Bos taurus Gene: FZD9 | |||||||||||||||
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Summary | |||||||||||||||
InnateDB Gene | IDBG-648723.3 | ||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||
Gene Symbol | FZD9 | ||||||||||||||
Gene Name | Uncharacterized protein | ||||||||||||||
Synonyms | |||||||||||||||
Species | Bos taurus | ||||||||||||||
Ensembl Gene | ENSBTAG00000020742 | ||||||||||||||
Encoded Proteins |
frizzled family receptor 9
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Protein Structure | |||||||||||||||
Useful resources | Stemformatics EHFPI ImmGen | ||||||||||||||
Entrez Gene | |||||||||||||||
Summary |
This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000188763:
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] 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] |
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Gene Information | |||||||||||||||
Type | Protein coding | ||||||||||||||
Genomic Location | Chromosome 25:34245429-34247198 | ||||||||||||||
Strand | Reverse strand | ||||||||||||||
Band | |||||||||||||||
Transcripts |
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Interactions | |||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
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Gene Ontology | |||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Orthologs | |||||||||||||||
Species
Homo sapiens
Mus musculus
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Gene ID
Gene Order
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Pathway Predictions based on Human Orthology Data | |||||||||||||||
NETPATH |
Wnt pathway
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REACTOME |
Class B/2 (Secretin family receptors) pathway
Signaling by GPCR pathway
Signal Transduction pathway
GPCR ligand binding pathway
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KEGG |
Wnt signaling pathway pathway
Basal cell carcinoma pathway
Melanogenesis pathway
Pathways in cancer pathway
Basal cell carcinoma pathway
Melanogenesis pathway
Wnt signaling pathway pathway
Pathways in cancer pathway
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INOH |
Wnt signaling pathway pathway
GPCR signaling pathway
Wnt signaling pathway pathway
GPCR signaling pathway
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PID NCI |
Wnt signaling network
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Cross-References | |||||||||||||||
SwissProt | |||||||||||||||
TrEMBL | F1MBL4 | ||||||||||||||
UniProt Splice Variant | |||||||||||||||
Entrez Gene | 521364 | ||||||||||||||
UniGene | Bt.26945 | ||||||||||||||
RefSeq | XM_002698189 XM_599625 | ||||||||||||||
HUGO | HGNC:4047 | ||||||||||||||
OMIM | |||||||||||||||
CCDS | |||||||||||||||
HPRD | |||||||||||||||
IMGT | |||||||||||||||
EMBL | DAAA02058197 | ||||||||||||||
GenPept | |||||||||||||||
RNA Seq Atlas | 521364 | ||||||||||||||