Gene: KITLG ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4254
Gene Symbol: KITLG
KITLG 		0.300 GermlineCausalMutation disease ORPHANET Gain-of-function mutation of KIT ligand on melanin synthesis causes familial progressive hyperpigmentation. 19375057 2009