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.
rs2230926
,
ERBB2
,
Response to oxidative stress
,
Obesity
,
Endothelial cell
,
Alcohol
)
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
aloxe3 protein, human
(compound)
Summary
General Info
Genetic Markers
Most Correlated Genes
No genes found
Explore Genetic Markers Results
Pathway Enrichment
Most Correlated Biogroups
No biogroups found
Explore Pathway Enrichment Results
Curated Studies
Most Correlated Studies
Expression changes in organotypic epidermis upon depletion of TINCR ncRNA or STAU1 protein
ZNF750 Drives Terminal Epidermal Differentiation via Induction of Klf4
Explore Curated Studies Results
Literature
Most Relevant Literature
The ALOXE3 gene variants from patients with Dravet syndrome decrease gene expression and enzyme acti…
Meta-Analysis of Mutations in ALOX12B or ALOXE3 Identified in a Large Cohort of 224 Patients.
Phenotypic suppression of acral peeling skin syndrome in a patient with autosomal recessive congenit…
Variants in NIPAL4 and ALOXE3 cause autosomal recessive congenital ichthyosis in Pakistani families.
Congenital Ichthyosis and Recurrent Eczema Associated with a Novel ALOXE3 Mutation.
Explore Literature Results
Clinical Trials
Most Relevant Clinical Trials
There were no clinical trials for aloxe3 protein, human
Explore Clinical Trials Results
search
→
result
search
→
result
See more about this page
See complete FAQ