Protein RFT1 homolog is a protein that in humans is encoded by the RFT1 gene.
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].
via MyGene.info
Protein RFT1 homolog is a protein that in humans is encoded by the RFT1 gene.
Defects are associated with congenital disorder of glycosylation type 1N.
Discovered by embedding cosine similarity (sentence-transformers MiniLM, 384-dim).