Gap Junction Protein Alpha 8 (GJa8)

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CAE; CAE1; CX50; CZP1; MP70; Connexin 50; Lens fiber protein MP70

Gap Junction Protein Alpha 8 (GJa8)
GJa8 encodes a transmembrane connexin protein that is necessary for lens growth and maturation of lens fiber cells. The encoded protein is a component of gap junction channels and functions in a calcium and pH-dependent manner. Mutations in this gene have been associated with zonular pulverulent cataracts, nuclear progressive cataracts, and cataract-microcornea syndrome.Defects in GJA8 are the cause of cataract-microcornea syndrome. Cataract-microcornea syndrome is characterized by the association of congenital cataract and microcornea without any other systemic anomaly or dysmorphism. Clinical findings include a corneal diameter inferior to 10 mm in both meridians in an otherwise normal eye, and an inherited cataract, which is most often bilateral posterior polar with opacification in the lens periphery.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Gap Junction Protein Alpha 8 (GJa8) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Gap Junction Protein Alpha 8 (GJa8) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Gap Junction Protein Alpha 8 (GJa8) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Gap Junction Protein Alpha 8 (GJa8) CLIA Kit Customized Service Offer
n/a ELISA Kit for Gap Junction Protein Alpha 8 (GJa8) ELISA Kit Customized Service Offer

Organism species: Mus musculus (Mouse)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Gap Junction Protein Alpha 8 (GJa8) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Gap Junction Protein Alpha 8 (GJa8) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Gap Junction Protein Alpha 8 (GJa8) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Gap Junction Protein Alpha 8 (GJa8) CLIA Kit Customized Service Offer
n/a ELISA Kit for Gap Junction Protein Alpha 8 (GJa8) ELISA Kit Customized Service Offer
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  2. ErratumCurr. Eye Res. 14:979-981(1995) [PubMed] [Europe PMC] [Abstract]
  3. "The DNA sequence and biological annotation of human chromosome 1." Nature 441:315-321(2006) [PubMed] [Europe PMC] [Abstract]
  4. "A missense mutation in the human connexin50 gene (GJA8) underlies autosomal dominant 'zonular pulverulent' cataract, on chromosome 1q."Am. J. Hum. Genet. 62:526-532(1998) [PubMed] [Europe PMC] [Abstract]
  5. "Connexin 50 mutation in a family with congenital 'zonular nuclear' pulverulent cataract of Pakistani origin."Hum. Genet. 105:168-170(1999) [PubMed] [Europe PMC] [Abstract]
  6. "Mutation in the connexin 50 gene (GJA8) in a Russian family with zonular pulverulent cataract."Clin. Genet. 60:476-478(2001) [PubMed] [Europe PMC] [Abstract]
  7. "A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataract."J. Med. Genet. 40:E124-E124(2003) [PubMed] [Europe PMC] [Abstract]
  8. "Two novel mutations of connexin genes in Chinese families with autosomal dominant congenital nuclear cataract."Br. J. Ophthalmol. 89:1535-1537(2005) [PubMed] [Europe PMC] [Abstract]
  9. ErratumBr. J. Ophthalmol. 90:125-125(2006)
  10. "Novel mutations in GJA8 associated with autosomal dominant congenital cataract and microcornea."Mol. Vis. 12:190-195(2006) [PubMed] [Europe PMC] [Abstract]
  11. "A novel connexin50 mutation associated with congenital nuclear pulverulent cataracts."J. Med. Genet. 45:155-160(2008) [PubMed] [Europe PMC] [Abstract]
  12. "The GJA8 allele encoding CX50I247M is a rare polymorphism, not a cataract-causing mutation."Mol. Vis. 15:1881-1885(2009) [PubMed] [Europe PMC] [Abstract]
  13. "Another evidence for a D47N mutation in GJA8 associated with autosomal dominant congenital cataract."Mol. Vis. 17:2380-2385(2011) [PubMed] [Europe PMC] [Abstract]
  14. "Genetic linkage analyses and Cx50 mutation detection in a large multiplex Chinese family with hereditary nuclear cataract."Ophthalmic Genet. 32:48-53(2011) [PubMed] [Europe PMC] [Abstract]
  15. "Whole exome sequencing in dominant cataract identifies a new causative factor, CRYBA2, and a variety of novel alleles in known genes."Hum. Genet. 132:761-770(2013) [PubMed] [Europe PMC] [Abstract]