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Kleefstra syndrome due to a point mutation
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Anaplastic ependymoma
2 associated genes
No signs/symptoms info
Kleefstra syndrome due to a point mutation
Anaplastic ependymoma

EHMT1
(UniProt - OMIM)
 C11ORF95
(UniProt - OMIM)
RELA
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
EHMT1
(0.75)
RELA


Citations in the biomedical literature:


Kleefstra syndrome due to a point mutation
EHMT1
Anaplastic ependymoma
C11ORF95 RELA



Kleefstra syndrome due to a point mutation
Anaplastic ependymoma

Synonym(s):
(no synonyms)

Synonym(s):
- High-grade ependymoma
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare neurologic disease
- Rare oncologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
(no data available)
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.