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  Domain Name: MFS_1
Major Facilitator Superfamily.
No pairwise interactions found for the domain MFS_1

Total Mutations Found: 188
Total Disease Mutations Found: 85
This domain occurred 80 times on human genes (146 proteins).



  ALLAN-HERNDON-DUDLEY SYNDROME
  ARTERIAL TORTUOSITY SYNDROME
  CARNITINE DEFICIENCY, SYSTEMIC PRIMARY
  CEROID LIPOFUSCINOSIS, NEURONAL, 7
  DEAFNESS, AUTOSOMAL DOMINANT 25
  DIABETES MELLITUS, NONINSULIN-DEPENDENT
  DYSTONIA 9
  DYSTONIA 9, INCLUDED
  EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 12
  ERYTHROCYTE LACTATE TRANSPORTER DEFECT
  FANCONI-BICKEL SYNDROME
  FOLATE MALABSORPTION, HEREDITARY
  GLUT1 DEFICIENCY SYNDROME 1
  GLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE
  GLUT1 DEFICIENCY SYNDROME 2
  GLUT1 DEFICIENCY SYNDROME 2, INCLUDED;;
  GLYCOGEN STORAGE DISEASE IB
  GLYCOGEN STORAGE DISEASE IC
  GOUT SUSCEPTIBILITY 4
  HYPOURICEMIA, RENAL, 1
  HYPOURICEMIA, RENAL, 2
  INFANTILE SIALIC ACID STORAGE DISORDER
  POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA
  PROLIFERATIVE VASCULOPATHY AND HYDRANENCEPHALY-HYDROCEPHALY SYNDROME
  SALLA DISEASE
  URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 4


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for MFS_1
























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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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