{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["CLF-1","CLF","CISS","CISS1"],"biotype":"protein_coding","hgnc_id":"HGNC:2364","gene_name":"cytokine receptor like factor 1","omim_gene":["604237"],"alias_name":["cold-induced sweating syndrome"],"gene_symbol":"CRLF1","hgnc_symbol":"CRLF1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"19:18683030-18718551","ensembl_id":"ENSG00000006016"}},"GRch38":{"90":{"location":"19:18572220-18607741","ensembl_id":"ENSG00000006016"}}},"hgnc_date_symbol_changed":"1999-02-26"},"entity_type":"gene","entity_name":"CRLF1","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["12509788"],"evidence":["Expert Review Green","Expert list"],"phenotypes":["Cold-induced sweating syndrome 1 272430"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":258,"hash_id":"55b75d5b22c1fc05fd2345c9","name":"Arthrogryposis","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Neuromuscular disorders","status":"public","version":"2.45","version_created":"2019-10-07T10:19:07.721001Z","relevant_disorders":["Arthrogrythsis"],"stats":{"number_of_genes":246,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"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"}]}},{"gene_data":{"alias":["CLF-1","CLF","CISS","CISS1"],"biotype":"protein_coding","hgnc_id":"HGNC:2364","gene_name":"cytokine receptor like factor 1","omim_gene":["604237"],"alias_name":["cold-induced sweating syndrome"],"gene_symbol":"CRLF1","hgnc_symbol":"CRLF1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"19:18683030-18718551","ensembl_id":"ENSG00000006016"}},"GRch38":{"90":{"location":"19:18572220-18607741","ensembl_id":"ENSG00000006016"}}},"hgnc_date_symbol_changed":"1999-02-26"},"entity_type":"gene","entity_name":"CRLF1","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["PAGE Additional Gene List","Expert Review Green"],"phenotypes":["Cold-induced sweating syndrome 1 272430"],"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."}]}}]}