This gene encodes a conserved proline-rich protein that is a component of the intraflagellar transport-B (IFT-B) core complex. The encoded protein is essential for the integrity of the IFT-B core complex, and for biosynthesis and maintenance of cilia. Mutations in this gene are associated with ciliopathy that affects the skeleton. [provided by RefSeq, Oct 2016]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| IFT52-20-RE | 20 (40 μL) | 200 μL |  |
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| IFT52-20-OR | 20 (40 μL) | 200 μL |  |
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| IFT52-20-GO | 20 (40 μL) | 200 μL |  |
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| IFT52-20-GR | 20 (40 μL) | 200 μL |  |
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| IFT52-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a conserved proline-rich protein that is a component of the intraflagellar transport-B (IFT-B) core complex. The encoded protein is essential for the integrity of the IFT-B core complex, and for biosynthesis and maintenance of cilia. Mutations in this gene are associated with ciliopathy that affects the skeleton. [provided by RefSeq, Oct 2016]
Gene Symbol : IFT52
Gene Name : Intraflagellar transport 52
Chromosome : CHR 20: 435,906,12-436,472,95
Locus : 20q13.12
Alt. Genes : FEM1B
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