| ACTG1 |
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| Identifiers |
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| Aliases | ACTG1, ACT, ACTG, BRWS2, DFNA20, DFNA26, HEL-176, actin gamma 1 |
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| External IDs | OMIM: 102560; MGI: 87906; GeneCards: ACTG1 |
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| Gene location (Mouse) |
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%3C%2Ftitle%3E%3Cdefs%3E%3CclipPath%20id%3D%22alt-text-clip%22%3E%3Crect%20x%3D%220%22%20y%3D%220%22%20width%3D%22100%25%22%20height%3D%22100%25%22%20%2F%3E%3C%2FclipPath%3E%3C%2Fdefs%3E%3Crect%20width%3D%22100%25%22%20height%3D%22100%25%22%20fill%3D%22transparent%22%2F%3E%3Cg%20clip-path%3D%22url(%23alt-text-clip)%22%3E%3Ctext%20x%3D%2250%25%22%20y%3D%2250%25%22%20text-anchor%3D%22middle%22%20dominant-baseline%3D%22middle%22%20fill%3D%22%2354595d%22%20font-size%3D%2216%22%20font-family%3D%22sans-serif%22%3EChromosome%2011%20(mouse)%3C%2Ftext%3E%3C%2Fg%3E%3C%2Fsvg%3E) | | Chr. | Chromosome 11 (mouse) |
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| | Band | 11|11 E2 | Start | 120,236,516 bp |
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| End | 120,239,368 bp |
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| Wikidata |
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Actin, cytoplasmic 2, or gamma-actin is a protein that in humans is encoded by the ACTG1 gene. Gamma-actin is widely expressed in cellular cytoskeletons of many tissues; in adult striated muscle cells, gamma-actin is localized to Z-discs and costamere structures, which are responsible for force transduction and transmission in muscle cells. Mutations in ACTG1 have been associated with nonsyndromic hearing loss and Baraitser-Winter syndrome, as well as susceptibility of adolescent patients to vincristine toxicity.