TRIM63, tripartite motif containing 63, 84676

N. diseases: 73; N. variants: 4
Disease: Muscular Atrophy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0026846
Disease: Muscular Atrophy
Muscular Atrophy 		0.510 Biomarker phenotype CTD_human Ouabain exacerbates botulinum neurotoxin-induced muscle paralysis via progression of muscle atrophy in mice. 21139329 2010
CUI: C0026846
Disease: Muscular Atrophy
Muscular Atrophy 		0.510 AlteredExpression phenotype LHGDN In catabolic states where proteolysis is increased, two genes specific to muscle atrophy, MuRf1 and MAFbx, are upregulated. 17977773 2008
CUI: C0026846
Disease: Muscular Atrophy
Muscular Atrophy 		0.510 Biomarker phenotype RGD Identification of ubiquitin ligases required for skeletal muscle atrophy. 11679633 2001