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VCGS."}],"child_panel_ids":[]},"transcript":null},{"gene_data":{"alias":["ZNEUROK1","NKB"],"biotype":"protein_coding","hgnc_id":"HGNC:11521","gene_name":"tachykinin 3","omim_gene":["162330"],"alias_name":["preprotachykinin-B"],"gene_symbol":"TAC3","hgnc_symbol":"TAC3","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"12:57403784-57422667","ensembl_id":"ENSG00000166863"}},"GRch38":{"90":{"location":"12:57010000-57028883","ensembl_id":"ENSG00000166863"}}},"hgnc_date_symbol_changed":"1986-01-01"},"entity_type":"gene","entity_name":"TAC3","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"","publications":["20332248, 20194706, 34403359, 19079066"],"evidence":["Expert List","Expert Review Green"],"phenotypes":["Hypogonadotropic hypogonadism 10 with or without anosmia, MIM# 614839"],"mode_of_inheritance":"BIALLELIC, autosomal or pseudoautosomal","tags":[],"panel":{"id":3166,"hash_id":null,"name":"Primary Ovarian Insufficiency_Premature Ovarian 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If FSH is low, the Hypogonadotropic hypogonadism panel should be used.\r\n\r\nPlease also consider the Differences of Sex Development panel where appropriate depending on clinical features.","status":"public","version":"0.414","version_created":"2026-04-13T17:24:24.650771+10:00","relevant_disorders":["Premature ovarian insufficiency","HP:0008209"],"stats":{"number_of_genes":164,"number_of_strs":2,"number_of_regions":0},"types":[{"name":"Royal Melbourne Hospital","slug":"royal-melbourne-hospital","description":"Royal Melbourne Hospital"},{"name":"Rare Disease","slug":"rare-disease","description":"Rare disease panels"},{"name":"Genetic Health Queensland","slug":"genetic-health-queensland","description":"Panel used by GHQ."},{"name":"Victorian Clinical Genetics Services","slug":"victorian-clinical-genetics-services","description":"Panel used by VCGS."}],"child_panel_ids":[]},"transcript":null}]}