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  Domain Name: Arp
FOG: Ankyrin repeat [General function prediction only]
No pairwise interactions found for the domain Arp

Total Mutations Found: 177
Total Disease Mutations Found: 24
This domain occurred 162 times on human genes (278 proteins).



  BARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP B
  BREAST CANCER, SUSCEPTIBILITY TO
  CEREBRAL CAVERNOUS MALFORMATIONS 1
  DOMINANT
  DOPAMINE RECEPTOR D2, REDUCED BRAIN DENSITY OF
  ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMAL
  GLAUCOMA 1, OPEN ANGLE, F
  LEFT VENTRICULAR NONCOMPACTION 7
  LONG QT SYNDROME 4 (LQT4)
  NEPHRONOPHTHISIS 16
  NEPHRONOPHTHISIS 2
  NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A
  PARKINSON DISEASE 14
  PHELAN-MCDERMID SYNDROME
  SPHEROCYTOSIS 1 (SPH1)


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for Arp


















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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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