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Gene: Dact3 (dishevelled-binding antagonist of beta-catenin 3) Rattus norvegicus
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Symbol: Dact3
Name: dishevelled-binding antagonist of beta-catenin 3
RGD ID: 1563892
Description: Predicted to have several functions, including delta-catenin binding activity; identical protein binding activity; and protein kinase C binding activity. Predicted to be involved in negative regulation of canonical Wnt signaling pathway; negative regulation of cell growth; and negative regulation of epithelial to mesenchymal transition. Predicted to localize to cytoplasm. Orthologous to human DACT3 (dishevelled binding antagonist of beta catenin 3); INTERACTS WITH flusilazole; furan; glyphosate.
Type: protein-coding
RefSeq Status: PROVISIONAL
Also known as: dapper homolog 3; dapper, antagonist of beta-catenin, homolog 3; dapper, antagonist of beta-catenin, homolog 3 (Xenopus laevis); LOC499088; RGD1563892; similar to MGC15476 protein
Orthologs:
Latest Assembly: Rnor_6.0 - RGSC Genome Assembly v6.0
Position:
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Rnor_6.0178,800,754 - 78,812,483 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl178,800,754 - 78,812,483 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0180,048,066 - 80,059,888 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4177,201,808 - 77,213,537 (+)NCBIRGSC3.4rn4RGSC3.4
Celera172,031,999 - 72,043,732 (+)NCBICelera
Cytogenetic Map1q21NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


References - curated
References - uncurated

Genomics

Comparative Map Data
Position Markers
QTLs in Region (Rnor_6.0)
miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Transcriptome
Promoters

Strain Variation

Strain Sequence Variants (Rnor 6.0)

Additional Information

External Database Links
Nomenclature History
 
More on Dact3
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: rn5 rn6
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1563892
Created: 2006-02-09
Species: Rattus norvegicus
Last Modified: 2020-08-20
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.