{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["TAFII70","TAFII80","MGC:8964","TAFII85"],"biotype":"protein_coding","hgnc_id":"HGNC:11540","gene_name":"TATA-box binding protein associated factor 6","omim_gene":["602955"],"alias_name":["TAF6 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 80 kD","transcription initiation factor TFIID 70 kD subunit"],"gene_symbol":"TAF6","hgnc_symbol":"TAF6","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"7:99704693-99717464","ensembl_id":"ENSG00000106290"}},"GRch38":{"90":{"location":"7:100107070-100119841","ensembl_id":"ENSG00000106290"}}},"hgnc_date_symbol_changed":"2001-12-07"},"entity_type":"gene","entity_name":"TAF6","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Red","SFARI"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":657,"hash_id":null,"name":"Autism","disease_group":"","disease_sub_group":"","status":"public","version":"0.15","version_created":"2019-06-20T15:10:14.437740Z","relevant_disorders":[],"stats":{"number_of_genes":733,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Research","slug":"research","description":"This is a gene panel used for research."}]}},{"gene_data":{"alias":["TAFII70","TAFII80","MGC:8964","TAFII85"],"biotype":"protein_coding","hgnc_id":"HGNC:11540","gene_name":"TATA-box binding protein associated factor 6","omim_gene":["602955"],"alias_name":["TAF6 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 80 kD","transcription initiation factor TFIID 70 kD subunit"],"gene_symbol":"TAF6","hgnc_symbol":"TAF6","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"7:99704693-99717464","ensembl_id":"ENSG00000106290"}},"GRch38":{"90":{"location":"7:100107070-100119841","ensembl_id":"ENSG00000106290"}}},"hgnc_date_symbol_changed":"2001-12-07"},"entity_type":"gene","entity_name":"TAF6","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":null,"publications":["25558065","25574841"],"evidence":["Victorian Clinical Genetics Services","Expert Review Green","Literature"],"phenotypes":["Alazami-Yuan syndrome, 617126","Intellectual disability"],"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"}]}}]}