Homo sapiens retinoid isomerohydrolase RPE65 (RPE65), RefSeqGene on ch - Nucleotide

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RPE65-Associated Retinal Dystrophies: Phenotypes and Treatment Effects with Voretigene Neparvovec. [Klin Monbl Augenheilkd. 2024]
RPE65-Associated Retinal Dystrophies: Phenotypes and Treatment Effects with Voretigene Neparvovec.
Stingl K, Priglinger C, Herrmann P. Klin Monbl Augenheilkd. 2024 Mar; 241(3):259-265. Epub 2024 Mar 20.
Development of a novel prediction model based on protein structure for identifying RPE65-associated inherited retinal disease (IRDs) of missense variants. [PeerJ. 2023]
Development of a novel prediction model based on protein structure for identifying RPE65-associated inherited retinal disease (IRDs) of missense variants.
Wu J, Sun Z, Zhang DW, Liu HL, Li T, Zhang S, Wu J. PeerJ. 2023; 11:e15702. Epub 2023 Aug 2.
Voretigene Neparvovec for the Treatment of RPE65-associated Retinal Dystrophy: Consensus and Recommendations from the Korea RPE65-IRD Consensus Paper Committee. [Korean J Ophthalmol. 2023]
Voretigene Neparvovec for the Treatment of RPE65-associated Retinal Dystrophy: Consensus and Recommendations from the Korea RPE65-IRD Consensus Paper Committee.
Han J, Joo K, Kim US, Woo SJ, Lee EK, Lee JY, Park TK, Kim SJ, Byeon SH. Korean J Ophthalmol. 2023 Apr; 37(2):166-186. Epub 2023 Mar 23.

RefSeq alternative splicing
See 6 reference mRNA sequence splice variants for the RPE65 gene.

Protein
Protein sequence from Nucleotide coding region
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Mannheimia haemolytica strain 1512 chromosome, complete genome
Mannheimia haemolytica strain 1512 chromosome, complete genome
gi|1724228713|ref|NZ_CP017532.1|

Nucleotide
LGR8 [Homo sapiens]
LGR8 [Homo sapiens]
gi|18702460|gb|AAL69324.2|AF403384_

Protein
PubChem Compound Links for Gene (Select 6121) (7)
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Nucleotide