SLC7A2, solute carrier family 7 member 2, 6542

N. diseases: 30; N. variants: 4
Disease: Cataract ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0086543
Disease: Cataract
Cataract 		0.010 GeneticVariation disease BEFREE The Cat2 mouse mutants are interesting models for human cataracts caused by mutations in the gamma-crystallin genes at human chromosome 2q32-35. 9932285 1999