Gene: IFITM5 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 387733
Gene Symbol: IFITM5
IFITM5 		0.020 GeneticVariation disease BEFREE The exception is a unique dominant defect in IFITM5, which encodes Bril and leads to hypertrophic callus and interosseous membrane ossification. 23771926 2013
Entrez Id: 387733
Gene Symbol: IFITM5
IFITM5 		0.020 GeneticVariation disease BEFREE A mutation in the 5'-UTR of IFITM5 creates an in-frame start codon and causes autosomal-dominant osteogenesis imperfecta type V with hyperplastic callus. 22863195 2012