Gene
rft1
- ID
- ZDB-GENE-110411-126
- Name
- RFT1 homolog
- Symbol
- rft1 Nomenclature History
- Previous Names
-
- si:dkey-265k7.6
- slc52a1 (1)
- Type
- protein_coding_gene
- Location
- Chr: 6 Mapping Details/Browsers
- Description
- Predicted to have lipid transporter activity. Predicted to be involved in glycolipid translocation. Predicted to localize to endoplasmic reticulum membrane. Human ortholog(s) of this gene implicated in congenital disorder of glycosylation In. Orthologous to human RFT1 (RFT1 homolog).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- No data available
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| congenital disorder of glycosylation In | Alliance | Congenital disorder of glycosylation, type In | 612015 |
Domain, Family, and Site Summary
| Type | InterPro ID | Name |
|---|---|---|
| Family | IPR007594 | RFT1 |
Domain Details Per Protein
| Protein | Length | RFT1 |
|---|---|---|
|
UniProtKB:E7EXE6
|
540 |
Interactions and Pathways
No data available
Plasmids
No data available