Fanconi Anemia Gene Set

Dataset	CTD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	A congenital hypoplastic anemia characterized by progressive pancytopenia with bone marrow failure, variable congenital malformations and predisposition to develop hematological or solid tumors. It is a result of a genetic defect in a cluster of proteins responsible for DNA repair. (Human Disease Ontology, DOID_13636)
External Link	http://ctdbase.org/detail.go?type=disease&acc=MESH:D005199
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Genes

15 genes/proteins associated with the disease Fanconi Anemia from the curated CTD Gene-Disease Associations dataset.

Symbol	Name	Standardized Value
BRIP1	BRCA1 interacting protein C-terminal helicase 1	2.88009
SLX4	SLX4 structure-specific endonuclease subunit	2.88009
FANCD2	Fanconi anemia, complementation group D2	2.88009
MX1	MX dynamin-like GTPase 1	2.88009
BRCA2	breast cancer 2, early onset	2.88009
TNF	tumor necrosis factor	2.88009
RAD51C	RAD51 paralog C	2.88009
FANCL	Fanconi anemia, complementation group L	2.88009
FANCM	Fanconi anemia, complementation group M	2.88009
FANCA	Fanconi anemia, complementation group A	2.88009
FANCB	Fanconi anemia, complementation group B	2.88009
FANCC	Fanconi anemia, complementation group C	2.88009
FANCE	Fanconi anemia, complementation group E	2.88009
FANCG	Fanconi anemia, complementation group G	2.88009
FANCF	Fanconi anemia, complementation group F	2.88009