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General Information



Gene_Symbol Gene_ID Gene_Name Chromosome Alias
WNT5A 7474 wingless-type MMTV integration site family, member 5A  3hWNT5A 







  • Evidence
  • Gene
  • mRNA
  • CDS
  • Protein
  • PTM
  • Enzyme
  • PPi
  • Pathway
  • Structural
  • Domain
  • Ontology
  • SNP
  • Drug
  • External Links



Evidence Information


Pubmed ID Year Sample Information Techniques Mechanism Fold Change Remark
18172252   2008Cell line : -

Source : -

Sample Type : CRC tumor and normal tissue

No. of Sample : 29 CRC and 15 normal tissue

Stage : -

real time RT-PCR,Methylation-specific PCR and bisulfite genomic sequencing,Western blottingMethylation-WNT5A is frequently inactivated in CRC by tumor-specific methylation, and thus, is a potential biomarker. WNT5A could act as a tumor suppressor for CRC by antagonizing the Wnt/beta-catenin signaling.

WNT5A methylation was frequently detected in CRC tumors (14 of 29, 48%), but only occasionally in paired normal colon tissues (2 of 15, 13%; P = 0.025).


Gene Details



Chromosome 3 - NC_000003.12 (55465715..55505261, complement)

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Gene Type protein coding
Gene Family Wingless-type MMTV integration sites, "Endogenous ligands"
Description 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 encodes a member of the WNT family that signals through both the canonical and non-canonical WNT pathways. This protein is a ligand for the seven transmembrane receptor frizzled-5 and the tyrosine kinase orphan receptor 2. This protein plays an essential role in regulating developmental pathways during embryogenesis. This protein may also play a role in oncogenesis. Mutations in this gene are the cause of autosomal dominant Robinow syndrome. Alternate splicing results in multiple transcript variants.  
Chromosome 3
Location 3p21-p14
Start 55465715  
End 55505261  
Strand -  
Gene Sequence

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Length 39547  
OMIM ID 164975   
HGNC ID HGNC:12784   
Unigene ID Hs.643085   
Ensembl ID ENSG00000114251   
PharmGKB ID -   

mRNA Information


mRNA ID XM_011534082.1
Exon join(1..64,3480..3663,7785..7873,11207..11432, 11515..15232,24344..24477,25698..25948,30633..30925, 34712..39547)  
mRNA Sequence

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Length 5599  



CDS Information


   
Locationjoin(18277..18282,24344..24477,25698..25948,30633..30925, 34712..35170)
CDS Sequence

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CCDS ID CCDS46850.1



Protein Information


      
Protein IDNP_001243034.1
Protein Namewingless-type MMTV integration site family, member 5A
Molecular Wt. (Da)37992
Protein Sequence

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Length 365  
Uniprot IDP05112
Ensembl Protein ID ENSP00000231449  



Post-translational Modification Information (Source : HPRD)


No matching records could be found.

Enzyme Information


No matching records could be found.

PPi Information


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No matching records from HPRD source could be found.

Pathway Information


                                                      
Pathway Name Pathway ID
Basal cell carcinoma hsa05217
Hedgehog signaling pathway hsa04340
Hippo signaling pathway hsa04390
HTLV-I infection hsa05166
Melanogenesis hsa04916
Pathways in cancer hsa05200
Proteoglycans in cancer hsa05205
Signaling pathways regulating pluripotency of stem cells hsa04550
Wnt signaling pathway hsa04310


Structure Information


No matching records could be found.

Domain Information




ID Location Description
smart0009771-380  WNT1
cl1956871-380  wnt superfamily
pfam0011068-380  wnt


Ontology Information


   
HPRD ID970
Molecular ClassLigand
Molecular FunctionCytokine activity (GO:0005125)
Biological ProcessImmune response (GO:0006955)  



SNP Information


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Drug Information


No matching records could be found.

External Links


                                 
ArrayExpressGO
ICGCGO
Cancer3DGO
COSMICGO
NCGGO
TSGeneGO
Tumor Gene Family of DatabasesGO
CCDBGO
G2SBCGO
Osteosarcoma DatabaseGO
RCDBGO