated with kidney function from analyses of a million individuals.

31152163

2019

dbSNP:

rs2273684

Entrez Id:	2937
Gene Symbol:	GSS

GSS

CUI:	C0017654
Disease:

Glomerular Filtration Rate

0.700

GeneticVariation

GWASCAT

Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies.

30604766

2019

dbSNP:

rs2273684

Entrez Id:	2937
Gene Symbol:	GSS

GSS

CUI:	C0017654
Disease:

Glomerular Filtration Rate

0.700

GeneticVariation

GWASCAT

Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis.

31015462

2019

dbSNP:

rs752560204

Entrez Id:	2937
Gene Symbol:	GSS

GSS

CUI:	C0398746
Disease:

Gluthathione synthetase deficiency

0.700

CausalMutation

CLINVAR

Mutations in the glutathione synthetase gene cause 5-oxoprolinuria.

8896573

1996

dbSNP:

rs28938472

Entrez Id:	2937
Gene Symbol:	GSS

GSS

CUI:	C0398746
Disease:

Gluthathione synthetase deficiency

0.800

CausalMutation

CLINVAR

dbSNP:

rs28938472

Entrez Id:	2937
Gene Symbol:	GSS

GSS

CUI:	C1856399
Disease:

Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to

0.700

CausalMutation

CLINVAR

dbSNP:

rs121909308

Entrez Id:	2937
Gene Symbol:	GSS

GSS

CUI:	C0398746
Disease:

Gluthathione synthetase deficiency

0.800

CausalMutation

CLINVAR

dbSNP:

rs121909309

Entrez Id:	2937
Gene Symbol:	GSS

GSS

CUI:	C0398746
Disease:

Gluthathione synthetase deficiency

0.800

CausalMutation

CLINVAR

dbSNP:

rs28936396

Entrez Id:	2937
Gene Symbol:	GSS

GSS

CUI:	C0398746
Disease:

Gluthathione synthetase deficiency

0.700

CausalMutation

CLINVAR

dbSNP:

rs75863437

Entrez Id:	2937
Gene Symbol:	GSS

GSS

CUI:	C0398746
Disease:

Gluthathione synthetase deficiency

0.700

CausalMutation

CLINVAR

dbSNP:

rs121909308

Entrez Id:	2937
Gene Symbol:	GSS

GSS

CUI:	C0398746
Disease:

Gluthathione synthetase deficiency

0.800

GeneticVariation

UNIPROT

Mutations in the glutathione synthetase gene cause 5-oxoprolinuria.

8896573

1996

dbSNP:

rs121909308

Entrez Id:	2937
Gene Symbol:	GSS

GSS

CUI:	C0398746
Disease:

Gluthathione synthetase deficiency

0.800

GeneticVariation

UNIPROT

Recurrent Isolated Neonatal Hemolytic Anemia: Think About Glutathione Synthetase Deficiency.

27581854

2016

dbSNP:

rs121909308

Entrez Id:	2937
Gene Symbol:	GSS

GSS

CUI:	C0398746
Disease:

Gluthathione synthetase deficiency

0.800

GeneticVariation

UNIPROT

Missense mutations in the human glutathione synthetase gene result in severe metabolic acidosis, 5-oxoprolinuria, hemolytic anemia and neurological dysfunction.

9215686

1997

dbSNP:

rs121909309

Entrez Id:	2937
Gene Symbol:	GSS

GSS

CUI:	C0398746
Disease:

Gluthathione synthetase deficiency

0.800

GeneticVariation

UNIPROT

Recurrent Isolated Neonatal Hemolytic Anemia: Think About Glutathione Synthetase Deficiency.

27581854

2016

dbSNP:

rs121909309

Entrez Id:	2937
Gene Symbol:	GSS

GSS

CUI:	C0398746
Disease:

Gluthathione synthetase deficiency

0.800

GeneticVariation

UNIPROT

Missense mutations in the human glutathione synthetase gene result in severe metabolic acidosis, 5-oxoprolinuria, hemolytic anemia and neurological dysfunction.

9215686

1997

dbSNP:

rs121909309

Entrez Id:	2937
Gene Symbol:	GSS

GSS

CUI:	C0398746
Disease:

Gluthathione synthetase deficiency

0.800

GeneticVariation

UNIPROT

Mutations in the glutathione synthetase gene cause 5-oxoprolinuria.

8896573

1996

dbSNP:

rs17310467

Entrez Id:	2937;57644
Gene Symbol:	GSS;MYH7B

GSS;MYH7B

CUI:	C0919677
Disease:

Protein C measurement

0.800

GeneticVariation

GWASDB

Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project.

22443383

2012

dbSNP:

rs17310467

Entrez Id:	2937;57644
Gene Symbol:	GSS;MYH7B

GSS;MYH7B

CUI:	C1168438
Disease:

Protein C antigen measurement

0.800

GeneticVariation

GWASCAT

Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project.

22443383

2012

dbSNP:

rs17310467

Entrez Id:	2937;57644
Gene Symbol:	GSS;MYH7B

GSS;MYH7B

CUI:	C0919677
Disease:

Protein C measurement

0.800

GeneticVariation

GWASCAT

Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project.

22443383

2012