TMEM47 (transmembrane protein 47)

symbol:
TMEM47
locus group:
protein-coding gene
location:
Xp21.1
gene_family:
alias symbol:
BCMP1|DKFZP761J17121|DKFZp564E153|VAB-9
alias name:
None
entrez id:
83604
ensembl gene id:
ENSG00000147027
ucsc gene id:
uc004ddh.3
refseq accession:
NM_031442
hgnc_id:
HGNC:18515
approved reserved:
2003-07-10
Xp21.1

TMEM47(跨膜蛋白47)是一种位于内质网膜上的跨膜蛋白,属于TMEM(跨膜蛋白)基因家族成员。该家族的特点是编码多种跨膜蛋白,参与细胞内膜运输、细胞器结构和功能维持等过程。TMEM47在内质网中发挥重要作用,可能参与蛋白质折叠、质量控制或钙离子稳态调节,但其具体生物学功能尚未完全阐明。研究表明,TMEM47在神经系统中表达较高,可能与神经元发育或功能有关。该基因突变可能导致内质网功能紊乱,影响蛋白质加工和分泌途径,进而引发细胞应激反应。有研究发现TMEM47与某些神经系统疾病可能存在关联,但具体机制仍需进一步研究。当TMEM47过表达时,可能干扰内质网的正常功能平衡,导致蛋白质折叠异常或内质网应激;而表达降低则可能影响内质网的结构完整性或运输功能。TMEM基因家族成员通常具有多个跨膜结构域,参与细胞内膜细胞器的形成和功能调控,在物质运输、信号转导和细胞器互作中起重要作用。目前对TMEM47的研究相对有限,需要更多实验证据来明确其精确的分子机制和病理生理作用。

中文English

该基因编码的PMP22 / EMP /紧密连接蛋白家族的一个成员。所编码的蛋白质被定位到ER和质膜。在狗中,该基因的转录物以高水平在大脑中存在。 [由RefSeq的,2008年7月提供]

TMEM47基因的碱基序列:[NCBI]
Loading Gene Browser...
蛋白质序列
1MASAGSGMEE VRVSVLTPLK LVGLVCIFLA LCLDLGAVLS
41PAWVTADHQY YLSLWESCRK PASLDIWHCE STLSSDWQIA
81 TLALLLGGA AIILIAFLVG LISICVGSRR RFYRPVAVML
121FAAVVLQVCS LVLYPIKFIE TVSLKIYHEF NWGYGLAWGA
161T IFSFGGAI LYCLNPKNYE DYY
结构预测来自 AlphaFold DB(UniProt: Q9BQJ4),颜色表示 pLDDT 置信度(深蓝高、黄橙低)。
TMEM47基因的碱基突变:           仅显示部分snp
rs3813160       rs4269688       rs4276835       rs4320691       rs4354457       rs4385612       rs4397576       rs4408051       rs4462052       rs4542095       rs5010895       rs5012459       rs5927297       rs5928614       rs5928615       rs5928617       rs5973217      

TMEM47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
TACTACCTGTCGTTGTGGG
59
GTAGCAATCTGCCAATCGC
60
CTACCTGTCGTTGTGGGAG
60
GTAGCAATCTGCCAATCGC
60
CTACCTGTCGTTGTGGGAG
60
TAGCAATCTGCCAATCGCT
60
      尚未收录相关数据

TMEM47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

TMEM47基因的本体(GO)信息:

GO库代码
对应的蛋白质
来源代码
GO:0003674
Q9BQJ4 (UniProtKB)
ND
GO:0005886
Q9BQJ4 (UniProtKB)
IDA
GO:0005911
Q9BQJ4 (UniProtKB)
IEA
GO:0005912
Q9BQJ4 (UniProtKB)
IEA
GO:0008150
Q9BQJ4 (UniProtKB)
ND
GO:0016021
Q9BQJ4 (UniProtKB)
IEA
GO:0030054
Q9BQJ4 (UniProtKB)
IBA
GO:0098609
Q9BQJ4 (UniProtKB)
IBA

可能调控 TMEM47基因的相关microRNA:     

String
加载中…
关联基因 作用方式 资源库来源/分值
疾病名称 关系值 NofPmids NofSnps 来源
疾病名称 关系值 NofPmids NofSnps 来源
Mental Retardation, X-Linked 0.002995792 1 0 BeFree_LHGDN
The SMARCA4-TMEM47 axis plays an essential role in chikungunya virus RNA replication.
Fu YZ, Luo FF, Yang L, Li JY, Zhang BW, Li ZQ, Zhao LX, Wang SY, Wang YY Proc Natl Acad Sci U S A IF: 9.5 2026-03-24
Organ-specific adaptive signaling pathway activation in metastatic breast cancer cells.
Burnett Riesa M, Craven Kelly E, Krishnamurthy Purna, Goswami Chirayu P, Badve Sunil, Crooks Peter, Mathews William P, Bhat-Nakshatri Poornima, Nakshatri Harikrishna Oncotarget IF: 5.168 2016-03-25
Detection of chromosomal breakpoints in patients with developmental delay and speech disorders.
Utami Kagistia H, Hillmer Axel M, Aksoy Irene, Chew Elaine G Y, Teo Audrey S M, Zhang Zhenshui, Lee Charlie W H, Chen Pauline J, Seng Chan Chee, Ariyaratne Pramila N, Rouam Sigrid L, Soo Lim Seong, Yousoof Saira, Prokudin Ivan, Peters Gregory, Collins Felicity, Wilson Meredith, Kakakios Alyson, Haddad Georges, Menuet Arnaud, Perche Olivier, Tay Stacey Kiat Hong, Sung Ken W K, Ruan Xiaoan, Ruan Yijun, Liu Edison T, Briault Sylvain, Jamieson Robyn V, Davila Sonia, Cacheux Valere PLoS One IF: 2.6 2015-02-12
Use of integrative epigenetic and cytogenetic analyses to identify novel tumor-suppressor genes in malignant melanoma.
Mithani Suhail K, Smith Ian M, Califano Joseph A Melanoma Res IF: 1.8 2011-10-28
Novel markers of subclinical disease for Ewing family tumors from gene expression profiling.
Cheung Irene Y, Feng Yi, Danis Karen, Shukla Neerav, Meyers Paul, Ladanyi Marc, Cheung Nai-Kong V Clin Cancer Res IF: 10.9 2008-05-07

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