HNMT (histamine N-methyltransferase)

symbol:
HNMT
locus group:
protein-coding gene
location:
2q22.1
gene_family:
alias symbol:
None
alias name:
None
entrez id:
3176
ensembl gene id:
ENSG00000150540
ucsc gene id:
uc002tvf.4
refseq accession:
NM_001024074
hgnc_id:
HGNC:5028
approved reserved:
1994-04-18
2q22.1
基因染色体位置图

HNMT(组胺N-甲基转移酶)是一种重要的代谢酶,主要负责催化组胺的甲基化反应,将其转化为N-甲基组胺,从而调控组胺的活性和降解。组胺是一种重要的生物活性分子,参与多种生理过程,如免疫反应、神经传递和胃酸分泌。HNMT主要在肝脏、肾脏、中枢神经系统和支气管等组织中表达,其活性直接影响组胺在体内的浓度和功能。HNMT的突变可能导致酶活性降低,进而引起组胺代谢障碍,增加组胺在体内的积累,与多种疾病相关,如过敏性疾病、哮喘、精神分裂症和神经退行性疾病(如帕金森病和阿尔茨海默病)。HNMT基因的多态性(如Thr105Ile)已被研究,某些变异可能影响酶的稳定性和活性,从而增加个体对组胺相关疾病的易感性。HNMT属于甲基转移酶基因家族,该家族的共性是通过转移甲基基团参与多种生物分子的代谢和调控,包括神经递质、激素和药物。如果HNMT过表达,可能会加速组胺的降解,导致组胺水平过低,影响免疫和神经功能;而HNMT表达降低则可能导致组胺积累,引发炎症反应或过敏症状。此外,HNMT的功能异常还可能影响其他依赖组胺的信号通路,如肥大细胞活化和H1-H4受体介导的生理反应。研究HNMT的调控机制和功能对于理解组胺相关疾病的发病机制和开发靶向治疗策略具有重要意义。

In mammals, histamine is metabolized by two major pathways: N(tau)-methylation via histamine N-methyltransferase and oxidative deamination via diamine oxidase. This gene encodes the first enzyme which is found in the cytosol and uses S-adenosyl-L-methionine as the methyl donor. In the mammalian brain, the neurotransmitter activity of histamine is controlled by N(tau)-methylation as diamine oxidase is not found in the central nervous system. A common genetic polymorphism affects the activity levels of this gene product in red blood cells. Multiple alternatively spliced transcript variants that encode different proteins have been found for this gene. [provided by RefSeq, Jul 2008]

None

HNMT基因的碱基序列:[NCBI]
Loading Gene Browser...
HNMT基因的碱基突变:           仅显示部分snp
rs2187       rs973013       rs985322       rs991788       rs993891       rs1020677       rs1020678       rs1050891       rs1050900       rs1156369       rs1156370       rs1156403       rs1349992       rs1378319       rs1378320       rs1378321       rs1378322      

HNMT基因在不同组织中的表达:    [UniProt]

基因在不同组织中的表达图
正向引物序列
正向Tm值
反向引物序列
反向Tm值
评分
TTTCTCAACCATTCCACGG
58
TCTCCAATCCTTCCTATTATGC
57
CAAATACAAAGAGCTTGTAGCC
58
TGGTATTCAGATGATGTCTCCT
58
GCCAGGCATAATAGGAAGG
58
CTACAAGCTCTTTGTATTTGGC
58
ATTCATGGACAAGAAGCTGC
59
TAATCCTCTTGCCTGCACC
60
TTTCTCAACCATTCCACGG
58
CAGCAATTCTGGTATCTTCCT
58
GCTGCCAGGCATAATAGGA
60
GATCAATTTCACCTGCACCTC
60
TTTCTCAACCATTCCACGG
58
CAGCAATTCTGGTATCTTCCT
58
TTGTTGTGTCAGGAAGCAG
58
ATACTGGCAGAGGTCATCC
59
TTGTTGTGTCAGGAAGCAG
58
ATACTGGCAGAGGTCATCC
59
GCTGCCAGGCATAATAGGA
60
ATGAGACAATCTGCACCTCC
60
      尚未收录相关数据

HNMT基因(以及对应的蛋白质)的细胞分布位置:

[UniProt]     [GenomeNet]

