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Literature summary extracted from

  • Simon-Sanchez, J.; Singleton, A.B.
    Sequencing analysis of OMI/HTRA2 shows previously reported pathogenic mutations in neurologically normal controls (2008), Hum. Mol. Genet., 17, 1988-1993.
    View publication on PubMed

Application

EC Number Application Comment Organism
3.4.21.108 medicine mutations of the OMI/HTRA2 gene are linked to Parkinsons disease Homo sapiens

Protein Variants

EC Number Protein Variants Comment Organism
3.4.21.108 A141S HtrA2 variant Homo sapiens
3.4.21.108 A227S HtrA2 variant Homo sapiens
3.4.21.108 F172V HtrA2 variant Homo sapiens
3.4.21.108 G399S HtrA2 variant Homo sapiens
3.4.21.108 L118L HtrA2 variant Homo sapiens
3.4.21.108 L367L HtrA2 variant Homo sapiens
3.4.21.108 additional information rs2231248, rs2241027 and rs2241028, HtrA2 variants Homo sapiens
3.4.21.108 P128L HtrA2 variant Homo sapiens
3.4.21.108 R209R HtrA2 variant Homo sapiens
3.4.21.108 V109V HtrA2 variant Homo sapiens
3.4.21.108 W12C HtrA2 variant Homo sapiens

Molecular Weight [Da]

EC Number Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
3.4.21.108 48840
-
-
 Homo sapiens

Organism

EC Number Organism UniProt Comment Textmining
3.4.21.108 Homo sapiens O43464
-
-

Synonyms

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