DisGeNET - a database of gene-disease associations

Source: GENOMICS_ENGLAND

Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP B ×

Gene: FANCB ×

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Gene

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	2187
Gene Symbol:	FANCB

FANCB

CUI:	C1845292
Disease:	FANCONI ANEMIA, COMPLEMENTATION GROUP B

FANCONI ANEMIA, COMPLEMENTATION GROUP B

0.600

Biomarker

GENOMICS_ENGLAND

X-linked recessive VACTERL-H due to a mutation in FANCB in a preterm boy.

26683739

2016

Entrez Id:	2187
Gene Symbol:	FANCB

FANCB

CUI:	C1845292
Disease:	FANCONI ANEMIA, COMPLEMENTATION GROUP B

FANCONI ANEMIA, COMPLEMENTATION GROUP B

0.600

Biomarker

GENOMICS_ENGLAND

X-linked inheritance of Fanconi anemia complementation group B.

15502827

2004

Entrez Id:	2187
Gene Symbol:	FANCB

FANCB

CUI:	C1845292
Disease:	FANCONI ANEMIA, COMPLEMENTATION GROUP B

FANCONI ANEMIA, COMPLEMENTATION GROUP B

0.600

Biomarker

GENOMICS_ENGLAND

Entrez Id:	2187
Gene Symbol:	FANCB

FANCB

CUI:	C1845292
Disease:	FANCONI ANEMIA, COMPLEMENTATION GROUP B

FANCONI ANEMIA, COMPLEMENTATION GROUP B

0.600

Biomarker

GENOMICS_ENGLAND