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BRENDA support

Literature summary for 3.3.2.10 extracted from

  • Kullmann, S.; Binner, P.; Rackebrandt, K.; Huge, A.; Haltern, G.; Lankisch, M.; Fueth, R.; von Hodenberg, E.; Bestehorn, H.P.; Scheffold, T.
    Variation in the human soluble epoxide hydrolase gene and risk of restenosis after percutaneous coronary intervention (2009), BMC Cardiovasc. Disord., 9, 48.
    View publication on PubMedView publication on EuropePMC

Cloned(Commentary)

Cloned (Comment) Organism
genotyping of coronary heart disease patients Homo sapiens

Protein Variants

Protein Variants Comment Organism
K55R naturally occuring polymorphism, rs41507953, the mutation is not associated with restenosis after percutaneous coronary intervention, with incidence of coronary heart disease, or with an increased risk of hypertension and therefore, can not serve as a predictor for risk of coronary heart disease or restenosis after percutaneous coronary intervention Homo sapiens

Localization

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

Organism

Organism UniProt Comment Textmining
Homo sapiens P34913 gene EPHX2
-