FANCB


Summary: This gene encodes a member of the Fanconi anemia complementation group B. This protein is assembled into a nucleoprotein complex that is involved in the repair of DNA lesions. Mutations in this gene can cause chromosome instability and VACTERL syndrome with hydrocephalus. [provided by RefSeq, Apr 2016].

NameOMIM IDEnsembl IDHGNC IDPHARMGKB IDMap Location
FA complementation group BMIM:300515Ensembl:ENSG00000181544HGNC:HGNC:3583PA27996Xp22.2

Gene Categories:

DNA REPAIR

GO terms in FANCB


Term TypeEvidence TypeGO Term IDGO Des.
MFIPIGO:0005515protein binding
BPTASGO:0036297interstrand cross-link repair
BPIBAGO:1905168positive regulation of double-strand break repair via homologous recombination
BPIBAGO:1990414replication-born double-strand break repair via sister chromatid exchange
BPIBAGO:2000042negative regulation of double-strand break repair via homologous recombination
CCTASGO:0005654nucleoplasm
CCIBAGO:0043240Fanconi anaemia nuclear complex
CCIDAGO:0043240Fanconi anaemia nuclear complex

Gene expression in normal tissue: FANCB

Gene-model tissue-cancer distribution: Bubble Plot

Gene-drug pathway distribution

Pathways in FANCB


DatabasePathway IDPathway Des.
pidfanconi_pathwayFanconi anemia pathway
kegghsa03460Fanconi anemia pathway - Homo sapiens (human)
reactomeR-HSA-6783310Fanconi Anemia Pathway
reactomeR-HSA-73894DNA Repair

Gene-Drug: Aster Plot


Drug IDDrug NameModel Num.
iGMDRD451Serdemetan3
iGMDRD300Tozasertib1
iGMDRD246NPC263
iGMDRD506Fedratinib1
iGMDRD74Idarubicin2
iGMDRD187BRD98761
iGMDRD782DC-45-A23
iGMDRD171Pemetrexed4
iGMDRD5Tyrphostin AG 14781
iGMDRD158NSC1415403
iGMDRD137Indisulam1
iGMDRD375GW-4058333
iGMDRD154NSC237663
iGMDRD211(1S,3R)-RSL33
iGMDRD466Chaetocin3
iGMDRD177Teniposide1
iGMDRD314Tanespimycin2
iGMDRD85Ursolic acid3
iGMDRD483SCH-5290743
iGMDRD670ML 2103
iGMDRD599Salermide3
iGMDRD126Tipifarnib6

Gene in drug-gene network: Network Plot

Gene-drug targets distribution

Gene Structure: PDB

Models in FANCB

​​​​