{"count":5,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:3687","gene_name":"fibroblast growth factor 9","omim_gene":["600921"],"alias_name":["glia-activating factor"],"gene_symbol":"FGF9","hgnc_symbol":"FGF9","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"13:22245522-22278637","ensembl_id":"ENSG00000102678"}},"GRch38":{"90":{"location":"13:21671383-21704498","ensembl_id":"ENSG00000102678"}}},"hgnc_date_symbol_changed":"1995-08-15"},"entity_type":"gene","entity_name":"FGF9","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":null,"publications":["19460469","28730625","28169396","19589401"],"evidence":["Expert Review Amber","London South East RGC GSTT","Viapath"],"phenotypes":["Multiple synostoses syndrome 3 612961"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":384,"hash_id":null,"name":"Limb disorders","disease_group":"","disease_sub_group":"","status":"public","version":"1.61","version_created":"2019-10-03T10:01:34.398179Z","relevant_disorders":[],"stats":{"number_of_genes":234,"number_of_strs":0,"number_of_regions":1},"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."},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}},{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:3687","gene_name":"fibroblast growth factor 9","omim_gene":["600921"],"alias_name":["glia-activating factor"],"gene_symbol":"FGF9","hgnc_symbol":"FGF9","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"13:22245522-22278637","ensembl_id":"ENSG00000102678"}},"GRch38":{"90":{"location":"13:21671383-21704498","ensembl_id":"ENSG00000102678"}}},"hgnc_date_symbol_changed":"1995-08-15"},"entity_type":"gene","entity_name":"FGF9","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["19589401"],"evidence":["NHS GMS","Expert Review Red",""],"phenotypes":["?Multiple synostoses syndrome type 3 612961"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":["watchlist"],"panel":{"id":309,"hash_id":"5693952f22c1fc251660fb1e","name":"Skeletal dysplasia","disease_group":"Skeletal disorders","disease_sub_group":"Skeletal dysplasias","status":"public","version":"1.203","version_created":"2019-10-03T09:38:50.417968Z","relevant_disorders":["Unexplained skeletal dysplasia","Skeletal dysplasia"],"stats":{"number_of_genes":546,"number_of_strs":1,"number_of_regions":6},"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."},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}},{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:3687","gene_name":"fibroblast growth factor 9","omim_gene":["600921"],"alias_name":["glia-activating factor"],"gene_symbol":"FGF9","hgnc_symbol":"FGF9","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"13:22245522-22278637","ensembl_id":"ENSG00000102678"}},"GRch38":{"90":{"location":"13:21671383-21704498","ensembl_id":"ENSG00000102678"}}},"hgnc_date_symbol_changed":"1995-08-15"},"entity_type":"gene","entity_name":"FGF9","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Amber","PAGE DD-Gene2Phenotype"],"phenotypes":["MULTIPLE SYNOSTOSES SYNDROME TYPE 3"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":478,"hash_id":null,"name":"Fetal anomalies","disease_group":"","disease_sub_group":"","status":"public","version":"0.344","version_created":"2019-09-17T09:38:10.568007Z","relevant_disorders":["R21"],"stats":{"number_of_genes":1721,"number_of_strs":0,"number_of_regions":0},"types":[{"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":[],"biotype":"protein_coding","hgnc_id":"HGNC:3687","gene_name":"fibroblast growth factor 9","omim_gene":["600921"],"alias_name":["glia-activating factor"],"gene_symbol":"FGF9","hgnc_symbol":"FGF9","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"13:22245522-22278637","ensembl_id":"ENSG00000102678"}},"GRch38":{"90":{"location":"13:21671383-21704498","ensembl_id":"ENSG00000102678"}}},"hgnc_date_symbol_changed":"1995-08-15"},"entity_type":"gene","entity_name":"FGF9","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["NHS GMS"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":168,"hash_id":"55b605f722c1fc05fd2345af","name":"Craniosynostosis","disease_group":"Skeletal disorders","disease_sub_group":"Craniosynostosis syndromes","status":"public","version":"2.0","version_created":"2019-09-17T13:00:09.542482Z","relevant_disorders":["Craniosynostosis syndromes","Craniosynostosis syndromes phenotypes","Rare syndromic craniosynostosis or isolated multisuture synostosis","R100"],"stats":{"number_of_genes":114,"number_of_strs":0,"number_of_regions":2},"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."},{"name":"GMS signed-off","slug":"gms-signed-off","description":"This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."}]}},{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:3687","gene_name":"fibroblast growth factor 9","omim_gene":["600921"],"alias_name":["glia-activating factor"],"gene_symbol":"FGF9","hgnc_symbol":"FGF9","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"13:22245522-22278637","ensembl_id":"ENSG00000102678"}},"GRch38":{"90":{"location":"13:21671383-21704498","ensembl_id":"ENSG00000102678"}}},"hgnc_date_symbol_changed":"1995-08-15"},"entity_type":"gene","entity_name":"FGF9","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["19589401"],"evidence":["DD-Gene2Phenotype","Expert Review Amber"],"phenotypes":["MULTIPLE SYNOSTOSES SYNDROME TYPE 3 612961"],"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"}]}}]}
