Gene: CFAP410 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 755
Gene Symbol: CFAP410
CFAP410 		0.320 GeneticVariation disease BEFREE Homozygous variant in C21orf2 in a case of Jeune syndrome with severe thoracic involvement: Extending the phenotypic spectrum. 28422394 2017
Entrez Id: 755
Gene Symbol: CFAP410
CFAP410 		0.320 GeneticVariation disease BEFREE C21orf2 mutations have been recently found to cause isolated retinal degeneration and Jeune syndrome. 26974433 2016
Entrez Id: 755
Gene Symbol: CFAP410
CFAP410 		0.320 Biomarker disease GENOMICS_ENGLAND An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes. 26167768 2015
Entrez Id: 755
Gene Symbol: CFAP410
CFAP410 		0.320 Biomarker disease GENOMICS_ENGLAND Autozygome-guided exome sequencing in retinal dystrophy patients reveals pathogenetic mutations and novel candidate disease genes. 23105016 2013