{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FLJ20311","MTB","CAP-G2","hCAP-G2"],"biotype":"protein_coding","hgnc_id":"HGNC:21904","gene_name":"non-SMC condensin II complex subunit G2","omim_gene":["608532"],"alias_name":null,"gene_symbol":"NCAPG2","hgnc_symbol":"NCAPG2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"7:158424003-158497520","ensembl_id":"ENSG00000146918"}},"GRch38":{"90":{"location":"7:158631311-158704829","ensembl_id":"ENSG00000146918"}}},"hgnc_date_symbol_changed":"2006-09-04"},"entity_type":"gene","entity_name":"NCAPG2","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":null,"publications":["30609410"],"evidence":["Expert Review Amber","Expert list"],"phenotypes":["Khan-Khan-Katsanis syndrome, 618460"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":384,"hash_id":null,"name":"Limb disorders","disease_group":"","disease_sub_group":"","status":"public","version":"1.61","version_created":"2019-10-03T10:01:34.398179Z","relevant_disorders":[],"stats":{"number_of_genes":234,"number_of_strs":0,"number_of_regions":1},"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"}]}},{"gene_data":{"alias":["FLJ20311","MTB","CAP-G2","hCAP-G2"],"biotype":"protein_coding","hgnc_id":"HGNC:21904","gene_name":"non-SMC condensin II complex subunit G2","omim_gene":["608532"],"alias_name":null,"gene_symbol":"NCAPG2","hgnc_symbol":"NCAPG2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"7:158424003-158497520","ensembl_id":"ENSG00000146918"}},"GRch38":{"90":{"location":"7:158631311-158704829","ensembl_id":"ENSG00000146918"}}},"hgnc_date_symbol_changed":"2006-09-04"},"entity_type":"gene","entity_name":"NCAPG2","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"Other - please provide details in the comments","publications":["30609410"],"evidence":["Expert Review Amber","DD-Gene2Phenotype"],"phenotypes":["Severe Neurodevelopmental Syndrome"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","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"}]}}]}