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13 OMIM references -
14 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 3
1 OMIM reference -
7 associated genes
No signs/symptoms info
Autosomal dominant nonsyndromic intellectual deficit
Translocation renal cell carcinoma

CACNG2 ASPSCR1
CDH15 CLTC
CTNNB1 NONO
DOCK8 PRCC
DYNC1H1 SFPQ
DYRK1A TFE3
EPB41L1 TFEB
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)
NONO
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
Translocation renal cell carcinoma
ASPSCR1 CLTC NONO PRCC SFPQ TFE3
TFEB



Autosomal dominant nonsyndromic intellectual deficit
Translocation renal cell carcinoma

Synonym(s):
(no synonyms)

Synonym(s):
- Carcinoma associated with MITF/TFE translocation
- Translocation carcinoma

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

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:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.