This gene encodes a subunit of the intraflagellar transport subcomplex IFT-B. Subcomplexes IFT-A and IFT-B are necessary for ciliary assembly and maintenance. Mutations in this gene have been associated with skeletal ciliopathies, with or without polydactyly, such as such short-rib thoracic dysplasias 1, 9 or 10. [provided by RefSeq, Mar 2014]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| IFT172-20-RE | 20 (40 μL) | 200 μL |  |
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| IFT172-20-OR | 20 (40 μL) | 200 μL |  |
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| IFT172-20-GO | 20 (40 μL) | 200 μL |  |
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| IFT172-20-GR | 20 (40 μL) | 200 μL |  |
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| IFT172-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a subunit of the intraflagellar transport subcomplex IFT-B. Subcomplexes IFT-A and IFT-B are necessary for ciliary assembly and maintenance. Mutations in this gene have been associated with skeletal ciliopathies, with or without polydactyly, such as such short-rib thoracic dysplasias 1, 9 or 10. [provided by RefSeq, Mar 2014]
Gene Symbol : IFT172
Gene Name : Intraflagellar transport 172
Chromosome : CHR 2: 274,898,18-274,443,72
Locus : 2p23.3
Alt. Genes : KIF20A
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