{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["CDw92","CTL1","CHTL1","CD92"],"biotype":"protein_coding","hgnc_id":"HGNC:18798","gene_name":"solute carrier family 44 member 1","omim_gene":["606105"],"alias_name":null,"gene_symbol":"SLC44A1","hgnc_symbol":"SLC44A1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"9:108006903-108201452","ensembl_id":"ENSG00000070214"}},"GRch38":{"90":{"location":"9:105244622-105439171","ensembl_id":"ENSG00000070214"}}},"hgnc_date_symbol_changed":"2005-09-06"},"entity_type":"gene","entity_name":"SLC44A1","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":"","publications":["29903433","28097321"],"evidence":["Expert list"],"phenotypes":["mild ID, macrocephaly, acanthosis nigricans, accessory mamilla, muscular hypotonia, frontotemporal cerebral atrophy"],"mode_of_inheritance":"","tags":[],"panel":{"id":112,"hash_id":"55928cf522c1fc4f7d26e960","name":"Mitochondrial disorders","disease_group":"Metabolic disorders","disease_sub_group":"Mitochondrial","status":"public","version":"2.1","version_created":"2019-10-01T15:59:44.993681Z","relevant_disorders":["Lactic acidosis","All recognised syndromes and those with suggestive features"],"stats":{"number_of_genes":467,"number_of_strs":2,"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"},{"name":"GMS signed-off","slug":"gms-signed-off","description":"This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."}]}}]}