This gene encodes a multi-pass transmembrane protein. Reduced expression of this gene in mouse fibroblasts causes short cilia and failure of ciliogenesis. Expression of this gene is tightly coordinated with expression of the neighboring gene TMEM216. Mutations in this gene are associated with the autosomal recessive neurodevelopmental disorder Joubert Syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2012]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| TMEM138-20-RE | 20 (40 μL) | 200 μL |  |
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| TMEM138-20-OR | 20 (40 μL) | 200 μL |  |
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| TMEM138-20-GO | 20 (40 μL) | 200 μL |  |
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| TMEM138-20-GR | 20 (40 μL) | 200 μL |  |
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| TMEM138-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a multi-pass transmembrane protein. Reduced expression of this gene in mouse fibroblasts causes short cilia and failure of ciliogenesis. Expression of this gene is tightly coordinated with expression of the neighboring gene TMEM216. Mutations in this gene are associated with the autosomal recessive neurodevelopmental disorder Joubert Syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2012]
Gene Symbol : TMEM138
Gene Name : Transmembrane protein 138
Chromosome : CHR 11: 613,620,00-613,765,01
Locus : 11q12.2
Alt. Genes : KIF20A
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