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Pubmed ID :20159112
Publication Date : //

Mutations in TSPAN12 cause autosomal-dominant familial exudative vitreoretinopathy.


Familial exudative vitreoretinopathy (FEVR) is an inherited blinding disorder of the retinal vascular system. Although mutations in three genes (LRP5, FZD4, and NDP) are known to cause FEVR, these account for only a fraction of FEVR cases. The proteins encoded by these FEVR genes form part of a signaling complex that activates the Norrin-beta-catenin signaling pathway. Recently, through a large-scale reverse genetic screen in mice, Junge and colleagues identified an additional member of this signaling complex, Tspan12. Here, we report that mutations in TSPAN12 also cause autosomal-dominant FEVR. We describe seven mutations identified in a cohort of 70 FEVR patients in whom we had already excluded the known FEVR genes. This study provides further evidence for the importance of the Norrin-beta-catenin signaling pathway in the development of the retinal vasculature and also indicates that more FEVR genes remain to be identified.

Authors : Poulter James A , Ali Manir , Gilmour David F , Rice Aine , Kondo Hiroyuki , Hayashi Kenshi , Mackey David A , Kearns Lisa S , Ruddle Jonathan B , Craig Jamie E , Pierce Eric A , Downey Louise M , Mohamed Moin D , Markham Alexander F , Inglehearn Chris F , Toomes Carmel ,

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RP9 RP9 Gene retinitis pigmentosa 9 (autosomal dominant)
RP1 RP1 Gene retinitis pigmentosa 1 (autosomal dominant)
DFNA51 DFNA49 Gene deafness, autosomal dominant 49
DFNA53 DFNA51 Gene deafness, autosomal dominant 51
DFNA49 DFNA46 Gene deafness, autosomal dominant 46
DFNA52 DFNA5 Gene deafness, autosomal dominant 5
DFNA47 DFNA45 Gene deafness, autosomal dominant 45
DFNA46 DFNA43 Gene deafness, autosomal dominant 43
DFNA45 DFNA42 Gene deafness, autosomal dominant 42
DFNA43 DFNA41 Gene deafness, autosomal dominant 41
DFNA42 DFNA40 Gene deafness, autosomal dominant 40
DFNA54 DFNA52 Gene deafness, autosomal dominant 52
DFNA57 DFNA53 Gene deafness, autosomal dominant 53
DFNA58 DFNA54 Gene deafness, autosomal dominant 54
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E2649h Human Deafness, Autosomal Dominant 5 ELISA Kit 96T
NYX NYS4 Gene nystagmus 4, congenital autosomal dominant
HULC HTX2 Gene heterotaxy 2 (autosomal dominant)


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