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Anaplastic ependymoma
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Beckwith-Wiedemann syndrome due to NSD1 mutation
1 associated gene
No signs/symptoms info
Anaplastic ependymoma
Beckwith-Wiedemann syndrome due to NSD1 mutation

C11ORF95
(UniProt - OMIM)
 NSD1
(UniProt - OMIM)
RELA
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
RELA
(0.63)
NSD1


Citations in the biomedical literature:


Anaplastic ependymoma
C11ORF95 RELA
Beckwith-Wiedemann syndrome due to NSD1 mutation
NSD1



Anaplastic ependymoma
Beckwith-Wiedemann syndrome due to NSD1 mutation

Synonym(s):
- High-grade ependymoma
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare neurologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare cardiac disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare maxillo-facial surgical disease
- Rare oncologic disease
- Rare otorhinolaryngologic disease
- Rare renal disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.