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Literature summary for 1.3.3.6 extracted from

  • Carrozzo, R.; Bellini, C.; Lucioli, S.; Deodato, F.; Cassandrini, D.; Cassanello, M.; Caruso, U.; Rizzo, C.; Rizza, T.; Napolitano, M.L.; Wanders, R.J.; Jakobs, C.; Bruno, C.; Santorelli, F.M.; Dionisi-Vici, C.; Bonioli, E.
    Peroxisomal acyl-CoA-oxidase deficiency: two new cases (2008), Am. J. Med. Genet. A, 146A, 1676-1681.
    View publication on PubMed

Protein Variants

Protein Variants Comment Organism
G231V the mutation in combination with skipping of exon 13 leads to peroxisomal acyl-CoA oxidase deficiency Homo sapiens

Localization

Localization Comment Organism GeneOntology No. Textmining
peroxisome
-
Homo sapiens 5777
-

Organism

Organism UniProt Comment Textmining
Homo sapiens Q15067
-
-

Source Tissue

Source Tissue Comment Organism Textmining
fibroblast
-
Homo sapiens
-

Synonyms

Synonyms Comment Organism
ACOX1
-
Homo sapiens
acyl-CoA-oxidase
-
Homo sapiens
straight chain acyl-CoA oxidase
-
Homo sapiens