1. Gene
  2. FMO4 - flavin containing dimethylaniline monoxygenase 4 Gene

FMO4 - flavin containing dimethylaniline monoxygenase 4 Gene

中文名称:含黄素的二甲基苯胺单加氧酶 4

种属: Homo sapiens

同用名: FMO2

基因 ID: 2329 | 基因类型: protein coding

关于 FMO4

Cytogenetic location: 1q24.3 Genomic coordinates (GRCh38): 1:171,314,183-171,342,084 (from NCBI)

This gene has 5 transcripts (splice variants), 140 orthologues and 5 paralogues. Ubiquitous expression in kidney (RPKM 11.6), liver (RPKM 9.8) and 23 other tissues.

功能概要

饮食来源的氨基三甲胺 (TMA) 的代谢 N-氧化由含黄素的单加氧酶介导,并受人类遗传性 FMO3 多态性的影响。这导致 TMA N-氧化能力降低的小亚群,并导致鱼腥味综合症 (三甲基胺尿症) 。三种形式的酶由聚集在 1q23-q25 区域的基因编码。含黄素的单加氧酶是 NADPH 依赖性黄素酶,可催化药物、杀虫剂和异生素中软亲核杂原子中心的氧化。[RefSeq 提供,2015 年 1 月]

Metabolic N-oxidation of diet-derived amino-trimethylamine (TMA) is mediated by flavin-containing monooxygenase and is subject to an inherited FMO3 polymorphism in man. This results in a small subpopulation with reduced TMA N-oxidation capacity and causes fish odor syndrome (Trimethylaminuria). Three forms of the Enzyme are encoded by genes clustered in the 1q23-q25 region. Flavin-containing monooxygenases are NADPH-dependent flavoenzymes that catalyzes the oxidation of soft nucleophilic heteroatom centers in drugs, pesticides, and xenobiotics. [provided by RefSeq, Jan 2015]

FMO4 基因产物(1)

mRNA Protein Name
NM_002022.3 NP_002013.1 dimethylaniline monooxygenase [N-oxide-forming] 4
基因本体论
  • 分子功能
分子功能 GO 注释 逻辑证据 参考文献 来源
enables protein binding IPI
IPI: 通过物理相互作用推断
32296183 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

FMO4 蛋白结构

FMO-like

FMO-like: Flavin-binding monooxygenase-like (2 - 531)

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  • 558 a.a.
蛋白主名 其他名称

dimethylaniline monooxygenase [N-oxide-forming] 4

FMO 4

关联疾病

疾病名称 别名
Trimethylaminuria

TMAU

Fish-Odor Syndrome

Fish Malodor Syndrome

Fish Odor Syndrome

Stale Fish Syndrome

Tmauria

Severe Primary Trimethylaminuria

Mesh

D008661

Fish Odour Syndrome

Prader-Willi Syndrome

Prader-Labhart-Willi Syndrome

PWS

Willi-Prader Syndrome

Prader-Willi Syndrome Due To Translocation

Prader-Willi Syndrome Due To Imprinting Mutation

Prader-Willi Syndrome Due To Maternal Uniparental Disomy Of Chromosome 15

Prader Willi Syndrome

Upd(15)Mat

疾病名称 别名
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

直系同源

种属 基因名 来源 基因 ID
Canis familiaris FMO4 VGNC VGNC:40919
Macaca mulatta FMO4 VGNC VGNC:72684
Rattus norvegicus FMO4 RGD RGD:628601
Mus musculus FMO4 MGD MGI:2429497
Bos taurus FMO4 VGNC VGNC:29052
Felis catus FMO4 VGNC VGNC:62310