{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["BTN6","BTNL11"],"biotype":"protein_coding","hgnc_id":"HGNC:7197","gene_name":"myelin oligodendrocyte glycoprotein","omim_gene":["159465"],"alias_name":null,"gene_symbol":"MOG","hgnc_symbol":"MOG","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"6:29624758-29640149","ensembl_id":"ENSG00000204655"}},"GRch38":{"90":{"location":"6:29656981-29672372","ensembl_id":"ENSG00000204655"}}},"hgnc_date_symbol_changed":"1994-03-30"},"entity_type":"gene","entity_name":"MOG","confidence_level":"2","penetrance":"Complete","mode_of_pathogenicity":"","publications":["21907016"],"evidence":["Expert Review Amber"],"phenotypes":["Narcolepsy 7, 614250"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":213,"hash_id":"55ace3c022c1fc7042059034","name":"Kleine-Levin syndrome","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Sleep disorders","status":"public","version":"1.4","version_created":"2019-06-20T15:15:12.561039Z","relevant_disorders":["Kleine-Levin syndrome and other inherited sleep disorders"],"stats":{"number_of_genes":12,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["BTN6","BTNL11"],"biotype":"protein_coding","hgnc_id":"HGNC:7197","gene_name":"myelin oligodendrocyte glycoprotein","omim_gene":["159465"],"alias_name":null,"gene_symbol":"MOG","hgnc_symbol":"MOG","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"6:29624758-29640149","ensembl_id":"ENSG00000204655"}},"GRch38":{"90":{"location":"6:29656981-29672372","ensembl_id":"ENSG00000204655"}}},"hgnc_date_symbol_changed":"1994-03-30"},"entity_type":"gene","entity_name":"MOG","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["21907016"],"evidence":["Expert Review Amber","NHS GMS","London North GLH","Wessex and West Midlands GLH"],"phenotypes":["Narcolepsy 7, 614250"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":541,"hash_id":null,"name":"Paroxysmal central nervous system disorders","disease_group":"","disease_sub_group":"","status":"public","version":"0.168","version_created":"2019-10-01T13:39:46.962209Z","relevant_disorders":["Paroxysmal neurological disorders","pain disorders and sleep disorders"],"stats":{"number_of_genes":83,"number_of_strs":5,"number_of_regions":1},"types":[{"name":"GMS Rare Disease","slug":"gms-rare-disease","description":"This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"}]}}]}