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CRMP1

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

CRMP1
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Collapsin response mediator protein 1, encoded by the CRMP1 gene, is a human protein of the CRMP family.[5]

Quick Facts Available structures, PDB ...

This gene encodes a member of a family of cytosolic phosphoproteins expressed exclusively in the nervous system. The encoded protein is thought to be a part of the semaphorin signal transduction pathway implicated in semaphorin-induced growth cone collapse during neural development. Alternative splicing results in multiple transcript variants.[5]

CRMP1 mediates reelin signaling in cortical neuronal migration.[6] Mice deficient in CRMP1 exhibit impaired long-term potentiation and impaired spatial learning and memory.[7]

CRMP1 gene overlaps with another gene called EVC.[8]

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Interactions

CRMP1 has been shown to interact with DPYSL2.[9]

References

Further reading

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