{"count":3,"next":null,"previous":null,"results":[{"gene_data":{"alias":["huASH1","ASH1","ASH1L1","KMT2H"],"biotype":"protein_coding","hgnc_id":"HGNC:19088","gene_name":"ASH1 like histone lysine methyltransferase","omim_gene":["607999"],"alias_name":null,"gene_symbol":"ASH1L","hgnc_symbol":"ASH1L","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:155305059-155532598","ensembl_id":"ENSG00000116539"}},"GRch38":{"90":{"location":"1:155335268-155562807","ensembl_id":"ENSG00000116539"}}},"hgnc_date_symbol_changed":"2003-08-06"},"entity_type":"gene","entity_name":"ASH1L","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["20212079","26185613","23042784","24267887","26166478","25989142","24090431","24581740","26167905","23999528","25294932"],"evidence":["Expert Review Green","SFARI"],"phenotypes":["ID, EPS, DD/NDD, ASD"],"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":["huASH1","ASH1","ASH1L1","KMT2H"],"biotype":"protein_coding","hgnc_id":"HGNC:19088","gene_name":"ASH1 like histone lysine methyltransferase","omim_gene":["607999"],"alias_name":null,"gene_symbol":"ASH1L","hgnc_symbol":"ASH1L","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:155305059-155532598","ensembl_id":"ENSG00000116539"}},"GRch38":{"90":{"location":"1:155335268-155562807","ensembl_id":"ENSG00000116539"}}},"hgnc_date_symbol_changed":"2003-08-06"},"entity_type":"gene","entity_name":"ASH1L","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"Other - please provide details in the comments","publications":["25961944","28394464","29753921","29276005"],"evidence":["DD-Gene2Phenotype","Expert Review Amber"],"phenotypes":["INTELLECTUAL DISABILITY"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":484,"hash_id":null,"name":"DDG2P","disease_group":"","disease_sub_group":"","status":"public","version":"1.137","version_created":"2019-10-08T15:56:59.220133Z","relevant_disorders":[],"stats":{"number_of_genes":1893,"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)"},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}},{"gene_data":{"alias":["huASH1","ASH1","ASH1L1","KMT2H"],"biotype":"protein_coding","hgnc_id":"HGNC:19088","gene_name":"ASH1 like histone lysine methyltransferase","omim_gene":["607999"],"alias_name":null,"gene_symbol":"ASH1L","hgnc_symbol":"ASH1L","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"1:155305059-155532598","ensembl_id":"ENSG00000116539"}},"GRch38":{"90":{"location":"1:155335268-155562807","ensembl_id":"ENSG00000116539"}}},"hgnc_date_symbol_changed":"2003-08-06"},"entity_type":"gene","entity_name":"ASH1L","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["25961944","26350204","29276005","29753921","28191889"],"evidence":["Victorian Clinical Genetics Services","Expert Review Green"],"phenotypes":["Mental retardation, autosomal dominant 52, 617796","intellectual disability"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":285,"hash_id":"558aa423bb5a16630e15b63c","name":"Intellectual disability","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Neurodevelopmental disorders","status":"public","version":"2.1065","version_created":"2019-10-07T13:42:16.019766Z","relevant_disorders":["Coarse facial features including Coffin-Siris-like disorders","ID","Moderate","severe or profound intellectual disability","Schizophrenia plus additional features","Intellectual disability - microarray","fragile X and sequencing"],"stats":{"number_of_genes":2253,"number_of_strs":11,"number_of_regions":57},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"name":"GMS Rare Disease Virtual","slug":"gms-rare-disease-virtual","description":"This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}
