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.
Rosiglitazone
,
rs2230926
,
PTEN
,
Coagulation
,
Leukemia
,
Endothelial cell
)
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
Eif2ak4
(gene)
Summary
General Info
Body Atlas
Most Correlated Tissues
Synovial membrane
Prostate gland
Joint synovium
Pituitary gland
Endometrium
Explore Body Atlas Results
Disease Atlas
Most Correlated Diseases
Muscle cachexia
Injury of integument
Bacterial septicemia
Infestation by Ixodidae
Disease due to Rhinovirus
Explore Disease Atlas Results
Pharmaco Atlas
Most Correlated Compounds
TGX 221
BAY 43-9006
ustekinumab
HC toxin
HIV Protease Inhibitors
Explore Pharmaco Atlas Results
Knockdown Atlas
Most Correlated Gene Perturbations
HRAS
PHO2
MIR376A1
RNF43
hsa-miR-365a-3p
Explore Knockdown Atlas Results
Curated Studies
Most Correlated Studies
Loading...
Explore Curated Studies Results
Literature
Most Relevant Literature
Downregulation of nutrition sensor GCN2 in macrophages contributes to poor wound healing in diabetes…
T-cell dysregulation and inflammatory process in Gcn2 (Eif2ak4-/-)-deficient rats in basal and stres…
Disruption of GCN2 Pathway Aggravates Vascular and Parenchymal Remodeling during Pulmonary Fibrosis.
GCN2 adapts protein synthesis to scavenging-dependent growth.
Modulation of GCN2 activity under excess light stress by osmoprotectants and amino acids.
Explore Literature Results
Clinical Trials
Most Relevant Clinical Trials
Screening of Pulmonary Veino Occlusive Disease in Heterozygous EIF2AK4 Mutation Carriers
Genetics of Pulmonary Hypertension
The PAH Platform for Deep Phenotyping in Korean Subjects
Explore Clinical Trials Results
search
→
result
search
→
result
See more about this page
See complete FAQ