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Results for Proteins associated with the Gene: GJB2
GJB2
2706


Known Diseases associated with this Protein:
  BART-PUMPHREY SYNDROME (BPS)
  DEAFNESS, AUTOSOMAL DOMINANT 3A
  DEAFNESS, AUTOSOMAL DOMINANT 3A, INCLUDED
  DEAFNESS, AUTOSOMAL DOMINANT, 3A (DFNA3A)
  DEAFNESS, AUTOSOMAL RECESSIVE 1A
  DEAFNESS, AUTOSOMAL RECESSIVE 1A, INCLUDED
  DEAFNESS, AUTOSOMAL RECESSIVE, 1A (DFNB1A)
  HYSTRIX-LIKE ICHTHYOSIS WITH DEAFNESS, INCLUDED
  KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME (KID SYNDROME)
  KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT
  KERATODERMA, PALMOPLANTAR, WITH DEAFNESS
  KERATODERMA, PALMOPLANTAR, WITH DEAFNESS (PPKDFN)
  KNUCKLE PADS, LEUKONYCHIA, AND SENSORINEURAL DEAFNESS
  VOHWINKEL SYNDROME
  VOHWINKEL SYNDROME (VS)
72
21
30
2
61
Tips:
 The Domains on the Default View are decided by HMMER's search E-Value of the Protein against the Domain model.
 Clicking a check box on the left will display or hide the corresponding domain(s).
 To view the Protein page, either click on the protein links in the box to the left or the blue bar above the Protein's graphic.


Default View:

Connexin - pfam00029
CNX - smart00037
Connexin_CCC - pfam10582


Swiss-Prot Protein: P29033
Identical to: NP_003995
   Default View:



Default View:

Connexin - pfam00029
CNX - smart00037
Connexin_CCC - pfam10582


RefSeq Protein: NP_003995
   Default View:




Domains found on the Proteins

Protein ↕Domain ↕Domain Accession ↕Start ↕End ↕E-Value ↕
P29033Connexinpfam0002921085.9e-77
P29033CNXsmart0003742751.6e-21
P29033Connexin_CCCpfam105821462133.5e-47
NP_003995Connexinpfam0002921085.9e-77
NP_003995CNXsmart0003742751.6e-21
NP_003995Connexin_CCCpfam105821462133.5e-47



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