1. Gene
  2. FBXW5 - F-box and WD repeat domain containing 5 Gene

FBXW5 - F-box and WD repeat domain containing 5 Gene

Homo sapiens

Also known as Fbw5

Gene ID: 54461 | Gene type: protein coding

About FBXW5

Cytogenetic location: 9q34.3 Genomic coordinates (GRCh38): 9:136,940,435-136,944,738 (from NCBI)

This gene has 8 transcripts (splice variants), 194 orthologues and 1 paralogue. Broad expression in testis (RPKM 77.8), colon (RPKM 28.1) and 25 other tissues.

Summary

This gene encodes a member of the F-box protein family, members of which are 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 three 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 contains WD-40 domains, in addition to an F-box motif, so it belongs to the Fbw class. Alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene, however, they were found to be nonsense-mediated mRNA decay (NMD) candidates, hence not represented. [provided by RefSeq, Jul 2008]

FBXW5 Products(1)

mRNA Protein Name
NM_018998.4 NP_061871.1 F-box/WD repeat-containing protein 5

FBXW5 Protein Structure

F-box-like

F-box-like: F-box-like (7 - 50)

WD40

WD40: WD domain, G-beta repeat (84 - 120)

WD40

WD40: WD domain, G-beta repeat (509 - 538)

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  • 566 a.a.
Protein Preferred Names Protein Names

F-box/WD repeat-containing protein 5

F-box and WD-40 domain-containing protein 5

Related Diseases

Diseases Alias
Localized Chondrosarcoma
Bardet-Biedl Syndrome 10

BBS10

Bardet-Biedl Syndrome

Bbs

Bardet-Biedl Syndrome, Type 10

Cockayne Syndrome A

Cockayne Syndrome Type 1

Cockayne Syndrome, Type A

Cockayne Syndrome Type I

CSA

Cockayne Syndrome Classic Form

Cockayne Syndrome Classical

Cockayne Syndrome Type A

Ckn1

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Bos taurus FBXW5 VGNC VGNC:28925
Canis familiaris FBXW5 VGNC VGNC:40796
Mus musculus FBXW5 MGD MGI:1354731
Felis catus FBXW5 VGNC VGNC:62203
Rattus norvegicus FBXW5 RGD RGD:1305661
Macaca mulatta FBXW5 VGNC VGNC:72503