CCDC151:Ensemblv90

coiled-coil domain containing 151
OMIM: 615956, ClinGen, DECIPHER

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green CCDC151 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, 30, MIM# 616037 Tags new gene name
Green CCDC151 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, 30, MIM# 616037 Tags new gene name
Green CCDC151 in Mendeliome Version 1.3802	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Ciliary dyskinesia, primary, 30, MIM# 616037 Tags new gene name
Green CCDC151 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 30, MONDO:0014465 Ciliary dyskinesia, primary, 30, OMIM:616037 Tags new gene name
Green CCDC151 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, 30, MIM# 616037 Tags new gene name
Green CCDC151 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, 30, MIM# 616037 Tags new gene name
Green CCDC151 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 30, MONDO:0014465 Ciliary dyskinesia, primary, 30, OMIM:616037 Tags new gene name