| Systematic Name | YDR282C |
|---|---|
| Feature Type | ORF, Uncharacterized |
| Description | Putative protein of unknown function; localizes to the inner mitochondrial membrane with the C terminus facing the intermembrane space; ortholog of human RMND1, mutation in which is implicated in infantile encephaloneuromyopathy and defective mitochondrial translation (1) |
| Chromosomal Location | |
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| Note: this feature is encoded on the Crick strand. | |
Gene Ontology Annotations All YDR282C GO evidence and references
| View Computational GO annotations for YDR282C | |
| Molecular Function | |
| Manually curated |
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| Biological Process | |
| Manually curated |
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| Cellular Component | |
| Manually curated |
Mutant phenotypes All YDR282C Phenotype evidence and references
| Classical genetics | |
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| null | |
| Large-scale survey | |
| null | |
| Resources |
interactions All YDR282C Interaction evidence and references
| 1 total interaction(s) for 1 unique genes/features. | |
| Genetic Interactions |
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| Resources |
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Expression Summary
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| Resources |
Protein Information All YDR282C Protein evidence and references
| Localization | |
|---|---|
| Phosphorylation | PhosphoGRID | PhosphoPep Database |
| Structure | |
| Homologs |
sequence information
| Note: this feature is encoded on the Crick strand. | |||||||||||||
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| Last Update | Coordinates: 2011-02-03 | Sequence: 1996-07-31 | ||||||||||||
| 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 | Entrez Gene | Entrez RefSeq Protein | MIPS | Search all NCBI (Entrez) | UniProtKB |
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| Primary SGDID | S000002690 |
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References cited on this page View Complete Literature Guide for
| 1) | Garcia-Diaz B, et al. (2012) Infantile encephaloneuromyopathy and defective mitochondrial translation are due to a homozygous RMND1 mutation. Am J Hum Genet 91(4):729-36 |




