Prickle planar cell polarity protein 1 is a protein that in humans is encoded by the PRICKLE1 gene. [5]

PRICKLE1
Identifiers
AliasesPRICKLE1, EPM1B, RILP, prickle planar cell polarity protein 1
External IDsOMIM: 608500; MGI: 1916034; HomoloGene: 17686; GeneCards: PRICKLE1; OMA:PRICKLE1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001144881
NM_001144882
NM_001144883
NM_153026

NM_001033217
NM_001364846

RefSeq (protein)

NP_001138353
NP_001138354
NP_001138355
NP_694571

NP_001028389
NP_001351775

Location (UCSC)Chr 12: 42.46 – 42.59 MbChr 15: 93.4 – 93.49 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Function

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This gene encodes a nuclear receptor that may be a negative regulator of the Wnt/beta-catenin signaling pathway. The encoded protein localizes to the nuclear membrane and has been implicated in the nuclear trafficking of the transcription repressors REST/NRSF and REST4. Mutations in this gene have been linked to progressive myoclonus epilepsy. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 3.

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000139174Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000036158Ensembl, 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: Prickle planar cell polarity protein 1". Retrieved 2017-08-08.

Further reading

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