The protein encoded by this gene localizes to the primary cilium and to the plasma membrane. The gene functions in centriole migration to the apical membrane and formation of the primary cilium. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Meckel syndrome type 3 (MKS3) and Joubert syndrome type 6 (JBTS6). [provided by RefSeq, Nov 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| TMEM67-20-RE | 20 (40 μL) | 200 μL |  |
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| TMEM67-20-OR | 20 (40 μL) | 200 μL |  |
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| TMEM67-20-GO | 20 (40 μL) | 200 μL |  |
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| TMEM67-20-GR | 20 (40 μL) | 200 μL |  |
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| TMEM67-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene localizes to the primary cilium and to the plasma membrane. The gene functions in centriole migration to the apical membrane and formation of the primary cilium. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Meckel syndrome type 3 (MKS3) and Joubert syndrome type 6 (JBTS6). [provided by RefSeq, Nov 2008]
Gene Symbol : TMEM67
Gene Name : Transmembrane protein 67
Chromosome : CHR 8: 937,548,43-938,326,52
Locus : 8q22.1
Alt. Genes : RAD50
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