This gene encodes an intracellular monovalent cation channel that functions in maintenance of intracellular calcium release. Mutations in this gene may be associated with autosomal recessive osteogenesis. [provided by RefSeq, Oct 2012]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| TMEM38B-20-RE | 20 (40 μL) | 200 μL |  |
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| TMEM38B-20-OR | 20 (40 μL) | 200 μL |  |
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| TMEM38B-20-GO | 20 (40 μL) | 200 μL |  |
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| TMEM38B-20-GR | 20 (40 μL) | 200 μL |  |
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| TMEM38B-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes an intracellular monovalent cation channel that functions in maintenance of intracellular calcium release. Mutations in this gene may be associated with autosomal recessive osteogenesis. [provided by RefSeq, Oct 2012]
Gene Symbol : TMEM38B
Gene Name : Transmembrane protein 38B
Chromosome : CHR 9: 105,694,524-105,776,610
Locus : 9q31.2
Alt. Genes : ZNF263
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