KEGG   DISEASE: Marinesco-Sjogren syndrome
Entry
H01284                      Disease                                
Name
Marinesco-Sjogren syndrome
Description
Marinesco-Sjogren syndrome is an autosomal recessive multisystem disorder which is characterized by cerebellar ataxia, progressive myopathy and cataracts. Mutations in the endoplasmic reticulum associated co-chaperone SIL1/BAP were identified to be the major cause of this syndrome.
Category
Nervous system disease
Brite
Human diseases in ICD-11 classification [BR:br08403]
 08 Diseases of the nervous system
  Diseases of neuromuscular junction or muscle
   Primary disorders of muscles
    8C70  Muscular dystrophy
     H01284  Marinesco-Sjogren syndrome
Pathway
hsa04141  Protein processing in endoplasmic reticulum
Gene
SIL1 [HSA:64374] [KO:K14001]
Other DBs
ICD-11: 8C70.6
ICD-10: G11.1
MeSH: D013132
OMIM: 248800
Reference
  Authors
Howes J, Shimizu Y, Feige MJ, Hendershot LM
  Title
C-terminal mutations destabilize SIL1/BAP and can cause Marinesco-Sjogren syndrome.
  Journal
J Biol Chem 287:8552-60 (2012)
DOI:10.1074/jbc.M111.333286
Reference
  Authors
Anttonen AK, Mahjneh I, Hamalainen RH, Lagier-Tourenne C, Kopra O, Waris L, Anttonen M, Joensuu T, Kalimo H, Paetau A, Tranebjaerg L, Chaigne D, Koenig M, Eeg-Olofsson O, Udd B, Somer M, Somer H, Lehesjoki AE
  Title
The gene disrupted in Marinesco-Sjogren syndrome encodes SIL1, an HSPA5 cochaperone.
  Journal
Nat Genet 37:1309-11 (2005)
DOI:10.1038/ng1677
Reference
  Authors
Senderek J, Krieger M, Stendel C, Bergmann C, Moser M, Breitbach-Faller N, Rudnik-Schoneborn S, Blaschek A, Wolf NI, Harting I, North K, Smith J, Muntoni F, Brockington M, Quijano-Roy S, Renault F, Herrmann R, Hendershot LM, Schroder JM, Lochmuller H, Topaloglu H, Voit T, Weis J, Ebinger F, Zerres K
  Title
Mutations in SIL1 cause Marinesco-Sjogren syndrome, a cerebellar ataxia with cataract and myopathy.
  Journal
Nat Genet 37:1312-4 (2005)
DOI:10.1038/ng1678
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