{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["NAPI-3B"],"biotype":"protein_coding","hgnc_id":"HGNC:11020","gene_name":"solute carrier family 34 member 2","omim_gene":["604217"],"alias_name":null,"gene_symbol":"SLC34A2","hgnc_symbol":"SLC34A2","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"4:25656923-25680370","ensembl_id":"ENSG00000157765"}},"GRch38":{"90":{"location":"4:25655301-25678748","ensembl_id":"ENSG00000157765"}}},"hgnc_date_symbol_changed":"1999-07-19"},"entity_type":"gene","entity_name":"SLC34A2","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["16960801","15331184"],"evidence":["Expert Review Green","Radboud University Medical Center, Nijmegen","Literature"],"phenotypes":["Pulmonary alveolar microlithiasis, 265100"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":200,"hash_id":"563259de22c1fc58285b2840","name":"Familial pulmonary fibrosis","disease_group":"Respiratory disorders","disease_sub_group":"Interstitial lung disorders","status":"public","version":"1.6","version_created":"2019-08-20T14:18:14.336659Z","relevant_disorders":[],"stats":{"number_of_genes":71,"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 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."}]}}]}