Sequence Detail

ID/Version

Q9R216 Q9R2B3 Q9CX16 O35494 (UniProt | EBI)

Last sequence update: 2000-05-01
Last annotation update: 2024-07-24

Sequence description from provider

RecName: Full=Frizzled-9; Short=Fz-9; Short=mFz3; Short=mFz9;AltName: CD_antigen=CD349;Flags: Precursor;

Provider

SWISS-PROT

Sequence

Polypeptide 592 aa

Source

Organism mouse

See UniProt | EBI for source

Annotated genes and markers

Follow the symbol links to get more information on the GO terms, expression assays, orthologs, phenotypic alleles, and other information for the genes or markers below.

Type	Symbol	Name	GO Terms	Expression Assays	Orthologs	Phenotypic Alleles
Gene	Fzd9	frizzled class receptor 9	56	123	4	11

Sequence references in MGI

J:49924 Wang YK, et al., Characterization and expression pattern of the frizzled gene Fzd9, the mouse homolog of FZD9 which is deleted in Williams-Beuren syndrome. Genomics. 1999 Apr 15;57(2):235-48
J:99680 The FANTOM Consortium and RIKEN Genome Exploration Research Group and Genome Science Group (Genome Network Project Core Group), The Transcriptional Landscape of the Mammalian Genome. Science. 2005;309(5740):1559-1563
J:99893 Zhao C, et al., Hippocampal and visuospatial learning defects in mice with a deletion of frizzled 9, a gene in the Williams syndrome deletion interval. Development. 2005 Jun;132(12):2917-27
J:169924 Albers J, et al., Control of bone formation by the serpentine receptor Frizzled-9. J Cell Biol. 2011 Mar 21;192(6):1057-72
J:211112 Heilmann A, et al., The Wnt serpentine receptor Frizzled-9 regulates new bone formation in fracture healing. PLoS One. 2013;8(12):e84232
J:236211 Aviles EC, et al., Frizzled-9 impairs acetylcholine receptor clustering in skeletal muscle cells. Front Cell Neurosci. 2014;8:110