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Results 1 - 10 of 198 > >>
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Show all pathways known for 2.6.1.44Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.44alanine-glyoxylate transaminase deficiency 1496924 Alanine glyoxylate aminotransferase deficiency: biochemical and molecular genetic lessons from the study of a human disease. causal interaction
ongoing research
unassigned
4
2
0
Show all pathways known for 2.6.1.44Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.44alanine-glyoxylate transaminase deficiency 1763934 [Hepatic and renal transplantation in the treatment of type I hyperoxaluria] causal interaction
unassigned
4
0
Show all pathways known for 2.6.1.44Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.44alanine-glyoxylate transaminase deficiency 12352890 Renal allograft survival in patients with oxalosis. causal interaction
diagnostic usage
unassigned
4
3
0
Show all pathways known for 2.6.1.44Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.44alanine-glyoxylate transaminase deficiency 16904473 Treatment of primary hyperoxaluria type 1 with sequential liver and kidney transplants from the same living donor. causal interaction
diagnostic usage
unassigned
4
3
0
Show all pathways known for 2.6.1.44Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.44alanine-glyoxylate transaminase deficiency 27512303 Recurrent truncating mutations in alanine-glyoxylate aminotransferase gene in two South Indian families with primary hyperoxaluria type 1 causing later onset end-stage kidney disease. causal interaction
unassigned
4
0
Show all pathways known for 2.6.1.44Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.44Arthritis, Rheumatoid 28357606 Genetic variations in the alanine-glyoxylate aminotransferase 2 (AGXT2) gene and dimethylarginines levels in rheumatoid arthritis. causal interaction
unassigned
2
0
Show all pathways known for 2.6.1.44Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.44Atherosclerosis 25620171 Missense variants of the alanine: glyoxylate aminotransferase 2 gene correlated with carotid atherosclerosis in the Japanese population. causal interaction
therapeutic application
unassigned
4
2
0
Show all pathways known for 2.6.1.44Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.44Atherosclerosis 34320345 Dysregulated oxalate metabolism is a driver and therapeutic target in atherosclerosis. ongoing research
therapeutic application
unassigned
3
2
0
Show all pathways known for 2.6.1.44Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.44Atrial Fibrillation 26984639 Associations of functional alanine-glyoxylate aminotransferase 2 gene variants with atrial fibrillation and ischemic stroke. causal interaction
ongoing research
therapeutic application
unassigned
3
2
1
0
Show all pathways known for 2.6.1.44Display the word mapDisplay the reaction diagram Show all sequences 2.6.1.44Carcinoma, Hepatocellular 26294768 AGXT2L1 is down-regulated in heptocellular carcinoma and associated with abnormal lipogenesis. causal interaction
diagnostic usage
ongoing research
therapeutic application
4
4
3
1
Results 1 - 10 of 198 > >>