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  Domain Name: Laminin_G_2
Laminin G domain. This family includes the Thrombospondin N-terminal-like domain, a Laminin G subfamily.
No pairwise interactions found for the domain Laminin_G_2

Total Mutations Found: 84
Total Disease Mutations Found: 37
This domain occurred 37 times on human genes (82 proteins).



  AUTISM, SUSCEPTIBILITY TO, 15
  LEBER CONGENITAL AMAUROSIS 8
  MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT
  MUSCULAR DYSTROPHY, CONGENITAL, DUE TO PARTIAL LAMA2 DEFICIENCY
  MYASTHENIA, LIMB-GIRDLE, FAMILIAL
  OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA
  PITT-HOPKINS-LIKE SYNDROME 2
  RETINITIS PIGMENTOSA 12
  RETINITIS PIGMENTOSA 12, INCLUDED
  RETINITIS PIGMENTOSA 25
  THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
  THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL RECESSIVE


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for Laminin_G_2











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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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