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Wd repeat containing planar cell polarity effector

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Protein-coding gene in the species Homo sapiens
WDPCP
Identifiers
AliasesWDPCP, BBS15, C2orf86, FRITZ, FRTZ, CHDTHP, WD repeat containing planar cell polarity effector, CPLANE5
External IDsOMIM: 613580; MGI: 2144467; HomoloGene: 9299; GeneCards: WDPCP; OMA:WDPCP - orthologs
Gene location (Human)
Chromosome 2 (human)
Chr.Chromosome 2 (human)
Chromosome 2 (human)Genomic location for WDPCPGenomic location for WDPCP
Band2p15Start63,119,559 bp
End63,827,843 bp
Gene location (Mouse)
Chromosome 11 (mouse)
Chr.Chromosome 11 (mouse)
Chromosome 11 (mouse)Genomic location for WDPCPGenomic location for WDPCP
Band11 A3.1|11 13.9 cMStart21,522,235 bp
End21,848,989 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • mucosa of paranasal sinus

  • palpebral conjunctiva

  • superficial temporal artery

  • sperm

  • cardiac muscle tissue of right atrium

  • myocardium of left ventricle

  • pancreatic epithelial cell

  • buccal mucosa cell

  • germinal epithelium

  • skin of arm
Top expressed in
  • fourth ventricle

  • choroid plexus of fourth ventricle

  • spermatocyte

  • spermatid

  • choroidal fissure

  • seminiferous tubule

  • nasolacrimal duct

  • lumbar spinal ganglion

  • right kidney

  • olfactory system
More reference expression data
BioGPS
n/a
Orthologs
SpeciesHumanMouse
Entrez

51057

216560

Ensembl

ENSG00000143951

ENSMUSG00000020319

UniProt

O95876

Q8C456

RefSeq (mRNA)

NM_001042692
NM_015910
NM_001354044
NM_001354045

NM_145425
NM_001364768

RefSeq (protein)

NP_001036157
NP_056994
NP_001340973
NP_001340974

NP_663400
NP_001351697

Location (UCSC)Chr 2: 63.12 – 63.83 MbChr 11: 21.52 – 21.85 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

WD repeat containing planar cell polarity effector is a protein that in humans is encoded by the WDPCP gene.

Function

This gene encodes a cytoplasmic WD40 repeat protein. A similar gene in frogs encodes a planar cell polarity protein that plays a critical role in collective cell movement and ciliogenesis by mediating septin localization. Mutations in this gene are associated with Bardet-Biedl syndrome 15 and may also play a role in Meckel-Gruber syndrome. Alternative splicing results in multiple transcript variants.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000143951Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000020319Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. "Entrez Gene: WD repeat containing planar cell polarity effector". Retrieved 2017-06-07.

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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