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.
Breast
,
Metabolism of nitric oxide
,
Rosiglitazone
,
rs3825942
,
PBX1
,
Angiogenesis
)
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
Russell-Silver syndrome
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
H19
RSS
FLG
KIAA0040
REPS2
No SNPs found
Explore Genetic Markers Results
Pathway Enrichment
Most Correlated Biogroups
MARKEY_RB1_CHRONIC_LOF_UP
DUTERTRE_ESTRADIOL_RESPONSE_24HR_UP
GOBERT_OLIGODENDROCYTE_DIFFERENTIATION_UP
FISCHER_DREAM_TARGETS
KOBAYASHI_EGFR_SIGNALING_24HR_DN
Explore Pathway Enrichment Results
Curated Studies
Most Correlated Studies
Skin fibroblasts of Silver-Russell syndrome with hypomethylation of ICR1 region in IGF2/H19 locus
Skin fibroblasts of Silver-Russell syndrome and Temple syndrome patients
OMIM - Congenital disorder
Explore Curated Studies Results
Literature
Most Relevant Literature
Generalized lichen nitidus in Russell-Silver syndrome.
Deletion of the paternal allele of the imprinted MEST/PEG1 region in a patient with Silver-Russell s…
Mosaic upd(7)mat in a patient with Silver-Russell syndrome.
Russell-Silver syndrome due to paternal H19/IGF2 hypomethylation in a patient conceived using intrac…
Methylation profiling in individuals with Russell-Silver syndrome.
Explore Literature Results
Clinical Trials
Most Relevant Clinical Trials
Prenatal Screening for Imprinting Anomalies Implicated in Beckwith Wiedemann and Silver Russell Synd…
Aromatase Inhibitor in Bone Maturation, Children With Silver Russell or Prader-Willi Syndrome
GROWing Up With Rare GENEtic Syndromes
Study to Assess the Efficacy and Safety of Eutropin in Prader-Willi Syndrome
Genetic Diagnosis and Human Growth Hormone Treatment in Small for Gestational Age Children With Shor…
Explore Clinical Trials Results
search
→
result
search
→
result
See more about this page
See complete FAQ