NQO1

GENERAL INFORMATION

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Gene name

NQO1

Gene description

NAD(P)H dehydrogenase, quinone 1

Protein class

Cancer-related genes
Enzymes
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

6
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (stomach)
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Cytoplasmic expression in several tissues.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Supportive based on 2 antibodies.
HPA007308 , CAB012421
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Stomach

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enhanced (stomach)

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

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Gene name

NQO1 (HGNC Symbol)

Synonyms

DHQU, DIA4, DTD, NMOR1, QR1

Description

NAD(P)H dehydrogenase, quinone 1 (HGNC Symbol)

Entrez gene summary

This gene is a member of the NAD(P)H dehydrogenase (quinone) family and encodes a cytoplasmic 2-electron reductase. This FAD-binding protein forms homodimers and reduces quinones to hydroquinones. This protein's enzymatic activity prevents the one electron reduction of quinones that results in the production of radical species. Mutations in this gene have been associated with tardive dyskinesia (TD), an increased risk of hematotoxicity after exposure to benzene, and susceptibility to various forms of cancer. Altered expression of this protein has been seen in many tumors and is also associated with Alzheimer's disease (AD). Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]

Chromosome

16

Cytoband

q22.1

Chromosome location (bp)

69706996 - 69726951

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000181019 (version 78.38)

Entrez gene

1728

UniProt

P15559 (UniProt - Evidence at protein level)

neXtProt

NX_P15559

Antibodypedia

NQO1 antibodies


PROTEIN BROWSER

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ENST00000320623
 
ENST00000379046
 
ENST00000379047
 
ENST00000439109
 
ENST00000561500
 
ENST00000564043
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

NQO1-001 ENSP00000319788
ENST00000320623
P15559
Show all »
Show » Show » 274 30.9 No 0
NQO1-002 ENSP00000368335
ENST00000379047
P15559
Show all »
Show » Show » 240 27.3 No 0
NQO1-003 ENSP00000456282
ENST00000561500
H3BRK3
Show all »
Show » 269 29.9 No 0
NQO1-004 ENSP00000368334
ENST00000379046
P15559
Show all »
Show » Show » 236 26.4 No 0
NQO1-005 ENSP00000455020
ENST00000564043
H3BNV2
Show all »
Show » Show » 253 28.5 No 0
NQO1-007 ENSP00000398330
ENST00000439109
B4DLR8
Show all »
Show » 202 22.8 No 0