RFT1, RFT1 homolog

RFT1, RFT1 homolog

• This gene encodes an enzyme which catalyzes the translocation of the Man(5)GlcNAc (2)-PP-Dol intermediate from the cytoplasmic to the luminal side of the endoplasmic reticulum membrane in the pathway for the N-glycosylation of proteins. Mutations in this gene are associated with congenital disorder of glycosylation type In.[provided by RefSeq, Dec 2008]

• Gene Synonyms (protein RFT1 homolog, RFT1, requiring fifty three 1 homolog, congenital disorder of glycosylation 1N, putative endoplasmic reticulum multispan transmembrane protein, CDG1N,)
• NCBI Gene ID: 91869
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q96AA3
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

RFT1 homolog interacts with:

• adhesion G protein-coupled receptor G5
  spindle and kinetochore associated complex subunit 1
  transmembrane protein 171
  zinc activated ion channel

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.