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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
5 OMIM references -
8 associated genes
No signs/symptoms info
BAP1-related tumor predisposition syndrome
Familial pancreatic carcinoma

BAP1 BRCA1
BRCA2
CDKN2A
KRAS
MANF
PALB2
SMAD4
TP53


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
BAP1
(0.89)
BRCA1



Citations in the biomedical literature:


BAP1-related tumor predisposition syndrome
BAP1
Familial pancreatic carcinoma
BRCA1 BRCA2 CDKN2A KRAS MANF PALB2
SMAD4 TP53



BAP1-related tumor predisposition syndrome
Familial pancreatic carcinoma

Synonym(s):
- Tumor susceptibility linked to germline BAP1 mutations

Synonym(s):
- Familial pancreatic cancer

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

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

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

External references:
1 OMIM reference -
No MeSH references
External references:
5 OMIM references -
1 MeSH reference: C535837

No signs/symptoms info available.