COQ2

GENERAL INFORMATION

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Gene name

COQ2

Gene description

Coenzyme Q2 4-hydroxybenzoate polyprenyltransferase

Protein class

Disease related genes
Enzymes
Mitochondrial proteins
Potential drug targets
Predicted membrane proteins

Predicted localization

Membrane

Number of transcripts

2
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Expressed in all
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

A majority of normal tissues showed moderate to strong cytoplasmic positivity. Lymphatic tissues and most squamous epithelia were negative.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 1 antibody.
HPA068727
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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
Nasopharynx
N/A
N/A
Bronchus
N/A
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Gallbladder

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

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Gene name

COQ2 (HGNC Symbol)

Synonyms

CL640, FLJ26072

Description

Coenzyme Q2 4-hydroxybenzoate polyprenyltransferase (HGNC Symbol)

Entrez gene summary

This gene encodes an enzyme that functions in the final steps in the biosynthesis of CoQ (ubiquinone), a redox carrier in the mitochondrial respiratory chain and a lipid-soluble antioxidant. This enzyme, which is part of the coenzyme Q10 pathway, catalyzes the prenylation of parahydroxybenzoate with an all-trans polyprenyl group. Mutations in this gene cause coenzyme Q10 deficiency, a mitochondrial encephalomyopathy, and also COQ2 nephropathy, an inherited form of mitochondriopathy with primary renal involvement. [provided by RefSeq, Oct 2009]

Chromosome

4

Cytoband

q21.23

Chromosome location (bp)

83261536 - 83284914

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000173085 (version 78.38)

Entrez gene

27235

UniProt

Q96H96 (UniProt - Evidence at protein level)

neXtProt

NX_Q96H96

Antibodypedia

COQ2 antibodies


PROTEIN BROWSER

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ENST00000311461
 
ENST00000311469
 
 
 
 


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)

COQ2-001 ENSP00000310873
ENST00000311469
Q96H96
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Show » Show » 421 45.6 No 8
COQ2-003 ENSP00000311835
ENST00000311461
E2QRG7
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Show » Show » 328 35.5 No 7