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8 OMIM references -
11 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
7 associated genes
No signs/symptoms info
Brugada syndrome
Translocation renal cell carcinoma

CACNA1C ASPSCR1
CACNB2 CLTC
GPD1L NONO
HCN4 PRCC
KCND3 SFPQ
KCNE3 TFE3
KCNJ8 TFEB
SCN1B
SCN3B
SCN5A
TRPM4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
KCND3
(0.63)
NONO



Citations in the biomedical literature:


Brugada syndrome
CACNA1C CACNB2 GPD1L HCN4 KCND3 KCNE3
KCNJ8 SCN1B SCN3B SCN5A TRPM4
Translocation renal cell carcinoma
ASPSCR1 CLTC NONO PRCC SFPQ TFE3
TFEB



Brugada syndrome
Translocation renal cell carcinoma

Synonym(s):
- Bangungut
- Dream disease
- Idiopathic ventricular fibrillation, Brugada type
- Pokkuri death syndrome
- SUNDS
- Sudden unexplained nocturnal death syndrome

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

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

Classification (ICD10):
- Diseases of the circulatory system -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

External references:
8 OMIM references -
1 MeSH reference: D053840
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.