RAN, RAN, member RAS oncogene family, 5901

N. diseases: 87; N. variants: 2
Disease: Myotonic Dystrophy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0027126
Disease: Myotonic Dystrophy
Myotonic Dystrophy 		0.020 Biomarker disease BEFREE RAN proteins, which were first described in spinocerebellar ataxia type 8 (SCA8) and myotonic dystrophy type 1 (DM1), have now been reported in a growing list of microsatellite expansion diseases. 29891563 2018
CUI: C0027126
Disease: Myotonic Dystrophy
Myotonic Dystrophy 		0.020 Biomarker disease BEFREE RAN proteins have been reported in a growing number of diseases, including spinocerebellar ataxia type 8 (SCA8), myotonic dystrophy type 1 (DM1), Fragile-X tremor ataxia syndrome (FXTAS), and C9ORF72 amyotrophic lateral sclerosis (ALS)/frontotemporal dementia (FTD). 24852074 2014