{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["Map80","KIAA0572","GANP","SAC3"],"biotype":"protein_coding","hgnc_id":"HGNC:6946","gene_name":"minichromosome maintenance complex component 3 associated protein","omim_gene":["603294"],"alias_name":["germinal-centre associated nuclear protein"],"gene_symbol":"MCM3AP","hgnc_symbol":"MCM3AP","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"21:47655047-47706211","ensembl_id":"ENSG00000160294"}},"GRch38":{"90":{"location":"21:46235126-46286297","ensembl_id":"ENSG00000160294"}}},"hgnc_date_symbol_changed":"1999-03-04"},"entity_type":"gene","entity_name":"MCM3AP","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["NHS GMS","London North GLH"],"phenotypes":["Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development, 618124"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":85,"hash_id":"55ad205422c1fc7041340234","name":"Hereditary neuropathy","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Motor and Sensory Disorders of the PNS","status":"public","version":"1.333","version_created":"2019-07-09T13:10:50.031506Z","relevant_disorders":["Charcot-Marie-Tooth disease"],"stats":{"number_of_genes":276,"number_of_strs":11,"number_of_regions":2},"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."}]}},{"gene_data":{"alias":["Map80","KIAA0572","GANP","SAC3"],"biotype":"protein_coding","hgnc_id":"HGNC:6946","gene_name":"minichromosome maintenance complex component 3 associated protein","omim_gene":["603294"],"alias_name":["germinal-centre associated nuclear protein"],"gene_symbol":"MCM3AP","hgnc_symbol":"MCM3AP","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"21:47655047-47706211","ensembl_id":"ENSG00000160294"}},"GRch38":{"90":{"location":"21:46235126-46286297","ensembl_id":"ENSG00000160294"}}},"hgnc_date_symbol_changed":"1999-03-04"},"entity_type":"gene","entity_name":"MCM3AP","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":null,"publications":["24123876","28633435","28969388","29982295"],"evidence":["Expert Review Green","Literature"],"phenotypes":["Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development, 618124"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","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"}]}}]}