CYP2C9 (cytochrome P450 family 2 subfamily C member 9)

symbol:
CYP2C9
locus group:
protein-coding gene
location:
10q23.33
gene_family:
Cytochrome P450s
alias symbol:
P450IIC9
alias name:
None
entrez id:
1559
ensembl gene id:
ENSG00000138109
ucsc gene id:
uc001kka.5
refseq accession:
NM_000771
hgnc_id:
HGNC:2623
approved reserved:
1992-04-06
10q23.33
基因染色体位置图

CYP2C9属于细胞色素P450(CYP450)基因家族,这是一个庞大的酶家族,主要参与药物代谢和内源性物质的生物转化。CYP2C9基因位于人类第10号染色体上,编码的CYP2C9酶主要在肝脏中表达,负责代谢多种药物,如华法林、苯妥英、甲苯磺丁脲和非甾体抗炎药(NSAIDs)。CYP2C9酶通过氧化反应使这些药物更易溶于水,从而促进其排泄。CYP2C9的突变可能显著影响其代谢能力,例如,CYP2C9*2和CYP2C9*3是常见的功能降低的等位基因,携带这些突变的个体对华法林等药物的代谢能力下降,可能导致药物在体内积累,增加出血风险。因此,CYP2C9基因型检测在个体化用药中具有重要意义,尤其是对于华法林等治疗窗窄的药物。CYP2C9的过表达可能加速药物代谢,导致药物疗效降低,而表达降低则可能延长药物作用时间或增加毒性。此外,CYP2C9还参与一些内源性物质的代谢,如花生四烯酸和维生素K的代谢。CYP2C9基因多态性与某些疾病的风险相关,例如,携带功能降低等位基因的个体可能对华法林更敏感,而某些突变可能与糖尿病或心血管疾病的易感性有关。CYP450基因家族的共性在于它们都是含血红素的单加氧酶,依赖NADPH和氧气催化底物的氧化反应,主要在外源性和内源性化合物的代谢中发挥作用。CYP450酶在药物代谢、毒素清除以及类固醇激素和胆汁酸的合成中具有关键作用。CYP2C9作为其中的一员,其功能异常可能影响多种药物的疗效和安全性,因此在临床用药中需要特别关注其遗传变异。

This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and its expression is induced by rifampin. The enzyme is known to metabolize many xenobiotics, including phenytoin, tolbutamide, ibuprofen and S-warfarin. Studies identifying individuals who are poor metabolizers of phenytoin and tolbutamide suggest that this gene is polymorphic. The gene is located within a cluster of cytochrome P450 genes on chromosome 10q24. [provided by RefSeq, Jul 2008]

该基因编码的酶的细胞色素P450超家族的成员。细胞色素P450蛋白是能催化涉及药物代谢和胆固醇,类固醇和其他脂类的合成许多反应单加氧酶。此蛋白质定位于内质网和它的表达是由利福平诱导。酶是已知的代谢许多生物异源物质,包括苯妥英,甲苯磺丁脲,布洛芬和S-华法林。研究确定个人谁是苯妥英和甲苯磺丁脲代谢不佳表明,这种基因是多态。该基因位于细胞色素P450基因在染色体10q24群集内。 [由RefSeq的,2008年7月提供]

CYP2C9基因的碱基序列:[NCBI]
Loading Gene Browser...
CYP2C9基因的碱基突变:           仅显示部分snp
rs1057909       rs1057910       rs1057911       rs1135654       rs1200312       rs1200313       rs1200314       rs1200315       rs1341161       rs1578438       rs1799853       rs1856908       rs1934959       rs1934960       rs1934962       rs1934963       rs1934964      

