RFT1
{{Short description|Protein-coding gene in the species Homo sapiens}}
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Protein RFT1 homolog is a protein that in humans is encoded by the RFT1 gene.{{cite web | title = Entrez Gene: RFT1 homolog (S. cerevisiae)| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=91869}}{{cite journal |vauthors=Haeuptle MA, Pujol FM, Neupert C, Winchester B, Kastaniotis AJ, Aebi M, Hennet T | title = Human RFT1 deficiency leads to a disorder of N-linked glycosylation | journal = Am. J. Hum. Genet. | volume = 82 | issue = 3 | pages = 600–6 |date=March 2008 | pmid = 18313027 | pmc = 2427296 | doi = 10.1016/j.ajhg.2007.12.021 }}
Defects are associated with congenital disorder of glycosylation type 1N.
See also
References
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Further reading
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- {{cite journal |vauthors=Helenius J, Ng DT, Marolda CL, etal |title=Translocation of lipid-linked oligosaccharides across the ER membrane requires Rft1 protein. |journal=Nature |volume=415 |issue= 6870 |pages= 447–50 |year= 2002 |pmid= 11807558 |doi= 10.1038/415447a |s2cid=4419970 }}
- {{cite journal |vauthors=Strausberg RL, Feingold EA, Grouse LH, etal |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2002 |pmid= 12477932 |doi= 10.1073/pnas.242603899 |pmc=139241|bibcode=2002PNAS...9916899M |doi-access=free }}
- {{cite journal |vauthors=Rose JE, Behm FM, Drgon T, etal |title=Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. |journal=Mol. Med. |volume=16 |issue= 7–8 |pages= 247–53 |year= 2010|pmid= 20379614 |doi= 10.2119/molmed.2009.00159 |pmc=2896464}}
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External links
- [https://www.ncbi.nlm.nih.gov/books/NBK1332/ GeneReviews/NCBI/NIH/UW entry on Congenital Disorders of Glycosylation Overview]
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