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]

See also

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000163933 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000052395 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "Entrez Gene: RFT1 homolog (S. cerevisiae)".
  6. ^ 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.

Further reading


Allikas: Https://en.wikipedia.org/wiki/RFT1
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