COMT

GENERAL INFORMATION

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Gene name

COMT

Gene description

Catechol-O-methyltransferase

Protein class

Enzymes
FDA approved drug targets
Plasma proteins
Predicted intracellular proteins
Predicted membrane proteins

Predicted localization

Intracellular,Membrane

Number of transcripts

8
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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

Cytoplasmic expression at variable levels in all tissues.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Supportive based on 2 antibodies.
HPA001169 , CAB011233
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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

Colon

Kidney

Testis

Placenta



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

COMT

Synonyms

Description

Catechol-O-methyltransferase (HGNC Symbol)

Entrez gene summary

Catechol-O-methyltransferase catalyzes the transfer of a methyl group from S-adenosylmethionine to catecholamines, including the neurotransmitters dopamine, epinephrine, and norepinephrine. This O-methylation results in one of the major degradative pathways of the catecholamine transmitters. In addition to its role in the metabolism of endogenous substances, COMT is important in the metabolism of catechol drugs used in the treatment of hypertension, asthma, and Parkinson disease. COMT is found in two forms in tissues, a soluble form (S-COMT) and a membrane-bound form (MB-COMT). The differences between S-COMT and MB-COMT reside within the N-termini. Several transcript variants are formed through the use of alternative translation initiation sites and promoters. [provided by RefSeq, Sep 2008]

Chromosome

22

Cytoband

q11.21

Chromosome location (bp)

19941607 - 19969975

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000093010 (version 78.38)

Entrez gene

1312

UniProt

P21964 (UniProt - Evidence at protein level)

neXtProt

NX_P21964

Antibodypedia

COMT antibodies


PROTEIN BROWSER

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ENST00000361682
 
ENST00000403184
 
ENST00000403710
 
ENST00000406520
 
ENST00000407537
 
ENST00000412786
 
ENST00000428707
 
ENST00000449653
 
 
 
 


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)

COMT-001 ENSP00000385150
ENST00000406520
P21964
Show all »
Show » Show » 271 30 No 0
COMT-002 ENSP00000385917
ENST00000403710
P21964
Show all »
Show » Show » 271 30 No 0
COMT-003 ENSP00000384654
ENST00000407537
P21964
Show all »
Show » Show » 271 30 No 0
COMT-004 ENSP00000383966
ENST00000403184
E7EUU8
Show all »
Show » Show » 235 26 No 0
COMT-005 ENSP00000403958
ENST00000412786
E7EMS6
Show all »
Show » Show » 223 24.8 No 0
COMT-008 ENSP00000387695
ENST00000428707
Show » Show » 152 16.8 No 1
COMT-011 ENSP00000354511
ENST00000361682
P21964
Show all »
Show » Show » 271 30 No 0
COMT-012 ENSP00000416778
ENST00000449653
P21964
Show all »
Show » Show » 221 24.4 No 0