Gene: IFT140 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9742
Gene Symbol: IFT140
IFT140 		0.400 GeneticVariation disease UNIPROT The ophthalmic phenotype of IFT140-related ciliopathy ranges from isolated to syndromic congenital retinal dystrophy. 26359340 2016
Entrez Id: 9742
Gene Symbol: IFT140
IFT140 		0.400 GeneticVariation disease UNIPROT Nonsyndromic Retinal Dystrophy due to Bi-Allelic Mutations in the Ciliary Transport Gene IFT140. 26968735 2016
Entrez Id: 9742
Gene Symbol: IFT140
IFT140 		0.400 GeneticVariation disease UNIPROT Mutations in human IFT140 cause non-syndromic retinal degeneration. 26216056 2015
Entrez Id: 9742
Gene Symbol: IFT140
IFT140 		0.400 CausalMutation disease CLINVAR