The protein encoded by this gene is part of the intraflagellar transport complex B and is necessary for the function of motile and sensory cilia. Defects in this gene are a cause of asphyxiating thoracic dystrophy 2 (ATD2). Three transcript variants encoding two different isoforms have been found for this gene.[provided by RefSeq, Jun 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| IFT80-20-RE | 20 (40 μL) | 200 μL |  |
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| IFT80-20-OR | 20 (40 μL) | 200 μL |  |
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| IFT80-20-GO | 20 (40 μL) | 200 μL |  |
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| IFT80-20-GR | 20 (40 μL) | 200 μL |  |
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| IFT80-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is part of the intraflagellar transport complex B and is necessary for the function of motile and sensory cilia. Defects in this gene are a cause of asphyxiating thoracic dystrophy 2 (ATD2). Three transcript variants encoding two different isoforms have been found for this gene.[provided by RefSeq, Jun 2010]
Gene Symbol : IFT80
Gene Name : Intraflagellar transport 80
Chromosome : CHR 3: 160,399,531-160,256,985
Locus : 3q25.33
Alt. Genes : OPTN
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