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Immunogen sequence: ERLNMDFWRL RATEQPCAAA AGPGGRRDCS LPGGSVPTVA VFMLKIFMSL VVGITSGVWV WSSKTFQTWQ SLCYRKIAAG RARAKACRAP GSYGRGTHCH YKAPTVVLHM TKTDPSLENP THL; Positive Samples: TE-1, 293T, HepG2, THP-1, U-251MG, Mouse heart, Mouse brain, Rat skeletal muscle; Cellular Location: Cell membrane, Multi-pass membrane protein
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.
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Protein Aliases: CD349; CD349 antigen; Frizzled 3; frizzled 9; frizzled 9, seven transmembrane spanning receptor; frizzled family receptor 9; frizzled homolog 9; Frizzled-9; Frizzled-like protein 9; Frizzled3; Frizzled9; Fz-9; FzE6; hFz9; mFz3; rFz9
Gene Aliases: CD349; FZD3; FZD9; mfz9
UniProt ID: (Human) O00144, (Rat) Q8K4C8, (Mouse) Q9R216
Entrez Gene ID: (Human) 8326, (Rat) 266608, (Mouse) 14371
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