A4GALT (alpha 1,4-galactosyltransferase (P blood group))

symbol:
A4GALT
locus group:
protein-coding gene
location:
22q13.2
gene_family:
Alpha 1,4-glycosyltransferases
alias symbol:
A14GALT|Gb3S|P(k)
alias name:
Gb3 synthase|CD77 synthase|globo...
entrez id:
53947
ensembl gene id:
ENSG00000128274
ucsc gene id:
uc062ewl.1
refseq accession:
NM_017436
hgnc_id:
HGNC:18149
approved reserved:
2002-02-06
22q13.2

A4GALT(Alpha 1,4-Galactosyltransferase)是一种编码糖基转移酶的基因,属于糖基转移酶家族(Glycosyltransferase family 29)。该基因的主要功能是催化糖脂和糖蛋白的生物合成,特别是在红细胞表面P抗原(也称为Gb3或CD77)的形成中起关键作用。P抗原是一种重要的糖鞘脂,参与细胞间识别和信号传导。A4GALT通过将半乳糖残基转移到乳糖神经酰胺(LacCer)上,生成Gb3,这是后续P1和P抗原合成的关键步骤。该基因的突变可能导致P血型系统的变异,例如在罕见的p表型个体中,A4GALT功能丧失会导致P抗原缺失,从而增加对某些细菌(如大肠杆菌)感染的易感性,也可能与流产风险相关。此外,Gb3的异常积累与Fabry病(一种溶酶体贮积症)有关,尽管Fabry病主要由GLA基因突变引起,但A4GALT的异常表达可能间接影响相关代谢途径。A4GALT的过表达可能导致Gb3水平升高,与某些癌症(如伯基特淋巴瘤)的发展相关,因为Gb3可作为细胞表面受体促进肿瘤生长和转移。相反,A4GALT表达降低可能导致P抗原减少,影响免疫应答和细胞黏附。糖基转移酶家族的共性在于它们都参与糖链的合成或修饰,通过转移糖分子(如半乳糖、葡萄糖等)到脂类、蛋白质或其他糖分子上,从而影响细胞表面特性、信号传导和分子识别。A4GALT作为该家族成员,其功能异常不仅影响血型抗原,还可能涉及感染、癌症和代谢疾病等多种病理过程。

中文English

由该基因编码的蛋白质催化的半乳糖转移到乳糖苷神经酰胺以形成globotriaosylceramide,这已被确定为在P血型系统中的P(k)的抗原。所编码的蛋白质,它是在高尔基体中发现II型膜蛋白,也需要在细菌vero毒素受体的合成。 [由RefSeq的,2008年7月提供]

A4GALT基因的碱基序列:[NCBI]
Loading Gene Browser...
蛋白质序列
1MSKPPDLLLR LLRGAPRQRV CTLFIIGFKF TFFVSIMIYW
41HVVGEPKEKG QLYNLPAEIP CPTLTPPTPP SHGPTPGNIF
81 FLETSDRTN PNFLFMCSVE SAARTHPESH VLVLMKGLPG
121GNASLPRHLG ISLLSCFPNV QMLPLDLREL FRDTPLADWY
161A AVQGRWEP YLLPVLSDAS RIALMWKFGG IYLDTDFIVL
201KNLRNLTNVL GTQSRYVLNG AFLAFERRHE FMALCMRDFV
241DH YNGWIWG HQGPQLLTRV FKKWCSIRSL AESRACRGVT
281TLPPEAFYPI PWQDWKKYFE DINPEELPRL LSATYAVHVW
321NKK SQGTRF EATSRALLAQ LHARYCPTTH EAMKMYL
结构预测来自 AlphaFold DB(UniProt: Q9NPC4),颜色表示 pLDDT 置信度(深蓝高、黄橙低)。
A4GALT基因的碱基突变:           仅显示部分snp
rs130392       rs130393       rs130394       rs130395       rs130396       rs130397       rs130398       rs130399       rs135106       rs135107       rs135108       rs738526       rs738527       rs910301       rs910302       rs910303       rs916231      

A4GALT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
TTCGTGTTGGCAAAGAAGG
59
GATGATGAACAGGGTGCAG
59
GTAGAAGTCAGAGTCGATGGT
59
GCTGGTCTGAACTGTATCGA
60
CAGTAGTACCAGTCAGCGT
59
GATGATGAACAGGGTGCAG
59
ATATCGAGATGGATTTGCAGC
59
TGTCACTGGCTGGTAACTG
60
TGTTGGCAAAGAAGACCAG
58
GAAGCCGATGATGAACAGG
59
GTGTTGGCAAAGAAGACCA
59
GATGATGAACAGGGTGCAG
59
AATATCGAGATGGATTTGCAGC
59
TCACTGGCTGGTAACTGAC
59
GTAGAAGTCAGAGTCGATGGT
59
GCTGGTCTGAACTGTATCG
58
CGTGTTGGCAAAGAAGGTC
60
GATGATGAACAGGGTGCAG
59
AGTAGTACCAGTCAGCGTC
59
GATGATGAACAGGGTGCAG
59
      尚未收录相关数据

A4GALT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

A4GALT基因的本体(GO)信息:

