{"count":5,"next":null,"previous":null,"results":[{"gene_data":{"alias":["MOX1"],"biotype":"protein_coding","hgnc_id":"HGNC:7013","gene_name":"mesenchyme homeobox 1","omim_gene":["600147"],"alias_name":null,"gene_symbol":"MEOX1","hgnc_symbol":"MEOX1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"17:41717756-41739322","ensembl_id":"ENSG00000005102"}},"GRch38":{"90":{"location":"17:43640388-43661954","ensembl_id":"ENSG00000005102"}}},"hgnc_date_symbol_changed":"1994-12-14"},"entity_type":"gene","entity_name":"MEOX1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Radboud University Medical Center, Nijmegen"],"phenotypes":["Klippel-Feil syndrome"],"mode_of_inheritance":"","tags":[],"panel":{"id":11,"hash_id":"57e3df7e8f62034b82c0d332","name":"Familial Neural Tube Defects","disease_group":"","disease_sub_group":"","status":"public","version":"1.5","version_created":"2017-11-05T02:37:19.836037Z","relevant_disorders":[],"stats":{"number_of_genes":44,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["MOX1"],"biotype":"protein_coding","hgnc_id":"HGNC:7013","gene_name":"mesenchyme homeobox 1","omim_gene":["600147"],"alias_name":null,"gene_symbol":"MEOX1","hgnc_symbol":"MEOX1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"17:41717756-41739322","ensembl_id":"ENSG00000005102"}},"GRch38":{"90":{"location":"17:43640388-43661954","ensembl_id":"ENSG00000005102"}}},"hgnc_date_symbol_changed":"1994-12-14"},"entity_type":"gene","entity_name":"MEOX1","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["NHS GMS","Expert Review Green","Expert list","Radboud University Medical Center, Nijmegen",""],"phenotypes":["Klippel-Feil syndrome 2 214300"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":309,"hash_id":"5693952f22c1fc251660fb1e","name":"Skeletal dysplasia","disease_group":"Skeletal disorders","disease_sub_group":"Skeletal dysplasias","status":"public","version":"1.203","version_created":"2019-10-03T09:38:50.417968Z","relevant_disorders":["Unexplained skeletal dysplasia","Skeletal dysplasia"],"stats":{"number_of_genes":546,"number_of_strs":1,"number_of_regions":6},"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":["MOX1"],"biotype":"protein_coding","hgnc_id":"HGNC:7013","gene_name":"mesenchyme homeobox 1","omim_gene":["600147"],"alias_name":null,"gene_symbol":"MEOX1","hgnc_symbol":"MEOX1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"17:41717756-41739322","ensembl_id":"ENSG00000005102"}},"GRch38":{"90":{"location":"17:43640388-43661954","ensembl_id":"ENSG00000005102"}}},"hgnc_date_symbol_changed":"1994-12-14"},"entity_type":"gene","entity_name":"MEOX1","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Amber","PAGE DD-Gene2Phenotype"],"phenotypes":["KLIPPEL-FEIL ANOMALY"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":478,"hash_id":null,"name":"Fetal anomalies","disease_group":"","disease_sub_group":"","status":"public","version":"0.344","version_created":"2019-09-17T09:38:10.568007Z","relevant_disorders":["R21"],"stats":{"number_of_genes":1721,"number_of_strs":0,"number_of_regions":0},"types":[{"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":["MOX1"],"biotype":"protein_coding","hgnc_id":"HGNC:7013","gene_name":"mesenchyme homeobox 1","omim_gene":["600147"],"alias_name":null,"gene_symbol":"MEOX1","hgnc_symbol":"MEOX1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"17:41717756-41739322","ensembl_id":"ENSG00000005102"}},"GRch38":{"90":{"location":"17:43640388-43661954","ensembl_id":"ENSG00000005102"}}},"hgnc_date_symbol_changed":"1994-12-14"},"entity_type":"gene","entity_name":"MEOX1","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["DD-Gene2Phenotype","Expert Review Amber"],"phenotypes":["KLIPPEL-FEIL ANOMALY 118100"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":484,"hash_id":null,"name":"DDG2P","disease_group":"","disease_sub_group":"","status":"public","version":"1.137","version_created":"2019-10-08T15:56:59.220133Z","relevant_disorders":[],"stats":{"number_of_genes":1893,"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"}]}},{"gene_data":{"alias":["MOX1"],"biotype":"protein_coding","hgnc_id":"HGNC:7013","gene_name":"mesenchyme homeobox 1","omim_gene":["600147"],"alias_name":null,"gene_symbol":"MEOX1","hgnc_symbol":"MEOX1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"17:41717756-41739322","ensembl_id":"ENSG00000005102"}},"GRch38":{"90":{"location":"17:43640388-43661954","ensembl_id":"ENSG00000005102"}}},"hgnc_date_symbol_changed":"1994-12-14"},"entity_type":"gene","entity_name":"MEOX1","confidence_level":"2","penetrance":"Complete","mode_of_pathogenicity":"","publications":["23290072","24073994"],"evidence":["Expert Review Amber"],"phenotypes":["KLIPPEL-FEIL SYNDROME 2, AUTOSOMAL RECESSIVE","KFS2"],"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"}]}}]}