Askja
Room N-132
Siddarth Banka, professor of Genomic Medicine and Rare Diseases at the University of Manchester, England, will give a talk in the BMC/GPMLS lecture series titled Analysis of R-loop forming regions identifies RNU2-2 and RNU5B-1 as neurodevelopmental disorder genes.
Abstract: R-loops are DNA–RNA hybrid structures that may promote mutagenesis. However, their contribution to human Mendelian disorders is unexplored. Here we show excess de novo variants in genomic regions that form R-loops (henceforth, ‘R-loop regions’) and demonstrate enrichment of R-loop region variants (RRVs) in ribozyme, snoRNA and snRNA genes, specifically in rare disease cohorts. Using this insight, we report neurodevelopmental disorders (NDDs) caused by rare variants in two major spliceosomal RNA encoding genes, RNU2-2 and RNU5B-1. These, along with the recently described RNU4-2-related ReNU syndrome, provide a genetic explanation for a substantial proportion of individuals with NDDs.
Bio: Sid is a Professor of Genomic Medicine and Rare Diseases at the University of Manchester, a Consultant Clinical Geneticist at the Manchester Centre for Genomic Medicine and Clinical Director of the Manchester Rare Conditions Centre. His research programs focus on novel disease-gene discovery; improving diagnosis through innovative data analysis and multi-omic approaches; understanding mechanisms and natural history of developmental diseases; and performing therapeutic clinical trials. He co-leads the Rare Conditions theme of the NIHR Manchester Biomedical Research Centre, the EpiGenRare node of the MRC UK Rare Disease Research Platform, and NHSE Rare Disease Genomics Network of Excellence.

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Buses 14, 1, 6, 3 and 12 stop at the University of Iceland in Vatnsmýri. Buses 11 and 15 also stop nearby. Let's travel in an ecological way!