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13 OMIM references -
14 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
6 associated genes
No signs/symptoms info
Autosomal dominant nonsyndromic intellectual deficit
Familial renal cell carcinoma

CACNG2 DIRC1
CDH15 DIRC2
CTNNB1 DIRC3
DOCK8 FHIT
DYNC1H1 HSPBAP1
DYRK1A RNF139
EPB41L1
GRIN1
GRIN2B
KIF1A
KIRREL3
MBD5
SYNGAP1
TCF4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CTNNB1
(0.78)
FHIT



Citations in the biomedical literature:


Autosomal dominant nonsyndromic intellectual deficit
CACNG2 CDH15 CTNNB1 DOCK8 DYNC1H1 DYRK1A
EPB41L1 GRIN1 GRIN2B KIF1A KIRREL3 MBD5
SYNGAP1 TCF4
Familial renal cell carcinoma
DIRC1 DIRC2 DIRC3 FHIT HSPBAP1 RNF139



Autosomal dominant nonsyndromic intellectual deficit
Familial renal cell carcinoma

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
(no data available)

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

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
1 MeSH reference: C536851

No signs/symptoms info available.