Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 383
Gene Symbol: ARG1
ARG1 		1.000 Biomarker phenotype CTD_human
Entrez Id: 383
Gene Symbol: ARG1
ARG1 		1.000 Biomarker phenotype CLINGEN On arginase and its participation in urea synthesis in the liver. 16747805 1944
Entrez Id: 383
Gene Symbol: ARG1
ARG1 		1.000 GeneticVariation phenotype BEFREE Molecular basis of argininemia. Identification of two discrete frame-shift deletions in the liver-type arginase gene. 2365823 1990
Entrez Id: 383
Gene Symbol: ARG1
ARG1 		1.000 Biomarker phenotype CLINGEN Molecular basis of argininemia. Identification of two discrete frame-shift deletions in the liver-type arginase gene. 2365823 1990
Entrez Id: 383
Gene Symbol: ARG1
ARG1 		1.000 GeneticVariation phenotype BEFREE Three novel mutations in the liver-type arginase gene in three unrelated Japanese patients with argininemia. 1463019 1992
Entrez Id: 383
Gene Symbol: ARG1
ARG1 		1.000 CausalMutation phenotype CLINVAR Molecular genetic study of human arginase deficiency. 1598908 1992
Entrez Id: 383
Gene Symbol: ARG1
ARG1 		1.000 GeneticVariation phenotype CLINVAR Molecular genetic study of human arginase deficiency. 1598908 1992
Entrez Id: 383
Gene Symbol: ARG1
ARG1 		1.000 Biomarker phenotype GENOMICS_ENGLAND Three novel mutations in the liver-type arginase gene in three unrelated Japanese patients with argininemia. 1463019 1992
Entrez Id: 383
Gene Symbol: ARG1
ARG1 		1.000 Biomarker phenotype CLINGEN Three novel mutations in the liver-type arginase gene in three unrelated Japanese patients with argininemia. 1463019 1992
Entrez Id: 383
Gene Symbol: ARG1
ARG1 		1.000 GeneticVariation phenotype UNIPROT Three novel mutations in the liver-type arginase gene in three unrelated Japanese patients with argininemia. 1463019 1992
Entrez Id: 383
Gene Symbol: ARG1
ARG1 		1.000 Biomarker phenotype CLINGEN Molecular genetic study of human arginase deficiency. 1598908 1992
Entrez Id: 383
Gene Symbol: ARG1
ARG1 		1.000 Biomarker phenotype GENOMICS_ENGLAND Molecular genetic study of human arginase deficiency. 1598908 1992
Entrez Id: 9439
Gene Symbol: MED23
MED23 		0.100 CausalMutation phenotype CLINVAR Molecular genetic study of human arginase deficiency. 1598908 1992
Entrez Id: 9439
Gene Symbol: MED23
MED23 		0.100 GeneticVariation phenotype CLINVAR Molecular genetic study of human arginase deficiency. 1598908 1992
Entrez Id: 383
Gene Symbol: ARG1
ARG1 		1.000 CausalMutation phenotype CLINVAR Identification of mutations (D128G, H141L) in the liver arginase gene of patients with hyperargininemia. 7981719 1994
Entrez Id: 9439
Gene Symbol: MED23
MED23 		0.100 CausalMutation phenotype CLINVAR Identification of mutations (D128G, H141L) in the liver arginase gene of patients with hyperargininemia. 7981719 1994
Entrez Id: 383
Gene Symbol: ARG1
ARG1 		1.000 GeneticVariation phenotype CLINVAR Molecular basis of phenotypic variation in patients with argininemia. 7649538 1995
Entrez Id: 383
Gene Symbol: ARG1
ARG1 		1.000 GeneticVariation phenotype UNIPROT Molecular basis of phenotypic variation in patients with argininemia. 7649538 1995
Entrez Id: 383
Gene Symbol: ARG1
ARG1 		1.000 CausalMutation phenotype CLINVAR Molecular basis of phenotypic variation in patients with argininemia. 7649538 1995
Entrez Id: 9439
Gene Symbol: MED23
MED23 		0.100 GeneticVariation phenotype CLINVAR Molecular basis of phenotypic variation in patients with argininemia. 7649538 1995
Entrez Id: 9439
Gene Symbol: MED23
MED23 		0.100 CausalMutation phenotype CLINVAR Molecular basis of phenotypic variation in patients with argininemia. 7649538 1995
Entrez Id: 383
Gene Symbol: ARG1
ARG1 		1.000 GeneticVariation phenotype CLINVAR Loss of function mutations in conserved regions of the human arginase I gene. 8902193 1996
Entrez Id: 383
Gene Symbol: ARG1
ARG1 		1.000 CausalMutation phenotype CLINVAR Loss of function mutations in conserved regions of the human arginase I gene. 8902193 1996
Entrez Id: 9439
Gene Symbol: MED23
MED23 		0.100 CausalMutation phenotype CLINVAR Loss of function mutations in conserved regions of the human arginase I gene. 8902193 1996
Entrez Id: 9439
Gene Symbol: MED23
MED23 		0.100 GeneticVariation phenotype CLINVAR Loss of function mutations in conserved regions of the human arginase I gene. 8902193 1996