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.
Valproic acid
,
rs6983267
,
BRCA1
,
Metabolism of xenobiotics
,
Influenza
,
Neuron
,
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
PLCG1;jsessionid=DB10E1116EB6D3FAC4ED8340478991D2
(gene)
Summary
General Info
Body Atlas
Most Correlated Tissues
Skeletal muscle psoas
Cerebellar vermis
Cerebellum
Cerebellar hemisphere
Ciliary ganglion
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
No studies found
Explore Curated Studies Results
Literature
Most Relevant Literature
A gain-of-function variation in PLCG1 causes a new immune dysregulation disease.
PLCγ1 suppression promotes the adaptation of KRAS-mutant lung adenocarcinomas to hypoxia.
The function of PLCγ1 in developing mouse mDA system.
Associating bovine herpesvirus 1 envelope glycoprotein gD with activated phospho-PLC-γ1(S1248).
A kinetic model of phospholipase C-γ1 linking structure-based insights to dynamics of enzyme autoinh…
Explore Literature Results
Clinical Trials
Most Relevant Clinical Trials
There were no clinical trials for PLCG1;jsessionid=DB10E1116EB6D3FAC4ED8340478991D2
Explore Clinical Trials Results
search
→
result
search
→
result
See more about this page
See complete FAQ