GJA5 (gap junction protein alpha 5)

symbol:
GJA5
locus group:
protein-coding gene
location:
1q21.2
gene_family:
Gap junction proteins
alias symbol:
CX40
alias name:
connexin 40
entrez id:
2702
ensembl gene id:
ENSG00000265107
ucsc gene id:
uc031uum.2
refseq accession:
NM_181703
hgnc_id:
HGNC:4279
approved reserved:
1991-07-11
1q21.2
基因染色体位置图

GJA5(间隙连接蛋白α5)是连接蛋白基因家族的一员,属于连接蛋白α亚家族(Connexin α family),该家族编码的蛋白质在细胞间形成间隙连接通道,介导细胞间的直接通讯。GJA5编码的蛋白称为连接蛋白40(Connexin 40,Cx40),主要在心脏、血管内皮和平滑肌细胞中表达,对心脏电传导和血管功能调节至关重要。Cx40形成的间隙连接通道允许小分子、离子和电信号在相邻细胞间传递,确保心肌细胞的同步收缩和血管张力的协调调控。GJA5突变可能导致通道功能异常,与心律失常(如心房颤动)、先天性心脏病(如房间隔缺损)及高血压相关。突变可能破坏电信号传导,导致心律不齐或血管功能紊乱。GJA5过表达可能增强细胞间耦合,改善电传导,但过度表达可能引发异常电活动;降低表达则可能导致传导延迟或阻滞,增加心律失常风险。GJA5与GJA1(Cx43)、GJA4(Cx37)等同家族成员共享四跨膜结构域和保守的胞内调控区域,共同维持组织电生理稳态。该基因家族通过间隙连接参与发育、代谢和疾病过程,尤其在心血管和神经系统中作用突出。

This gene is a member of the connexin gene family. The encoded protein is a component of gap junctions, which are composed of arrays of intercellular channels that provide a route for the diffusion of low molecular weight materials from cell to cell. Mutations in this gene may be associated with atrial fibrillation. Alternatively spliced transcript variants encoding the same isoform have been described. [provided by RefSeq, Jul 2008]

此基因是连接蛋白基因家族的一个成员。所编码的蛋白质是间隙连接,这是由提供用于低分子量物质从细胞到细胞的扩散的路径间的通道阵列的一个组成部分。在这个基因的突变可以与房颤相关联。编码相同同种型的可变剪接转录物变体已有描述。 [由RefSeq的,2008年7月提供]

GJA5基因的碱基序列:[NCBI]
Loading Gene Browser...
GJA5基因的碱基突变:           仅显示部分snp
rs791269       rs791270       rs791271       rs791272       rs791273       rs791274       rs791275       rs791276       rs791277       rs791278       rs791279       rs791280       rs791281       rs791282       rs791283       rs791284       rs791285      

GJA5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
AAGGAAAGTCCAGGGAGGA
60
AAATTTCCCAGGAAGCTCCA
60
ATTACAACACAAGGCAGCA
58
AAATTTCCCAGGAAGCTCCA
60
AAGGAAAGTCCAGGGAGGA
60
AAATTTCCCAGGAAGCTCCA
60
GAAGGAAAGTCCAGGGAGG
59
AATTTCCCAGGAAGCTCCA
59
GAAGGAAAGTCCAGGGAGG
59
AATTTCCCAGGAAGCTCCA
59
GATTACAACACAAGGCAGCA
59
AATTTCCCAGGAAGCTCCA
59
AAGGAAAGTCCAGGGAGGA
60
AATTTCCCAGGAAGCTCCA
59
AAGGAAAGTCCAGGGAGGA
60
AATTTCCCAGGAAGCTCCA
59
ATTACAACACAAGGCAGCA
58
AATTTCCCAGGAAGCTCCA
59
转录因子
影响基因
影响类型
参考文献链接(PubMed)
TBX5
GJA5
Activation

GJA5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

GJA5基因的本体(GO)信息:

