Views provided by UsageCountsEYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosa
EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosa
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.
- University of Oxford United Kingdom
- Sorbonne University France
- Wellcome Sanger Institute United Kingdom
- Spanish National Research Council Spain
- Wellcome Trust United Kingdom
Photoreceptors, Sequence Homology, Amino Acid, Gene Expression Profiling, Genes, Recessive, Retinal architecture, Cell Line, Protein Structure, Tertiary, Retinitis pigmentosa, Protein Transport, EYS, Drosophila melanogaster, Gene Expression Regulation, Mutation, Animals, Drosophila Proteins, Humans, Eye-specific gene, Chromosomes, Human, Pair 6, Eye Proteins, Retinitis Pigmentosa
Photoreceptors, Sequence Homology, Amino Acid, Gene Expression Profiling, Genes, Recessive, Retinal architecture, Cell Line, Protein Structure, Tertiary, Retinitis pigmentosa, Protein Transport, EYS, Drosophila melanogaster, Gene Expression Regulation, Mutation, Animals, Drosophila Proteins, Humans, Eye-specific gene, Chromosomes, Human, Pair 6, Eye Proteins, Retinitis Pigmentosa
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