Homo sapiens Gene: WNT6
Summary
InnateDB Gene IDBG-81171.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol WNT6
Gene Name wingless-type MMTV integration site family, member 6
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000115596
Encoded Proteins
wingless-type MMTV integration site family, member 6
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
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 embryogenesis. This gene is a member of the WNT gene family. It is overexpressed in cervical cancer cell line and strongly coexpressed with another family member, WNT10A, in colorectal cancer cell line. The gene overexpression may play key roles in carcinogenesis. This gene and the WNT10A gene are clustered in the chromosome 2q35 region. The protein encoded by this gene is 97% identical to the mouse Wnt6 protein at the amino acid level. [provided by RefSeq, Jul 2008]
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 embryogenesis. This gene is a member of the WNT gene family. It is overexpressed in cervical cancer cell line and strongly coexpressed with another family member, WNT10A, in colorectal cancer cell line. The gene overexpression may play key roles in carcinogenesis. This gene and the WNT10A gene are clustered in the chromosome 2q35 region. The protein encoded by this gene is 97%% identical to the mouse Wnt6 protein at the amino acid level. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 2:218859821-218874233
Strand Forward strand
Band q35
Transcripts
ENST00000233948 ENSP00000233948
ENST00000486233
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.
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005102 receptor binding
GO:0005109 frizzled binding
Biological Process
GO:0001658 branching involved in ureteric bud morphogenesis
GO:0007275 multicellular organismal development
GO:0009798 axis specification
GO:0010628 positive regulation of gene expression
GO:0016055 Wnt signaling pathway
GO:0030182 neuron differentiation
GO:0042475 odontogenesis of dentin-containing tooth
GO:0045165 cell fate commitment
GO:0045893 positive regulation of transcription, DNA-templated
GO:0060684 epithelial-mesenchymal cell signaling
GO:0061303 cornea development in camera-type eye
GO:0070172 positive regulation of tooth mineralization
GO:0071300 cellular response to retinoic acid
GO:0072079 nephron tubule formation
GO:0072080 nephron tubule development
Cellular Component
GO:0005576 extracellular region
GO:0005578 proteinaceous extracellular matrix
GO:0005615 extracellular space
GO:0005788 endoplasmic reticulum lumen
GO:0005796 Golgi lumen
GO:0005886 plasma membrane
GO:0009986 cell surface
GO:0031012 extracellular matrix
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
Wnt pathway
REACTOME
Class B/2 (Secretin family receptors) pathway
Signaling by WNT in cancer pathway
Signaling by Wnt pathway
Signaling by GPCR pathway
WNT ligand secretion is abrogated by the PORCN inhibitor LGK974 pathway
Signal Transduction pathway
WNT ligand biogenesis and trafficking pathway
GPCR ligand binding pathway
Disease pathway
KEGG
Wnt signaling pathway pathway
Hedgehog signaling pathway pathway
Basal cell carcinoma pathway
Melanogenesis pathway
Pathways in cancer pathway
INOH
Wnt signaling pathway pathway
GPCR signaling pathway
PID NCI
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.29764
RefSeq NM_006522
HUGO
OMIM
CCDS CCDS2425
HPRD 05233
IMGT
EMBL
GenPept
RNA Seq Atlas