{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["TNFSF2","DIF","TNF-alpha"],"biotype":"protein_coding","hgnc_id":"HGNC:11892","gene_name":"tumor necrosis factor","omim_gene":["191160"],"alias_name":["TNF superfamily, member 2"],"gene_symbol":"TNF","hgnc_symbol":"TNF","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"6:31543344-31546113","ensembl_id":"ENSG00000232810"}},"GRch38":{"90":{"location":"6:31575567-31578336","ensembl_id":"ENSG00000232810"}}},"hgnc_date_symbol_changed":"1986-01-01"},"entity_type":"gene","entity_name":"TNF","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["23106544"],"evidence":["Expert Review Red","Literature"],"phenotypes":["predisposition to hidradenitis suppurativa"],"mode_of_inheritance":"Unknown","tags":["promoter"],"panel":{"id":23,"hash_id":"5885e9db8f620309044f8a0a","name":"Familial hidradenitis suppurativa","disease_group":"Dermatological disorders","disease_sub_group":"Skin adnexa disorders","status":"public","version":"1.1","version_created":"2017-11-05T02:37:19.861127Z","relevant_disorders":[],"stats":{"number_of_genes":11,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["TNFSF2","DIF","TNF-alpha"],"biotype":"protein_coding","hgnc_id":"HGNC:11892","gene_name":"tumor necrosis factor","omim_gene":["191160"],"alias_name":["TNF superfamily, member 2"],"gene_symbol":"TNF","hgnc_symbol":"TNF","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"6:31543344-31546113","ensembl_id":"ENSG00000232810"}},"GRch38":{"90":{"location":"6:31575567-31578336","ensembl_id":"ENSG00000232810"}}},"hgnc_date_symbol_changed":"1986-01-01"},"entity_type":"gene","entity_name":"TNF","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":null,"publications":["28787010"],"evidence":["Literature"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":394,"hash_id":null,"name":"Familial Meniere Disease","disease_group":"Hearing and ear disorders","disease_sub_group":"Other hearing and ear disorders","status":"public","version":"1.1","version_created":"2018-01-17T16:26:29.432517Z","relevant_disorders":[],"stats":{"number_of_genes":130,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}