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Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
PROTEIN INTERACTIONS: 3
Familial pancreatic carcinoma
5 OMIM references -
8 associated genes
No signs/symptoms info
Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations
Familial pancreatic carcinoma

BRCA2
(UniProt - OMIM)
 BRCA1
(UniProt - OMIM)
BRCA2
(UniProt - OMIM)
CDKN2A
(UniProt - OMIM)
KRAS
(UniProt - OMIM)
MANF
(UniProt - OMIM)
PALB2
(UniProt - OMIM)
SMAD4
(UniProt - OMIM)
TP53
(UniProt - OMIM)

COMMON
GENES 		BRCA2
INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
BRCA2
BRCA2
BRCA2
(0.9)
(0.9)
(0.89)
BRCA1
PALB2
TP53


Citations in the biomedical literature:


Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations
BRCA2
Familial pancreatic carcinoma
BRCA1 CDKN2A KRAS MANF PALB2
SMAD4 TP53



Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations
Familial pancreatic carcinoma

Synonym(s):
(no synonyms)

Synonym(s):
- Familial pancreatic cancer
Classification (Orphanet):
- Rare genetic disease
- Rare oncologic disease
- Rare renal disease
Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
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.