Trafficking protein particle complex 11: Difference between revisions
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{{cite web | {{cite web | ||
| title = Entrez Gene: Trafficking protein particle complex 11 | | title = Entrez Gene: Trafficking protein particle complex 11 | ||
| url = | | url = https://www.ncbi.nlm.nih.gov/gene/60684 | ||
| accessdate = 2017-10-11 | | accessdate = 2017-10-11 | ||
}}</ref> | }}</ref> |
Latest revision as of 12:11, 10 January 2019
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External IDs | GeneCards: [1] | ||||||
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Species | Human | Mouse | |||||
Entrez |
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Ensembl |
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UniProt |
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RefSeq (mRNA) |
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RefSeq (protein) |
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Location (UCSC) | n/a | n/a | |||||
PubMed search | n/a | n/a | |||||
Wikidata | |||||||
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Trafficking protein particle complex 11 is a protein that in humans is encoded by the TRAPPC11 gene. [1]
Function
The protein encoded by this gene is a subunit of the TRAPP (transport protein particle) tethering complex, which functions in intracellular vesicle trafficking. This subunit is involved in early stage endoplasmic reticulum-to-Golgi vesicle transport. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2013].
References
- ↑ "Entrez Gene: Trafficking protein particle complex 11". Retrieved 2017-10-11.
Further reading
- Bögershausen N, Shahrzad N, Chong JX, von Kleist-Retzow JC, Stanga D, Li Y, Bernier FP, Loucks CM, Wirth R, Puffenberger EG, Hegele RA, Schreml J, Lapointe G, Keupp K, Brett CL, Anderson R, Hahn A, Innes AM, Suchowersky O, Mets MB, Nürnberg G, McLeod DR, Thiele H, Waggoner D, Altmüller J, Boycott KM, Schoser B, Nürnberg P, Ober C, Heller R, Parboosingh JS, Wollnik B, Sacher M, Lamont RE (2013). "Recessive TRAPPC11 mutations cause a disease spectrum of limb girdle muscular dystrophy and myopathy with movement disorder and intellectual disability". Am. J. Hum. Genet. 93 (1): 181–90. doi:10.1016/j.ajhg.2013.05.028. PMC 3710757. PMID 23830518.
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This article incorporates text from the United States National Library of Medicine, which is in the public domain.