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  Domain Name: FAS1
Four repeated domains in the Fasciclin I family of proteins, present in many other contexts.
No pairwise interactions found for the domain FAS1

Total Mutations Found: 6
Total Disease Mutations Found: 4
This domain occurred 4 times on human genes (13 proteins).



  CORNEAL DYSTROPHY, GROENOUW TYPE I
  CORNEAL DYSTROPHY, LATTICE TYPE IIIA
  CORNEAL DYSTROPHY, REIS-BUCKLERS TYPE
  CORNEAL DYSTROPHY, THIEL-BEHNKE TYPE


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for FAS1










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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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