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FZD9
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.
Protein class
CD markers, G-protein coupled receptors, Human disease related genes
Predicted location
Membrane
Single cell type specificity
Group enriched (Oligodendrocyte precursor cells, Late spermatids, Early spermatids, Sertoli cells, Muller glia cells)
Immune cell specificity
Not detected in immune cells
Cell line specificity
Cell line enhanced (HEK93, MCF7, NTERA-2)
Molecular function
Developmental protein, G-protein coupled receptor, Receptor, Transducer
More Types Infomation
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- Derivation: Phage display library
- Species Reactivity: Human
- Type: Rabbit IgG
- Application: WB
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For Research Use Only. Not For Clinical Use.