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

Total Mutations Found: 114
Total Disease Mutations Found: 50
This domain occurred 63 times on human genes (128 proteins).



  ASPHYXIATING THORACIC DYSTROPHY 4
  ASPHYXIATING THORACIC DYSTROPHY 4 (ATD4)
  BARDET-BIEDL SYNDROME (BBS)
  BARDET-BIEDL SYNDROME 4
  BONE MARROW FAILURE, FAMILIAL
  CILIARY DYSKINESIA, PRIMARY, 28, WITH SITUS INVERSUS
  CILIARY DYSKINESIA, PRIMARY, 28, WITHOUT SITUS INVERSUS
  DEFICIENCY
  FETAL AKINESIA DEFORMATION SEQUENCE
  FETAL AKINESIA DEFORMATION SEQUENCE (FADS)
  INTESTINAL ATRESIA, MULTIPLE
  JOUBERT SYNDROME 11 (JBTS11)
  MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR
  MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY (CMS-ACHRD)
  NEPHRONOPHTHISIS 12
  NEPHRONOPHTHISIS 12 (NPHP12)
  PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER)
  PEROXISOME BIOGENESIS DISORDER 2B
  RETINITIS PIGMENTOSA 60
  TRICHOHEPATOENTERIC SYNDROME 1


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for NrfG






























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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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