This gene encodes a subunit of the intraflagellar transport complex A (IFT-A). IFT-A is a multiprotein complex that plays an important role in cilia assembly and maintenance by mediating retrograde ciliary transport. Mutations in this gene are a cause of cranioectodermal dysplasia-3 (CED3), also known as Sensenbrenner syndrome. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| IFT43-20-RE | 20 (40 μL) | 200 μL |  |
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| IFT43-20-OR | 20 (40 μL) | 200 μL |  |
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| IFT43-20-GO | 20 (40 μL) | 200 μL |  |
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| IFT43-20-GR | 20 (40 μL) | 200 μL |  |
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| IFT43-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a subunit of the intraflagellar transport complex A (IFT-A). IFT-A is a multiprotein complex that plays an important role in cilia assembly and maintenance by mediating retrograde ciliary transport. Mutations in this gene are a cause of cranioectodermal dysplasia-3 (CED3), also known as Sensenbrenner syndrome. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]
Gene Symbol : IFT43
Gene Name : Intraflagellar transport 43
Chromosome : CHR 14: 759,857,52-760,840,72
Locus : 14q24.3
Alt. Genes : OPTN
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