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.
Angiogenesis
,
HIV infection
,
Breast
,
Avian flu virus
,
Acetaminophen
,
rs7903146
,
GATA1
)
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
UGT1A1;jsessionid=DB6DD9AE4AB208D0288016333C4F7653
(gene)
Summary
General Info
Body Atlas
Most Correlated Tissues
Kidney
Liver
Kidney cortex
Bladder
Ileum mucosa
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
A family study of the compound heterozygous mutation of the UGT1A1 gene causing Crigler-Najjar syndr…
Dutch pharmacogenetics working group (DPWG) guideline for the gene-drug interaction between UGT1A1 a…
TaqMan real time PCR for the Detection of the Gilbert's Syndrome Markers UGT1A1*28; UGT1A1*36 and UG…
Epigenetics and microRNAs in UGT1As.
Novel mutations in Uridyl-diphosphate-glucuronosyl-transferase 1A1 (UGT1A1) gene in Tunisian patient…
Explore Literature Results
Clinical Trials
Most Relevant Clinical Trials
There were no clinical trials for UGT1A1;jsessionid=DB6DD9AE4AB208D0288016333C4F7653
Explore Clinical Trials Results
search
→
result
search
→
result
See more about this page
See complete FAQ