{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["KIAA0591","KLP","HMSNII"],"biotype":"protein_coding","hgnc_id":"HGNC:16636","gene_name":"kinesin family member 1B","omim_gene":["605995"],"alias_name":null,"gene_symbol":"KIF1B","hgnc_symbol":"KIF1B","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"1:10270863-10441661","ensembl_id":"ENSG00000054523"}},"GRch38":{"90":{"location":"1:10210805-10381603","ensembl_id":"ENSG00000054523"}}},"hgnc_date_symbol_changed":"2001-11-14"},"entity_type":"gene","entity_name":"KIF1B","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","Radboud University Medical Center, Nijmegen"],"phenotypes":["Charcot-Marie-Tooth disease, type 2A1, 118210Pheochromocytoma, 171300{Neuroblastoma, susceptibility to, 1}, 256700"],"mode_of_inheritance":"","tags":[],"panel":{"id":97,"hash_id":"553f9599bb5a1616e5ed45b1","name":"Inherited phaeochromocytoma and paraganglioma","disease_group":"Tumour syndromes","disease_sub_group":"Breast and endocrine","status":"public","version":"1.5","version_created":"2019-03-05T14:07:55.639077Z","relevant_disorders":["Neuro-endocrine Tumours- PCC and PGL"],"stats":{"number_of_genes":20,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["KIAA0591","KLP","HMSNII"],"biotype":"protein_coding","hgnc_id":"HGNC:16636","gene_name":"kinesin family member 1B","omim_gene":["605995"],"alias_name":null,"gene_symbol":"KIF1B","hgnc_symbol":"KIF1B","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"1:10270863-10441661","ensembl_id":"ENSG00000054523"}},"GRch38":{"90":{"location":"1:10210805-10381603","ensembl_id":"ENSG00000054523"}}},"hgnc_date_symbol_changed":"2001-11-14"},"entity_type":"gene","entity_name":"KIF1B","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["11389829","25802885"],"evidence":["NHS GMS","South West GLH","Expert Review Red","Emory Genetics Laboratory","UKGTN","Expert list","Radboud University Medical Center, Nijmegen","Illumina TruGenome Clinical Sequencing Services"],"phenotypes":["Charcot Marie Tooth disease, type 2A1, 118210"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","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."}]}}]}
