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Splenic hypoplasia
Splenic hypoplasia
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
SPLENIC HYPOPLASIA
C0685889
NKX2-5
Unknown
—
Disgenet
YAP1- and WWTR1 (TAZ)-stimulated gene expression
Physiological factors
RPSA
Unknown
—
Disgenet
Ribosome
Coronavirus disease - COVID-19
L13a-mediated translational silencing of Ceruloplasmin expression
SRP-dependent cotranslational protein targeting to membrane
Viral mRNA Translation
Major pathway of rRNA processing in the nucleolus and cytosol
Translation initiation complex formation
Formation of a pool of free 40S subunits
Formation of the ternary complex, and subsequently, the 43S complex
Ribosomal scanning and start codon recognition
GTP hydrolysis and joining of the 60S ribosomal subunit
Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC)
Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC)
+10 more
All
2
Causal
0
Unknown
2
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
2
CTD
0
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
0
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Related via 2 shared genes including NKX2-5, RPSA.
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1 shared gene
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Related via 1 shared gene including NKX2-5.
NKX2.5-related congenital, conduction and myopathic heart disease
1 shared gene
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Related via 1 shared gene including NKX2-5.
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1 shared gene
RPSA
Related via 1 shared gene including RPSA.
Deletion 5q35 syndrome
1 shared gene
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Related via 1 shared gene including NKX2-5.
1
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