FZD9

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Frizzled homolog 9 (Drosophila)
Identifiers
SymbolsFZD9; FZD3
External IDsOMIM601766 MGI1313278 HomoloGene2619 IUPHAR: FZD9 GeneCards: FZD9 Gene
RNA expression pattern
250px
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez832614371
EnsemblENSG00000188763ENSMUSG00000049551
UniProtO00144Q9R216
RefSeq (mRNA)NM_003508XM_284144
RefSeq (protein)NP_003499XP_284144
Location (UCSC)Chr 7:
72.49 - 72.49 Mb
Chr 5:
135.53 - 135.54 Mb
PubMed search[1][2]

Frizzled-9 is a protein that in humans is encoded by the FZD9 gene.[1][2][3] FZD9 has also been designated as CD349 (cluster of differentiation 349).

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.[3]

See also

References

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Further reading

External links

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

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  3. 3.0 3.1 "Entrez Gene: FZD9 frizzled homolog 9 (Drosophila)".