Wnt signaling in kidney disease (Mus musculus)

From WikiPathways

Revision as of 21:20, 6 August 2016 by AlexanderPico (Talk | contribs)
Jump to: navigation, search
1, 2Cytoskeleton/planar cell PolarityCanonical TranscriptionNon-Canonical RhoaNphp3CalciumNphp2 (Invs)beta-cateninLrp5Lrp6Wnt1Wnt10aWnt10bWnt7aWnt16Wnt6Wnt5aWnt2bWnt11Wnt4Wnt3aWnt5bWnt9bWnt2Wnt3Wnt7bFzd1Fzd8Fzd4Fzd2Fzd7Fzd9Fzd5Fzd6Fzd3Fzd1Fzd8Fzd4Fzd2Fzd7Fzd9Fzd5Fzd6Fzd3Dvl2Dvl3Dvl1Mapk9Mapk10Mapk8Dvl2Dvl3Dvl1cytoplasmicdisheveledmembrane-bounddisheveled


Description

This pathway is modeled after Figure 5 of the article "Glomerulocystic kidney disease" (Bissler, et al. 2010). The gene product Wnt signals two different paths titled canonical and non-canonical. The non-canonical path is mediated by the membrane bound protein Disheveled (Dvl) which then controls the planar cell Polarity. The canonical path on the other hand is mediated by the cytoplasmic protein Disheveled (Dvl) and then is effected through b-catenin transcription. The complex of Nphp2 and Nphp3 seem to help facilitate the process by controlling the Wnt signaling. Bergmann, et al. (2008) showed that Nphp3 deficiency in Xenopus resulted to planar cell polarity defects.

Try the New WikiPathways

View approved pathways at the new wikipathways.org.

Quality Tags

Ontology Terms

 

Bibliography

  1. Stamos JL, Weis WI; ''The β-catenin destruction complex.''; Cold Spring Harb Perspect Biol, 2013 PubMed Europe PMC Scholia
  2. Bissler JJ, Siroky BJ, Yin H; ''Glomerulocystic kidney disease.''; Pediatr Nephrol, 2010 PubMed Europe PMC Scholia
  3. Bergmann C, Fliegauf M, Brüchle NO, Frank V, Olbrich H, Kirschner J, Schermer B, Schmedding I, Kispert A, Kränzlin B, Nürnberg G, Becker C, Grimm T, Girschick G, Lynch SA, Kelehan P, Senderek J, Neuhaus TJ, Stallmach T, Zentgraf H, Nürnberg P, Gretz N, Lo C, Lienkamp S, Schäfer T, Walz G, Benzing T, Zerres K, Omran H; ''Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia.''; Am J Hum Genet, 2008 PubMed Europe PMC Scholia

History

View all...
CompareRevisionActionTimeUserComment
129329view14:09, 26 March 2024Mkutmonfix publication reference encoding issue
129328view14:06, 26 March 2024MkutmonOntology Term : 'disease pathway' added !
128390view03:05, 4 February 2024EweitzStandardize case
118851view09:54, 2 June 2021EweitzOntology Term : 'PW:0000003' removed !
117952view10:46, 23 May 2021EweitzModified title
107767view17:38, 1 November 2019AgustinGVPathway disappeared on previous update attempt
107766view17:21, 1 November 2019AgustinGV
107765view17:16, 1 November 2019AgustinGVFix alignment
107764view17:14, 1 November 2019AgustinGVAdd literature
107763view17:12, 1 November 2019AgustinGVUpdate annotation to NCBI
107762view17:09, 1 November 2019AgustinGVAdd beta-catenin destruction complex
107761view16:52, 1 November 2019AgustinGVcorrect alignments
106887view13:36, 17 September 2019MaintBotHMDB identifier normalization
90797view17:25, 14 December 2016KhanspersModified title
90183view18:28, 21 October 2016Khanspersupdated lit ref
88437view21:20, 6 August 2016AlexanderPicoUpdated references
88436view21:19, 6 August 2016AlexanderPicoModified description
88435view21:11, 6 August 2016AlexanderPicoUpdated title, lit ref and label
88434view21:02, 6 August 2016AlexanderPicoOntology Term : 'signaling pathway' added !
88433view21:00, 6 August 2016AlexanderPicoAdded paralogs, Lrp5/6, cell compartments and Dvl labels
88380view01:21, 2 August 2016AAR&CoOntology Term : 'Wnt signaling, the planar cell polarity pathway' added !
88379view01:20, 2 August 2016AAR&CoOntology Term : 'kidney disease' added !
88217view00:37, 1 August 2016AAR&CoAdded Identifier
88216view00:35, 1 August 2016AAR&CoAdded Identifiers
87416view11:31, 22 July 2016MkutmonOntology Term : 'Wnt signaling pathway' added !
87279view16:47, 20 July 2016AAR&CoIdentifiers Added
87277view16:43, 20 July 2016AAR&CoModified description
87268view16:08, 20 July 2016AAR&CoNew pathway

External references

DataNodes

View all...
NameTypeDatabase referenceComment
CalciumMetaboliteHMDB00464 (HMDB)
Dvl1GeneProduct13542 (Entrez Gene)
Dvl2GeneProduct13543 (Entrez Gene)
Dvl3GeneProduct13544 (Entrez Gene)
Fzd1GeneProduct14362 (Entrez Gene)
Fzd2GeneProduct57265 (Entrez Gene)
Fzd3GeneProduct14365 (Entrez Gene)
Fzd4GeneProduct14366 (Entrez Gene)
Fzd5GeneProduct14367 (Entrez Gene)
Fzd6GeneProduct14368 (Entrez Gene)
Fzd7GeneProduct14369 (Entrez Gene)
Fzd8GeneProduct14370 (Entrez Gene)
Fzd9GeneProduct14371 (Entrez Gene)
Lrp5GeneProductENSMUSG00000024913 (Ensembl)
Lrp6GeneProductENSMUSG00000030201 (Ensembl)
Mapk10GeneProduct26414 (Entrez Gene)
Mapk8GeneProduct26419 (Entrez Gene)
Mapk9GeneProduct26420 (Entrez Gene)
Nphp2 (Invs)GeneProductENSMUSG00000028344 (Ensembl)
Nphp3GeneProductENSMUSG00000032558 (Ensembl)
RhoaGeneProductENSMUSG00000007815 (Ensembl)
Wnt10aGeneProduct22409 (Entrez Gene)
Wnt10bGeneProduct22410 (Entrez Gene)
Wnt11GeneProduct22411 (Entrez Gene)
Wnt1GeneProduct22408 (Entrez Gene)
Wnt16GeneProduct93735 (Entrez Gene)
Wnt2GeneProduct22413 (Entrez Gene)
Wnt2bGeneProduct22414 (Entrez Gene)
Wnt3GeneProduct22415 (Entrez Gene)
Wnt3aGeneProduct22416 (Entrez Gene)
Wnt4GeneProduct22417 (Entrez Gene)
Wnt5aGeneProduct22418 (Entrez Gene)
Wnt5bGeneProduct22419 (Entrez Gene)
Wnt6GeneProduct22420 (Entrez Gene)
Wnt7aGeneProduct22421 (Entrez Gene)
Wnt7bGeneProduct22422 (Entrez Gene)
Wnt9bGeneProduct22412 (Entrez Gene)
beta-cateninGeneProductENSMUSG00000006932 (Ensembl)

Annotated Interactions

No annotated interactions

Personal tools