This gene is a member of the kelch-like family. The encoded protein contains a BACK domain, a BTB/POZ domain, and 5 Kelch repeats. This protein is thought to function in skeletal muscle development and maintenance. Mutations in this gene have been associated with nemaline myopathy (NM), a rare congenital muscle disorder. [provided by RefSeq, Mar 2015]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| KLHL41-20-RE | 20 (40 μL) | 200 μL |  |
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| KLHL41-20-OR | 20 (40 μL) | 200 μL |  |
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| KLHL41-20-GO | 20 (40 μL) | 200 μL |  |
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| KLHL41-20-GR | 20 (40 μL) | 200 μL |  |
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| KLHL41-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene is a member of the kelch-like family. The encoded protein contains a BACK domain, a BTB/POZ domain, and 5 Kelch repeats. This protein is thought to function in skeletal muscle development and maintenance. Mutations in this gene have been associated with nemaline myopathy (NM), a rare congenital muscle disorder. [provided by RefSeq, Mar 2015]
Gene Symbol : KLHL41
Gene Name : Kelch like family member 41
Chromosome : CHR 2: 169,509,701-169,526,261
Locus : 2q31.1
Alt. Genes : TRIM28
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