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Literature summary extracted from

  • Ross, O.A.; Soto, A.I.; Vilarino-Gueell, C.; Heckman, M.G.; Diehl, N.N.; Hulihan, M.M.; Aasly, J.O.; Sando, S.; Gibson, J.M.; Lynch, T.; Krygowska-Wajs, A.; Opala, G.; Barcikowska, M.; Czyzewski, K.; Uitti, R.J.; Wszolek, Z.K.; Farrer, M.J.
    Genetic variation of Omi/HtrA2 and Parkinsons disease (2008), Parkinsonism Relat. Disord., 14, 539-543.
    View publication on PubMed

Application

EC Number Application Comment Organism
3.4.21.108 medicine the study does not support a role of HtrA2 variants in the pathogenesis of Parkinsons disease Homo sapiens

Localization

EC Number Localization Comment Organism GeneOntology No. Textmining
3.4.21.108 mitochondrion
-
 Homo sapiens 5739
-

Organism

EC Number Organism UniProt Comment Textmining
3.4.21.108 Homo sapiens
-
-
-

Synonyms

EC Number Synonyms Comment Organism
3.4.21.108 Omi/HtrA2
-
 Homo sapiens
3.4.21.108 serine protease
-
 Homo sapiens