{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["DKFZp586J0619","KIAA1440","INT1","NET28"],"biotype":"protein_coding","hgnc_id":"HGNC:24555","gene_name":"integrator complex subunit 1","omim_gene":["611345"],"alias_name":null,"gene_symbol":"INTS1","hgnc_symbol":"INTS1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"7:1509913-1545489","ensembl_id":"ENSG00000164880"}},"GRch38":{"90":{"location":"7:1470277-1504367","ensembl_id":"ENSG00000164880"}}},"hgnc_date_symbol_changed":"2006-03-15"},"entity_type":"gene","entity_name":"INTS1","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":null,"publications":[],"evidence":["Victorian Clinical Genetics Services"],"phenotypes":["Cleft palate"],"mode_of_inheritance":"","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":["DKFZp586J0619","KIAA1440","INT1","NET28"],"biotype":"protein_coding","hgnc_id":"HGNC:24555","gene_name":"integrator complex subunit 1","omim_gene":["611345"],"alias_name":null,"gene_symbol":"INTS1","hgnc_symbol":"INTS1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"7:1509913-1545489","ensembl_id":"ENSG00000164880"}},"GRch38":{"90":{"location":"7:1470277-1504367","ensembl_id":"ENSG00000164880"}}},"hgnc_date_symbol_changed":"2006-03-15"},"entity_type":"gene","entity_name":"INTS1","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":null,"publications":["28542170","30622326","17544522"],"evidence":["Expert Review Green","Victorian Clinical Genetics Services","Literature"],"phenotypes":["Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies, 618571","Hypotonia","Global developmental delay","Cataract","Abnormality of the skeletal system"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","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"}]}}]}
