Gene Gene information from NCBI Gene database.
Entrez ID 147906
Gene name Dishevelled binding antagonist of beta catenin 3
Gene symbol DACT3
Synonyms (NCBI Gene)
DAPPER3RRR1
Chromosome 19
Chromosome location 19q13.32
miRNA miRNA information provided by mirtarbase database.
36
miRTarBase ID miRNA Experiments Reference
MIRT005875 hsa-miR-31-5p ImmunoprecipitaionLuciferase reporter assayMicroarrayqRT-PCRWestern blot 21048943
MIRT005875 hsa-miR-31-5p ImmunoprecipitaionLuciferase reporter assayMicroarrayqRT-PCRWestern blot 21048943
MIRT005875 hsa-miR-31-5p ImmunoprecipitaionLuciferase reporter assayMicroarrayqRT-PCRWestern blot 21048943
MIRT005875 hsa-miR-31-5p ImmunoprecipitaionLuciferase reporter assayMicroarrayqRT-PCRWestern blot 21048943
MIRT005875 hsa-miR-31-5p ImmunoprecipitaionLuciferase reporter assayMicroarrayqRT-PCRWestern blot 21048943
Transcription factors Transcription factors information provided by TRRUST V2 database.
2
Transcription factor Regulation Reference
EZH2 Repression 22144423
NKX2-5 Repression 19479054
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
18
GO ID Ontology Definition Evidence Reference
GO:0001837 Process Epithelial to mesenchymal transition IEA
GO:0005080 Function Protein kinase C binding IEA
GO:0005080 Function Protein kinase C binding ISS
GO:0005737 Component Cytoplasm IBA
GO:0005737 Component Cytoplasm IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
611112 30745 ENSG00000197380
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96B18
Protein name Dapper homolog 3 (Antagonist of beta-catenin Dapper homolog 3) (Arginine-rich region 1 protein) (Dapper antagonist of catenin 3)
Protein function May be involved in regulation of intracellular signaling pathways during development. Specifically thought to play a role in canonical and/or non-canonical Wnt signaling pathways through interaction with DSH (Dishevelled) family proteins. {ECO:0
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15268 Dapper 19 166 Dapper Family
PF15268 Dapper 543 629 Dapper Family
Sequence
MIRAFSFPVSPERGRLRGWLEGSLAGLCELHWLRERQEYRVQQALRLAQPGMGGAEAEDE
EDADEDEDAAAARRAAAALEEQLEALPGLVWDLGQQLGDLSLESGGLEQESGRSSGFYED
PSSTGGPDSPPSTFCGDSGFSGSSSYGRLGPSEPRGIYASERPKSL
GDASPSAPEVVGAR
AAVPRSFSAPYPTAGGSAGPEACSSAERRARAGPFLTPSPLHAVAMRSPRPCGRPPTDSP
DAGGAGRPLDGYISALLRRRRRRGAGQPRTSPGGADGGPRRQNSVRQRPPDASPSPGSAR
PAREPSLERVGGHPTSPAALSRAWASSWESEAAPEPAAPPAAPSPPDSPAEGRLVKAQYI
PGAQAATRGLPGRAARRKPPPLTRGRSVEQSPPRERPRAAGRRGRMAEASGRRGSPRARK
ASRSQSETSLLGRASAVPSGPPKYPTAEREEPRPPRPRRGPAPTLAAQAAGSCRRWRSTA
EIDAADGRRVRPRAPAARVPGPGPSPSAPQRRLLYGCAGSDSECSAGRLGPLGRRGPAGG
VGGGYGESESSASEGESPAFSSASSDSDGSGGLVWPQQLVAATAASGGGAGAGAPAGPAK
VFVKIKASHALKKKILRFRSGSLKVMTTV
Sequence length 629
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
Intellectual disability Uncertain significance ClinVar
Disgenet
★★★☆☆
Reported in Unknown/Other Associations (≥2 sources)
POLYCYSTIC OVARY SYNDROME CTD, Disgenet
CTD, Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Progressive spastic paraparesis Uncertain significance ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Asthma Asthma BEFREE 29456669
★☆☆☆☆
Found in Text Mining only
Carcinoma Carcinoma BEFREE 24809775
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Hepatocellular carcinoma Pubtator 35764883 Associate
★☆☆☆☆
Found in Text Mining only
Colorectal Carcinoma Colorectal Cancer BEFREE 18538736
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Colorectal Neoplasms LHGDN 18538736
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Colorectal neoplasm Pubtator 18538736 Associate
★☆☆☆☆
Found in Text Mining only
Esophageal carcinoma Esophageal Carcinoma BEFREE 28077137
★☆☆☆☆
Found in Text Mining only
Esophageal Neoplasms Esophagus Neoplasm BEFREE 28077137
★☆☆☆☆
Found in Text Mining only
Esophageal Neoplasms Esophageal neoplasm Pubtator 28077137 Inhibit
★☆☆☆☆
Found in Text Mining only
Hypoxia Hypoxia Pubtator 35764883 Stimulate
★☆☆☆☆
Found in Text Mining only