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  Domain Name: Sulfate_transp
Sulfate transporter family. Mutations in human SLC26A2 lead to several human diseases.
No pairwise interactions found for the domain Sulfate_transp

Total Mutations Found: 14
Total Disease Mutations Found: 5
This domain occurred 8 times on human genes (20 proteins).



  ACHONDROGENESIS, TYPE IB
  ATELOSTEOGENESIS, TYPE II
  DE LA CHAPELLE DYSPLASIA
  DIASTROPHIC DYSPLASIA, BROAD BONE-PLATYSPONDYLIC VARIANT
  DIASTROPHIC DYSPLASIA, INCLUDED
  DIASTROPHIC DYSPLASIA, INCLUDED;;
  EPIPHYSEAL DYSPLASIA, MULTIPLE, 4, INCLUDED


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for Sulfate_transp













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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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