Jump to content
 







Main menu
   


Navigation  



Main page
Contents
Current events
Random article
About Wikipedia
Contact us
Donate
 




Contribute  



Help
Learn to edit
Community portal
Recent changes
Upload file
 








Search  

































Create account

Log in
 









Create account
 Log in
 




Pages for logged out editors learn more  



Contributions
Talk
 



















Contents

   



(Top)
 


1 Function  





2 References  





3 Further reading  














CD96






Deutsch
Русский
Татарча / tatarça
Українська
 

Edit links
 









Article
Talk
 

















Read
Edit
View history
 








Tools
   


Actions  



Read
Edit
View history
 




General  



What links here
Related changes
Upload file
Special pages
Permanent link
Page information
Cite this page
Get shortened URL
Download QR code
Wikidata item
 




Print/export  



Download as PDF
Printable version
 
















Appearance
   

 






From Wikipedia, the free encyclopedia
 


CD96
Identifiers
AliasesCD96, TACTILE, CD96 molecule
External IDsOMIM: 606037; MGI: 1934368; HomoloGene: 68489; GeneCards: CD96; OMA:CD96 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_005816
NM_198196
NM_001318889

NM_032465

RefSeq (protein)

NP_001305818
NP_005807
NP_937839
NP_001305818.1

NP_115854

Location (UCSC)Chr 3: 111.29 – 111.67 MbChr 16: 45.86 – 45.94 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

CD96 (Cluster of Differentiation96) or Tactile (T cell activation, increased late expression) is a protein that in humans is encoded by the CD96 gene.[5] CD96 is a receptor protein which is expressed on T cells and NK cells and shares sequence similarity with CD226 (also known as DNAM-1).[6] The protein encoded by this gene belongs to the immunoglobulin superfamily. It is a type I membrane protein. The protein may play a role in the adhesion of activated T and NK cells to their target cells during the late phase of the immune response. It may also function in antigen presentation[citation needed]. Alternative splicing occurs at this locus and two transcript variants encoding distinct isoforms have been identified. CD96 is a transmembrane glycoprotein that has three extracellular immunoglobulin-like domains and is expressed by all resting human and mouse NK cells. CD96 main ligandisCD155. CD 96 has approximately 20% homology with CD226 and competed for binding to CD155 with CD226.[7]

Function

[edit]

The protein encoded by this gene belongs to the immunoglobulin superfamily. It is a type I membrane protein. The protein may play a role in the adhesive interactions of activated T and NK cells during the late phase of the immune response. It may also function in antigen presentation. Alternative splicing generates multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jan 2016].

References

[edit]
  • ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  • ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  • ^ "Entrez Gene: CD96 molecule". Retrieved 2018-07-03.
  • ^ Fuchs A, Colonna M (October 2006). "The role of NK cell recognition of nectin and nectin-like proteins in tumor immunosurveillance". Seminars in Cancer Biology. 16 (5): 359–366. doi:10.1016/j.semcancer.2006.07.002. PMID 16904340.
  • ^ Martinet L, Smyth MJ (April 2015). "Balancing natural killer cell activation through paired receptors". Nature Reviews. Immunology. 15 (4): 243–254. doi:10.1038/nri3799. PMID 25743219. S2CID 20825600.
  • Further reading

    [edit]
  • Hosen N, Park CY, Tatsumi N, Oji Y, Sugiyama H, Gramatzki M, et al. (June 2007). "CD96 is a leukemic stem cell-specific marker in human acute myeloid leukemia". Proceedings of the National Academy of Sciences of the United States of America. 104 (26): 11008–11013. Bibcode:2007PNAS..10411008H. doi:10.1073/pnas.0704271104. PMC 1904175. PMID 17576927.
  • Kaname T, Yanagi K, Chinen Y, Makita Y, Okamoto N, Maehara H, et al. (October 2007). "Mutations in CD96, a member of the immunoglobulin superfamily, cause a form of the C (Opitz trigonocephaly) syndrome". American Journal of Human Genetics. 81 (4): 835–841. doi:10.1086/522014. PMC 2227933. PMID 17847009.
  • Meyer D, Seth S, Albrecht J, Maier MK, du Pasquier L, Ravens I, et al. (January 2009). "CD96 interaction with CD155 via its first Ig-like domain is modulated by alternative splicing or mutations in distal Ig-like domains". The Journal of Biological Chemistry. 284 (4): 2235–2244. doi:10.1074/jbc.M807698200. PMID 19056733.
  • Davila S, Froeling FE, Tan A, Bonnard C, Boland GJ, Snippe H, et al. (April 2010). "New genetic associations detected in a host response study to hepatitis B vaccine". Genes and Immunity. 11 (3): 232–238. doi:10.1038/gene.2010.1. PMID 20237496. S2CID 11183658.
  • Wu Y, Xiao M, Zhu L, Zhou XX, Gong Q, Xin X, et al. (June 2011). "[CD96 expression on bone marrow mononuclear cells in 91 patients with acute leukemia]". Zhongguo Shi Yan Xue Ye Xue Za Zhi (in Chinese). 19 (3): 585–588. PMID 21729528.
  • Mohseni Nodehi S, Repp R, Kellner C, Bräutigam J, Staudinger M, Schub N, et al. (2012). "Enhanced ADCC activity of affinity maturated and Fc-engineered mini-antibodies directed against the AML stem cell antigen CD96". PLOS ONE. 7 (8): e42426. Bibcode:2012PLoSO...742426M. doi:10.1371/journal.pone.0042426. PMC 3411760. PMID 22879978.
  • Eriksson EM, Keh CE, Deeks SG, Martin JN, Hecht FM, Nixon DF (2012). "Differential expression of CD96 surface molecule represents CD8⁺ T cells with dissimilar effector function during HIV-1 infection". PLOS ONE. 7 (12): e51696. Bibcode:2012PLoSO...751696E. doi:10.1371/journal.pone.0051696. PMC 3521672. PMID 23272144.
  • Chávez-González A, Dorantes-Acosta E, Moreno-Lorenzana D, Alvarado-Moreno A, Arriaga-Pizano L, Mayani H (May 2014). "Expression of CD90, CD96, CD117, and CD123 on different hematopoietic cell populations from pediatric patients with acute myeloid leukemia". Archives of Medical Research. 45 (4): 343–350. doi:10.1016/j.arcmed.2014.04.001. PMID 24751333.
  • t
  • e
  • t
  • e
  • t
  • e
  • This article incorporates text from the United States National Library of Medicine, which is in the public domain.


    Retrieved from "https://en.wikipedia.org/w/index.php?title=CD96&oldid=1196788546"

    Categories: 
    Genes on human chromosome 3
    Clusters of differentiation
    Immunology stubs
    Biochemistry stubs
    Human chromosome 3 gene stubs
    Hidden categories: 
    Articles with short description
    Short description matches Wikidata
    All articles with unsourced statements
    Articles with unsourced statements from February 2018
    CS1 Chinese-language sources (zh)
    All stub articles
    Wikipedia articles incorporating text from the United States National Library of Medicine
     



    This page was last edited on 18 January 2024, at 13:21 (UTC).

    Text is available under the Creative Commons Attribution-ShareAlike License 4.0; additional terms may apply. By using this site, you agree to the Terms of Use and Privacy Policy. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc., a non-profit organization.



    Privacy policy

    About Wikipedia

    Disclaimers

    Contact Wikipedia

    Code of Conduct

    Developers

    Statistics

    Cookie statement

    Mobile view



    Wikimedia Foundation
    Powered by MediaWiki