TY - JOUR T1 - Homozygous variants in <em>SYCP2L</em> cause premature ovarian insufficiency JF - Journal of Medical Genetics JO - J Med Genet DO - 10.1136/jmedgenet-2019-106789 SP - jmedgenet-2019-106789 AU - Wen-Bin He AU - Chen Tan AU - Ya-Xin Zhang AU - Lan-Lan Meng AU - Fei Gong AU - Guang-Xiu Lu AU - Ge Lin AU - Juan Du AU - Yue-Qiu Tan Y1 - 2020/04/17 UR - http://jmg.bmj.com/content/early/2020/04/17/jmedgenet-2019-106789.abstract N2 - Background The genetic causes of the majority of cases of female infertility caused by premature ovarian insufficiency (POI) are unknown.Objective To identify the genetic causes of POI in 110 patients.Methods Whole-exome sequencing was performed on 110 patients with POI, and putative disease-causative variants were validated by Sanger sequencing. Bioinformatic and in vitro functional analyses were performed for functional characterisation of the identified candidate disease-causative variants.Results We identified two homozygous variants (NM_001040274: c.150_151del (p.Ser52Profs*7), c.999A&gt;G (p.Ile333Met)) in SYCP2L in two patients, which had co-segregated with POI in these families. Bioinformatic analysis predicted that the two variants are deleterious, and in vitro functional analysis showed that mutant SYCP2L proteins exhibited mislocalisation and loss of function.Conclusions SYCP2L is a novel gene found to be responsible for human POI. Our findings provide a potential molecular marker for POI and improve the understanding of the genetic basis of female infertility. ER -