| Standard Name | DFG10 1 |
|---|---|
| Systematic Name | YIL049W |
| Feature Type | ORF, Verified |
| Description | Probable polyprenol reductase that catalyzes conversion of polyprenol to dolichol, the precursor for N-glycosylation; involved in filamentous growth; mutations in human ortholog SRD5A3 confer CDG (Congenital Disorders of Glycosylation) (1, 2) |
| Name Description | Defective for Filamentous Growth 1 |
| Chromosomal Location | |
|---|---|
Gene Ontology Annotations All DFG10 GO evidence and references
| View Computational GO annotations for DFG10 | |
| Molecular Function | |
| Manually curated | |
| Biological Process | |
| Manually curated | |
| Cellular Component | |
| High-throughput |
Mutant phenotypes All DFG10 Phenotype evidence and references
| Classical genetics | |
|---|---|
| null | |
| unspecified | |
| Large-scale survey | |
| null |
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| Resources |
interactions All DFG10 Interaction evidence and references
| 11 total interaction(s) for 11 unique genes/features. | |
| Physical Interactions |
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| Genetic Interactions |
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| Resources |
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Expression Summary
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| Resources |
Protein Information All DFG10 Protein evidence and references
| Localization | |
|---|---|
| Phosphorylation | PhosphoGRID | PhosphoPep Database |
| Structure | |
| Homologs |
sequence information
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| Last Update | Coordinates: 2011-02-03 | Sequence: 1994-12-10 | ||||||||||||
| Subfeature details |
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| Retrieve sequences | |||||||||||||
Analyze Sequence
| S288C only | |
|---|---|
| S288C vs. other species | |
| S288C vs. other strains |
Resources
| External Links | All Associated Seq | E.C. | Entrez Gene | Entrez RefSeq Protein | MIPS | Search all NCBI (Entrez) | UniProtKB |
|---|
| Primary SGDID | S000001311 |
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References cited on this page View Complete Literature Guide for DFG10
| 1) | Mosch HU and Fink GR (1997) Dissection of filamentous growth by transposon mutagenesis in Saccharomyces cerevisiae. Genetics 145(3):671-84 |
| 2) | Cantagrel V, et al. (2010) SRD5A3 is required for converting polyprenol to dolichol and is mutated in a congenital glycosylation disorder. Cell 142(2):203-17 |




