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.
Retina
,
Amniocentesis
,
Trichostatin A
,
rs4950928
,
IL1A
,
Angiogenesis
,
Leukemia
)
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
COL4A5
(gene)
Summary
General Info
Body Atlas
Most Correlated Tissues
Myometrium
Corpus callosum
Cervix
Nodose nucleus
Urethra
Explore Body Atlas Results
Disease Atlas
Most Correlated Diseases
Hutchinson-Gilford syndrome
Nephrotic syndrome
Herpes simplex type 2 infection
Atherosclerotic occlusive disease
Disease due to Rotavirus
Explore Disease Atlas Results
Pharmaco Atlas
Most Correlated Compounds
sporidesmin
saikosaponin
astragaloside IV
puerarin
ainsliadimer A
Explore Pharmaco Atlas Results
Knockdown Atlas
Most Correlated Gene Perturbations
PDGFC
ZRSR2
HSP90AA1
CPT2
NOVA1
Explore Knockdown Atlas Results
Curated Studies
Most Correlated Studies
Loading...
Explore Curated Studies Results
Literature
Most Relevant Literature
Decorin in the spatial control of collagen mineralization.
COL4A5 genotypes and clinical characteristics of children with Alport syndrome].
Trimerization profile of type IV collagen COL4A5 exon deletion in X-linked Alport syndrome.
Exploring the link between Alport syndrome and multiple intracranial artery stenoses: A case report …
A novel COL4A5 splicing mutation causes alport syndrome in a Chinese family.
Explore Literature Results
Clinical Trials
Most Relevant Clinical Trials
Safety and Efficacy of ACEI in Alport Syndrome Patients With COL4A3/COL4A4/COL4A5 Variants
Genotype-Phenotype Correlations in Patients With Alport Syndrome
A Study of ELX-02 in Patients With Alport Syndrome
Study of Hydroxychloroquine in Patients With X-linked Alport Syndrome in China (CHXLAS)
Treatment With Metformin in Chinese Children With Alport Syndrome
Explore Clinical Trials Results
search
→
result
search
→
result
See more about this page
See complete FAQ