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Gene: FANCB (FA complementation group B) Homo sapiens
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Symbol: FANCB
Name: FA complementation group B
Description: 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]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: FA2; FAAP90; FAAP95; FAB; FACB; Fanconi anemia complementation group B; Fanconi anemia group B protein; Fanconi anemia, complementation group B; fanconi anemia-associated polypeptide of 95 kDa; type 2 Fanconi pancytopenia
Orthologs:
Mus musculus (house mouse) : Fancb (Fanconi anemia, complementation group B)  MGI  Alliance
Rattus norvegicus (Norway rat) : Fancb (FA complementation group B)  Alliance
Chinchilla lanigera (long-tailed chinchilla) : Fancb (FA complementation group B)
Pan paniscus (bonobo/pygmy chimpanzee) : FANCB (FA complementation group B)
Canis lupus familiaris (dog) : FANCB (FA complementation group B)
Ictidomys tridecemlineatus (thirteen-lined ground squirrel) : Fancb (FA complementation group B)
Sus scrofa (pig) : FANCB (FA complementation group B)
more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38X14,690,863 - 14,873,255 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X14,861,529 - 14,891,184 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X14,771,450 - 14,801,105 (-)NCBINCBI36hg18NCBI36
Build 34X14,621,185 - 14,650,848NCBI
CeleraX18,976,913 - 19,006,568 (-)NCBI
Cytogenetic MapXp22.2NCBI
HuRefX12,620,535 - 12,649,320 (-)NCBIHuRef
CHM1_1X14,891,941 - 14,921,601 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
Phenotype Annotations
References - curated
References - uncurated

Genomics

Comparative Map Data
miRNA Target Status

Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on FANCB
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1351449
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2019-07-09
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.