{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["DKFZp761A078","SAS-6","FLJ22097","SAS6"],"biotype":"protein_coding","hgnc_id":"HGNC:25403","gene_name":"SAS-6 centriolar assembly protein","omim_gene":["609321"],"alias_name":null,"gene_symbol":"SASS6","hgnc_symbol":"SASS6","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"1:100549119-100598511","ensembl_id":"ENSG00000156876"}},"GRch38":{"90":{"location":"1:100083563-100132955","ensembl_id":"ENSG00000156876"}}},"hgnc_date_symbol_changed":"2005-10-13"},"entity_type":"gene","entity_name":"SASS6","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["24951542"],"evidence":["NHS GMS","Other","Literature"],"phenotypes":["autosomal recessive primary microcephaly (MCPH)","?Microcephaly 14, primary, autosomal recessive, 616402"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":162,"hash_id":"568f860222c1fc1c79ca1769","name":"Severe microcephaly","disease_group":"Dysmorphic and congenital abnormality syndromes","disease_sub_group":"DNA repair disorders","status":"public","version":"1.72","version_created":"2019-08-19T16:58:29.143286Z","relevant_disorders":["Primary Microcephaly - Microcephalic Dwarfism Spectrum","Severe microcephaly"],"stats":{"number_of_genes":122,"number_of_strs":0,"number_of_regions":5},"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":["DKFZp761A078","SAS-6","FLJ22097","SAS6"],"biotype":"protein_coding","hgnc_id":"HGNC:25403","gene_name":"SAS-6 centriolar assembly protein","omim_gene":["609321"],"alias_name":null,"gene_symbol":"SASS6","hgnc_symbol":"SASS6","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:100549119-100598511","ensembl_id":"ENSG00000156876"}},"GRch38":{"90":{"location":"1:100083563-100132955","ensembl_id":"ENSG00000156876"}}},"hgnc_date_symbol_changed":"2005-10-13"},"entity_type":"gene","entity_name":"SASS6","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["24951542"],"evidence":["Expert Review Amber","Exper Review Amber","PAGE Additional Gene List"],"phenotypes":["?Microcephaly 14, primary, autosomal recessive 616402"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":478,"hash_id":null,"name":"Fetal anomalies","disease_group":"","disease_sub_group":"","status":"public","version":"0.344","version_created":"2019-09-17T09:38:10.568007Z","relevant_disorders":["R21"],"stats":{"number_of_genes":1721,"number_of_strs":0,"number_of_regions":0},"types":[{"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."}]}}]}
