Gene: KRT12 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3859
Gene Symbol: KRT12
KRT12 		0.110 GeneticVariation disease BEFREE We have identified a novel missense mutation within the highly conserved helix-initiation motif of KRT12 causing Meesmann;s corneal dystrophy in a German family. 20577595 2010
Entrez Id: 3859
Gene Symbol: KRT12
KRT12 		0.110 Biomarker disease HPO