{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["GMAP","GAL-GMAP","GLNN"],"biotype":"protein_coding","hgnc_id":"HGNC:4114","gene_name":"galanin and GMAP prepropeptide","omim_gene":["137035"],"alias_name":["galanin-message-associated peptide"],"gene_symbol":"GAL","hgnc_symbol":"GAL","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"11:68451247-68458643","ensembl_id":"ENSG00000069482"}},"GRch38":{"90":{"location":"11:68683779-68691175","ensembl_id":"ENSG00000069482"}}},"hgnc_date_symbol_changed":"1993-06-22"},"entity_type":"gene","entity_name":"GAL","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["22325380"],"evidence":["Expert Review Red","Literature"],"phenotypes":["Hirschsprung disease","HD"],"mode_of_inheritance":"Unknown","tags":[],"panel":{"id":63,"hash_id":"58c7f5008f620328d77ce70f","name":"Familial Hirschsprung Disease","disease_group":"Gastroenterological disorders","disease_sub_group":"Gastrointestinal disorders","status":"public","version":"1.6","version_created":"2019-06-20T15:11:10.292595Z","relevant_disorders":[],"stats":{"number_of_genes":62,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["GMAP","GAL-GMAP","GLNN"],"biotype":"protein_coding","hgnc_id":"HGNC:4114","gene_name":"galanin and GMAP prepropeptide","omim_gene":["137035"],"alias_name":["galanin-message-associated peptide"],"gene_symbol":"GAL","hgnc_symbol":"GAL","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"11:68451247-68458643","ensembl_id":"ENSG00000069482"}},"GRch38":{"90":{"location":"11:68683779-68691175","ensembl_id":"ENSG00000069482"}}},"hgnc_date_symbol_changed":"1993-06-22"},"entity_type":"gene","entity_name":"GAL","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":null,"publications":["25691535"],"evidence":["Wessex and West Midlands GLH","NHS GMS","Expert Review Red","Literature"],"phenotypes":["?Epilepsy, familial temporal lobe, 8 616461"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":402,"hash_id":null,"name":"Genetic epilepsy syndromes","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Inherited Epilepsy Syndromes","status":"public","version":"1.363","version_created":"2019-10-08T10:06:11.607307Z","relevant_disorders":["Epilepsy Plus","Epilepsy plus other features","Genetic Epilepsy Syndromes","Epileptic encephalopathy","Familial Focal Epilepsies","Familial Genetic Generalised Epilepsies","Genetic Epilepsies with Febrile Seizures Plus (GEFS+)","Genetic Epilepsies with Febrile Seizures Plus"],"stats":{"number_of_genes":614,"number_of_strs":2,"number_of_regions":13},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"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)"},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}
