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  Domain Name: Laminin_N
Laminin N-terminal (Domain VI).
No pairwise interactions found for the domain Laminin_N

Total Mutations Found: 48
Total Disease Mutations Found: 14
This domain occurred 13 times on human genes (26 proteins).



  CORTICAL MALFORMATIONS, OCCIPITAL
  EPIDERMOLYSIS BULLOSA, JUNCTIONAL, HERLITZ TYPE
  EPIDERMOLYSIS BULLOSA, JUNCTIONAL, NON-HERLITZ TYPE
  EPIDERMOLYSIS BULLOSA, JUNCTIONAL, NON-HERLITZ TYPE, INCLUDED
  EPIDERMOLYSIS BULLOSA, JUNCTIONAL, NON-HERLITZ TYPE, SOMATIC MOSAIC
  MEROSIN-DEFICIENT CONGENITAL MUSCULAR DYSTROPHY 1A (MDC1A)
  NEPHROTIC SYNDROME, TYPE 5, WITH OCULAR ABNORMALITIES
  NEPHROTIC SYNDROME, TYPE 5, WITHOUT OCULAR ABNORMALITIES
  PIERSON SYNDROME
  PIERSON SYNDROME (PIERSS)
  REVERTANT
  USHER SYNDROME, TYPE IIA


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for Laminin_N











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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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