Gene: MIP ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4284
Gene Symbol: MIP
MIP 		0.300 GermlineCausalMutation disease ORPHANET A novel MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family. 24405844 2014
Entrez Id: 4284
Gene Symbol: MIP
MIP 		0.300 GermlineCausalMutation disease ORPHANET A novel mutation in the major intrinsic protein (MIP) associated with autosomal dominant congenital cataracts in a Chinese family. 20361015 2010