The protein encoded by this gene is a mitochondrial membrane protein of unknown function. Defects in this gene are a cause of optic atrophy type 7 (OPA7). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| TMEM126A-20-RE | 20 (40 μL) | 200 μL |  |
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| TMEM126A-20-OR | 20 (40 μL) | 200 μL |  |
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| TMEM126A-20-GO | 20 (40 μL) | 200 μL |  |
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| TMEM126A-20-GR | 20 (40 μL) | 200 μL |  |
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| TMEM126A-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is a mitochondrial membrane protein of unknown function. Defects in this gene are a cause of optic atrophy type 7 (OPA7). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]
Gene Symbol : TMEM126A
Gene Name : Transmembrane protein 126A
Chromosome : CHR 11: 856,479,18-856,565,52
Locus : 11q14.1
Alt. Genes : PLXNC1
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