FBXW10

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

F-box/WD repeat-containing protein 10 is a protein that in humans is encoded by the FBXW10 gene.[5][6][7]

AliasesFBXW10, Fbw10, HREP, SM25H2, SM2SH2, F-box and WD repeat domain containing 10
End18,779,349 bp[1]
Quick facts Identifiers, Aliases ...
FBXW10
Identifiers
AliasesFBXW10, Fbw10, HREP, SM25H2, SM2SH2, F-box and WD repeat domain containing 10
External IDsOMIM: 611679; MGI: 3052463; HomoloGene: 32757; GeneCards: FBXW10; OMA:FBXW10 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001267585
NM_001267586
NM_031456

NM_001033669
NM_001291441

RefSeq (protein)

NP_001254514
NP_001254515

Location (UCSC)Chr 17: 18.74 – 18.78 MbChr 11: 62.74 – 62.77 Mb
PubMed search[3][4]
Wikidata
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Members of the F-box protein family, such as FBXW10, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603034), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004).[supplied by OMIM][7] Increased expression of the gene has been associated with laminopathies, and in degradation of chromatin associated proteins such as HP1, ATR kinases (Chaturvedi and ParnaiK, 2010, PMID 20498703).

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