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FMO2

From Wikipedia, the free encyclopedia
Protein-coding gene in the species Homo sapiens
FMO2
Identifiers
Aliases FMO2 , FMO1B1, flavin containing monooxygenase 2, flavin containing dimethylaniline monoxygenase 2
External IDsOMIM: 603955; MGI: 1916776; HomoloGene: 86882; GeneCards: FMO2; OMA:FMO2 - orthologs
Gene location (Human)
Chromosome 1 (human)
Chr. Chromosome 1 (human) [1]
Band 1q24.3Start171,185,249 bp [1]
End171,212,686 bp [1]
Gene location (Mouse)
Chromosome 1 (mouse)
Chr. Chromosome 1 (mouse)[2]
Band 1|1 H2.1Start162,701,886 bp [2]
End162,726,295 bp [2]
RNA expression pattern
Bgee
Human Mouse (ortholog)
  • pericardium

  • right lung

  • lower lobe of lung

  • Descending thoracic aorta

  • lactiferous duct

  • ascending aorta

  • vena cava

  • upper lobe of lung

  • upper lobe of left lung

  • abdominal fat
  • lumbar spinal ganglion

  • ascending aorta

  • right lung

  • left lung lobe

  • aortic valve

  • right lung lobe

  • pericardium

  • esophagus

  • right kidney

  • human kidney
More reference expression data
BioGPS
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

2327

55990

Ensembl

ENSG00000094963

ENSMUSG00000040170

UniProt

Q99518

Q8K2I3

RefSeq (mRNA)

NM_001301347
NM_001460
NM_001365900

NM_018881
NM_001360913
NM_001360914

RefSeq (protein)

NP_001288276
NP_001451
NP_001352829

NP_061369
NP_001347842
NP_001347843

Location (UCSC)Chr 1: 171.19 – 171.21 Mb Chr 1: 162.7 – 162.73 Mb
PubMed search[3] [4]
Wikidata

Dimethylaniline monooxygenase [N-oxide-forming] 2 is an enzyme that in humans is encoded by the FMO2 gene.[5] [6] [7]

The flavin-containing monooxygenases are NADPH-dependent enzymes that catalyze the oxidation of many drugs and xenobiotics. In most mammals, there is a flavin-containing monooxygenase that catalyzes the N-oxidation of some primary alkylamines through an N-hydroxylamine intermediate. However, in humans, this enzyme is truncated and is probably rapidly degraded. The protein encoded by this gene represents the truncated form and apparently has no catalytic activity. A functional allele found in African Americans has been reported, but no sequence evidence has been deposited to support the finding. This gene is found in a cluster with the FMO1, FMO3, and FMO4 genes on chromosome 1.[7]

References

[edit ]
  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000094963Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000040170Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Dolphin CT, Shephard EA, Povey S, Smith RL, Phillips IR (Nov 1992). "Cloning, primary sequence and chromosomal localization of human FMO2, a new member of the flavin-containing mono-oxygenase family". Biochem J. 287. ( Pt 1) (Pt 1): 261–7. doi:10.1042/bj2870261. PMC 1133153 . PMID 1417778.
  6. ^ Dolphin CT, Beckett DJ, Janmohamed A, Cullingford TE, Smith RL, Shephard EA, Phillips IR (Dec 1998). "The flavin-containing monooxygenase 2 gene (FMO2) of humans, but not of other primates, encodes a truncated, nonfunctional protein". J Biol Chem. 273 (46): 30599–607. doi:10.1074/jbc.273.46.30599 . PMID 9804831.
  7. ^ a b "Entrez Gene: FMO2 flavin containing monooxygenase 2 (non-functional)".

Further reading

[edit ]
1.14.11: 2-oxoglutarate
1.14.13: NADH or NADPH
1.14.14: reduced flavin or flavoprotein
1.14.15: reduced iron–sulfur protein
1.14.16: reduced pteridine (BH4 dependent)
1.14.17: reduced ascorbate
1.14.18-19: other
1.14.99 - miscellaneous


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