Gene: CCDC151 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 115948
Gene Symbol: CCDC151
CCDC151 		0.100 CausalMutation phenotype CLINVAR Nonsense mutation in coiled-coil domain containing 151 gene (CCDC151) causes primary ciliary dyskinesia. 25224326 2014
Entrez Id: 115948
Gene Symbol: CCDC151
CCDC151 		0.100 CausalMutation phenotype CLINVAR Laterality defects other than situs inversus totalis in primary ciliary dyskinesia: insights into situs ambiguus and heterotaxy. 24577564 2014
Entrez Id: 115948
Gene Symbol: CCDC151
CCDC151 		0.100 CausalMutation phenotype CLINVAR CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formation. 25192045 2014
Entrez Id: 115948
Gene Symbol: CCDC151
CCDC151 		0.100 CausalMutation phenotype CLINVAR Primary ciliary dyskinesia: diagnostic and phenotypic features. 14656747 2004
Entrez Id: 115948
Gene Symbol: CCDC151
CCDC151 		0.100 CausalMutation phenotype CLINVAR Mild fetal cerebral ventriculomegaly as a prenatal sonographic marker for Kartagener syndrome. 12627427 2003
Entrez Id: 115948
Gene Symbol: CCDC151
CCDC151 		0.100 CausalMutation phenotype CLINVAR Treatment of otitis media with effusion in children with primary ciliary dyskinesia. 9298603 1997
Entrez Id: 115948
Gene Symbol: CCDC151
CCDC151 		0.100 CausalMutation phenotype CLINVAR Unusual inheritance of primary ciliary dyskinesia (Kartagener's syndrome). 8071978 1994