FANCB

FANCB
Identifiers
Aliases	FANCB, FA2, FAAP90, FAAP95, FAB, FACB, Fanconi anemia complementation group B, FA complementation group B
External IDs	OMIM: 300515; MGI: 2448558; HomoloGene: 51880; GeneCards: FANCB; OMA:FANCB - orthologs
Gene location (Human)
Chr.	X chromosome (human)
End	14,873,255 bp
Gene location (Mouse)
Chr.	X chromosome (mouse)
End	163,780,268 bp
RNA expression pattern
	Top expressed in
	testicle; ; gonad; ; buccal mucosa cell; ; internal globus pallidus; ; ventricular zone; ; bone marrow cells; ; ganglionic eminence; ; stromal cell of endometrium; ; monocyte; ; secondary oocyte;
	Top expressed in
	hand; ; primitive streak; ; secondary oocyte; ; epiblast; ; dermis; ; primary oocyte; ; medullary collecting duct; ; zygote; ; Paneth cell; ; tail of embryo;
	More reference expression data
	; ;
	More reference expression data
Gene ontology
Molecular function	protein binding;
Cellular component	nucleus; nucleoplasm; Fanconi anaemia nuclear complex;
Biological process	interstrand cross-link repair; cellular response to DNA damage stimulus; DNA repair; positive regulation of double-strand break repair via homologous recombination; replication-born double-strand break repair via sister chromatid exchange; negative regulation of double-strand break repair via homologous recombination;
	Sources:Amigo / QuickGO
Orthologs
	2187
	237211
	ENSG00000181544
	ENSMUSG00000047757
	Q8NB91
	Q5XJY6
	NM_001018113; NM_152633; NM_001324162
	NM_001146081; NM_175027
	NP_001018123; NP_001311091; NP_689846
	NP_001139553; NP_778192
	Wikidata
View/Edit Human	View/Edit Mouse

Fanconi anemia group B protein is a protein that in humans is encoded by the FANCB gene.