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Autism, x-linked
Autism, x-linked
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
AUTISM, SUSCEPTIBILITY TO, X-LINKED 5
MONDO:0010449
RPL10
Unknown
—
ClinVar
,
GenCC
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
Formation of a pool of free 40S subunits
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)
+7 more
AUTISM, SUSCEPTIBILITY TO, X-LINKED 6
C3550875
TMLHE
Unknown
—
Disgenet
Lysine degradation
Metabolic pathways
Carnitine synthesis
All
6
Causal
4
Unknown
2
Select all
Clear
ClinVar
1
Orphanet
0
Disgenet
1
CTD
0
HPO
0
GWAS catalog
0
GenCC
1
ClinGen
0
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Diseases that share the most curated genes with Autism, x-linked.
5
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Central apnea
1 shared gene
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Related via 1 shared gene including MECP2.
Neonatal encephalopathy
1 shared gene
MECP2
Related via 1 shared gene including MECP2.
X-linked myopathy with excessive autophagy
1 shared gene
RPL10
Related via 1 shared gene including RPL10.
Bruxism
1 shared gene
MECP2
Related via 1 shared gene including MECP2.
Bulbar palsy
1 shared gene
MECP2
Related via 1 shared gene including MECP2.
1
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