{"count":3,"next":null,"previous":null,"results":[{"gene_data":{"alias":["HSST2"],"biotype":"protein_coding","hgnc_id":"HGNC:11459","gene_name":"sulfotransferase family 2B member 1","omim_gene":["604125"],"alias_name":null,"gene_symbol":"SULT2B1","hgnc_symbol":"SULT2B1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"19:49055332-49102682","ensembl_id":"ENSG00000088002"}},"GRch38":{"90":{"location":"19:48552075-48599425","ensembl_id":"ENSG00000088002"}}},"hgnc_date_symbol_changed":"1998-08-18"},"entity_type":"gene","entity_name":"SULT2B1","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["28575648"],"evidence":["Expert Review Green","Literature"],"phenotypes":["Ichthyosis, congenital, autosomal recessive 14\t617571"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":282,"hash_id":"562e5d2622c1fc582756e3b5","name":"Autosomal recessive congenital ichthyosis","disease_group":"Dermatological disorders","disease_sub_group":"Ichthyoses","status":"public","version":"1.9","version_created":"2019-06-20T15:14:56.521067Z","relevant_disorders":[],"stats":{"number_of_genes":14,"number_of_strs":0,"number_of_regions":1},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["HSST2"],"biotype":"protein_coding","hgnc_id":"HGNC:11459","gene_name":"sulfotransferase family 2B member 1","omim_gene":["604125"],"alias_name":null,"gene_symbol":"SULT2B1","hgnc_symbol":"SULT2B1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"19:49055332-49102682","ensembl_id":"ENSG00000088002"}},"GRch38":{"90":{"location":"19:48552075-48599425","ensembl_id":"ENSG00000088002"}}},"hgnc_date_symbol_changed":"1998-08-18"},"entity_type":"gene","entity_name":"SULT2B1","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["28575648"],"evidence":["Expert Review Green"],"phenotypes":["Ichthyosis, congenital, autosomal recessive 14 617571"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":555,"hash_id":null,"name":"Ichthyosis and erythrokeratoderma","disease_group":"","disease_sub_group":"","status":"public","version":"0.10","version_created":"2019-09-09T15:38:37.080974Z","relevant_disorders":[],"stats":{"number_of_genes":64,"number_of_strs":0,"number_of_regions":1},"types":[{"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":["HSST2"],"biotype":"protein_coding","hgnc_id":"HGNC:11459","gene_name":"sulfotransferase family 2B member 1","omim_gene":["604125"],"alias_name":null,"gene_symbol":"SULT2B1","hgnc_symbol":"SULT2B1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"19:49055332-49102682","ensembl_id":"ENSG00000088002"}},"GRch38":{"90":{"location":"19:48552075-48599425","ensembl_id":"ENSG00000088002"}}},"hgnc_date_symbol_changed":"1998-08-18"},"entity_type":"gene","entity_name":"SULT2B1","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["London North GLH","NHS GMS","Expert Review Green"],"phenotypes":["Ichthyosis, congenital, autosomal recessive 14","617571"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":556,"hash_id":null,"name":"Palmoplantar keratodermas","disease_group":"","disease_sub_group":"","status":"public","version":"0.9","version_created":"2019-09-09T15:38:38.871976Z","relevant_disorders":[],"stats":{"number_of_genes":69,"number_of_strs":0,"number_of_regions":0},"types":[{"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"}]}}]}