{"count":4,"next":null,"previous":null,"results":[{"gene_data":{"alias":["KE04","Erlin-1","SPG62"],"biotype":"protein_coding","hgnc_id":"HGNC:16947","gene_name":"ER lipid raft associated 1","omim_gene":["611604"],"alias_name":["Band_7 23-211 Keo4 (Interim) similar to C.elegans protein C42C1.9"],"gene_symbol":"ERLIN1","hgnc_symbol":"ERLIN1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"10:101909851-101948091","ensembl_id":"ENSG00000107566"}},"GRch38":{"90":{"location":"10:100150094-100188334","ensembl_id":"ENSG00000107566"}}},"hgnc_date_symbol_changed":"2007-01-26"},"entity_type":"gene","entity_name":"ERLIN1","confidence_level":"3","penetrance":"unknown","mode_of_pathogenicity":null,"publications":["24482476"],"evidence":["Expert Review Green","Other"],"phenotypes":["Hereditary spastic paraplegia","Spastic paraplegia 62, 615681"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":165,"hash_id":"55ad019f22c1fc7042059038","name":"Hereditary spastic paraplegia","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Motor Disorders of the CNS","status":"public","version":"1.205","version_created":"2019-06-20T15:15:08.031188Z","relevant_disorders":[],"stats":{"number_of_genes":109,"number_of_strs":10,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["KE04","Erlin-1","SPG62"],"biotype":"protein_coding","hgnc_id":"HGNC:16947","gene_name":"ER lipid raft associated 1","omim_gene":["611604"],"alias_name":["Band_7 23-211 Keo4 (Interim) similar to C.elegans protein C42C1.9"],"gene_symbol":"ERLIN1","hgnc_symbol":"ERLIN1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"10:101909851-101948091","ensembl_id":"ENSG00000107566"}},"GRch38":{"90":{"location":"10:100150094-100188334","ensembl_id":"ENSG00000107566"}}},"hgnc_date_symbol_changed":"2007-01-26"},"entity_type":"gene","entity_name":"ERLIN1","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["24482476"],"evidence":["Yorkshire and North East GLH","NHS GMS","London North GLH","Expert Review Green","Other"],"phenotypes":["Hereditary spastic paraplegia","Spastic paraplegia 62, 615681"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":568,"hash_id":null,"name":"Hereditary spastic paraplegia - childhood onset","disease_group":"","disease_sub_group":"","status":"public","version":"1.179","version_created":"2019-09-30T12:40:08.803161Z","relevant_disorders":["Childhood onset hereditary spastic paraplegia;R61"],"stats":{"number_of_genes":98,"number_of_strs":10,"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":["KE04","Erlin-1","SPG62"],"biotype":"protein_coding","hgnc_id":"HGNC:16947","gene_name":"ER lipid raft associated 1","omim_gene":["611604"],"alias_name":["Band_7 23-211 Keo4 (Interim) similar to C.elegans protein C42C1.9"],"gene_symbol":"ERLIN1","hgnc_symbol":"ERLIN1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"10:101909851-101948091","ensembl_id":"ENSG00000107566"}},"GRch38":{"90":{"location":"10:100150094-100188334","ensembl_id":"ENSG00000107566"}}},"hgnc_date_symbol_changed":"2007-01-26"},"entity_type":"gene","entity_name":"ERLIN1","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["24482476"],"evidence":["Yorkshire and North East GLH","South West GLH","Expert Review Green","NHS GMS","London North GLH"],"phenotypes":["Hereditary spastic paraplegia","Spastic paraplegia 62, 615681"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":567,"hash_id":null,"name":"Hereditary spastic paraplegia - adult onset","disease_group":"","disease_sub_group":"","status":"public","version":"0.156","version_created":"2019-09-30T12:38:14.427158Z","relevant_disorders":["R60"],"stats":{"number_of_genes":97,"number_of_strs":10,"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)"}]}},{"gene_data":{"alias":["KE04","Erlin-1","SPG62"],"biotype":"protein_coding","hgnc_id":"HGNC:16947","gene_name":"ER lipid raft associated 1","omim_gene":["611604"],"alias_name":["Band_7 23-211 Keo4 (Interim) similar to C.elegans protein C42C1.9"],"gene_symbol":"ERLIN1","hgnc_symbol":"ERLIN1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"10:101909851-101948091","ensembl_id":"ENSG00000107566"}},"GRch38":{"90":{"location":"10:100150094-100188334","ensembl_id":"ENSG00000107566"}}},"hgnc_date_symbol_changed":"2007-01-26"},"entity_type":"gene","entity_name":"ERLIN1","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":null,"publications":["24482476"],"evidence":["Expert Review Red","Wessex and West Midlands GLH","NHS GMS","Yorkshire and North East GLH","Expert list"],"phenotypes":["Hereditary spastic paraplegia","Spastic paraplegia 62, 615681"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":474,"hash_id":null,"name":"Neurodegenerative disorders - adult onset","disease_group":"","disease_sub_group":"","status":"public","version":"1.106","version_created":"2019-09-20T16:19:10.101841Z","relevant_disorders":["R58"],"stats":{"number_of_genes":395,"number_of_strs":18,"number_of_regions":4},"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."}]}}]}
