RFT1

RFT1 homolog
Identifiers
Symbols RFT1 ; CDG1N
External IDs OMIM: 611908 MGI: 3607791 HomoloGene: 5343 GeneCards: RFT1 Gene
Orthologs
Species Human Mouse
Entrez 91869 328370
Ensembl ENSG00000163933 ENSMUSG00000052395
UniProt Q96AA3 Q8C3B8
RefSeq (mRNA) NM_052859 NM_177815
RefSeq (protein) NP_443091 NP_808483
Location (UCSC) Chr 3:
53.09 – 53.13 Mb
Chr 14:
30.65 – 30.69 Mb
PubMed search

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]

See also

References

  1. "Entrez Gene: RFT1 homolog (S. cerevisiae)".
  2. 1 2 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


External links


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