{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["LOC124512"],"biotype":"protein_coding","hgnc_id":"HGNC:26988","gene_name":"methyltransferase like 23","omim_gene":["615262"],"alias_name":null,"gene_symbol":"METTL23","hgnc_symbol":"METTL23","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"17:74722912-74730018","ensembl_id":"ENSG00000181038"}},"GRch38":{"90":{"location":"17:76726830-76733936","ensembl_id":"ENSG00000181038"}}},"hgnc_date_symbol_changed":"2011-03-03"},"entity_type":"gene","entity_name":"METTL23","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["24501276"],"evidence":["Expert Review Red"],"phenotypes":["Mental retardation, autosomal recessive 44,  615942","MRT44"],"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":["LOC124512"],"biotype":"protein_coding","hgnc_id":"HGNC:26988","gene_name":"methyltransferase like 23","omim_gene":["615262"],"alias_name":null,"gene_symbol":"METTL23","hgnc_symbol":"METTL23","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"17:74722912-74730018","ensembl_id":"ENSG00000181038"}},"GRch38":{"90":{"location":"17:76726830-76733936","ensembl_id":"ENSG00000181038"}}},"hgnc_date_symbol_changed":"2011-03-03"},"entity_type":"gene","entity_name":"METTL23","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":null,"publications":["24501276","24626631"],"evidence":["Expert Review Green","Literature"],"phenotypes":["Mental retardation, autosomal recessive 44, 615942"],"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"}]}}]}