{"count":2,"next":null,"previous":null,"results":[{"gene_data":{"alias":["P2Y5"],"biotype":"protein_coding","hgnc_id":"HGNC:15520","gene_name":"lysophosphatidic acid receptor 6","omim_gene":["609239"],"alias_name":null,"gene_symbol":"LPAR6","hgnc_symbol":"LPAR6","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"13:48963707-49018840","ensembl_id":"ENSG00000139679"}},"GRch38":{"90":{"location":"13:48389567-48444704","ensembl_id":"ENSG00000139679"}}},"hgnc_date_symbol_changed":"2009-06-23"},"entity_type":"gene","entity_name":"LPAR6","confidence_level":"3","penetrance":"Complete","mode_of_pathogenicity":"","publications":["21070332","21426374","18461368"],"evidence":["Expert Review Green","Other","Radboud University Medical Center, Nijmegen"],"phenotypes":["Hypotrichosis 8, 278150","Hereditary hypotrichosis simplex (HHS)","Hypotrichosis simplex (HS)","localized autosomal recessive hypotrichosis-3 (LAH3)","Autosomal recessive hypotrichosis","Hypotrichosis 8","HYPT8","Woolly hair, autosomal recessive 1, with or without hypotrichosis, 278150"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":189,"hash_id":"56937d0d22c1fc25158f3c9e","name":"Non-syndromic hypotrichosis","disease_group":"Dermatological disorders","disease_sub_group":"Skin adnexa disorders","status":"public","version":"1.2","version_created":"2019-06-20T15:15:14.478586Z","relevant_disorders":[],"stats":{"number_of_genes":11,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["P2Y5"],"biotype":"protein_coding","hgnc_id":"HGNC:15520","gene_name":"lysophosphatidic acid receptor 6","omim_gene":["609239"],"alias_name":null,"gene_symbol":"LPAR6","hgnc_symbol":"LPAR6","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"13:48963707-49018840","ensembl_id":"ENSG00000139679"}},"GRch38":{"90":{"location":"13:48389567-48444704","ensembl_id":"ENSG00000139679"}}},"hgnc_date_symbol_changed":"2009-06-23"},"entity_type":"gene","entity_name":"LPAR6","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["21426374","21070332","18461368"],"evidence":["Expert Review Green"],"phenotypes":["Hypotrichosis 8","Woolly hair, autosomal recessive 1, with or without hypotrichosis, 278150","HYPT8","localized autosomal recessive hypotrichosis-3 (LAH3)","Autosomal recessive hypotrichosis","Hereditary hypotrichosis simplex (HHS)","Hypotrichosis simplex (HS)","Hypotrichosis 8, 278150"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":553,"hash_id":null,"name":"Ectodermal dysplasia","disease_group":"","disease_sub_group":"","status":"public","version":"0.22","version_created":"2019-09-17T19:00:33.930109Z","relevant_disorders":[],"stats":{"number_of_genes":71,"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"}]}}]}