CYP2C9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
CTGATTGATCTTGGAGAGGAG
58
TTCCAAATCCTCTGTTAGCTC
58
TATCTCATTCCCAAGGGCA
58
CAAACATCTCTGGGTTGGG
59
GACATCAGCAAATCCTTAACCA
59
AATACAGAGTGAACACAGGG
57
TGCAATGTGATCTGCTCCA
60
TATTGCAGATCTGGATCCAGG
60
TGCAATGTGATCTGCTCCA
60
TATTGCAGATCTGGATCCAGG
60
CTGCAATGTGATCTGCTCC
59
ATTGCAGATCTGGATCCAGG
60
CTGCAATGTGATCTGCTCC
59
ATTGCAGATCTGGATCCAGG
60
GACATCAGCAAATCCTTAACC
57
AATACAGAGTGAACACAGGG
57
CTGATTGATCTTGGAGAGGAG
58
TCCAAATCCTCTGTTAGCTC
57
CTATCTCATTCCCAAGGGCA
59
AAACATCTCTGGGTTGGGA
59
转录因子
影响基因
影响类型
参考文献链接(PubMed)
HNF4A
CYP2C9
Activation
HNF4A
CYP2C9
Unknown
NCOA6
CYP2C9
Unknown
NR1I2
CYP2C9
Unknown
NR1I3
CYP2C9
Unknown
PPARA
CYP2C9
Repression
PPARGC1A
CYP2C9
Unknown

CYP2C9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

CYP2C9基因的本体(GO)信息:

GO库代码
对应的蛋白质
来源代码
GO:0001567
P11712 (UniProtKB)
IEA
GO:0004497
P11712 (UniProtKB)
IDA
GO:0004497
P11712 (UniProtKB)
NAS
GO:0004497
P11712 (UniProtKB)
TAS
GO:0004497
P11712 (UniProtKB)
TAS
GO:0005506
P11712 (UniProtKB)
IEA
GO:0005789
P11712 (UniProtKB)
TAS
GO:0005789
P11712 (UniProtKB)
TAS
GO:0005789
P11712 (UniProtKB)
TAS
GO:0006805
P11712 (UniProtKB)
TAS
GO:0008144
P11712 (UniProtKB)
IDA
GO:0008202
P11712 (UniProtKB)
IMP
GO:0008392
P11712 (UniProtKB)
IBA
GO:0008395
P11712 (UniProtKB)
IMP
GO:0016098
P11712 (UniProtKB)
IDA
GO:0016491
P11712 (UniProtKB)
IDA
GO:0016491
P11712 (UniProtKB)
IDA
GO:0017144
P11712 (UniProtKB)
IDA
GO:0017144
P11712 (UniProtKB)
IDA
GO:0017144
P11712 (UniProtKB)
IMP
GO:0018675
P11712 (UniProtKB)
IEA
GO:0018676
P11712 (UniProtKB)
IEA
GO:0019373
P11712 (UniProtKB)
IBA
GO:0019373
P11712 (UniProtKB)
TAS
GO:0019627
P11712 (UniProtKB)
IDA
GO:0019825
P11712 (UniProtKB)
TAS
GO:0020037
P11712 (UniProtKB)
IEA
GO:0032787
P11712 (UniProtKB)
IDA
GO:0034875
P11712 (UniProtKB)
IDA
GO:0042737
P11712 (UniProtKB)
IMP
GO:0042738
P11712 (UniProtKB)
IDA
GO:0043231
P11712 (UniProtKB)
TAS
GO:0043231
P11712 (UniProtKB)
TAS
GO:0043231
P11712 (UniProtKB)
IDA
GO:0043603
P11712 (UniProtKB)
IDA
GO:0052741
P11712 (UniProtKB)
IEA
GO:0055114
P11712 (UniProtKB)
IDA
GO:0055114
P11712 (UniProtKB)
IDA
GO:0070989
P11712 (UniProtKB)
IDA
GO:0097267
P11712 (UniProtKB)
TAS

可能调控 CYP2C9基因的相关microRNA:     

Reactome

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
Hemorrhage 0.153495766 13 0 CTD_human_GAD_LHGDN
Drug-Induced Liver Injury 0.127101096 5 0 CTD_human_GAD
Drug Allergy 0.124734064 3 0 CTD_human_GAD
Peptic Ulcer Hemorrhage 0.122367032 1 0 CTD_human_GAD
Coumarin Resistance 0.120542884 2 0 BeFree_CTD_human
Brain Neoplasms 0.120271442 1 0 BeFree_CTD_human
Cardiomyopathies 0.12 1 0 CTD_human
Acute kidney injury 0.12 1 0 CTD_human
Adverse reaction to drug 0.12 2 0 CTD_human
Nephritis, Interstitial 0.12 1 0 CTD_human

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