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CRMP1
Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia
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Collapsin response mediator protein 1, encoded by the CRMP1 gene, is a human protein of the CRMP family.[5]
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]
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