Gene: FBXW7 (F-box and WD repeat domain containing 7, E3 ubiquitin protein ligase)  Homo sapiens

Symbol: FBXW7
Name: F-box and WD repeat domain containing 7, E3 ubiquitin protein ligase
Description: This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene was previously referred to as FBX30, and belongs to the Fbws class; in addition to an F-box, this protein contains 7 tandem WD40 repeats. This protein binds directly to cyclin E and probably targets cyclin E for ubiquitin-mediated degradation. Mutations in this gene are detected in ovarian and breast cancer cell lines, implicating the gene's potential role in the pathogenesis of human cancers. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2012]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: AGO; archipelago; archipelago homolog; archipelago, Drosophila, homolog of; CDC4; DKFZp686F23254; f-box and wd-40 domain protein 7 (archipelago homolog, drosophila); F-box and WD-40 domain protein 7 (archipelago homolog, Drosophila); F-box and WD-40 domain-containing protein 7; F-box protein FBW7; F-box protein FBX30; F-box protein SEL-10; F-box/WD repeat-containing protein 7; FBW6; FBW7; FBX30; FBXO30; FBXW6; FLJ16457; hAgo; hAgo; hCdc4; hCdc4; homolog of C elegans sel-10; SEL-10; SEL10
Orthologs: Mus musculus : Fbxw7 (F-box and WD-40 domain protein 7)  MGI
Rattus norvegicus : Fbxw7 (F-box and WD repeat domain containing 7, E3 ubiquitin protein ligase)
Latest Assembly: Human Genome Assembly GRCh37
Position:
MapChrPositionStrandSource
Human Alternate Assembly CHM1_14153,027,150 - 153,241,136-NCBI
Human Genome Assembly HuRef4148,968,491 - 149,182,492-NCBI
Human Genome Assembly GRCh374153,242,410 - 153,456,393-NCBI
Human Genome Assembly Build 364153,461,860 - 153,675,622-NCBI
Human Cytogenetic Map4q31.3 NCBI
Human Genome Assembly4153,601,099 - 153,690,635 NCBI
Model

Launch Genome Browser (GBrowse) : build 36 (hg18) build 37 (hg19)


Gene-Chemical Interaction Annotations
Gene Ontology Annotations
Molecular Pathway Annotations
References - curated
References - uncurated
RGD Disease Portals

Genomics

Comparative Map Data
Position Markers
QTLs in Region (Human Genome Assembly GRCh37)

Sequence

Nucleotide Sequences
Protein Sequences
Promoters

Additional Information

External Database Links
Nomenclature History
 
More on FBXW7
Entrez Gene
Ensembl Gene
Genome Browser: (hg18) (hg19)
HGNC Report
NCBI Map Viewer
Vista
Vista + UCSC

RGD Object Information
RGD ID: 1347453
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2013-05-14
Status: ACTIVE