FZD9, frizzled class receptor 9

FZD9, frizzled class receptor 9

• 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 Synonyms (frizzled-9, frizzled 9, seven transmembrane spanning receptor, frizzled family receptor 9, frizzled homolog 9, fz-9, fzE6, hFz9, CD349, FZD3,)
• NCBI Gene ID: 8326
• Species: Homo sapiens (Human)
• UNIPROT ID#>>O00144
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

frizzled class receptor 9 interacts with:

• keratin associated protein 10-3

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.