This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| MYO7A-20-RE | 20 (40 μL) | 200 μL |  |
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| MYO7A-20-OR | 20 (40 μL) | 200 μL |  |
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| MYO7A-20-GO | 20 (40 μL) | 200 μL |  |
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| MYO7A-20-GR | 20 (40 μL) | 200 μL |  |
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| MYO7A-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]
Gene Symbol : MYO7A
Gene Name : Myosin VIIA
Chromosome : CHR 11: 771,281,91-772,152,40
Locus : 11q13.5
Alt. Genes : FAM13A
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