From Wikipedia, the free encyclopedia
Protein-coding gene in the species Homo sapiens
Protein RFT1 homolog is a protein that in humans is encoded by the RFT1 gene .[ 5] [ 6]
Defects are associated with congenital disorder of glycosylation type 1N.[ 6]
^ a b c GRCh38: Ensembl release 89: ENSG00000163933 – Ensembl , May 2017^ a b c GRCm38: Ensembl release 89: ENSMUSG00000052395 – Ensembl , May 2017^ "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: RFT1 homolog (S. cerevisiae)" .^ a b 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 .
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 . S2CID 4419970 . 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. Bibcode :2002PNAS...9916899M . doi :10.1073/pnas.242603899 PMC 139241 PMID 12477932 . Rose JE, Behm FM, Drgon T, et al. (2010). "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 .
