The protein encoded by this gene is a tetraspanin protein that is thought to be involved in WNT signaling. Defects in this gene are a cause of Joubert syndrome-14. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| TMEM237-20-RE | 20 (40 μL) | 200 μL |  |
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| TMEM237-20-OR | 20 (40 μL) | 200 μL |  |
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| TMEM237-20-GO | 20 (40 μL) | 200 μL |  |
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| TMEM237-20-GR | 20 (40 μL) | 200 μL |  |
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| TMEM237-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is a tetraspanin protein that is thought to be involved in WNT signaling. Defects in this gene are a cause of Joubert syndrome-14. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]
Gene Symbol : TMEM237
Gene Name : Transmembrane protein 237
Chromosome : CHR 2: 201,643,528-201,620,183
Locus : 2q33.1
Alt. Genes : CELA3A
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