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Translocation renal cell carcinoma
1 OMIM reference -
7 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Limb-mammary syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
Translocation renal cell carcinoma
Limb-mammary syndrome

ASPSCR1
(UniProt - OMIM)
 TP63
(UniProt - OMIM)
CLTC
(UniProt - OMIM)
NONO
(UniProt - OMIM)
PRCC
(UniProt - OMIM)
SFPQ
(UniProt - OMIM)
TFE3
(UniProt - OMIM)
TFEB
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
NONO
(0.72)
TP63


Citations in the biomedical literature:


Translocation renal cell carcinoma
ASPSCR1 CLTC NONO PRCC SFPQ TFE3
TFEB
Limb-mammary syndrome
TP63



Translocation renal cell carcinoma
Limb-mammary syndrome

Synonym(s):
- Carcinoma associated with MITF/TFE translocation
- Translocation carcinoma
Synonym(s):
- LMS
Classification (Orphanet):
- Rare oncologic disease
- Rare renal disease
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
- Rare gynecologic or obstetric disease
- Rare skin disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: no data available
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: C535903
No signs/symptoms info available.