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  Domain Name: fn3
Fibronectin type III domain.

Total Mutations Found: 164
Total Disease Mutations Found: 30
This domain occurred 120 times on human genes (231 proteins).



  CARDIOMYOPATHY, DILATED, 1MM
  CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4
  CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4, INCLUDED
  COLD-INDUCED SWEATING SYNDROME 1
  EHLERS-DANLOS SYNDROME, HYPERMOBILITY TYPE
  EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE
  EPIDERMOLYSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA
  GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS
  GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2
  HOLOPROSENCEPHALY 11
  HYPOGONADOTROPIC HYPOGONADISM 1 WITH ANOSMIA
  LEFT VENTRICULAR NONCOMPACTION 10
  RETINITIS PIGMENTOSA 39


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for fn3








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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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