The protein encoded by this gene, together with IFT74, forms a tubulin-binding module of intraflagellar transport complex B. This module is involved in transport of tubulin within the cilium, and the encoded protein is required for ciliogenesis. Mutations in this gene are a cause of short-rib polydactyly syndromes. [provided by RefSeq, Dec 2016]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| IFT81-20-RE | 20 (40 μL) | 200 μL |  |
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| IFT81-20-OR | 20 (40 μL) | 200 μL |  |
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| IFT81-20-GO | 20 (40 μL) | 200 μL |  |
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| IFT81-20-GR | 20 (40 μL) | 200 μL |  |
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| IFT81-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene, together with IFT74, forms a tubulin-binding module of intraflagellar transport complex B. This module is involved in transport of tubulin within the cilium, and the encoded protein is required for ciliogenesis. Mutations in this gene are a cause of short-rib polydactyly syndromes. [provided by RefSeq, Dec 2016]
Gene Symbol : IFT81
Gene Name : Intraflagellar transport 81
Chromosome : CHR 12: 110,124,334-110,218,794
Locus : 12q24.11
Alt. Genes : SGK2
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