WNT1

Wnt family member 1

Ensembl:
ENSG00000125084
UniProt:
P04628
OMIM:
164820
Synonyms:
INT1

Cilia effects upon perturbation of WNT1

Ciliogenesis screen results (4 screens)

  • Kim2016: No effect
  • Wheway et al. 2015 (siRNA) [siRNA]: No effect PMID:26167766
  • Breslow et al. 2018 (CRISPR) [CRISPR]: No Significant Effect PMID:29459680
  • Roosing et al. 2015 (siRNA) [siRNA]: Hyper-ciliogenesis (robust z=2.18, ciliated=54.3%) PMID:26595381

Phenotypes

Mouse phenotype:
preweaning lethality, incomplete penetrance, preweaning lethality, complete penetrance, increased circulating cholesterol level
Mouse ciliopathy phenotype:
increased circulating creatinine level

Subcellular localization

cilia associated gene, lysosomes

Functional category

  • Ciliary assembly/disassembly
  • Actin & cytoskeleton regulation
  • T cell biology
  • Protein processing & maturation
  • Cell migration & adhesion
  • Signaling (Hedgehog, GPCRs, ion channels)
  • Cardiac & muscle development
  • Transcription regulation

Function

Using the Kif3af/f ,Wnt1-Cre ciliopathic mouse model to prevent Shh sig l transduction by means of the loss of primary cilia in neural crest cells, mesenchymal Shh activity is necessary for gland development ( 29532549).

Model organism evidence

Mus musculus (2 references)

METHODS AND RESULTS: Here, we disrupted primary cilia by deleting the ciliary gene Ift88 in the main progenitor cells forming the aortic valve using specific Cre drivers: Wnt1-Cre for neural crest cells, Isl1-Cre for second heart field (SHF) cells, Tie2-Cre for endocardial-derived cells, and Tnnt

Primary Cilium in Neural Crest Cells Crucial for Anterior Segment Development and Corneal Avascularity.

PMIDs: 40498626, 38517430