This gene encodes an intracellular receptor for inositol 1,4,5-trisphosphate. Upon stimulation by inositol 1,4,5-trisphosphate, this receptor mediates calcium release from the endoplasmic reticulum. Mutations in this gene cause spinocerebellar ataxia type 15, a disease associated with an heterogeneous group of cerebellar disorders. Multiple transcript variants have been identified for this gene. [provided by RefSeq, Nov 2009]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ITPR1-20-RE | 20 (40 μL) | 200 μL |  |
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| ITPR1-20-OR | 20 (40 μL) | 200 μL |  |
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| ITPR1-20-GO | 20 (40 μL) | 200 μL |  |
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| ITPR1-20-GR | 20 (40 μL) | 200 μL |  |
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| ITPR1-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes an intracellular receptor for inositol 1,4,5-trisphosphate. Upon stimulation by inositol 1,4,5-trisphosphate, this receptor mediates calcium release from the endoplasmic reticulum. Mutations in this gene cause spinocerebellar ataxia type 15, a disease associated with an heterogeneous group of cerebellar disorders. Multiple transcript variants have been identified for this gene. [provided by RefSeq, Nov 2009]
Gene Symbol : ITPR1
Gene Name : Inositol 1,4,5-trisphosphate receptor type 1
Chromosome : CHR 3: 449,334,7-484,783,9
Locus : 3p26.1
Alt. Genes : LRPPRC
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