| GFM1 |
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| Identifiers |
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| Aliases | GFM1, COXPD1, EFG, EFG1, EFGM, EGF1, GFM, hEFG1, G elongation factor, mitochondrial 1, G elongation factor mitochondrial 1, mtEF-G1 |
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| External IDs | OMIM: 606639; MGI: 107339; HomoloGene: 6449; GeneCards: GFM1; OMA:GFM1 - orthologs |
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| Gene location (Mouse) |
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| | Chr. | Chromosome 3 (mouse) |
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| | Band | 3 E1|3 30.96 cM | Start | 67,337,429 bp |
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| End | 67,383,862 bp |
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| RNA expression pattern |
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| Bgee | | Human | Mouse (ortholog) |
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| Top expressed in | - endothelial cell
- biceps brachii
- Brodmann area 23
- Skeletal muscle tissue of biceps brachii
- retinal pigment epithelium
- Skeletal muscle tissue of rectus abdominis
- right ventricle
- germinal epithelium
- mucosa of sigmoid colon
- parietal pleura
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| | Top expressed in | - myocardium of ventricle
- otic placode
- right kidney
- cardiac muscles
- cardiac muscle tissue of left ventricle
- digastric muscle
- masseter muscle
- right ventricle
- proximal tubule
- temporal muscle
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| | More reference expression data |
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| BioGPS | |
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| Wikidata |
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Elongation factor G 1, mitochondrial is a protein that in humans is encoded by the GFM1 gene. It is an EF-G homolog.
Eukaryotes contain two protein translational systems, one in the cytoplasm and one in the mitochondria. Mitochondrial translation is crucial for maintaining mitochondrial function and mutations in this system lead to a breakdown in the respiratory chain-oxidative phosphorylation system and to impaired maintenance of mitochondrial DNA. This gene encodes one of the mitochondrial translation elongation factors. Its role in the regulation of normal mitochondrial function and in different disease states attributed to mitochondrial dysfunction is not known.