{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["DKFZP564K1964"],"biotype":"protein_coding","hgnc_id":"HGNC:24529","gene_name":"transmembrane protein 98","omim_gene":["615949"],"alias_name":null,"gene_symbol":"TMEM98","hgnc_symbol":"TMEM98","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"17:31254928-31272124","ensembl_id":"ENSG00000006042"}},"GRch38":{"90":{"location":"17:32927910-32945106","ensembl_id":"ENSG00000006042"}}},"hgnc_date_symbol_changed":"2005-12-16"},"entity_type":"gene","entity_name":"TMEM98","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["24852644","26392740"],"evidence":["Expert Review Green","Literature"],"phenotypes":["Nanophthalmos 4, 615972","NNO4"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":34,"hash_id":"553f97abbb5a1616e5ed45f9","name":"Anophthalmia or microphthalmia","disease_group":"Ophthalmological disorders","disease_sub_group":"Ocular malformations","status":"public","version":"1.21","version_created":"2019-06-20T15:14:55.669056Z","relevant_disorders":["Anophthalmia or microphthamia","Anophthalmia/microphthamia","Anophthalmia/microphthalmia"],"stats":{"number_of_genes":58,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["DKFZP564K1964"],"biotype":"protein_coding","hgnc_id":"HGNC:24529","gene_name":"transmembrane protein 98","omim_gene":["615949"],"alias_name":null,"gene_symbol":"TMEM98","hgnc_symbol":"TMEM98","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"17:31254928-31272124","ensembl_id":"ENSG00000006042"}},"GRch38":{"90":{"location":"17:32927910-32945106","ensembl_id":"ENSG00000006042"}}},"hgnc_date_symbol_changed":"2005-12-16"},"entity_type":"gene","entity_name":"TMEM98","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"Other - please provide details in the comments","publications":["24852644","26392740"],"evidence":["NHS GMS","Expert Review Green"],"phenotypes":["NNO4 Nanophthalmos 4, 615972"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","tags":[],"panel":{"id":509,"hash_id":null,"name":"Structural eye disease","disease_group":"","disease_sub_group":"","status":"public","version":"0.93","version_created":"2019-10-09T13:18:12.923145Z","relevant_disorders":["R36"],"stats":{"number_of_genes":456,"number_of_strs":0,"number_of_regions":2},"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)"}]}}]}