ODCs

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2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Anaplastic ependymoma

Polymicrogyria due to TUBB2B mutation

C11ORF95	(UniProt - OMIM)		TUBB2B	(UniProt - OMIM)
RELA	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	RELA	(0.72)	TUBB2B

Citations in the biomedical literature:

Anaplastic ependymoma		Polymicrogyria due to TUBB2B mutation
	Synonym(s): - High-grade ependymoma		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare neurologic disease - Rare oncologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.