SLC24A3, solute carrier family 24 member 3, 57419

N. diseases: 34; N. variants: 11
Disease: Amelogenesis Imperfecta ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0002452
Disease: Amelogenesis Imperfecta
Amelogenesis Imperfecta 		0.010 Biomarker disease BEFREE Identification of mutations in SLC24A4, encoding a potassium-dependent sodium/calcium exchanger, as a cause of amelogenesis imperfecta. 23375655 2013