Table2: Genes linked to inherited kidney diseases and their extrarenal manifestations: an OMIM-based exploration of nuclear genes.

Displayed genes were identified using the Genomics England Panel App website (https://panelapp.genomicsengland.co.uk/). Genes identified as being listed in the following panels were used: renal superpanel broad and narrow, renal tubulopathies, renal ciliopathies, neurological ciliopathies, rare multisystem ciliopathies, cystic kidney disease, atypical hemolytic uremic syndrome, CAKUT, extreme-early onset hypertension, membranoproliferative glomerulonephritis including C3 glomerulopathy, proteinuric renal disease, unexplained kidney failure in young people, nephrocalcinosis or nephrolithiasis, skeletal ciliopathies. Only genes curated as green or amber from each panel with a higher confidence of association with inherited kidney diseases were chosen for display. Missing entries in the “kidney” were due to no listings for kidney in OMIM, but these genes were still kept because of their association with secondary kidney disease.