Literature summary for 3.3.2.10 extracted from

Gschwendtner, A.; Ripke, S.; Freilinger, T.; Lichtner, P.; Mueller-Myhsok, B.; Wichmann, H.E.; Meitinger, T.; Dichgans, M.
Genetic variation in soluble epoxide hydrolase (EPHX2) is associated with an increased risk of ischemic stroke in white Europeans (2008), Stroke, 39, 1593-1596.

Search for more literature for 3.3.2.10

Application

Application	Comment	Organism
medicine	genetic variation in or near the EPHX2 gene contributes to the risk of ischemic stroke	Homo sapiens

Protein Variants

Protein Variants	Comment	Organism
R287Q	the mutation reduces the activity of sEH, there is an association with increased risk for ischemic stroke for the 287Q allele	Homo sapiens

Organism

Organism	UniProt	Comment	Textmining
Homo sapiens	-	-	-

Synonyms

Synonyms	Comment	Organism
EPHX2	-	Homo sapiens
SEH	-	Homo sapiens

Use of this online version of BRENDA is free under the CC BY 4.0 license. See terms of use for full details.

Release 2023.1 (January 2023)