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Literature summary for 3.3.2.9 extracted from

  • Kiran, M.; Chawla, Y.K.; Jain, M.; Kaur, J.
    Haplotypes of microsomal epoxide hydrolase and x-ray cross-complementing group 1 genes in Indian hepatocellular carcinoma patients (2009), DNA Cell Biol., 28, 573-577.
    View publication on PubMed

Cloned(Commentary)

Cloned (Comment) Organism
genotyping Homo sapiens

Protein Variants

Protein Variants Comment Organism
H139R the naturally occuring mutation is a risk factor for hepatocellular carcinoma with both control and chronic hepatitis-infected individuals, association of GSTT1 and GSTM1 null genotypes and mEPHX polymorphisms with hepatitis virus-related HCC risk in an Indian population. Frequencies in hepatocellular carcinoma, controls, and the chronic viral hepatitis subjects, respectively, overview Homo sapiens
Y133H naturally occuring mutation, frequencies in hepatocellular carcinoma, controls, and the chronic viral hepatitis subjects, respectively, overview Homo sapiens

Localization

Localization Comment Organism GeneOntology No. Textmining
microsome
-
Homo sapiens
-
-

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
Indian hepatocellular carcinoma patients
-

Source Tissue

Source Tissue Comment Organism Textmining
hepatoma cell
-
Homo sapiens
-
liver
-
Homo sapiens
-

Synonyms

Synonyms Comment Organism
mEPHX
-
Homo sapiens

General Information

General Information Comment Organism
malfunction association of GSTT1 and GSTM1 null genotypes and mEPHX polymorphisms with hepatitis virus-related HCC risk in an Indian population Homo sapiens