RecName: Full=Retinol dehydrogenase 8; AltName: Full=Photoreceptor out - Protein

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A Splicing Variant in RDH8 Is Associated with Autosomal Recessive Stargardt Macular Dystrophy. [Genes (Basel). 2023]
A Splicing Variant in RDH8 Is Associated with Autosomal Recessive Stargardt Macular Dystrophy.
Zampatti S, Peconi C, Calvino G, Ferese R, Gambardella S, Cascella R, Sebastiani J, Falsini B, Cusumano A, Giardina E. Genes (Basel). 2023 Aug 21; 14(8). Epub 2023 Aug 21.
Investigation of the association between all-trans-retinol dehydrogenase (RDH8) polymorphisms and high myopia in Chinese. [J Zhejiang Univ Sci B. 2010]
Investigation of the association between all-trans-retinol dehydrogenase (RDH8) polymorphisms and high myopia in Chinese.
Yu YS, Wang LL, Shen Y, Yap MK, Yip SP, Han W. J Zhejiang Univ Sci B. 2010 Nov; 11(11):836-41.
An outer segment localization signal at the C terminus of the photoreceptor-specific retinol dehydrogenase. [J Neurosci. 2004]
An outer segment localization signal at the C terminus of the photoreceptor-specific retinol dehydrogenase.
Luo W, Marsh-Armstrong N, Rattner A, Nathans J. J Neurosci. 2004 Mar 17; 24(11):2623-32.

RefSeq genomic sequence
See the genomic reference sequence for the RDH8 gene (NG_033979.1).
RefSeq protein
See the reference protein sequence for retinol dehydrogenase 8 (NP_056540.3).

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Q9NYR8 [Domain Mapping of Disease Mut...]
Q9NYR8
Domain Mapping of Disease Mutations
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RecName: Full=Retinol dehydrogenase 8; AltName: Full=Photoreceptor outer segment...
RecName: Full=Retinol dehydrogenase 8; AltName: Full=Photoreceptor outer segment all-trans retinol dehydrogenase; AltName: Full=Short chain dehydrogenase/reductase family 28C member 2
gi|74753074|sp|Q9NYR8.1|RDH8_HUMAN

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