BaseSpace
Correlation
Engine-Public
Sign In
Register
Correlation Engine 2.0
Home
My Data
Bookmarks
Collaborations
Inbox
Import Your Data
QuickView
FAQ
What is QuickView?
What can my QuickView results tell me?
What are the sources for the General Info tab in QuickView?
More QuickView FAQs
Back to top
QuickView
Curated
Studies
Body
Atlas
Disease
Atlas
Pharmaco
Atlas
Knockdown
Atlas
Genetic
Markers
Pathway
Enrichment
Literature
Clinical
Trials
0
Meta-
Analysis
QuickView
Search sequence regions
(e.g.
Lung
,
Neocentromeres
,
Fenofibrate
,
rs6983267
,
ERBB2
,
Response to oxidative stress
)
Organisms
Chromosomes
Start
Stop
Homo Sapiens
Mus Musculus
Rattus Norvegicus
C. Elegans
D. Melanogaster
Saccharomyces Cerevisiae
QuickView
Go back to main search
Bookmark
Forward
QuickView
for
RPE65
(gene)
Summary
General Info
Body Atlas
Most Correlated Tissues
Loading...
Explore Body Atlas Results
Disease Atlas
Most Correlated Diseases
Loading...
Explore Disease Atlas Results
Pharmaco Atlas
Most Correlated Compounds
Loading...
Explore Pharmaco Atlas Results
Knockdown Atlas
Most Correlated Gene Perturbations
Loading...
Explore Knockdown Atlas Results
Curated Studies
Most Correlated Studies
Loading...
Explore Curated Studies Results
Literature
Most Relevant Literature
Retinal pigment epithelium 65 kDa protein (RPE65): An update.
Generation of two induced pluripotent stem cell lines (LVPEIi004-A and LVPEIi005-A) from probands wi…
Pathogenicity reclassification of the RPE65 c.1580A>G (p.His527Arg) - a case report.
A Molecular Genetic Analysis of RPE65-Associated Forms of Inherited Retinal Degenerations in the Rus…
Leukemia Inhibitory Factor Protects against Degeneration of Cone Photoreceptors Caused by RPE65 Defi…
Explore Literature Results
Clinical Trials
Most Relevant Clinical Trials
Gene Therapy in Subjects With Biallelic RPE65 Mutation-associated Retinal Dystrophy
Safety Study of RPE65 Gene Therapy to Treat Leber Congenital Amaurosis
Study of Efficacy and Safety of Voretigene Neparvovec in Japanese Patients With Biallelic RPE65 Muta…
Natural History Study in Inherited Retinal Disease Subjects Caused by Mutations in RPE65 or LRAT
Natural History Study of Patients With Leber Congenital Amaurosis Associated With Mutations in RPE65
Explore Clinical Trials Results
search
→
result
search
→
result
See more about this page
See complete FAQ