{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["OlfC","NOE2"],"biotype":"protein_coding","hgnc_id":"HGNC:17189","gene_name":"olfactomedin 2","omim_gene":["617492"],"alias_name":["noelin 2"],"gene_symbol":"OLFM2","hgnc_symbol":"OLFM2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"19:9964394-10047228","ensembl_id":"ENSG00000105088"}},"GRch38":{"90":{"location":"19:9853718-9936552","ensembl_id":"ENSG00000105088"}}},"hgnc_date_symbol_changed":"2002-01-11"},"entity_type":"gene","entity_name":"OLFM2","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["27844144","17122126"],"evidence":["London North GLH","Expert Review Amber","NHS GMS"],"phenotypes":["Bilateral microphthalmia, short stature and facial dysmorphism","No OMIM"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":509,"hash_id":null,"name":"Structural eye disease","disease_group":"","disease_sub_group":"","status":"public","version":"0.93","version_created":"2019-10-09T13:18:12.923145Z","relevant_disorders":["R36"],"stats":{"number_of_genes":456,"number_of_strs":0,"number_of_regions":2},"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)"}]}}]}