{"count":3,"next":null,"previous":null,"results":[{"gene_data":{"alias":["eIF3-delta","eIF3-p44","eIF3g"],"biotype":"protein_coding","hgnc_id":"HGNC:3274","gene_name":"eukaryotic translation initiation factor 3 subunit G","omim_gene":["603913"],"alias_name":null,"gene_symbol":"EIF3G","hgnc_symbol":"EIF3G","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"19:10225693-10230596","ensembl_id":"ENSG00000130811"}},"GRch38":{"90":{"location":"19:10115017-10119918","ensembl_id":"ENSG00000130811"}}},"hgnc_date_symbol_changed":"2007-07-27"},"entity_type":"gene","entity_name":"EIF3G","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["25669430"],"evidence":["Literature"],"phenotypes":["Narcolepsy"],"mode_of_inheritance":"Unknown","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":["eIF3-delta","eIF3-p44","eIF3g"],"biotype":"protein_coding","hgnc_id":"HGNC:3274","gene_name":"eukaryotic translation initiation factor 3 subunit G","omim_gene":["603913"],"alias_name":null,"gene_symbol":"EIF3G","hgnc_symbol":"EIF3G","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"19:10225693-10230596","ensembl_id":"ENSG00000130811"}},"GRch38":{"90":{"location":"19:10115017-10119918","ensembl_id":"ENSG00000130811"}}},"hgnc_date_symbol_changed":"2007-07-27"},"entity_type":"gene","entity_name":"EIF3G","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","SFARI"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":657,"hash_id":null,"name":"Autism","disease_group":"","disease_sub_group":"","status":"public","version":"0.15","version_created":"2019-06-20T15:10:14.437740Z","relevant_disorders":[],"stats":{"number_of_genes":733,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Research","slug":"research","description":"This is a gene panel used for research."}]}},{"gene_data":{"alias":["eIF3-delta","eIF3-p44","eIF3g"],"biotype":"protein_coding","hgnc_id":"HGNC:3274","gene_name":"eukaryotic translation initiation factor 3 subunit G","omim_gene":["603913"],"alias_name":null,"gene_symbol":"EIF3G","hgnc_symbol":"EIF3G","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"19:10225693-10230596","ensembl_id":"ENSG00000130811"}},"GRch38":{"90":{"location":"19:10115017-10119918","ensembl_id":"ENSG00000130811"}}},"hgnc_date_symbol_changed":"2007-07-27"},"entity_type":"gene","entity_name":"EIF3G","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":["25669430"],"evidence":["Expert Review Red","NHS GMS","London North GLH","Wessex and West Midlands GLH"],"phenotypes":["Narcolepsy"],"mode_of_inheritance":"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)"}]}}]}