SCUBA

NQO1 — NAD(P)H quinone dehydrogenase 1

NQO1 belongs to a gene co-expression module in 3 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.

NQO1's module in each cell type

Cell typeModuleShares the module with
EndothelialVenous Endothelial Identity
Endothelial cell development
ABI3, CCDC85B, DOCK4, EHD4, EVA1B, EXOC3L2, HDAC7, ITGA6 +8 moreView in SCUBA
FibroblastsLamina Propria ECM
ECM production
ADAMTS7, ADGRL4, ANGPTL6, BMP2, CBLN2, CYTL1, DHRS7C, FAM135B +14 moreView in SCUBA
PericytesVascular Permeability
Migration & adhesion
ABI3, FLT1, GALNT18, ITGA6, PLVAP, PRKCH, TM4SF18View in SCUBA

About the gene

SynonymsDHQU, DIA4, DTD, NMOR1, QR1
Chromosome16: 69706996-69726668
Predicted locationIntracellular
Essential geneNo
Protein classCancer-related genes, Enzymes, Metabolic proteins, Predicted intracellular proteins
Molecular functionOxidoreductase

Function

Flavin-containing quinone reductase that catalyzes two- electron reduction of quinones to hydroquinones using either NADH or NADPH as electron donors. In a ping-pong kinetic mechanism, the electrons are sequentially transferred from NAD(P)H to flavin cofactor and then from reduced flavin to the quinone, bypassing the formation of semiquinone and reactive oxygen species (By similarity). Regulates cellular redox state primarily through quinone detoxification. Reduces components of plasma membrane redox system such as coenzyme Q and vitamin quinones, producing antioxidant hydroquinone forms. In the process may function as superoxide scavenger to prevent hydroquinone oxidation and facilitate excretion. Alternatively, can activate quinones and their derivatives by generating redox reactive hydroquinones with DNA cross-linking antitumor potential. Acts as a gatekeeper of the core 20S proteasome known to degrade proteins with unstructured regions. Upon oxidative stress, interacts with tumor suppressors TP53 and TP73 in a NADH-dependent way and inhibits their ubiquitin-independent degradation by the 20S proteasome.

Human Protein Atlas · Open Targets · UniProt

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