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  Domain Name: GLE1
GLE1-like protein. The members of this family are sequences that are similar to the human protein GLE1. This protein is localised at the nuclear pore complexes and functions in poly(A)+ RNA export to the cytoplasm.
No pairwise interactions found for the domain GLE1

Total Mutations Found: 4
Total Disease Mutations Found: 2
This domain occurred 1 times on human genes (3 proteins).



  LETHAL ARTHROGRYOPOSIS WITH ANTERIOR HORN CELL DISEASE
  LETHAL CONGENITAL CONTRACTURE SYNDROME 1


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for GLE1













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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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