C21orf59:Ensemblv90

chromosome 21 open reading frame 59
OMIM: 615494, ClinGen, DECIPHER

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green C21orf59 in Ciliary Dyskinesia Level 2: Respiratory disorders Version 1.68	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Ciliary dyskinesia, primary, 26, MIM# 615500 Tags founder new gene name
Green C21orf59 in Heterotaxy Level 2: Dysmorphic and congenital abnormality syndromes Version 1.44	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Ciliary dyskinesia, primary, 26, MIM# 615500 Tags founder new gene name
Green C21orf59 in Mendeliome Version 1.3802	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Ciliary dyskinesia, primary, 26, MIM# 615500 Tags founder new gene name
Green C21orf59 in Fetal anomalies Version 1.482	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Victorian Clinical Genetics Services Phenotypes Primary ciliary dyskinesia 26, MONDO:0014211 Ciliary dyskinesia, primary, 26, OMIM:615500 Tags founder new gene name
Green C21orf59 in Ciliary Dyskinesia Level 2: Respiratory disorders Version 2.0	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Victorian Clinical Genetics Services Expert Review Green Phenotypes Ciliary dyskinesia, primary, 26, MIM# 615500 Tags founder new gene name
Green C21orf59 in Heterotaxy Level 2: Dysmorphic and congenital abnormality syndromes Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Victorian Clinical Genetics Services Expert Review Green Phenotypes Ciliary dyskinesia, primary, 26, MIM# 615500 Tags founder new gene name
Green C21orf59 in Fetal anomalies Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Victorian Clinical Genetics Services Genomics England PanelApp Expert Review Green Phenotypes Primary ciliary dyskinesia 26, MONDO:0014211 Ciliary dyskinesia, primary, 26, OMIM:615500 Tags founder new gene name