SCUBA

FBXW7 — F-box and WD repeat domain containing 7

FBXW7 belongs to a gene co-expression module in 4 of 28 SCUBA cell types. Each module groups genes that rise and fall together in that cell type; the genes it shares a module with are its closest co-expression partners there.

FBXW7's module in each cell type

Cell typeModuleShares the module with
Gamma-delta T cellsChromatin Remodeling Signaling
DNA/chromatin regulation
AKAP13, BPTF, CARNMT1, CCDC6, CFLAR, CLASP1, CLASP2, DOCK10 +23 more
MacrophagesUbiquitin Proteasome Regulation
Housekeeping
ARIH1, BTAF1, CLASP2, DENND4A, DYRK1A, FBXO11, GATAD2B, LMBR1 +8 moreView in SCUBA
Mucosal-associated invariant T cellRAS-GEF Signaling
TCR Signaling
ASCC3, GPATCH8, HERC1, RASGRF2, RASGRP1, TLK1, TNRC6B, TRAPPC9 +2 more
NeutrophilsUbiquitin Regulatory Signaling
Housekeeping
ARID4B, CYRIB, GRB2, QKI, RAB1A, SIK3, STK10, USP9X

About the gene

SynonymsAGO, CDC4, FBW7, FBX30, FBXW6, FLJ11071, SEL-10, SEL10
Chromosome4: 152320544-152536092
Predicted locationIntracellular
Essential geneNo
Protein classCancer-related genes, Predicted intracellular proteins
Biological processBiological rhythms, DNA damage, DNA repair, Host-virus interaction, Ubl conjugation pathway

Function

Substrate recognition component of a SCF (SKP1-CUL1-F-box protein) E3 ubiquitin-protein ligase complex which mediates the ubiquitination and subsequent proteasomal degradation of target proteins. Recognizes and binds phosphorylated sites/phosphodegrons within target proteins and thereafter brings them to the SCF complex for ubiquitination. Identified substrates include cyclin-E (CCNE1 or CCNE2), DISC1, JUN, MYC, NOTCH1 released notch intracellular domain (NICD), NFE2L1, NOTCH2, MCL1, MLST8, RICTOR, and probably PSEN1. Acts as a negative regulator of JNK signaling by binding to phosphorylated JUN and promoting its ubiquitination and subsequent degradation. Involved in bone homeostasis and negative regulation of osteoclast differentiation. Regulates the amplitude of the cyclic expression of hepatic core clock genes and genes involved in lipid and glucose metabolism via ubiquitination and proteasomal degradation of their transcriptional repressor NR1D1; CDK1-dependent phosphorylation of NR1D1 is necessary for SCF(FBXW7)-mediated ubiquitination. Also able to promote 'Lys-63'-linked ubiquitination in response to DNA damage. The SCF(FBXW7) complex facilitates double-strand break repair following phosphorylation by ATM: phosphorylation promotes localization to sites of double-strand breaks and 'Lys-63'-linked ubiquitination of phosphorylated XRCC4, enhancing DNA non-homologous end joining.

Human Protein Atlas · Open Targets · UniProt

Gene annotation from the Human Protein Atlas and UniProt; see sources & licences.