这个基因编码一个叉头转录因子。该蛋白包含一个叉头DNA结合域,可能在卵巢发育和功能中发挥作用。该基因的突变是引起睑裂综合征和卵巢早衰的原因3。
This gene encodes a forkhead transcription factor. The protein contains a fork-head DNA-binding domain and may play a role in ovarian development and function. Mutations in this gene are a cause of blepharophimosis syndrome and premature ovarian failure 3.

基因名:FOXL2
别名:BPES,BPES1,PFRK,PINTO,POF3
基因ID:668
Chromosome:
(GRCh37)
3 Start: 138663066 End: 138665982 Strand: -1
信号通路: 基因组不稳定