{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["OP-1"],"biotype":"protein_coding","hgnc_id":"HGNC:1074","gene_name":"bone morphogenetic protein 7","omim_gene":["112267"],"alias_name":["osteogenic protein 1"],"gene_symbol":"BMP7","hgnc_symbol":"BMP7","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"20:55743804-55841685","ensembl_id":"ENSG00000101144"}},"GRch38":{"90":{"location":"20:57168748-57266629","ensembl_id":"ENSG00000101144"}}},"hgnc_date_symbol_changed":"1991-06-05"},"entity_type":"gene","entity_name":"BMP7","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["20506283"],"evidence":["Literature"],"phenotypes":[],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":294,"hash_id":"5550a166bb5a161bf644a3b6","name":"Ocular coloboma","disease_group":"Ophthalmological disorders","disease_sub_group":"Ocular malformations","status":"public","version":"1.34","version_created":"2019-06-20T15:15:14.600523Z","relevant_disorders":[],"stats":{"number_of_genes":63,"number_of_strs":0,"number_of_regions":2},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["OP-1"],"biotype":"protein_coding","hgnc_id":"HGNC:1074","gene_name":"bone morphogenetic protein 7","omim_gene":["112267"],"alias_name":["osteogenic protein 1"],"gene_symbol":"BMP7","hgnc_symbol":"BMP7","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"20:55743804-55841685","ensembl_id":"ENSG00000101144"}},"GRch38":{"90":{"location":"20:57168748-57266629","ensembl_id":"ENSG00000101144"}}},"hgnc_date_symbol_changed":"1991-06-05"},"entity_type":"gene","entity_name":"BMP7","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"other - please provide details in the comments","publications":["20506283","7590254"],"evidence":["Expert Review Amber","NHS GMS"],"phenotypes":["Microphthalmia, anophthalmia, systemic abnormalities, intellectual disability","None"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","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)"}]}}]}