{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["TSG"],"biotype":"protein_coding","hgnc_id":"HGNC:12429","gene_name":"twisted gastrulation BMP signaling modulator 1","omim_gene":["605049"],"alias_name":null,"gene_symbol":"TWSG1","hgnc_symbol":"TWSG1","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"18:9334765-9402418","ensembl_id":"ENSG00000128791"}},"GRch38":{"90":{"location":"18:9334767-9402420","ensembl_id":"ENSG00000128791"}}},"hgnc_date_symbol_changed":"2000-02-16"},"entity_type":"gene","entity_name":"TWSG1","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":["10866189","11260715","11260716","11260717"],"evidence":["Expert Review Red","Expert list"],"phenotypes":["Bilateral Microtia"],"mode_of_inheritance":"Unknown","tags":[],"panel":{"id":251,"hash_id":"57f4dbd18f62036d37cfe4e4","name":"Deafness and congenital structural abnormalities","disease_group":"Hearing and ear disorders","disease_sub_group":"Deafness and congenital structural abnormalities","status":"public","version":"1.17","version_created":"2019-06-20T15:10:56.166309Z","relevant_disorders":["Bilateral microtia","Ear malformations with hearing impairment","Ear malformations","Familial hemifacial microsomia"],"stats":{"number_of_genes":54,"number_of_strs":0,"number_of_regions":3},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}}]}