이 유전자, CYP2B6는 효소들의 사이토크롬 P450의 구성원을 암호화하고 있다.시토크롬 P450 단백질은 약물 대사 및 콜레스테롤, 스테로이드 및 기타 지질의 합성에 관련된 많은 반응을 촉진하는 단옥시겐이다.이 단백질은 소포체 망막까지 국소화되며 그 발현이 페노바르비탈에 의해 유도된다.이 효소는 항암제 사이클로인산아미드, 이프인산아미드와 같은 일부 외국균제를 대사하는 것으로 알려져 있다.[5]null
유전자
이 유전자에 대한 대본 변형은 설명되었지만, 이 대본이 실제로 이 유전자에 의해 생성되는지 아니면 밀접하게 연관된 유사 유전자인 CYP2B7에 의해 생성되는지는 확인되지 않았다.유전자와 유사유전자는 모두 19q 염색체의 CYP2A, CYP2B, CYP2F 하위가족에서 나온 사이토크롬 P450 유전자의 큰 군집 안에서 발견되는 CYP2A 유사유전자의 중간에 위치한다.[5]
^알카탄, A, & 알살라멘, E.(2021년).Clopidogrel 치료의 임상적 효과와 안전에 영향을 미치는 Phase-I 대사 효소와 관련된 유전자의 다형성.약물 대사 및 독성학에 대한 전문가 의견, 10.1080/17425255.2021.1925249.온라인 게시를 진행하십시오.https://doi.org/10.1080/17425255.2021.1925249
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