1. Gene
  2. Comt - catechol-O-methyltransferase Gene

Comt - catechol-O-methyltransferase Gene

Rattus norvegicus
Gene ID: 24267 | Gene type: protein coding

About Comt

Primary_assembly 11: 82,568,025-82,587,642 forward strand.mRatBN7.2:CM026984.1

This gene has 3 transcripts (splice variants), 276 orthologues, 2 paralogues and is associated with 68 phenotypes. Biased expression in Liver (RPKM 255.1), Kidney (RPKM 1227.4) and 5 other tissues.

Summary

Enables catechol O-methyltransferase activity. Involved in several processes, including learning or memory; negative regulation of smooth muscle cell proliferation; and regulation of cellular amine metabolic process. Located in several cellular components, including cell body; dendritic spine; and postsynaptic membrane. Used to study Parkinsonism and hypertension. Biomarker of hypertension. Human ortholog(s) of this gene implicated in several diseases, including attention deficit hyperactivity disorder; autoimmune disease of skin and connective tissue (multiple); bulimia nervosa; cognitive disorder (multiple); and reproductive organ Cancer (multiple). Orthologous to human COMT (catechol-O-methyltransferase). [provided by Alliance of Genome Resources, Apr 2022]

Comt Products(1)

mRNA Protein Name
NM_012531.2 NP_036663.1 catechol O-methyltransferase
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables catechol O-methyltransferase activity IDA
IDA: Inferred from direct assay
12584150 RGD
Biological Process GO Annotation Evidence Reference Source
involved in estrogen metabolic process IMP
IMP: Inferred from mutant phenotype
11071850 RGD
involved in female pregnancy IMP
IMP: Inferred from mutant phenotype
18042640 RGD
involved in learning IMP
IMP: Inferred from mutant phenotype
15190105 RGD
involved in negative regulation of dopamine metabolic process IMP
IMP: Inferred from mutant phenotype
15190105 RGD
involved in negative regulation of smooth muscle cell proliferation IMP
IMP: Inferred from mutant phenotype
11071850 RGD
involved in positive regulation of homocysteine metabolic process IMP
IMP: Inferred from mutant phenotype
15779086 RGD
involved in response to estrogen IEP
IEP: Inferred from expression pattern
22100850 RGD
involved in response to lipopolysaccharide IEP
IEP: Inferred from expression pattern
17573159 RGD
involved in response to organic cyclic compound IEP
IEP: Inferred from expression pattern
15964593 RGD
involved in response to pain IMP
IMP: Inferred from mutant phenotype
17084978 RGD
involved in response to xenobiotic stimulus IEP
IEP: Inferred from expression pattern
17868501 RGD
involved in short-term memory IMP
IMP: Inferred from mutant phenotype
22815336 RGD
Cellular Component GO Annotation Evidence Reference Source
located in axon IDA
IDA: Inferred from direct assay
21846718 RGD
located in cell body IDA
IDA: Inferred from direct assay
21846718 RGD
located in dendrite IDA
IDA: Inferred from direct assay
21846718 RGD
located in dendritic spine IDA
IDA: Inferred from direct assay
7617303 RGD
is active in glutamatergic synapse IDA
IDA: Inferred from direct assay
7617303 RGD
is active in postsynapse IDA
IDA: Inferred from direct assay
7617303 RGD
located in postsynaptic membrane IDA
IDA: Inferred from direct assay
7617303 RGD
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

Comt Protein Structure

YrrM

YrrM: cl28097 (44 - 238)

  • 0
  • 100
  • 200
  • 265 a.a.
Protein Preferred Names Protein Names

catechol O-methyltransferase

catecholamine-O-methyltransferase

Orthologs Information

Species Symbol Source ID
Homo sapiens Comt NCBI NCBI:1312