Members of the 'frizzled' gene family encode 7-transmembrane domain proteins that are receptors for Wnt signaling proteins. The FZD9 gene is located within the Williams syndrome common deletion region of chromosome 7, and heterozygous deletion of the FZD9 gene may contribute to the Williams syndrome phenotype. FZD9 is expressed predominantly in brain, testis, eye, skeletal muscle, and kidney. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| FZD9-20-RE | 20 (40 μL) | 200 μL |  |
Request Pricing |
| FZD9-20-OR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| FZD9-20-GO | 20 (40 μL) | 200 μL |  |
Request Pricing |
| FZD9-20-GR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| FZD9-20-AQ | 20 (40 μL) | 200 μL |  |
Request Pricing |
Members of the 'frizzled' gene family encode 7-transmembrane domain proteins that are receptors for Wnt signaling proteins. The FZD9 gene is located within the Williams syndrome common deletion region of chromosome 7, and heterozygous deletion of the FZD9 gene may contribute to the Williams syndrome phenotype. FZD9 is expressed predominantly in brain, testis, eye, skeletal muscle, and kidney. [provided by RefSeq, Jul 2008]
Gene Symbol : FZD9
Gene Name : Frizzled class receptor 9
Chromosome : CHR 7: 734,337,78-734,361,19
Locus : 7q11.23
Alt. Genes : TRAP1
Lorem Ipsum is simply dummy text of the printing and typesetting industry.
Lorem Ipsum is simply dummy text of the printing and typesetting industry.