GO库代码
对应的蛋白质
来源代码
GO:0005922
A0A0B4J1Y3 (UniProtKB)
IEA
GO:0007154
A0A0B4J1Y3 (UniProtKB)
IEA
GO:0016021
A0A0B4J1Y3 (UniProtKB)
IEA
GO:0001501
P36382 (UniProtKB)
IEA
GO:0001525
P36382 (UniProtKB)
IEP
GO:0003105
P36382 (UniProtKB)
IEA
GO:0003151
P36382 (UniProtKB)
IMP
GO:0003158
P36382 (UniProtKB)
IEA
GO:0003161
P36382 (UniProtKB)
IEA
GO:0003174
P36382 (UniProtKB)
IMP
GO:0003193
P36382 (UniProtKB)
IMP
GO:0003281
P36382 (UniProtKB)
IMP
GO:0003283
P36382 (UniProtKB)
IMP
GO:0003284
P36382 (UniProtKB)
IEA
GO:0003294
P36382 (UniProtKB)
IEA
GO:0005887
P36382 (UniProtKB)
IDA
GO:0005921
P36382 (UniProtKB)
IDA
GO:0005922
P36382 (UniProtKB)
IDA
GO:0006813
P36382 (UniProtKB)
IEA
GO:0010643
P36382 (UniProtKB)
IEA
GO:0010652
P36382 (UniProtKB)
IEA
GO:0014704
P36382 (UniProtKB)
IDA
GO:0014704
P36382 (UniProtKB)
TAS
GO:0016264
P36382 (UniProtKB)
IMP
GO:0016264
P36382 (UniProtKB)
IDA
GO:0030326
P36382 (UniProtKB)
IEA
GO:0035050
P36382 (UniProtKB)
IEA
GO:0035922
P36382 (UniProtKB)
IEA
GO:0042995
P36382 (UniProtKB)
IEA
GO:0045776
P36382 (UniProtKB)
IEA
GO:0045907
P36382 (UniProtKB)
IEA
GO:0045909
P36382 (UniProtKB)
IEA
GO:0048844
P36382 (UniProtKB)
ISS
GO:0051259
P36382 (UniProtKB)
IEA
GO:0055077
P36382 (UniProtKB)
IDA
GO:0055085
P36382 (UniProtKB)
IEA
GO:0055117
P36382 (UniProtKB)
IMP
GO:0055117
P36382 (UniProtKB)
IMP
GO:0055117
P36382 (UniProtKB)
IMP
GO:0060307
P36382 (UniProtKB)
IEA
GO:0060371
P36382 (UniProtKB)
IMP
GO:0060371
P36382 (UniProtKB)
IMP
GO:0060373
P36382 (UniProtKB)
IEA
GO:0060412
P36382 (UniProtKB)
IEA
GO:0060413
P36382 (UniProtKB)
IEA
GO:0071253
P36382 (UniProtKB)
IEA
GO:0086005
P36382 (UniProtKB)
IEA
GO:0086015
P36382 (UniProtKB)
IEA
GO:0086053
P36382 (UniProtKB)
IMP
GO:0086054
P36382 (UniProtKB)
IMP
GO:0086064
P36382 (UniProtKB)
IDA
GO:0086064
P36382 (UniProtKB)
IDA
GO:0086075
P36382 (UniProtKB)
IMP
GO:0086075
P36382 (UniProtKB)
IDA
GO:0086077
P36382 (UniProtKB)
IDA
GO:0086091
P36382 (UniProtKB)
IEA
GO:0098904
P36382 (UniProtKB)
IMP
GO:0098905
P36382 (UniProtKB)
IMP
GO:0098906
P36382 (UniProtKB)
IMP
GO:0098910
P36382 (UniProtKB)
IMP
GO:1900133
P36382 (UniProtKB)
IEA
GO:1900825
P36382 (UniProtKB)
IEA
GO:1990029
P36382 (UniProtKB)
IEA

可能调控 GJA5基因的相关microRNA:     

BioGrid

IntAct

mentha

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
CARDIOMYOPATHY, FAMILIAL, WITH CONDUCTION DISTURBANCE 0.241085767 5 1 BeFree_CTD_human_UNIPROT
ATRIAL FIBRILLATION, FAMILIAL, 11 0.24 1 6 CLINVAR_UNIPROT
Hypertensive disease 0.20554839 7 0 BeFree_CTD_human_GAD_RGD
Tetralogy of Fallot 0.200542884 2 0 BeFree_MGD_ORPHANET
ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder) 0.12 0 0 CTD_human
Overactive Bladder 0.08 1 0 RGD
Ureteral obstruction 0.08 1 0 RGD
Shock, Hemorrhagic 0.08 1 0 RGD
Glomerulonephritis 0.08 1 0 RGD
Hypertension, Renovascular 0.08 1 0 RGD

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