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Results 1 - 10 of 177 > >>
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Show all pathways known for 2.2.1.2Display the word mapDisplay the reaction diagram Show all sequences 2.2.1.2Acatalasia 11390181 Relationship between posttranslational modification of transaldolase and catalase deficiency in UV-sensitive repair-deficient xeroderma pigmentosum fibroblasts and SV40-transformed human cells. causal interaction
ongoing research
unassigned
2
2
0
Show all pathways known for 2.2.1.2Display the word mapDisplay the reaction diagram Show all sequences 2.2.1.2Alopecia 28409271 Unique presentation of cutis laxa with Leigh-like syndrome due to ECHS1 deficiency. causal interaction
unassigned
4
0
Show all pathways known for 2.2.1.2Display the word mapDisplay the reaction diagram Show all sequences 2.2.1.2Anemia 19299175 Transaldolase deficiency in two new patients with a relative mild phenotype. causal interaction
unassigned
4
0
Show all pathways known for 2.2.1.2Display the word mapDisplay the reaction diagram Show all sequences 2.2.1.2Anemia 24497183 Clinical and molecular characteristics of two transaldolase-deficient patients. causal interaction
diagnostic usage
unassigned
4
4
0
Show all pathways known for 2.2.1.2Display the word mapDisplay the reaction diagram Show all sequences 2.2.1.2Anemia 26238251 Transaldolase Deficiency: A New Case Expands the Phenotypic Spectrum. causal interaction
diagnostic usage
unassigned
4
3
0
Show all pathways known for 2.2.1.2Display the word mapDisplay the reaction diagram Show all sequences 2.2.1.2Anemia, Hemolytic 21913417 [A newly discovered metabolic diseases due to defects in the pentose pathway]. causal interaction
unassigned
4
0
Show all pathways known for 2.2.1.2Display the word mapDisplay the reaction diagram Show all sequences 2.2.1.2arylsulfatase (type i) deficiency 27106218 Antenatal manifestations of inborn errors of metabolism: autopsy findings suggestive of a metabolic disorder. causal interaction
unassigned
4
0
Show all pathways known for 2.2.1.2Display the word mapDisplay the reaction diagram Show all sequences 2.2.1.2aspartate-ammonia ligase deficiency 27106218 Antenatal manifestations of inborn errors of metabolism: autopsy findings suggestive of a metabolic disorder. causal interaction
unassigned
4
0
Show all pathways known for 2.2.1.2Display the word mapDisplay the reaction diagram Show all sequences 2.2.1.2Autoimmune Diseases 33848380 High Transaldolase 1 expression predicts poor survival of patients with upper tract urothelial carcinoma. causal interaction
diagnostic usage
ongoing research
therapeutic application
4
4
4
2
Show all pathways known for 2.2.1.2Display the word mapDisplay the reaction diagram Show all sequences 2.2.1.2Breast Neoplasms 34282517 SLC1A5 co-expression with TALDO1 associates with endocrine therapy failure in estrogen receptor-positive breast cancer. causal interaction
diagnostic usage
ongoing research
therapeutic application
3
4
2
4
Results 1 - 10 of 177 > >>