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EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosa.

Authors :
Abd El-Aziz, Mai M
Barragan, Isabel
O'Driscoll, Ciara A
Goodstadt, Leo
Prigmore, Elena
Borrego, Salud
Mena, Marcela
Pieras, Juan I
El-Ashry, Mohamed F
Safieh, Leen Abu
Shah, Amna
Cheetham, Michael E
Carter, Nigel P
Chakarova, Christina
Ponting, Chris P
Bhattacharya, Shomi S
Antinolo, Guillermo
Source :
Nature Genetics; Nov2008, Vol. 40 Issue 11, p1285-1287, 3p, 2 Color Photographs, 1 Diagram, 1 Chart
Publication Year :
2008

Abstract

Using a positional cloning approach supported by comparative genomics, we have identified a previously unreported gene, EYS, at the RP25 locus on chromosome 6q12 commonly mutated in autosomal recessive retinitis pigmentosa. Spanning over 2 Mb, this is the largest eye-specific gene identified so far. EYS is independently disrupted in four other mammalian lineages, including that of rodents, but is well conserved from Drosophila to man and is likely to have a role in the modeling of retinal architecture. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10614036
Volume :
40
Issue :
11
Database :
Complementary Index
Journal :
Nature Genetics
Publication Type :
Academic Journal
Accession number :
34962109
Full Text :
https://doi.org/10.1038/ng.241