{"count":5,"next":null,"previous":null,"results":[{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:12660","gene_name":"ventral anterior homeobox 1","omim_gene":["604294"],"alias_name":null,"gene_symbol":"VAX1","hgnc_symbol":"VAX1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"10:118888032-118897812","ensembl_id":"ENSG00000148704"}},"GRch38":{"90":{"location":"10:117128521-117138301","ensembl_id":"ENSG00000148704"}}},"hgnc_date_symbol_changed":"1999-08-27"},"entity_type":"gene","entity_name":"VAX1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Emory Genetics Laboratory"],"phenotypes":["Eye Disorders"],"mode_of_inheritance":"","tags":[],"panel":{"id":249,"hash_id":"55507b25bb5a161bf644a3b2","name":"Glaucoma (developmental)","disease_group":"Ophthalmological disorders","disease_sub_group":"Anterior segment abnormalities","status":"public","version":"1.5","version_created":"2019-06-20T15:15:07.662717Z","relevant_disorders":[],"stats":{"number_of_genes":224,"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:12660","gene_name":"ventral anterior homeobox 1","omim_gene":["604294"],"alias_name":null,"gene_symbol":"VAX1","hgnc_symbol":"VAX1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"10:118888032-118897812","ensembl_id":"ENSG00000148704"}},"GRch38":{"90":{"location":"10:117128521-117138301","ensembl_id":"ENSG00000148704"}}},"hgnc_date_symbol_changed":"1999-08-27"},"entity_type":"gene","entity_name":"VAX1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["22095910"],"evidence":["Expert Review Red"],"phenotypes":["MICROPHTHALMIA, SYNDROMIC 11","MCOPS11"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":81,"hash_id":"57acb8268f620364dc61afd3","name":"Clefting","disease_group":"Dysmorphic and congenital abnormality syndromes","disease_sub_group":"Dysmorphic disorders","status":"public","version":"1.59","version_created":"2019-09-03T09:03:20.170928Z","relevant_disorders":["Familial non-syndromic cleft lip and or familial cleft palate","Familial non-syndromic clefting","Syndromic cleft lip and or cleft palate","Syndromic clefting"],"stats":{"number_of_genes":258,"number_of_strs":0,"number_of_regions":5},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"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."},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}},{"gene_data":{"alias":[],"biotype":"protein_coding","hgnc_id":"HGNC:12660","gene_name":"ventral anterior homeobox 1","omim_gene":["604294"],"alias_name":null,"gene_symbol":"VAX1","hgnc_symbol":"VAX1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"10:118888032-118897812","ensembl_id":"ENSG00000148704"}},"GRch38":{"90":{"location":"10:117128521-117138301","ensembl_id":"ENSG00000148704"}}},"hgnc_date_symbol_changed":"1999-08-27"},"entity_type":"gene","entity_name":"VAX1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","Emory Genetics Laboratory","Radboud University Medical Center, Nijmegen"],"phenotypes":["Microphthalmia, syndromic 11, 614402"],"mode_of_inheritance":"","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":[],"biotype":"protein_coding","hgnc_id":"HGNC:12660","gene_name":"ventral anterior homeobox 1","omim_gene":["604294"],"alias_name":null,"gene_symbol":"VAX1","hgnc_symbol":"VAX1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"10:118888032-118897812","ensembl_id":"ENSG00000148704"}},"GRch38":{"90":{"location":"10:117128521-117138301","ensembl_id":"ENSG00000148704"}}},"hgnc_date_symbol_changed":"1999-08-27"},"entity_type":"gene","entity_name":"VAX1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["NHS GMS","Expert Review Red"],"phenotypes":["Eye Disorders"],"mode_of_inheritance":"","tags":[],"panel":{"id":307,"hash_id":"56e0238b22c1fc09c97a6e46","name":"Retinal disorders","disease_group":"Ophthalmological disorders","disease_sub_group":"Posterior segment abnormalities","status":"public","version":"1.199","version_created":"2019-10-08T09:22:18.436205Z","relevant_disorders":["Posterior segment abnormalities","Cone Dysfunction Syndrome","Developmental macular and foveal dystrophy","Inherited macular dystrophy","Leber Congenital Amaurosis Early-Onset Severe Retinal Dystrophy","Leber Congenital Amaurosis / Early-Onset Severe Retinal Dystrophy","Leber Congenital Amaurosis or Early-Onset Severe Retinal Dystrophy","Rod Dysfunction Syndrome","Rod-cone dystrophy","Familial exudative vitreoretinopathy","Familial exudative retinopathy","R32","R33","R34","R35"],"stats":{"number_of_genes":320,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"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":[],"biotype":"protein_coding","hgnc_id":"HGNC:12660","gene_name":"ventral anterior homeobox 1","omim_gene":["604294"],"alias_name":null,"gene_symbol":"VAX1","hgnc_symbol":"VAX1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"10:118888032-118897812","ensembl_id":"ENSG00000148704"}},"GRch38":{"90":{"location":"10:117128521-117138301","ensembl_id":"ENSG00000148704"}}},"hgnc_date_symbol_changed":"1999-08-27"},"entity_type":"gene","entity_name":"VAX1","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["10601035","22095910"],"evidence":["Expert Review Amber","NHS GMS"],"phenotypes":["Microphthalmia, syndromic 11, 614402"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","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)"}]}}]}