Gene Gene information from NCBI Gene database.
Entrez ID 7473
Gene name Wnt family member 3
Gene symbol WNT3
Synonyms (NCBI Gene)
INT4TETAMS
Chromosome 17
Chromosome location 17q21.31-q21.32
Summary 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 embryog
miRNA miRNA information provided by mirtarbase database.
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miRTarBase ID miRNA Experiments Reference
MIRT018503 hsa-miR-335-5p Microarray 18185580
MIRT024672 hsa-miR-215-5p Microarray 19074876
MIRT026683 hsa-miR-192-5p Microarray 19074876
MIRT036062 hsa-miR-1301-3p CLASH 23622248
MIRT696724 hsa-miR-1255b-2-3p HITS-CLIP 23313552
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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GO ID Ontology Definition Evidence Reference
GO:0000902 Process Cell morphogenesis IMP 15588944
GO:0001707 Process Mesoderm formation IEA
GO:0005102 Function Signaling receptor binding IEA
GO:0005109 Function Frizzled binding IBA
GO:0005109 Function Frizzled binding IPI 10557084, 18313787
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
165330 12782 ENSG00000108379
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P56703
Protein name Proto-oncogene Wnt-3 (Proto-oncogene Int-4 homolog)
Protein function Ligand for members of the frizzled family of seven transmembrane receptors (Probable). Functions in the canonical Wnt signaling pathway that results in activation of transcription factors of the TCF/LEF family (PubMed:26902720). Required for nor
PDB 6AHY
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00110 wnt 47 355 wnt family Family
Sequence
Sequence length 355
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  mTOR signaling pathway
Wnt signaling pathway
Hippo signaling pathway
Signaling pathways regulating pluripotency of stem cells
Melanogenesis
Cushing syndrome
Alzheimer disease
Pathways of neurodegeneration - multiple diseases
Human papillomavirus infection
Pathways in cancer
Proteoglycans in cancer
MicroRNAs in cancer
Basal cell carcinoma
Breast cancer
Hepatocellular carcinoma
Gastric cancer
  TCF dependent signaling in response to WNT
WNT ligand biogenesis and trafficking
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
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Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Bladder exstrophy-epispadias-cloacal extrophy complex Likely pathogenic rs786205887 RCV000172899
Tetraamelia syndrome 1 Pathogenic rs104894653 RCV000014823
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
WNT3-related disorder Likely benign; Benign rs150717986, rs143605657, rs767605103 RCV003971108
RCV003958862
RCV004758926
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Acute Radiation Syndrome Associate 33476246, 35680903, 37676284, 38499035
Alzheimer Disease Associate 31504236, 36191742
Amyotrophic Lateral Sclerosis Stimulate 30924074
Aortic Valve Stenosis Associate 29227539
Autism Spectrum Disorder Associate 37907504
Bladder Exstrophy Associate 34355505
Breast Neoplasms Associate 23071104, 30651373
Carcinogenesis Associate 17767013, 29565490
Carcinoma Hepatocellular Associate 18313787, 18577996, 36275697
Carcinoma Non Small Cell Lung Stimulate 29565490