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1 OMIM reference -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 3
12 associated genes
No signs/symptoms info
Cree leukoencephalopathy
Giant cell glioblastoma

EIF2B1 EGFR
EIF2B2 FGFR1
EIF2B3 FGFR3
EIF2B4 IDH1
EIF2B5 LZTR1
MGMT
NFKBIA
PPARG
SEPT14
TACC1
TACC3
TP53


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
EIF2B3
EIF2B2
EIF2B5
(0.82)
(0.63)
(0.63)
EGFR
EGFR
EGFR



Citations in the biomedical literature:


Cree leukoencephalopathy
EIF2B1 EIF2B2 EIF2B3 EIF2B4 EIF2B5
Giant cell glioblastoma
EGFR FGFR1 FGFR3 IDH1 LZTR1 MGMT
NFKBIA PPARG SEPT14 TACC1 TACC3 TP53



Cree leukoencephalopathy
Giant cell glioblastoma

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare neurologic disease
- Rare oncologic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
(no data available)

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: adulthood
Average age of death: -
Type of inheritance: sporadic

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

No signs/symptoms info available.