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13 OMIM references -
14 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 3
6 associated genes
No signs/symptoms info
Autosomal dominant nonsyndromic intellectual deficit
Inflammatory myofibroblastic tumor

CACNG2 ALK
CDH15 CARS
CTNNB1 CLTC
DOCK8 RANBP2
DYNC1H1 TPM3
DYRK1A TPM4
EPB41L1
GRIN1
GRIN2B
KIF1A
KIRREL3
MBD5
SYNGAP1
TCF4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CTNNB1
DYRK1A
GRIN1
(0.63)
(0.63)
(0.59)
RANBP2
CLTC
CLTC



Citations in the biomedical literature:


Autosomal dominant nonsyndromic intellectual deficit
CACNG2 CDH15 CTNNB1 DOCK8 DYNC1H1 DYRK1A
EPB41L1 GRIN1 GRIN2B KIF1A KIRREL3 MBD5
SYNGAP1 TCF4
Inflammatory myofibroblastic tumor
ALK CARS CLTC RANBP2 TPM3 TPM4



Autosomal dominant nonsyndromic intellectual deficit
Inflammatory myofibroblastic tumor

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

Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)

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

External references:
13 OMIM references -
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.