RPS6KA3, ribosomal protein S6 kinase A3, 6197

N. diseases: 315; N. variants: 37
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0424230
Disease: Motor retardation
Motor retardation
0.300 Biomarker phenotype CTD_human Mutations in the kinase Rsk-2 associated with Coffin-Lowry syndrome. 8955270 1996