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