A novel KNL1 intronic splicing variant likely destabilizes the KMN complex, causing primary microcephaly
Bridget J Fellows1, Giovanna Cantini Tolezano2, Sara Ferreira Pires2
1Department of Biochemistry, University of Otago, Dunedin, New Zealand.
American Journal of Medical Genetics. Part A
|November 8, 2023
Summary
Genetic variants in the KNL1 gene cause primary microcephaly (MCPH). A novel splicing variant in KNL1 disrupts the kinetochore, leading to MCPH and intellectual disability in siblings.
Area of Science:
- Genetics
- Molecular Biology
- Cell Biology
Background:
- Primary microcephaly (MCPH) is a neurodevelopmental disorder defined by a significantly smaller head circumference.
- MCPH4 is linked to biallelic variants in the KNL1 gene, a crucial component of the kinetochore KMN network.
- The KMN network is essential for accurate chromosome segregation during cell division (mitosis).
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