{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["DKFZP434G099"],"biotype":"protein_coding","hgnc_id":"HGNC:16075","gene_name":"RAB33B, member RAS oncogene family","omim_gene":["605950"],"alias_name":null,"gene_symbol":"RAB33B","hgnc_symbol":"RAB33B","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"4:140374386-140397763","ensembl_id":"ENSG00000172007"}},"GRch38":{"90":{"location":"4:139453232-139476609","ensembl_id":"ENSG00000172007"}}},"hgnc_date_symbol_changed":"2001-09-14"},"entity_type":"gene","entity_name":"RAB33B","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["22652534","16470731","23042644","28127940"],"evidence":["Expert Review Green","NHS GMS","Expert list","Illumina TruGenome Clinical Sequencing Services","Radboud University Medical Center, Nijmegen",""],"phenotypes":["Smith-McCort dysplasia 2 615222"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":309,"hash_id":"5693952f22c1fc251660fb1e","name":"Skeletal dysplasia","disease_group":"Skeletal disorders","disease_sub_group":"Skeletal dysplasias","status":"public","version":"1.203","version_created":"2019-10-03T09:38:50.417968Z","relevant_disorders":["Unexplained skeletal dysplasia","Skeletal dysplasia"],"stats":{"number_of_genes":546,"number_of_strs":1,"number_of_regions":6},"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"}]}}]}