{"count":5,"next":null,"previous":null,"results":[{"gene_data":{"alias":["DXS8237E","KIAA0122","GPATC9","ZRANB5","GPATCH9"],"biotype":"protein_coding","hgnc_id":"HGNC:9896","gene_name":"RNA binding motif protein 10","omim_gene":["300080"],"alias_name":null,"gene_symbol":"RBM10","hgnc_symbol":"RBM10","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"X:47004268-47046212","ensembl_id":"ENSG00000182872"}},"GRch38":{"90":{"location":"X:47144869-47186813","ensembl_id":"ENSG00000182872"}}},"hgnc_date_symbol_changed":"2000-02-21"},"entity_type":"gene","entity_name":"RBM10","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":null,"publications":["21910224","20451169","24259342"],"evidence":["Victorian Clinical Genetics Services"],"phenotypes":["Polydactyly","TARP syndrome 311900"],"mode_of_inheritance":"X-LINKED: hemizygous mutation in males, biallelic mutations in females","tags":[],"panel":{"id":384,"hash_id":null,"name":"Limb disorders","disease_group":"","disease_sub_group":"","status":"public","version":"1.61","version_created":"2019-10-03T10:01:34.398179Z","relevant_disorders":[],"stats":{"number_of_genes":234,"number_of_strs":0,"number_of_regions":1},"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":["DXS8237E","KIAA0122","GPATC9","ZRANB5","GPATCH9"],"biotype":"protein_coding","hgnc_id":"HGNC:9896","gene_name":"RNA binding motif protein 10","omim_gene":["300080"],"alias_name":null,"gene_symbol":"RBM10","hgnc_symbol":"RBM10","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"X:47004268-47046212","ensembl_id":"ENSG00000182872"}},"GRch38":{"90":{"location":"X:47144869-47186813","ensembl_id":"ENSG00000182872"}}},"hgnc_date_symbol_changed":"2000-02-21"},"entity_type":"gene","entity_name":"RBM10","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Amber","PAGE DD-Gene2Phenotype"],"phenotypes":["TARP SYNDROME"],"mode_of_inheritance":"X-LINKED: hemizygous mutation in males, biallelic mutations in females","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":["DXS8237E","KIAA0122","GPATC9","ZRANB5","GPATCH9"],"biotype":"protein_coding","hgnc_id":"HGNC:9896","gene_name":"RNA binding motif protein 10","omim_gene":["300080"],"alias_name":null,"gene_symbol":"RBM10","hgnc_symbol":"RBM10","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"X:47004268-47046212","ensembl_id":"ENSG00000182872"}},"GRch38":{"90":{"location":"X:47144869-47186813","ensembl_id":"ENSG00000182872"}}},"hgnc_date_symbol_changed":"2000-02-21"},"entity_type":"gene","entity_name":"RBM10","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["20451169","5410571"],"evidence":["DD-Gene2Phenotype","Expert Review Amber"],"phenotypes":["TARP SYNDROME 311900"],"mode_of_inheritance":"X-LINKED: hemizygous mutation in males, biallelic mutations in females","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":["DXS8237E","KIAA0122","GPATC9","ZRANB5","GPATCH9"],"biotype":"protein_coding","hgnc_id":"HGNC:9896","gene_name":"RNA binding motif protein 10","omim_gene":["300080"],"alias_name":null,"gene_symbol":"RBM10","hgnc_symbol":"RBM10","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"X:47004268-47046212","ensembl_id":"ENSG00000182872"}},"GRch38":{"90":{"location":"X:47144869-47186813","ensembl_id":"ENSG00000182872"}}},"hgnc_date_symbol_changed":"2000-02-21"},"entity_type":"gene","entity_name":"RBM10","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["20451169"],"evidence":["Victorian Clinical Genetics Services","Expert Review Green"],"phenotypes":["TARP SYNDROME","TARPS","Cleft palate"],"mode_of_inheritance":"X-LINKED: hemizygous mutation in males, biallelic mutations in females","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":["DXS8237E","KIAA0122","GPATC9","ZRANB5","GPATCH9"],"biotype":"protein_coding","hgnc_id":"HGNC:9896","gene_name":"RNA binding motif protein 10","omim_gene":["300080"],"alias_name":null,"gene_symbol":"RBM10","hgnc_symbol":"RBM10","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"X:47004268-47046212","ensembl_id":"ENSG00000182872"}},"GRch38":{"90":{"location":"X:47144869-47186813","ensembl_id":"ENSG00000182872"}}},"hgnc_date_symbol_changed":"2000-02-21"},"entity_type":"gene","entity_name":"RBM10","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Victorian Clinical Genetics Services","Expert Review Green","Radboud University Medical Center, Nijmegen","Emory Genetics Laboratory"],"phenotypes":["TARP syndrome, 311900","TARP SYNDROME"],"mode_of_inheritance":"X-LINKED: hemizygous mutation in males, biallelic mutations in females","tags":[],"panel":{"id":285,"hash_id":"558aa423bb5a16630e15b63c","name":"Intellectual disability","disease_group":"Neurology and neurodevelopmental disorders","disease_sub_group":"Neurodevelopmental disorders","status":"public","version":"2.1065","version_created":"2019-10-07T13:42:16.019766Z","relevant_disorders":["Coarse facial features including Coffin-Siris-like disorders","ID","Moderate","severe or profound intellectual disability","Schizophrenia plus additional features","Intellectual disability - microarray","fragile X and sequencing"],"stats":{"number_of_genes":2253,"number_of_strs":11,"number_of_regions":57},"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"}]}}]}