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General Information
ZIRC
ZFIN ID: ZDB-GENE-060328-3
Gene Name: wingless-type MMTV integration site family, member 5a
Gene Symbol: wnt5a
Sequence Ontology ID : SO:0000704

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Location: Chr: 8 Mapping Details/Browsers
Nomenclature History
AUTOMATED DESCRIPTION
Predicted to have frizzled binding activity. Involved in pronephros development. Predicted to localize to the extracellular space. Human ortholog(s) of this gene implicated in autosomal dominant  ...
MUTATIONS AND SEQUENCE TARGETING REAGENTS
Allele Type Localization Consequence Mutagen Suppliers
sa93 Point Mutation Unknown Missense ENU
sa44695 Point Mutation Unknown Unknown ENU
Targeting reagents:
DISEASE ASSOCIATED WITH wnt5a HUMAN ORTHOLOG
Disease Ontology Term OMIM Term OMIM Phenotype ID
autosomal dominant Robinow syndrome 1 Robinow syndrome, autosomal dominant 1 180700
DISEASE ASSOCIATED WITH wnt5a VIA EXPERIMENTAL MODELS No data available
GENE ONTOLOGY
Ontology GO Term
Biological Process pronephros development (more)
Cellular Component extracellular region (more)
Molecular Function signaling receptor binding (more)
GO Terms (all 11)
TRANSCRIPTS No data available
GENE PRODUCT DESCRIPTION
INTERACTIONS AND PATHWAYS
ANTIBODIESNo data available
PLASMIDSNo data available
CONSTRUCTS WITH SEQUENCES FROM wnt5a No data available
MARKER RELATIONSHIPS
wnt5aEncodes: [cDNA] MGC:165375 (1) (order this), MGC:194820 (1) (order this), MGC:194832 (1) (order this)
SEQUENCE INFORMATION
Type Accession # Length (bp/aa) Analysis
RNA RefSeq:NM_001079834 (1) 1320bp
Genomic GenBank:CABZ01074186 (1) 30693bp
Select Tool
Polypeptide UniProtKB:A1BPR0 (1) 374aa
Sequence Clusters UniGene:108590 (1)
Sequence Information (all 23)
OTHER wnt5a GENE PAGES
  • Alliance (1)
  • Gene:568191 (1)
  • Ensembl(GRCz11):ENSDARG00000104973 (1)
  • ORTHOLOGY for wnt5a (Chr: 8)
    CITATIONS (54)