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Published on: August 15, 2019
Nonsense variants of STAG2 result in distinct congenital anomalies
Hiromi Aoi1,2, Ming Lei1, Takeshi Mizuguchi1
1Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Abstract:
Herein, we report two female cases with novel nonsense mutations of STAG2 at Xq25, encoding stromal antigen 2, a component of the cohesion complex. Exome analysis identified c.3097 C>T, p.(Arg1033*) in Case 1 (a fetus with multiple congenital anomalies) and c.2229 G>A, p.(Trp743*) in Case 2 (a 7-year-old girl with white matter hypoplasia and cleft palate). X inactivation was highly skewed in both cases.
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