FMO3 - flavin containing dimethylaniline monoxygenase 3 Gene
Also Known as TMAU; FMOII; dJ127D3.1
Species: Homo sapiens
About FMO3
This gene has 6 transcripts (splice variants), 131 orthologues, 5 paralogues and is associated with 3 phenotypes. Biased expression in liver (RPKM 241.9) and adrenal (RPKM 8.6).
Summary
Flavin-containing monooxygenases (FMO) are an important class of drug-metabolizing Enzymes that catalyze the NADPH-dependent oxygenation of various nitrogen-,sulfur-, and phosphorous-containing xenobiotics such as therapeutic drugs, dietary compounds, pesticides, and Other foreign compounds. The human FMO gene family is composed of 5 genes and multiple pseudogenes. FMO members have distinct developmental- and tissue-specific expression patterns. The expression of this FMO3 gene, the major FMO expressed in adult liver, can vary up to 20-fold between individuals. This inter-individual variation in FMO3 expression levels is likely to have significant effects on the rate at which xenobiotics are metabolised and, therefore, is of considerable interest to the pharmaceutical industry. This transmembrane protein localizes to the endoplasmic reticulum of many tissues. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. Mutations in this gene cause the disorder trimethylaminuria (TMAu) which is characterized by the accumulation and excretion of unmetabolized trimethylamine and a distinctive body odor. In healthy individuals, trimethylamine is primarily converted to the non odorous trimethylamine N-oxide.[provided by RefSeq, Jan 2016]
FMO3 Products (4)
| mRNA | Protein | Name |
|---|---|---|
| NM_001002294.3 | NP_001002294.1 | dimethylaniline monooxygenase [N-oxide-forming] 3 isoform a |
| NM_001319173.2 | NP_001306102.1 | dimethylaniline monooxygenase [N-oxide-forming] 3 isoform b |
| NM_001319174.2 | NP_001306103.1 | dimethylaniline monooxygenase [N-oxide-forming] 3 isoform c |
| NM_006894.6 | NP_008825.4 | dimethylaniline monooxygenase [N-oxide-forming] 3 isoform a |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables hypotaurine monooxygenase activity |
IDA
IDA: Inferred from direct assay
|
32156684 | GOA |
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
25910212 | GOA |
| Biological Process GO Annotation | Evidence | References | Source |
|---|---|---|---|
| involved in taurine biosynthetic process |
IDA
IDA: Inferred from direct assay
|
32156684 | GOA |
FMO3 Protein Structure
FMO-like: Flavin-binding monooxygenase-like (3 - 531)
- 0
- 100
- 200
- 300
- 400
- 500
- 532 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
dimethylaniline monooxygenase [N-oxide-forming] 3 |
|
FMO3 Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Intra
|
FMO3 | P31513 | CLEC10A | Homo sapiens | Q8IUN9 | 32296183 | |
|
Intra
|
FMO3 | P31513 | CLEC10A | Homo sapiens | Q8IUN9 | 32296183 | |
|
Intra
|
FMO3 | P31513 | CLEC10A | Homo sapiens | Q8IUN9 | 32296183 | |
|
Intra
|
FMO3 | P31513 | SACM1L | Homo sapiens | Q9NTJ5 | 32296183 | |
|
Intra
|
FMO3 | P31513 | CREB3 | Homo sapiens | O43889-2 | 25910212 | |
|
Intra
|
FMO3 | P31513 | CREB3 | Homo sapiens | O43889-2 | 25910212 | |
|
Intra
|
FMO3 | P31513 | CREB3 | Homo sapiens | O43889-2 | 25910212 | |
|
Intra
|
FMO3 | P31513 | CREB3 | Homo sapiens | O43889-2 | 31515488 | |
|
Intra
|
FMO3 | P31513 | SGSM3 | Homo sapiens | Q96HU1 | 32296183 | |
|
Intra
|
FMO3 | P31513 | SGSM3 | Homo sapiens | Q96HU1 | 32296183 | |
|
Intra
|
FMO3 | P31513 | SGSM3 | Homo sapiens | Q96HU1 | 32296183 |
FMO3 Antibodies
| Cat. No. | Product Name | Application | Reactivity |
|---|---|---|---|
| HY-P82247 | FMO3 Antibody (YA1992) | WB, IHC-P, ICC/IF | Human, Mouse, Rat |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Trimethylaminuria |
|
|
| Primary Trimethylaminuria |
|
|
| Familial Adenomatous Polyposis |
|
|
| Sudden Infant Death Syndrome |
|
|
| Choline Deficiency Disease |
|
|
| Arteriosclerosis |
|
Orthologs Information
| Species | Symbol | Source | ID |
|---|---|---|---|
| Bos taurus | FMO3 | VGNC | VGNC:29051 |
| Mus musculus | FMO3 | MGD | MGI:1100496 |
| Canis familiaris | FMO3 | VGNC | VGNC:40918 |
| Rattus norvegicus | FMO3 | RGD | RGD:619761 |
| Macaca mulatta | FMO3 | VGNC | VGNC:99953 |
| Felis catus | FMO3 | VGNC | VGNC:62309 |
| Others | FMO3 | NCBI |