Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 60681
Gene Symbol: FKBP10
FKBP10
CUI: C1850168
Disease: Bruck syndrome 1
Bruck syndrome 1 		0.700 GeneticVariation UNIPROT Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen. 22949511

2013
Entrez Id: 60681
Gene Symbol: FKBP10
FKBP10
CUI: C1850168
Disease: Bruck syndrome 1
Bruck syndrome 1 		0.700 GeneticVariation UNIPROT Mutations in FKBP10 cause recessive osteogenesis imperfecta and Bruck syndrome. 20839288

2011