Tetraspanin 9: Difference between revisions
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{{cite web | {{cite web | ||
| title = Entrez Gene: Tetraspanin 9 | | title = Entrez Gene: Tetraspanin 9 | ||
| url = | | url = https://www.ncbi.nlm.nih.gov/gene/10867 | ||
| accessdate = 2017-11-30 | | accessdate = 2017-11-30 | ||
}}</ref> | }}</ref> | ||
Latest revision as of 16:07, 28 January 2018
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Tetraspanin 9 is a protein that in humans is encoded by the TSPAN9 gene. [1]
Function
The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. Alternatively spliced transcripts encoding the same protein have been identified. [provided by RefSeq, Nov 2009].
References
- ↑ "Entrez Gene: Tetraspanin 9". Retrieved 2017-11-30.
Further reading
- Protty MB, Watkins NA, Colombo D, Thomas SG, Heath VL, Herbert JM, Bicknell R, Senis YA, Ashman LK, Berditchevski F, Ouwehand WH, Watson SP, Tomlinson MG (2009). "Identification of Tspan9 as a novel platelet tetraspanin and the collagen receptor GPVI as a component of tetraspanin microdomains". Biochem. J. 417 (1): 391–400. doi:10.1042/BJ20081126. PMC 2652832. PMID 18795891.
- Kotha J, Zhang C, Longhurst CM, Lu Y, Jacobs J, Cheng Y, Jennings LK (2009). "Functional relevance of tetraspanin CD9 in vascular smooth muscle cell injury phenotypes: a novel target for the prevention of neointimal hyperplasia". Atherosclerosis. 203 (2): 377–86. doi:10.1016/j.atherosclerosis.2008.07.036. PMID 18799160.
- Chapuis J, Hot D, Hansmannel F, Kerdraon O, Ferreira S, Hubans C, Maurage CA, Huot L, Bensemain F, Laumet G, Ayral AM, Fievet N, Hauw JJ, DeKosky ST, Lemoine Y, Iwatsubo T, Wavrant-Devrièze F, Dartigues JF, Tzourio C, Buée L, Pasquier F, Berr C, Mann D, Lendon C, Alpérovitch A, Kamboh MI, Amouyel P, Lambert JC (2009). "Transcriptomic and genetic studies identify IL-33 as a candidate gene for Alzheimer's disease". Mol. Psychiatry. 14 (11): 1004–16. doi:10.1038/mp.2009.10. PMC 2860783. PMID 19204726.
- Oguri M, Kato K, Yokoi K, Yoshida T, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nozawa Y, Yamada Y (2010). "Assessment of a polymorphism of SDK1 with hypertension in Japanese Individuals". Am. J. Hypertens. 23 (1): 70–7. doi:10.1038/ajh.2009.190. PMID 19851296.
- Yoshida T, Kato K, Yokoi K, Oguri M, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nozawa Y, Yamada Y (2010). "Association of genetic variants with hemorrhagic stroke in Japanese individuals". Int. J. Mol. Med. 25 (4): 649–56. PMID 20198315.
- Stiles KM, Kielian M (2016). "Role of TSPAN9 in Alphavirus Entry and Early Endosomes". J. Virol. 90 (9): 4289–97. doi:10.1128/JVI.00018-16. PMC 4836341. PMID 26865714.
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This article incorporates text from the United States National Library of Medicine, which is in the public domain.