{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:4947","gene_name":"major histocompatibility complex, class II, DR alpha","omim_gene":["142860"],"alias_name":null,"gene_symbol":"HLA-DRA","hgnc_symbol":"HLA-DRA","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"6:32407619-32412823","ensembl_id":"ENSG00000204287"}},"GRch38":{"90":{"location":"6:32439842-32445046","ensembl_id":"ENSG00000204287"}}},"hgnc_date_symbol_changed":"2001-06-22"},"entity_type":"gene","entity_name":"HLA-DRA","confidence_level":"2","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Amber","Other"],"phenotypes":["Graham Little-Piccardi-Lassueur syndrome","Graham Little syndrome","lichen planopilaris","progressive cicatricial (scarring) alopecia"],"mode_of_inheritance":"Unknown","tags":[],"panel":{"id":305,"hash_id":"568e844522c1fc1c78b67156","name":"Familial cicatricial alopecia","disease_group":"Dermatological disorders","disease_sub_group":"Skin adnexa disorders","status":"public","version":"1.2","version_created":"2019-06-20T15:15:02.358694Z","relevant_disorders":[],"stats":{"number_of_genes":25,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:4947","gene_name":"major histocompatibility complex, class II, DR alpha","omim_gene":["142860"],"alias_name":null,"gene_symbol":"HLA-DRA","hgnc_symbol":"HLA-DRA","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"6:32407619-32412823","ensembl_id":"ENSG00000204287"}},"GRch38":{"90":{"location":"6:32439842-32445046","ensembl_id":"ENSG00000204287"}}},"hgnc_date_symbol_changed":"2001-06-22"},"entity_type":"gene","entity_name":"HLA-DRA","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Amber"],"phenotypes":["lichen planopilaris","progressive cicatricial (scarring) alopecia","Graham Little syndrome","Graham Little-Piccardi-Lassueur syndrome"],"mode_of_inheritance":"Unknown","tags":[],"panel":{"id":553,"hash_id":null,"name":"Ectodermal dysplasia","disease_group":"","disease_sub_group":"","status":"public","version":"0.22","version_created":"2019-09-17T19:00:33.930109Z","relevant_disorders":[],"stats":{"number_of_genes":71,"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"}]}}]}
