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  Domain Name: Connexin
Connexin.
No pairwise interactions found for the domain Connexin

Total Mutations Found: 138
Total Disease Mutations Found: 93
This domain occurred 21 times on human genes (35 proteins).



  ATRIAL FIBRILLATION, FAMILIAL, 11
  ATRIAL FIBRILLATION, FAMILIAL, 11 (ATFB11)
  ATRIAL FIBRILLATION, SOMATIC
  CATARACT 1 WITH MICROCORNEA
  CATARACT 1, MULTIPLE TYPES
  CATARACT 1, MULTIPLE TYPES (CTRCT1)
  CATARACT 1, NUCLEAR PROGRESSIVE
  CATARACT 1, ZONULAR PULVERULENT
  CATARACT 14, MULTIPLE TYPES (CTRCT14)
  CATARACT 14, ZONULAR PULVERULENT
  CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE (CMDR)
  DEAFNESS, AUTOSOMAL DOMINANT 3A
  DEAFNESS, AUTOSOMAL DOMINANT 3A, INCLUDED
  DEAFNESS, AUTOSOMAL DOMINANT 3B
  DEAFNESS, AUTOSOMAL DOMINANT, 2B (DFNA2B)
  DEAFNESS, AUTOSOMAL DOMINANT, 3A (DFNA3A)
  DEAFNESS, AUTOSOMAL RECESSIVE 1A
  DEAFNESS, AUTOSOMAL RECESSIVE 1A, INCLUDED
  DEAFNESS, AUTOSOMAL RECESSIVE, 1A (DFNB1A)
  ECTODERMAL DYSPLASIA, HIDROTIC
  ERYTHROKERATODERMIA VARIABILIS (EKV)
  ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA
  HYPOPLASTIC LEFT HEART SYNDROME 1 (HLHS1)
  HYSTRIX-LIKE ICHTHYOSIS WITH DEAFNESS, INCLUDED
  KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT
  KERATODERMA, PALMOPLANTAR, WITH DEAFNESS
  KNUCKLE PADS, LEUKONYCHIA, AND SENSORINEURAL DEAFNESS
  LEUKODYSTROPHY, HYPOMYELINATING, 2
  LEUKODYSTROPHY, HYPOMYELINATING, 2 (HLD2)
  LYMPHEDEMA, HEREDITARY, IC
  OCULODENTODIGITAL DYSPLASIA
  OCULODENTODIGITAL DYSPLASIA (ODDD)
  OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE
  SPASTIC PARAPLEGIA 44
  VOHWINKEL SYNDROME


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for Connexin








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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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