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PRICKLE1, prickle planar cell polarity protein 1

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  • Interaction Network
  • Sequence Verification

PRICKLE1, prickle planar cell polarity protein 1

  • 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. [provided by RefSeq, Sep 2009]

  • Gene Synonyms (EPM1B, RILP, prickle-like protein 1, REST (RE-1 silencing transcription factor)/NRSF (neuron-restrictive silencer factor)-interacting LIM domain protein, REST/NRSF interacting LIM domain protein, REST/NRSF-interacting LIM domain protein 1, prickle homolog 1, prickle-like 1,)
  • NCBI Gene ID: 144165
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>B3KVG3
    UNIPROT ID#>>B3KVG6
    UNIPROT ID#>>Q96MT3
    UNIPROT ID#>>A0A024R0W7
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

prickle planar cell polarity protein 1 interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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