" d="M482.414,245.296c3.539,4.293,4.455,10.009,0.202,11 c-4.244,0.996-4.983-10.983-8.293-8.438c-5.271,4.08,9.834,12.271,5.144,17.287c-3.717,3.607-6.172-5.75-10.839-1.976 c-4.673,3.776,6.781,7.299,2.831,11.326c-4.354,4.045-6.979-1.449-9.837-5.517c-1.193-1.742-2.059-3.851-3.595-2.748 c-1.516,1.078-1.854,1.795-0.938,3.666c2.374,4.854,9.235,10.119,5.156,12.535c-5.636,3.346-5.044-8.871-9.426-7.574 c-4.388,1.291,2.557,10.66-1.245,11.141c-4.089,0.545-3.483-10.239-6.979-8.575c-2.522,1.206-0.929,3.071-0.938,4.899 c0.004,1.32-0.964,3.6-2.372,4.062c-3.593,1.171-8.544-1.065-10.251-3.59c-6.04-8.93,0.396-15.997,4.639-7.015 c3.023,4.642,5.182,0.834,2.839-2.219c-1.032-1.354-4.309-5.901-0.781-7.252c2.904-1.113,4.271,1.941,5.985,4.592 c2.61,4.016,5.485,0.117,3.031-3.414c-1.828-2.633-2.74-3.803,3.156-7.42c6.405-4.369,6.52,3.869,10.077,0.646 c2.309-1.832-4.783-5.149,0.06-8.995c2.896-2.293,5.18,6.207,7.961,3.516c3.523-2.737-7.717-7.369,0.117-11.736 C473.413,240.77,480.519,242.891,482.414,245.296z"/> Extracellular space Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi Apparatus Nucleus Mitochondrion 0 1 2 3 4 5 Confidence
  • 质膜
  • 细胞质
  • 细胞外
  • 高尔基体
  • 囊泡
  • 细胞骨架
  • 内质网
  • 细胞核
  • 内体
  • 溶酶体
  • 线粒体

HNMT基因的本体(GO)信息:

GO库代码
对应的蛋白质
来源代码
GO:0002347
P50135 (UniProtKB)
IEA
GO:0005654
P50135 (UniProtKB)
IDA
GO:0005737
P50135 (UniProtKB)
IDA
GO:0005829
P50135 (UniProtKB)
TAS
GO:0006548
P50135 (UniProtKB)
TAS
GO:0006972
P50135 (UniProtKB)
IEA
GO:0007420
P50135 (UniProtKB)
IBA
GO:0007585
P50135 (UniProtKB)
TAS
GO:0014075
P50135 (UniProtKB)
IEA
GO:0032259
P50135 (UniProtKB)
IBA
GO:0035902
P50135 (UniProtKB)
IEA
GO:0042220
P50135 (UniProtKB)
IEA
GO:0043005
P50135 (UniProtKB)
IBA
GO:0046539
P50135 (UniProtKB)
IBA
GO:0046539
P50135 (UniProtKB)
TAS
GO:0051384
P50135 (UniProtKB)
IEA
GO:0070062
P50135 (UniProtKB)
IDA
GO:0070555
P50135 (UniProtKB)
IEA
GO:1903955
P50135 (UniProtKB)
IMP

可能调控 HNMT基因的相关microRNA:     

BioGrid

IntAct

mentha

String

基因与其他基因之间的相互作用关系图
序号 作用方式 资源库来源/分值 基因名称 基因名称
疾病名称 关系值 NofPmids NofSnps 来源
疾病名称 关系值 NofPmids NofSnps 来源
Asthma 0.131096779 8 0 BeFree_CTD_human_GAD
Urticaria 0.122638474 3 0 BeFree_CTD_human_GAD
Rhinitis 0.120271442 1 0 BeFree_CTD_human
Drug Allergy 0.12 1 0 CTD_human
ASTHMA, SUSCEPTIBILITY TO (finding) 0.12 0 1 CLINVAR
Brain Infarction 0.08 2 0 RGD
Alcoholic Intoxication, Chronic 0.00554839 3 1 BeFree_GAD
Dermatitis, Atopic 0.005362824 1 1 BeFree_GAD_LHGDN
Bronchial Hyperreactivity 0.002638474 2 0 BeFree_GAD
Migraine Disorders 0.002638474 1 0 BeFree_GAD

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