This gene encodes a transmembrane protein, which is a component of the B9 complex involved in the formation of the diffusion barrier between the cilia and plasma membrane. Mutations in this gene cause Joubert syndrome (JBTS). Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2013]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| TMEM231-20-RE | 20 (40 μL) | 200 μL |  |
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| TMEM231-20-OR | 20 (40 μL) | 200 μL |  |
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| TMEM231-20-GO | 20 (40 μL) | 200 μL |  |
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| TMEM231-20-GR | 20 (40 μL) | 200 μL |  |
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| TMEM231-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a transmembrane protein, which is a component of the B9 complex involved in the formation of the diffusion barrier between the cilia and plasma membrane. Mutations in this gene cause Joubert syndrome (JBTS). Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2013]
Gene Symbol : TMEM231
Gene Name : Transmembrane protein 231
Chromosome : CHR 16: 755,562,85-755,381,16
Locus : 16q23.1
Alt. Genes : PREB
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