FANCB
Sign in to saveAlso known as FA2, FAAP90, FAAP95, FAB, FACB, Fanconi anemia complementation group B, FA complementation group B
Fanconi anemia group B protein is a protein that in humans is encoded by the FANCB gene.
Gene data
FANCB- Name
- FA complementation group B
- Type
- protein-coding
- Chromosome
- X
- Position
- 14,690,388–14,873,255 (−)
- Aliases
- FA2, FAAP90, FAAP95, FAB, FACB
- Ensembl
- ENSG00000181544
- RefSeq RNA
- NM_001018113.3, NM_001324162.2, NM_001410764.1, NM_152633.4, NR_136707.2
- RefSeq protein
- NP_001018123.1, NP_001311091.1, NP_001397693.1, NP_689846.1, XP_016884845.1
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].
Gene Ontology
Biological process
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
FA complementation group B
- Symbol
- FANCB
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- Chr X:14,690,388-14,873,255
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 7 more facts
- HomoloGene ID
- 51880
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/2187
- chromosome
- human X chromosome
- genomic end
- 14873255
- genomic start
- 14690388
- cytogenetic location
- Xp22.2
Sources (3)
via Wikidata · CC0
~3 min read
Encyclopedic overview
6 sectionsContents
- Function
- Gene
- Protein
- Meiosis
- References
- External links
Fanconi anemia group B protein is a protein that in humans is encoded by the FANCB gene.
== Function ==
Excerpted from Wikipedia’s “FANCB” article, available under the CC BY-SA 4.0 licence.