C21orf59

chromosome 21 open reading frame 59
OMIM: 615494, Gene2Phenotype

6 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Green C21orf59 in Primary ciliary disorders Level 3: Respiratory ciliopathies Level 2: Ciliopathies Version 1.42	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green UKGTN Radboud University Medical Center, Nijmegen Phenotypes Ciliary dyskinesia, primary, 26, 615500 Tags new-gene-name
Green C21orf59 in Laterality disorders and isomerism Version 3.10 Latest signed off version: v3.9 (1 May 2024)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green NHS GMS Phenotypes Ciliary dyskinesia, primary, 26, 615500 Tags new-gene-name
Green C21orf59 in Respiratory ciliopathies including non-CF bronchiectasis Version 3.11 Latest signed off version: v3.10 (1 May 2024)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green NHS GMS Phenotypes Ciliary dyskinesia, primary, 26, 615500 Tags new-gene-name
Green C21orf59 in Fetal anomalies Version 4.1 Latest signed off version: v4.0 (1 May 2024)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green PAGE DD-Gene2Phenotype Phenotypes Ciliary dyskinesia, primary, 26, OMIM:615500 Primary ciliary dyskinesia 26, MONDO:0014211 Tags new-gene-name
Green C21orf59 in DDG2P Version 4.1 Latest signed off version: v4.0 (1 May 2024) Component of the following Super Panels: Paediatric disorders	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green DD-Gene2Phenotype Phenotypes PRIMARY CILIARY DYSKINESIA Tags new-gene-name
Red C21orf59 in Rare multisystem ciliopathy disorders Level 3: Congenital malformations caused by ciliopathies Level 2: Ciliopathies Version 1.172	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Radboud University Medical Center, Nijmegen Expert list Phenotypes Ciliary dyskinesia, primary, 26, 615500 Tags new-gene-name