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EC Number Disease PubMed ID Title of Publication Category Confidence Level
Show all pathways known for 2.9.1.2Display the word mapDisplay the reaction diagram Show all sequences 2.9.1.2Brain Diseases 26115735 Selenoprotein biosynthesis defect causes progressive encephalopathy with elevated lactate. causal interaction
unassigned
3
0
Show all pathways known for 2.9.1.2Display the word mapDisplay the reaction diagram Show all sequences 2.9.1.2Brain Diseases 26805434 Pontocerebellar hypoplasia type 2D and optic nerve atrophy further expand the spectrum associated with selenoprotein biosynthesis deficiency. causal interaction
unassigned
4
0
Show all pathways known for 2.9.1.2Display the word mapDisplay the reaction diagram Show all sequences 2.9.1.2Infections 26975431 Selenoproteins of African trypanosomes are dispensable for parasite survival in a mammalian host. ongoing research
therapeutic application
unassigned
3
1
0
Show all pathways known for 2.9.1.2Display the word mapDisplay the reaction diagram Show all sequences 2.9.1.2Hepatitis, Autoimmune 28690845 Diagnostic autoantibodies for autoimmune liver diseases. causal interaction
unassigned
1
0
Show all pathways known for 2.9.1.2Display the word mapDisplay the reaction diagram Show all sequences 2.9.1.2Infections 28810614 Evolution of correlation between Helicobacter pylori infection and autoimmune liver disease. diagnostic usage
unassigned
2
0
Show all pathways known for 2.9.1.2Display the word mapDisplay the reaction diagram Show all sequences 2.9.1.2Cerebellar Ataxia 29464431 A SEPSECS mutation in a 23-year-old woman with microcephaly and progressive cerebellar ataxia. causal interaction
ongoing research
unassigned
2
1
0
Show all pathways known for 2.9.1.2Display the word mapDisplay the reaction diagram Show all sequences 2.9.1.2Microcephaly 29464431 A SEPSECS mutation in a 23-year-old woman with microcephaly and progressive cerebellar ataxia. causal interaction
ongoing research
unassigned
2
1
0
Show all pathways known for 2.9.1.2Display the word mapDisplay the reaction diagram Show all sequences 2.9.1.2Neurodegenerative Diseases 29709707 Consequences of mutations and inborn errors of selenoprotein biosynthesis and functions. causal interaction
unassigned
4
0
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