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RFT1

Gene

RFT1 glycolipid translocator homolog

HGNCHGNC:30220EnsemblENSG00000163933NCBI Gene91869
Locus: gene with protein productLocation: 3p21.1

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asCDG1N · SLC76A1
View full nomenclature history (6)
Alias symbolsCDG1N, SLC76A1
Previous namesRFT1 homolog, RFT1 homolog (S. cerevisiae), RFT1, requiring fifty three 1 homolog (S. cerevisiae)
Alias namescongenital disorder of glycosylation 1N

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Congenital disorder of glycosylation
Crohn's Disease
Neurodegenerative Diseases
Ovarian dysfunction

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

Solute carrier family 76

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2025-02-05.
Open TargetsGene–disease associations from the Open Targets Platform.