GO库代码
对应的蛋白质
来源代码
GO:0001576
Q9NPC4 (UniProtKB)
IEA
GO:0006486
Q9NPC4 (UniProtKB)
IEA
GO:0006688
Q9NPC4 (UniProtKB)
NAS
GO:0007009
Q9NPC4 (UniProtKB)
IDA
GO:0008378
Q9NPC4 (UniProtKB)
IDA
GO:0008378
Q9NPC4 (UniProtKB)
IDA
GO:0008378
Q9NPC4 (UniProtKB)
IDA
GO:0015643
Q9NPC4 (UniProtKB)
IEA
GO:0016020
Q9NPC4 (UniProtKB)
IDA
GO:0030173
Q9NPC4 (UniProtKB)
NAS
GO:0050512
Q9NPC4 (UniProtKB)
IEA
GO:0070062
Q9NPC4 (UniProtKB)
IDA

可能调控 A4GALT基因的相关microRNA:     

String
BioGrid
mentha
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
Blood group p phenotype (finding) 0.12 0 7 CLINVAR
Cortical Congenital Hyperostosis 0.12 0 0 CLINVAR
Burkitt Lymphoma 0.12 1 0 CTD_human
Hemolytic-Uremic Syndrome 0.00272435 1 0 LHGDN
leukemia 0.00272435 1 0 LHGDN
Uremia syndrome 0.000271442 1 0 BeFree
Teratocarcinoma 0.000271442 1 0 BeFree
Hematopoietic Neoplasms 0.000271442 1 0 BeFree
Acute Megakaryocytic Leukemias 0.000271442 1 0 BeFree
The Gb3-synthase A4GALT is an epigenetically regulated driver of tumor invasiveness in gastrointestinal cancer.
Hirsch ND, Perl M, Holzinger S, Barz C, Enßle S, Johannes W, Conrad A, Unterholzner JJ, Obermeier V, Tschurtschenthaler M, Johannes L, Janssen KP BMC Cancer IF: 3.288 2026-01-27
Unraveling A4GALT Mechanism and Its Modulation With Adamantyl-Galactosylceramide Analogues: Advancing Fabry Disease Therapeutic Strategies.
de Koster N, Vidal-Gironès Ò, de Graaf R, Kok K, Lelieveld LT, Hoogervorst J, Ferraz MJ, Rivas-Fernández JP, Lammers RF, Overkleeft HS, Aerts JMFG, Boot RG, Rovira C, Artola M Angew Chem Int Ed Engl 2026-08-06
Expression of a human Gb3/CD77 synthase in insect and human cells: comparison of activity and glycosylation.
Mikolajczyk K, Szymczak-Kulus K, Bereznicka A, Kaczmarek R, Sobala LF, Jakubiak-Augustyn A, Czerwinski M Protein Expr Purif IF: 1.8 2025-12-00
Comprehensive red blood cell and platelet antigen prediction from whole genome sequencing: proof of principle.
Lane William J, Westhoff Connie M, Uy Jon Michael, Aguad Maria, Smeland-Wagman Robin, Kaufman Richard M, Rehm Heidi L, Green Robert C, Silberstein Leslie E, Transfusion IF: 2.0 2016-08-01
Human Gb3/CD77 synthase reveals specificity toward two or four different acceptors depending on amino acid at position 211, creating P(k), P1 and NOR blood group antigens.
Kaczmarek Radoslaw, Duk Maria, Szymczak Katarzyna, Korchagina Elena, Tyborowska Jolanta, Mikolajczyk Krzysztof, Bovin Nicolai, Szewczyk Boguslaw, Jaskiewicz Ewa, Czerwinski Marcin Biochem Biophys Res Commun IF: 2.5 2016-06-07
Acquired genetic alterations in tumor cells dictate the development of high-risk neuroblastoma and clinical outcomes.
Khan Faizan H, Pandian Vijayabaskar, Ramraj Satishkumar, Natarajan Mohan, Aravindan Sheeja, Herman Terence S, Aravindan Natarajan BMC Cancer IF: 3.288 2016-03-24
[Molecular basis for an individual with rare p phenotype in P1Pk blood group system].
Ma Kairong, Lan Xiaofei, Xu Xianguo, Hong Xiaozhen, Chen Shu, Liu Ying, Ying Yanling, He Ji, Zhu Faming, Lyu Hangjun Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2015-06-18
A systematic study of single-nucleotide polymorphisms in the A4GALT gene suggests a molecular genetic basis for the P1/P2 blood groups.
Lai Yin-Ju, Wu Wan-Yi, Yang Chen-Ming, Yang Li-Rong, Chu Chen-Chung, Chan Yung-Syu, Lin Marie, Yu Lung-Chih Transfusion IF: 2.0 2015-02-12
P1/P2 genotyping of known and novel null alleles in the P1PK and GLOB histo-blood group systems.
Westman Julia S, Hellberg Asa, Peyrard Thierry, Hustinx Hein, Thuresson Britt, Olsson Martin L Transfusion IF: 2.0 2014-01-30
Large deletions involving the regulatory upstream regions of A4GALT give rise to principally novel P1PK-null alleles.
Westman Julia S, Hellberg Asa, Peyrard Thierry, Thuresson Britt, Olsson Martin L Transfusion IF: 2.0 2014-09-29

评论加载中...

登录后即可发表评论 登录 注册

联系地址

山东省济南市章丘区文博路2号

齐鲁师范学院 genelibs生信实验室

山东省济南市高新区舜华路750号

大学科技园北区F座4单元2楼

电话: 0531-88819269

微信公众号

关注微信订阅号,实时查看信息,关注医学生物学动态。


商务邮箱

E-mail: product@genelibs.com