在患有多种先天性异常和发育迟缓的个体中发现ARHGEF40中p.a g225残基的错义变异。

IF 3.3 Q2 GENETICS & HEREDITY HGG Advances Pub Date : 2025-01-20 DOI:10.1016/j.xhgg.2025.100408
Melanie P Napier, Erin Ryan, Adi Reich, Joshua A Suhl, Diane Masser-Frye, Marilyn Jones, Celese Beaudreau, Nathaniel Robin, Dana Goodloe, Leandra Folk, Michelle M Morrow, Deanna Alexis Carere
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引用次数: 0

摘要

ARHGEF40基因,也被称为SOLO,编码rhoa靶向鸟嘌呤核苷酸交换因子(GEF),目前被认为是与疾病有潜在关系的候选基因。我们的实验室已经在多个不相关的个体中证实了ARHGEF40蛋白p.a g225位点的变异,这些个体的表型包括畸形特征、先天性异常和神经发育异常。在这里,我们提供了两个携带p.a g225从头变异体并共享高度相似表型的个体的遗传和表型信息。该报告提示该氨基酸位置的变异与常染色体显性疾病之间的关系,需要进一步的研究来表征这种疾病-基因关系并阐明疾病机制。
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Missense variants at the p.Arg225 residue in ARHGEF40 identified in individuals with multiple congenital anomalies and developmental delay.

The ARHGEF40 gene, also known as SOLO, encodes a RhoA-targeting guanine nucleotide exchange factor (GEF) and is currently considered a candidate gene with a potential relationship to disease. Our laboratory has confirmed variants at position p.Arg225 of the ARHGEF40 protein in multiple unrelated individuals with a phenotype including dysmorphic features, congenital anomalies and neurodevelopmental abnormalities. Here, we provide genetic and phenotypic information for two individuals harboring de novo variants at p.Arg225 and sharing a highly similar phenotype. This report suggests a relationship between variants at this amino acid position and autosomal dominant disease, and further studies will be needed to characterize this disease-gene relationship and elucidate the disease mechanism.

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来源期刊
HGG Advances
HGG Advances Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
4.30
自引率
4.50%
发文量
69
审稿时长
14 weeks
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