{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["KCa2.3","hSK3","SKCA3"],"biotype":"protein_coding","hgnc_id":"HGNC:6292","gene_name":"potassium calcium-activated channel subfamily N member 3","omim_gene":["602983"],"alias_name":["small conductance calcium-activated potassium channel 3"],"gene_symbol":"KCNN3","hgnc_symbol":"KCNN3","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:154669931-154842756","ensembl_id":"ENSG00000143603"}},"GRch38":{"90":{"location":"1:154697455-154870280","ensembl_id":"ENSG00000143603"}}},"hgnc_date_symbol_changed":"1998-04-07"},"entity_type":"gene","entity_name":"KCNN3","confidence_level":"1","penetrance":"unknown","mode_of_pathogenicity":null,"publications":["26658685"],"evidence":["Expert Review Red","Literature"],"phenotypes":["No OMIM number","portal hypertension","varices","splenomegaly"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":["watchlist"],"panel":{"id":209,"hash_id":"58c8066b8f6203413360f1cf","name":"Ductal plate malformation","disease_group":"","disease_sub_group":"","status":"public","version":"1.10","version_created":"2019-06-20T15:10:58.988548Z","relevant_disorders":["Ductal plate malformation (DPM)","Polycystic liver disease"],"stats":{"number_of_genes":150,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["KCa2.3","hSK3","SKCA3"],"biotype":"protein_coding","hgnc_id":"HGNC:6292","gene_name":"potassium calcium-activated channel subfamily N member 3","omim_gene":["602983"],"alias_name":["small conductance calcium-activated potassium channel 3"],"gene_symbol":"KCNN3","hgnc_symbol":"KCNN3","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:154669931-154842756","ensembl_id":"ENSG00000143603"}},"GRch38":{"90":{"location":"1:154697455-154870280","ensembl_id":"ENSG00000143603"}}},"hgnc_date_symbol_changed":"1998-04-07"},"entity_type":"gene","entity_name":"KCNN3","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"Other - please provide details in the comments","publications":["31155282"],"evidence":["DD-Gene2Phenotype","Expert Review Amber"],"phenotypes":["ZIMMERMANN-LABAND SYNDROME"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":484,"hash_id":null,"name":"DDG2P","disease_group":"","disease_sub_group":"","status":"public","version":"1.137","version_created":"2019-10-08T15:56:59.220133Z","relevant_disorders":[],"stats":{"number_of_genes":1893,"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"}]}}]}