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Overrepresentation of genetic variation in the AnkyrinG interactome is related to a range of neurodevelopmental disorders.

Ilse M van der WerfSandra JansenPetra F de VriesAmber GerstmansMaartje van de VorstAnke Van DijckBert B A de VriesChristian GilissenAlexander HoischenLisenka E L M VissersR Frank KooyGeert Vandeweyer
Published in: European journal of human genetics : EJHG (2020)
Upon the discovery of numerous genes involved in the pathogenesis of neurodevelopmental disorders, several studies showed that a significant proportion of these genes converge on common pathways and protein networks. Here, we used a reversed approach, by screening the AnkyrinG protein-protein interaction network for genetic variation in a large cohort of 1009 cases with neurodevelopmental disorders. We identified a significant enrichment of de novo potentially disease-causing variants in this network, confirming that this protein network plays an important role in the emergence of several neurodevelopmental disorders.
Keyphrases
  • protein protein
  • small molecule
  • congenital heart disease
  • genome wide
  • binding protein
  • copy number
  • case control
  • single cell