This protein is part of a large family of nuclear receptor transcription factors involved in signaling pathways. Nuclear receptors have been shown to regulate pathways involved in embryonic development, as well as in maintenance of proper cell function in adults. Members of this family are characterized by discrete domains that function in DNA and ligand binding. This gene encodes a retinal nuclear receptor that is a ligand-dependent transcription factor. Defects in this gene are a cause of enhanced S cone syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| NR2E3-20-RE | 20 (40 μL) | 200 μL |  |
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| NR2E3-20-OR | 20 (40 μL) | 200 μL |  |
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| NR2E3-20-GO | 20 (40 μL) | 200 μL |  |
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| NR2E3-20-GR | 20 (40 μL) | 200 μL |  |
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| NR2E3-20-AQ | 20 (40 μL) | 200 μL |  |
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This protein is part of a large family of nuclear receptor transcription factors involved in signaling pathways. Nuclear receptors have been shown to regulate pathways involved in embryonic development, as well as in maintenance of proper cell function in adults. Members of this family are characterized by discrete domains that function in DNA and ligand binding. This gene encodes a retinal nuclear receptor that is a ligand-dependent transcription factor. Defects in this gene are a cause of enhanced S cone syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
Gene Symbol : NR2E3
Gene Name : Nuclear receptor subfamily 2 group E member 3
Chromosome : CHR 15: 718,105,47-718,182,58
Locus : 15q23
Alt. Genes : RBM12
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