RFT1
Sign in to saveAlso known as CDG1N, RFT1 homolog
Protein RFT1 homolog is a protein that in humans is encoded by the RFT1 gene.
Gene data
RFT1- Name
- RFT1 glycolipid translocator homolog
- Type
- protein-coding
- Aliases
- CDG1N, SLC76A1
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
Gene · Ensembl
RFT1 glycolipid translocator homolog
- Symbol
- RFT1
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 3:53,048,135-53,130,661
- Strand
- Reverse (−)
- Assembly
- GRCh38
View on Ensembl →
via Ensembl · EMBL-EBI
Wikidata facts
Show 5 more facts
- HomoloGene ID
- 5343
- exact match
- identifiers.org/ncbigene/91869
- genomic end
- 53130453
- genomic start
- 53122499
- cytogenetic location
- 3p21.1
via Wikidata · CC0
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Article
4 sectionsContents
- See also
- References
- Further reading
- External links
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.
Connections
Q180686
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human chromosome 3
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Ensembl genome database project
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protein
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Wikidata
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gene
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chromosome
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bibcode
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human genome
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Q229883
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base pair
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locus
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gene expression
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Online Mendelian Inheritance in Man
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Gene Ontology
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