{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["SP-A","SP-A1","COLEC4"],"biotype":"protein_coding","hgnc_id":"HGNC:10798","gene_name":"surfactant protein A1","omim_gene":["178630"],"alias_name":["surfactant, pulmonary-associated protein A1A"],"gene_symbol":"SFTPA1","hgnc_symbol":"SFTPA1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"10:81370695-81375196","ensembl_id":"ENSG00000122852"}},"GRch38":{"90":{"location":"10:79610939-79615455","ensembl_id":"ENSG00000122852"}}},"hgnc_date_symbol_changed":"2001-06-22"},"entity_type":"gene","entity_name":"SFTPA1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["26792177","13680361","22884059"],"evidence":["Expert Review Red","Radboud University Medical Center, Nijmegen"],"phenotypes":["{Pulmonary fibrosis, idiopathic, susceptibility to}, 178500","familial idiopathic pulmonary fibrosis"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","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."}]}}]}