| Literature DB >> 26299366 |
Akemi J Tanaka1, Megan T Cho2, Francisca Millan2, Jane Juusola2, Kyle Retterer2, Charuta Joshi3, Dmitriy Niyazov4, Adolfo Garnica5, Edward Gratz6, Matthew Deardorff7, Alisha Wilkins7, Xilma Ortiz-Gonzalez8, Katherine Mathews3, Karin Panzer9, Eva Brilstra10, Koen L I van Gassen10, Catharina M L Volker-Touw10, Ellen van Binsbergen10, Nara Sobreira11, Ada Hamosh11, Dianalee McKnight2, Kristin G Monaghan2, Wendy K Chung12.
Abstract
Using whole-exome sequencing, we have identified in ten families 14 individuals with microcephaly, developmental delay, intellectual disability, hypotonia, spasticity, seizures, sensorineural hearing loss, cortical visual impairment, and rare autosomal-recessive predicted pathogenic variants in spermatogenesis-associated protein 5 (SPATA5). SPATA5 encodes a ubiquitously expressed member of the ATPase associated with diverse activities (AAA) protein family and is involved in mitochondrial morphogenesis during early spermatogenesis. It might also play a role in post-translational modification during cell differentiation in neuronal development. Mutations in SPATA5 might affect brain development and function, resulting in microcephaly, developmental delay, and intellectual disability.Entities:
Mesh:
Substances:
Year: 2015 PMID: 26299366 PMCID: PMC4564988 DOI: 10.1016/j.ajhg.2015.07.014
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.025