ADGRV1 is implicated in myoclonic epilepsy

Summary Objective To investigate the significance of variation in ADGRV 1 (also known as GPR 98 , MASS 1 , and VLGR 1 ), MEF 2C , and other genes at the 5q14.3 chromosomal locus in myoclonic epilepsy. Methods We studied the epilepsy phenotypes of 4 individuals with 5q14.3 deletion and found that all had myoclonic seizures. We then screened 6 contiguous genes at 5q14.3, MEF 2C, CETN 3 , MBLAC 2 , POLR 3G , LYSMD 3 , and ADGRV 1 , in a 95‐patient cohort with epilepsy and myoclonic seizures. Of these genes, point mutations in MEF 2C cause a phenotype involving seizures and intellectual disability. A role for ADGRV 1 in epilepsy has been proposed previously, based on a recessive mutation in the Frings mouse model of audiogenic seizures, as well as a shared homologous region with another epilepsy gene, LGI 1 . Results Six patients from the myoclonic epilepsy cohort had likely pathogenic ultra‐rare ADGRV 1 variants, and statistical analysis showed that ultra‐rare variants were significantly overrepresented when compared to healthy population data from the Genome Aggregation Database. Of the remaining genes, no definite pathogenic variants were identified. Significance Our data suggest that the ADGRV 1 variation contributes to epilepsy with myoclonic seizures, although the inheritance pattern may be complex in many cases. In patients with 5q14.3 deletion and epilepsy, ADGRV 1 haploinsufficiency likely contributes to seizure development. The latter is a shift from current thinking, as MEF 2C haploinsufficiency has been considered the main cause of epilepsy in 5q14.3 deletion syndrome. In cases of 5q14.3 deletion and epilepsy, seizures likely occur due to haploinsufficiency of one or both of ADGRV 1 and MEF 2C .