{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FLJ14813","THC2","Gwl"],"biotype":"protein_coding","hgnc_id":"HGNC:19042","gene_name":"microtubule associated serine/threonine kinase like","omim_gene":["608221"],"alias_name":["greatwall kinase homolog"],"gene_symbol":"MASTL","hgnc_symbol":"MASTL","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"10:27443753-27475853","ensembl_id":"ENSG00000120539"}},"GRch38":{"90":{"location":"10:27154824-27186924","ensembl_id":"ENSG00000120539"}}},"hgnc_date_symbol_changed":"2004-02-10"},"entity_type":"gene","entity_name":"MASTL","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["12890928","21211618","26136524"],"evidence":["Expert Review Red","Illumina TruGenome Clinical Sequencing Services","Radboud University Medical Center, Nijmegen"],"phenotypes":["Thrombocytopenia","severe aplastic anemia"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":159,"hash_id":"58a70e858f62037e8779b2e8","name":"Cytopenias and congenital anaemias","disease_group":"Haematological disorders","disease_sub_group":"Anaemias and red cell disorders","status":"public","version":"1.73","version_created":"2019-09-23T11:25:32.403071Z","relevant_disorders":["Aplastic anaemia with or without paroxysmal nocturnal haemoglobinuria","Apparent aplastic anaemia or paroxysmal nocturnal haemoglobinuria","Congenital anaemias","Early onset pancytopenia and red cell disorders","Anaemias and red cell disorders","Cytopaenias and congenital anaemias","Cytopenia and pancytopenia"],"stats":{"number_of_genes":219,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["FLJ14813","THC2","Gwl"],"biotype":"protein_coding","hgnc_id":"HGNC:19042","gene_name":"microtubule associated serine/threonine kinase like","omim_gene":["608221"],"alias_name":["greatwall kinase homolog"],"gene_symbol":"MASTL","hgnc_symbol":"MASTL","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"10:27443753-27475853","ensembl_id":"ENSG00000120539"}},"GRch38":{"90":{"location":"10:27154824-27186924","ensembl_id":"ENSG00000120539"}}},"hgnc_date_symbol_changed":"2004-02-10"},"entity_type":"gene","entity_name":"MASTL","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["10891439","26136524","22102272"],"evidence":["London South GLH","NHS GMS","Expert Review Amber","Wessex and West Midlands GLH"],"phenotypes":["severe aplastic anemia","Thrombocytopenia"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":519,"hash_id":null,"name":"Cytopenia - NOT Fanconi anaemia","disease_group":"","disease_sub_group":"","status":"public","version":"0.120","version_created":"2019-09-23T10:29:43.892929Z","relevant_disorders":["R91","R258"],"stats":{"number_of_genes":84,"number_of_strs":0,"number_of_regions":0},"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)"}]}}]}