CSK, C-terminal Src kinase, 1445

N. diseases: 91; N. variants: 8
Disease: 15q24 Microdeletion ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3697269
Disease: 15q24 Microdeletion
15q24 Microdeletion 		0.010 Biomarker disease BEFREE There are several candidate genes within the SRO, including CYP11A1, SEMA7A, CPLX3, ARID3B, STRA6, SIN3A and CSK, that may predispose to many of the clinical features observed in individuals with 15q24 deletion syndrome. 22216833 2012