SACS, sacsin molecular chaperone, 26278

N. diseases: 106; N. variants: 252
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004134
Disease: Ataxia
Ataxia
0.100 Biomarker phenotype BEFREE ARSACS seems to be an important cause of ataxia and many different types of mutations have been identified, mainly located in exon 10. 31701440 2020
CUI: C0004134
Disease: Ataxia
Ataxia
0.100 GeneticVariation phenotype BEFREE Increasing expression of heat shock proteins also resolved neurofilament bundles, indicating that this endogenous chaperone system can compensate to some extent for sacsin deficiency.-Gentil, B. J., Lai, G.-T., Menade, M., Larivière, R., Minotti, S., Gehring, K., Chapple, J.-P., Brais, B., Durham, H. D. Sacsin, mutated in the ataxia ARSACS, regulates intermediate filament assembly and dynamics. 30332300 2019
CUI: C0004134
Disease: Ataxia
Ataxia
0.100 GeneticVariation phenotype BEFREE Sequencing of SACS in 22 patients with unexplained early-onset ataxia, assessment of novel SACS variants in 3.500 European control chromosomes and extensive phenotypic investigations of all SACS carriers. 23497566 2013
CUI: C0004134
Disease: Ataxia
Ataxia
0.100 Biomarker phenotype BEFREE Novel SACS mutation in a Belgian family with sacsin-related ataxia. 17716690 2008
CUI: C0004134
Disease: Ataxia
Ataxia
0.100 GeneticVariation phenotype BEFREE With the collaboration of the clinical European and Mediterranean SPATAX network, we identified 15 families with 34 affected members presenting with ataxia and pyramidal signs or spasticity that were not linked to the ARSACS locus on chromosome 13. 17273843 2007
CUI: C0004134
Disease: Ataxia
Ataxia
0.100 Biomarker phenotype BEFREE Sacsinopathies: sacsin-related ataxia. 17853117 2007
CUI: C0004134
Disease: Ataxia
Ataxia
0.100 Biomarker phenotype BEFREE A phenotype without spasticity in sacsin-related ataxia. 15985586 2005
CUI: C0004134
Disease: Ataxia
Ataxia
0.100 GeneticVariation phenotype BEFREE Novel compound heterozygous mutations in sacsin-related ataxia. 16198375 2005
CUI: C0004134
Disease: Ataxia
Ataxia
0.100 GeneticVariation phenotype LHGDN Identification of a SACS gene missense mutation in ARSACS. 14718708 2004
CUI: C0004134
Disease: Ataxia
Ataxia
0.100 GeneticVariation phenotype BEFREE Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in Tunisia. 12873855 2003