{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["SP-A2","COLEC5"],"biotype":"protein_coding","hgnc_id":"HGNC:10799","gene_name":"surfactant protein A2","omim_gene":["178642"],"alias_name":["surfactant, pulmonary-associated protein A2A"],"gene_symbol":"SFTPA2","hgnc_symbol":"SFTPA2","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"10:81315608-81320153","ensembl_id":"ENSG00000185303"}},"GRch38":{"90":{"location":"10:79555852-79560402","ensembl_id":"ENSG00000185303"}}},"hgnc_date_symbol_changed":"1997-04-16"},"entity_type":"gene","entity_name":"SFTPA2","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["20301408","19100526","26568241"],"evidence":["Expert Review Green","Radboud University Medical Center, Nijmegen"],"phenotypes":["Pulmonary fibrosis, idiopathic, 178500"],"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."}]}},{"gene_data":{"alias":["SP-A2","COLEC5"],"biotype":"protein_coding","hgnc_id":"HGNC:10799","gene_name":"surfactant protein A2","omim_gene":["178642"],"alias_name":["surfactant, pulmonary-associated protein A2A"],"gene_symbol":"SFTPA2","hgnc_symbol":"SFTPA2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"10:81315608-81320153","ensembl_id":"ENSG00000185303"}},"GRch38":{"90":{"location":"10:79555852-79560402","ensembl_id":"ENSG00000185303"}}},"hgnc_date_symbol_changed":"1997-04-16"},"entity_type":"gene","entity_name":"SFTPA2","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":null,"publications":["19100526","26568241"],"evidence":["Expert Review Amber","Expert list"],"phenotypes":["Pulmonary fibrosis, idiopathic, 178500"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":551,"hash_id":null,"name":"Surfactant deficiency","disease_group":"","disease_sub_group":"","status":"public","version":"0.28","version_created":"2019-09-04T16:26:46.384759Z","relevant_disorders":["R192"],"stats":{"number_of_genes":8,"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)"}]}}]}