This gene encodes a member of the glutamate receptor subfamily of G protein-coupled receptors. The encoded protein has an EGF-like calcium binding domain and a seven transmembrane domain in the N-terminal region of the protein. Mutations in this gene are associated with congenital stationary night blindness type 1E. [provided by RefSeq, Apr 2012]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| GPR179-20-RE | 20 (40 μL) | 200 μL |  |
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| GPR179-20-OR | 20 (40 μL) | 200 μL |  |
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| GPR179-20-GO | 20 (40 μL) | 200 μL |  |
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| GPR179-20-GR | 20 (40 μL) | 200 μL |  |
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| GPR179-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the glutamate receptor subfamily of G protein-coupled receptors. The encoded protein has an EGF-like calcium binding domain and a seven transmembrane domain in the N-terminal region of the protein. Mutations in this gene are associated with congenital stationary night blindness type 1E. [provided by RefSeq, Apr 2012]
Gene Symbol : GPR179
Gene Name : G protein-coupled receptor 179
Chromosome : CHR 17: 383,438,09-383,256,09
Locus : 17q12
Alt. Genes : AKAP9
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