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Results 1 - 10 of 41 > >>
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Show all pathways known for 2.4.2.26Display the word mapDisplay the reaction diagram Show all sequences 2.4.2.26Adenoma, Pleomorphic 27732748 The relationship between proteoglycan inhibition via xylosyltransferase II silencing and the implantation of salivary pleomorphic adenoma. ongoing research
unassigned
2
0
Show all pathways known for 2.4.2.26Display the word mapDisplay the reaction diagram Show all sequences 2.4.2.26Astrocytoma 29157673 Circulating microRNAs as Biomarkers for Pediatric Astrocytomas. unassigned 0
Show all pathways known for 2.4.2.26Display the word mapDisplay the reaction diagram Show all sequences 2.4.2.26Cardiomyopathy, Dilated 17635914 Transforming growth factor beta1-regulated xylosyltransferase I activity in human cardiac fibroblasts and its impact for myocardial remodeling. ongoing research
unassigned
4
0
Show all pathways known for 2.4.2.26Display the word mapDisplay the reaction diagram Show all sequences 2.4.2.26Cataract 26027496 Homozygosity for frameshift mutations in XYLT2 result in a spondylo-ocular syndrome with bone fragility, cataracts, and hearing defects. causal interaction
unassigned
4
0
Show all pathways known for 2.4.2.26Display the word mapDisplay the reaction diagram Show all sequences 2.4.2.26Cataract 26987875 Spondyloocular Syndrome - Novel Mutations in XYLT2 Gene and Expansion of the Phenotypic Spectrum. causal interaction
diagnostic usage
ongoing research
unassigned
2
3
3
0
Show all pathways known for 2.4.2.26Display the word mapDisplay the reaction diagram Show all sequences 2.4.2.26Cataract 27320698 Corneal clouding, cataract, and colobomas with a novel missense mutation in B4GALT7-a review of eye anomalies in the linkeropathy syndromes. causal interaction
unassigned
4
0
Show all pathways known for 2.4.2.26Display the word mapDisplay the reaction diagram Show all sequences 2.4.2.26Cataract 27871115 Abnormal Proteoglycan Synthesis Due to Gene Defects Causes Skeletal Diseases with Overlapping Phenotypes. causal interaction
unassigned
3
0
Show all pathways known for 2.4.2.26Display the word mapDisplay the reaction diagram Show all sequences 2.4.2.26Cysts 17517600 Polycystic disease caused by deficiency in xylosyltransferase 2, an initiating enzyme of glycosaminoglycan biosynthesis. causal interaction
therapeutic application
unassigned
1
1
0
Show all pathways known for 2.4.2.26Display the word mapDisplay the reaction diagram Show all sequences 2.4.2.26Diabetes Complications 18789912 Identification of a xylosyltransferase II gene haplotype marker for diabetic nephropathy in type 1 diabetes. causal interaction
diagnostic usage
therapeutic application
unassigned
4
3
1
0
Show all pathways known for 2.4.2.26Display the word mapDisplay the reaction diagram Show all sequences 2.4.2.26Diabetes Mellitus, Type 1 16164625 Impact of polymorphisms in the genes encoding xylosyltransferase I and a homologue in type 1 diabetic patients with and without nephropathy. ongoing research
therapeutic application
unassigned
1
1
0
Results 1 - 10 of 41 > >>