Symbol: Name: ID: |
WNT11 wingless-type MMTV integration site family, member 11 GFS:2535 |
Gene name: | WNT11 |
Chromosome: | 11q13.5 |
Previous Symbols: | |
Previous Names: | |
Aliases: | |
Name Aliases: | |
Locus Type: | gene with protein product |
Mouse Genome Database ID: | MGI:101948 | Rat Genome Database ID: | RGD:621463 |
HGNC ID: | HGNC:12776 | RefSeq IDs: | NM_004626 |
Entrez Gene ID: | 7481 | Ensembl Gene ID: | ENSG00000085741 |
VEGA IDs: | UniProt ID: | O96014 | |
UCSC ID: | uc001oxe.2 | OMIM ID: | 603699 |
Pubmed: | PMID9757009 | ||
CCDS IDs: | CCDSCCDS8242.1 |
Protein Wnt-11 is a protein that in humans is encoded by the WNT11 gene.
The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It encodes a protein which shows 97%, 85%, and 63% amino acid identity with mouse, chicken, and Xenopus Wnt11 protein, respectively. This gene may play roles in the development of skeleton, kidney and lung, and is considered to be a plausible candidate gene for High Bone Mass Syndrome. [provided by RefSeq]. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications.
Function: Ligand for members of the frizzled family of seven transmembrane receptors. Probable developmental protein. May be a signaling molecule which affects the development of discrete regions of tissues. Is likely to signal over only few cell diameters.
Products for WNT11 gene
Catalog | Product Name | Application | Company |
GFS:E02535 | wingless-type MMTV integration site family, member 11; ELISA kit | ELISA | n/a |
GFS:A02535 | wingless-type MMTV integration site family, member 11; Anti | ANTIBODIES | n/a |
GFS:P02535 | wingless-type MMTV integration site family, member 11; Protien | Protien | n/a |