This gene encodes a kinesin family member 1 binding protein that is characterized by two tetratrico peptide repeats. The encoded protein localizes to the mitochondria and may be involved in regulating transport of the mitochondria. Mutations in this gene are associated with Goldberg-Shprintzen megacolon syndrome. [provided by RefSeq, Mar 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| KIF1BP-20-RE | 20 (40 μL) | 200 μL |  |
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| KIF1BP-20-OR | 20 (40 μL) | 200 μL |  |
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| KIF1BP-20-GO | 20 (40 μL) | 200 μL |  |
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| KIF1BP-20-GR | 20 (40 μL) | 200 μL |  |
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| KIF1BP-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a kinesin family member 1 binding protein that is characterized by two tetratrico peptide repeats. The encoded protein localizes to the mitochondria and may be involved in regulating transport of the mitochondria. Mutations in this gene are associated with Goldberg-Shprintzen megacolon syndrome. [provided by RefSeq, Mar 2010]
Gene Symbol : KIF1BP
Gene Name : KIF1 binding protein
Chromosome : CHR 10: 689,887,20-690,169,82
Locus : 10q22.1
Alt. Genes : KIF20A
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