Literature DB >> 17601931

Mutation of the gap junction protein alpha 8 (GJA8) gene causes autosomal recessive cataract.

Surya Prakash G Ponnam1, Kekunnaya Ramesha, Sushma Tejwani, Balasubramanya Ramamurthy, Chitra Kannabiran.   

Abstract

BACKGROUND: GJA8 encodes connexin-50, a gap junction protein in the eye lens. Mutations in GJA8 have been reported in families with autosomal dominant cataract.
OBJECTIVE: To identify the disease gene in a family with congenital cataract of autosomal recessive inheritance.
METHODS: Eight candidate genes were screened for pathogenic alterations in affected and unaffected family members and in normal unrelated controls.
RESULTS: A single base insertion leading to frameshift at codon 203 of connexin 50 was found to co-segregate with disease in the family.
CONCLUSIONS: These results confirm involvement of GJA8 in autosomal recessive cataract.

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Year:  2007        PMID: 17601931      PMCID: PMC2598012          DOI: 10.1136/jmg.2007.050138

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  30 in total

1.  A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataract.

Authors:  C E Willoughby; Sara Arab; R Gandhi; S Zeinali; Seddigheh Arab; D Luk; G Billingsley; F L Munier; E Héon
Journal:  J Med Genet       Date:  2003-11       Impact factor: 6.318

Review 2.  Structural and functional diversity of connexin genes in the mouse and human genome.

Authors:  Klaus Willecke; Jürgen Eiberger; Joachim Degen; Dominik Eckardt; Alessandro Romualdi; Martin Güldenagel; Urban Deutsch; Goran Söhl
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4.  Mutation in the connexin 50 gene (GJA8) in a Russian family with zonular pulverulent cataract.

Authors:  A V Polyakov; I A Shagina; O V Khlebnikova; O V Evgrafov
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6.  Connexin46 mutations linked to congenital cataract show loss of gap junction channel function.

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7.  A Gja8 (Cx50) point mutation causes an alteration of alpha 3 connexin (Cx46) in semi-dominant cataracts of Lop10 mice.

Authors:  Bo Chang; Xin Wang; Norman L Hawes; Ryan Ojakian; Muriel T Davisson; Woo-Kuen Lo; Xiaohua Gong
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10.  Dominant cataracts result from incongruous mixing of wild-type lens connexins.

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  51 in total

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Review 2.  Gap junctions or hemichannel-dependent and independent roles of connexins in cataractogenesis and lens development.

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Review 5.  Homeostasis in the vertebrate lens: mechanisms of solute exchange.

Authors:  Ralf Dahm; Jan van Marle; Roy A Quinlan; Alan R Prescott; Gijs F J M Vrensen
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6.  Exome sequencing in developmental eye disease leads to identification of causal variants in GJA8, CRYGC, PAX6 and CYP1B1.

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8.  Autosomal recessive congenital cataract in consanguineous Pakistani families is associated with mutations in GALK1.

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9.  A novel GJA8 mutation (p.I31T) causing autosomal dominant congenital cataract in a Chinese family.

Authors:  Kaijie Wang; Binbin Wang; Jing Wang; Shiyi Zhou; Bo Yun; Peisu Suo; Jie Cheng; Xu Ma; Siquan Zhu
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10.  A new locus for autosomal recessive congenital cataract identified in a Pakistani family.

Authors:  Haiba Kaul; S Amer Riazuddin; Afshan Yasmeen; Sadia Mohsin; Mohsin Khan; Idrees A Nasir; Shaheen N Khan; Tayyab Husnain; Javed Akram; J Fielding Hejtmancik; Sheikh Riazuddin
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