이 유전자는 막 관련 효소인 아데닐시클라아제6를 암호화하고 2차 메신저 순환 아데노신 모노인산염(cAMP)의 형성을 촉진한다.이 유전자의 발현은 일부 종양뿐만 아니라 정상 갑상선과 뇌 조직에서도 발견되며, 하나의 과기능 갑상선 종양에서 정상 갑상선 조직보다 현저하게 더 높다.대체 스플리싱은 2가지 대본 변형을 생성한다.[5]
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