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.
Doxycycline
,
rs2230926
,
FGF21
,
calcium channel activity
,
Diabetes mellitus
,
Stem 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
XM_900787
(gene)
Summary
General Info
Body Atlas
Most Correlated Tissues
Appendix
Superior cervical ganglion
Skeletal muscle
T Lymphocyte (regulatory) of peripheral blood
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
Loading...
Explore Curated Studies Results
Literature
Most Relevant Literature
Inherited thrombocytopenia associated with a variant in the FLI1 binding site in the 5' UTR of ANKRD…
ANKRD26-Related Thrombocytopenia and Predisposition to Myeloid Neoplasms.
Analysis of clinical characteristics and treatment efficacy in two pediatric cases of ANKRD26-relate…
Prevalence and natural history of variants in the ANKRD26 gene: a short review and update of reporte…
ANKRD26 is a new regulator of type I cytokine receptor signaling in normal and pathological hematopo…
Explore Literature Results
Clinical Trials
Most Relevant Clinical Trials
There were no clinical trials for XM_900787
Explore Clinical Trials Results
search
→
result
search
→
result
See more about this page
See complete FAQ