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Results for Proteins associated with the Gene: GJA1
GJA1
2697


Known Diseases associated with this Protein:
  ATRIOVENTRICULAR SEPTAL DEFECT 3, INCLUDED
  CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE
  CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE (CMDR)
  HALLERMANN-STREIFF SYNDROME (HSS)
  HYPOPLASTIC LEFT HEART SYNDROME 1
  HYPOPLASTIC LEFT HEART SYNDROME 1 (HLHS1)
  OCULODENTODIGITAL DYSPLASIA
  OCULODENTODIGITAL DYSPLASIA (ODDD)
  OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE
  SYNDACTYLY 3 (SDTY3)
  SYNDACTYLY, TYPE III
61
17
16
1
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
Connexin43 - pfam03508


Swiss-Prot Protein: P17302
Identical to: NP_000156
   Default View:



Default View:

Connexin - pfam00029
CNX - smart00037
Connexin_CCC - pfam10582
Connexin43 - pfam03508


RefSeq Protein: NP_000156
   Default View:




Domains found on the Proteins

Protein ↕Domain ↕Domain Accession ↕Start ↕End ↕E-Value ↕
NP_000156Connexin43pfam035082933125.6e-09
NP_000156CNXsmart0003743762.8e-21
NP_000156Connexin_CCCpfam105821652312.7e-44



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