Health Dictionary
Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
RFT1
Introduction
Protein RFT1 homolog is a protein that in humans is encoded by the RFT1 gene.[1][2]
Defects are associated with congenital disorder of glycosylation type 1N.[2]
References
References
- ↑ “Entrez Gene: RFT1 homolog (S. cerevisiae)”.
- ↑ 2.0 2.1 Haeuptle MA, Pujol FM, Neupert C, Winchester B, Kastaniotis AJ, Aebi M, Hennet T (March 2008). “Human RFT1 deficiency leads to a disorder of N-linked glycosylation”. Am. J. Hum. Genet. 82 (3): 600–6. doi:10.1016/j.ajhg.2007.12.021. PMC 2427296. PMID 18313027.
Further reading
Further reading
- Helenius J, Ng DT, Marolda CL, et al. (2002). “Translocation of lipid-linked oligosaccharides across the ER membrane requires Rft1 protein”. Nature. 415 (6870): 447–50. doi:10.1038/415447a. PMID 11807558.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2002). “Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences”. Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- Rose JE, Behm FM, Drgon T, et al. “Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score”. Mol. Med. 16 (7–8): 247–53. doi:10.2119/molmed.2009.00159. PMC 2896464. PMID 20379614.