The protein encoded by this gene catalyzes the conversion of sn-glycerol 3-phosphate to glycerone phosphate. The encoded protein is found in the cytoplasm, associated with the plasma membrane, where it binds the sodium channel, voltage-gated, type V, alpha subunit (SCN5A). Defects in this gene are a cause of Brugada syndrome type 2 (BRS2) as well as sudden infant death syndrome (SIDS). [provided by RefSeq, Jul 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| GPD1L-20-RE | 20 (40 μL) | 200 μL |  |
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| GPD1L-20-OR | 20 (40 μL) | 200 μL |  |
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| GPD1L-20-GO | 20 (40 μL) | 200 μL |  |
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| GPD1L-20-GR | 20 (40 μL) | 200 μL |  |
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| GPD1L-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene catalyzes the conversion of sn-glycerol 3-phosphate to glycerone phosphate. The encoded protein is found in the cytoplasm, associated with the plasma membrane, where it binds the sodium channel, voltage-gated, type V, alpha subunit (SCN5A). Defects in this gene are a cause of Brugada syndrome type 2 (BRS2) as well as sudden infant death syndrome (SIDS). [provided by RefSeq, Jul 2010]
Gene Symbol : GPD1L
Gene Name : Glycerol-3-phosphate dehydrogenase 1 like
Chromosome : CHR 3: 321,065,10-321,687,14
Locus : 3p22.3
Alt. Genes : RBM12
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