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
- Aliases
- FA2, FAAP90, FAAP95, FAB, FACB
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].
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
View on Ensembl →
via Ensembl · EMBL-EBI
Wikidata facts
Show 5 more facts
- HomoloGene ID
- 51880
- exact match
- identifiers.org/ncbigene/2187
- genomic end
- 14873255
- genomic start
- 14690388
- cytogenetic location
- Xp22.2
Sources (3)
via Wikidata · CC0
~3 min read
Article
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 ==
Connections
Q180686
Entity
X chromosome
Entity
Ensembl genome database project
Entity
cryptochrome
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nucleotide-excision repair
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protein
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Wikidata
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gene
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testicle
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chromosome
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digital object identifier
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embryo
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meiosis
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DNA replication
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fertility
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human genome
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Q229883
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base pair
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locus
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gene expression
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