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RFT1

From Wikipedia, the free encyclopedia
RFT1
Identifiers
AliasesRFT1, CDG1N, RFT1 homolog
External IDsOMIM: 611908; MGI: 3607791; HomoloGene: 5343; GeneCards: RFT1; OMA:RFT1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_052859

NM_177815

RefSeq (protein)

NP_443091

NP_808483

Location (UCSC)Chr 3: 53.09 – 53.13 MbChr 14: 30.38 – 30.41 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

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

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References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000163933Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000052395Ensembl, 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

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