Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 215
Gene Symbol: ABCD1
ABCD1
0.010 Biomarker phenotype BEFREE This report examines links between biochemical markers (ammonia, glutamine, arginine, citrulline) and primary neuropsychological endpoints in three distal disorders, argininosuccinic acid synthetase deficiency (ASD or citrullinemia type I), argininosuccinic acid lyase deficiency (ASA or ALD), and arginase deficiency (ARGD). 29423830 2018
Entrez Id: 414
Gene Symbol: ARSD
ARSD
0.010 GeneticVariation phenotype BEFREE Laboratory results and test scores from neuropsychological evaluations were assessed in 145 study participants, ages 3 years and older, with ASD (n = 64), ASA (n = 65) and ARGD (n = 16). 29423830 2018
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
0.010 AlteredExpression phenotype BEFREE Blocking arginases using <i>S</i>-(2-boronoethyl)-l-cysteine (BEC) 18 h before ischemia mimicked arginase deficiency by reducing kidney injury, histopathological changes and kidney injury marker-1 expression, renal apoptosis, kidney inflammatory cell recruitment and inflammatory cytokines, and kidney oxidative stress; increasing kidney nitric oxide (NO) production and endothelial NO synthase (eNOS) phosphorylation, kidney peroxisome proliferator-activated receptor-γ coactivator-1α expression, and mitochondrial ATP; and preserving kidney mitochondrial ultrastructure compared with vehicle-treated IRI mice. 28515179 2017
Entrez Id: 435
Gene Symbol: ASL
ASL
0.010 GeneticVariation phenotype BEFREE We found a total of 55 cases of UCDs in Finland by 2007: 30 cases of ornithine transcarbamylase (OTC) deficiency, 20 of argininosuccinate lyase (ASL) deficiency, 3 of carbamyl phosphate synthetase (CPS-I) deficiency, 1 of type 1 citrullinaemia and 1 of argininaemia. 18616627 2008
Entrez Id: 5009
Gene Symbol: OTC
OTC
0.010 GeneticVariation phenotype BEFREE We found a total of 55 cases of UCDs in Finland by 2007: 30 cases of ornithine transcarbamylase (OTC) deficiency, 20 of argininosuccinate lyase (ASL) deficiency, 3 of carbamyl phosphate synthetase (CPS-I) deficiency, 1 of type 1 citrullinaemia and 1 of argininaemia. 18616627 2008
Entrez Id: 4843
Gene Symbol: NOS2
NOS2
0.010 AlteredExpression phenotype BEFREE These results suggest that L-Cit formed by nNOS in L-Arg-loaded neuronal cells inhibits NOS activity and nNOS in these L-Arg-loaded cells functions as a NADPH oxidase to produce ROS, which may cause neurotoxicity in argininemia. 9742507 1998
Entrez Id: 4842
Gene Symbol: NOS1
NOS1
0.010 AlteredExpression phenotype BEFREE These results suggest that L-Cit formed by nNOS in L-Arg-loaded neuronal cells inhibits NOS activity and nNOS in these L-Arg-loaded cells functions as a NADPH oxidase to produce ROS, which may cause neurotoxicity in argininemia. 9742507 1998
Entrez Id: 1666
Gene Symbol: DECR1
DECR1
0.010 Biomarker phenotype BEFREE These results suggest that L-Cit formed by nNOS in L-Arg-loaded neuronal cells inhibits NOS activity and nNOS in these L-Arg-loaded cells functions as a NADPH oxidase to produce ROS, which may cause neurotoxicity in argininemia. 9742507 1998
Entrez Id: 9439
Gene Symbol: MED23
MED23
0.100 GeneticVariation phenotype CLINVAR Clinical phenotype, biochemical profile, and treatment in 19 patients with arginase 1 deficiency. 27038030 2016
Entrez Id: 9439
Gene Symbol: MED23
MED23
0.100 CausalMutation phenotype CLINVAR Clinical phenotype, biochemical profile, and treatment in 19 patients with arginase 1 deficiency. 27038030 2016
Entrez Id: 9439
Gene Symbol: MED23
MED23
0.100 CausalMutation phenotype CLINVAR Characterization and mRNA expression analysis of a novel ARG1 splicing mutation causing hyperargininemia. 26169240 2015
Entrez Id: 9439
Gene Symbol: MED23
MED23
0.100 GeneticVariation phenotype CLINVAR Novel complex re-arrangement of ARG1 commonly shared by unrelated patients with hyperargininemia. 24103480 2014
Entrez Id: 9439
Gene Symbol: MED23
MED23
0.100 CausalMutation phenotype CLINVAR Novel complex re-arrangement of ARG1 commonly shared by unrelated patients with hyperargininemia. 24103480 2014
Entrez Id: 9439
Gene Symbol: MED23
MED23
0.100 GeneticVariation phenotype CLINVAR Five novel mutations in ARG1 gene in Chinese patients of argininemia. 23859858 2013
Entrez Id: 9439
Gene Symbol: MED23
MED23
0.100 CausalMutation phenotype CLINVAR Arginase I deficiency: severe infantile presentation with hyperammonemia: more common than reported? 21802329 2012
Entrez Id: 9439
Gene Symbol: MED23
MED23
0.100 GeneticVariation phenotype CLINVAR Studies on the functional significance of a C-terminal S-shaped motif in human arginase type I: essentiality for cooperative effects. 18957279 2009
Entrez Id: 9439
Gene Symbol: MED23
MED23
0.100 CausalMutation phenotype CLINVAR Amino acids in CSF and plasma in hyperammonaemic coma due to arginase1 deficiency. 19052914 2008
Entrez Id: 9439
Gene Symbol: MED23
MED23
0.100 GeneticVariation phenotype CLINVAR Functional consequences of the G235R mutation in liver arginase leading to hyperargininemia. 11883902 2002
Entrez Id: 9439
Gene Symbol: MED23
MED23
0.100 CausalMutation phenotype CLINVAR Mouse model for human arginase deficiency. 12052859 2002
Entrez Id: 9439
Gene Symbol: MED23
MED23
0.100 CausalMutation phenotype CLINVAR Identification of a novel R21X mutation in the liver-type arginase gene (ARG1) in four Portuguese patients with argininemia. 10502833 1999
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
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: 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