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  Domain Name: TSPN
Thrombospondin N-terminal -like domains. Heparin-binding and cell adhesion domain of thrombospondin
No pairwise interactions found for the domain TSPN

Total Mutations Found: 43
Total Disease Mutations Found: 7
This domain occurred 23 times on human genes (54 proteins).



  DEAFNESS, AUTOSOMAL DOMINANT, 13 (DFNA13)
  EHLERS-DANLOS SYNDROME 1 (EDS1)
  EHLERS-DANLOS SYNDROME 2 (EDS2)
  FIBROCHONDROGENESIS 1 (FBCG1)
  OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA
  STICKLER SYNDROME, TYPE II
  WEISSENBACHER-ZWEYMUELLER SYNDROME (WZS)


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for TSPN











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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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