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  Domain Name: RPT1
ATP-dependent 26S proteasome regulatory subunit [Posttranslational modification, protein turnover, chaperones]
No pairwise interactions found for the domain RPT1

Total Mutations Found: 31
Total Disease Mutations Found: 22
This domain occurred 27 times on human genes (48 proteins).



  AMYOTROPHIC LATERAL SCLEROSIS 14 WI
  AMYOTROPHIC LATERAL SCLEROSIS 14 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA
  AMYOTROPHIC LATERAL SCLEROSIS 14 WITHOUT FRONTOTEMPORAL DEMENTIA
  DEMENTIA
  INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL
  SPASTIC PARAPLEGIA 4
  SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
  SPINOCEREBELLAR ATAXIA 28


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for RPT1

















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Please Cite: Peterson, T.A., Adadey, A., Santana-Cruz ,I., Sun, Y., Winder A, Kann, M.G., (2010) DMDM: Domain Mapping of Disease Mutations. Bioinformatics 26 (19), 2458-2459.

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