CeGaT has updated its Diagnostic Panels for Ciliopathies, Epilepsy & Migraine, Eye Diseases, Ion Channel Diseases, Mitochondriopathies, and Neuromuscular Diseases. A new subpanel for Eye Diseases is available, designated EYE22, which is specific for Septo-optical dysplasia. Fifty-five genes have been added to the Mitochondriopathies panel, which now has a total of 266 of nuclear-encoded genes, and five subpanels have been updated on the panel for Neuromuscular Diseases.
The table below gives you an overview of all updated subpanels:
|Diseases||Total of genes
old / new*
|Ciliopathies||71 / 72||CIL01, CIL02, CIL03|
|Epilepsy & Migraine||413 / 414||EPI07|
|Eye Diseases||258 / 274||EYE02, EYE03, EYE05, EYE07, EYE13, EYE20, new EYE22|
|Ion Channel Diseases||114 / 115||ION06|
|Mitochondriopathies||211 / 303||MIT02|
|Neuromuscular Diseases||229 / 267||NMD01, NMD02, NMD03, NMD06, NMD08|
|* Genes in multiple subpanels are only counted once|
You can find an overview of all available panels on the Diagnostic Panels page.