CRMP1

Source: Wikipedia, the free encyclopedia.
CRMP1
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Ensembl
UniProt
RefSeq (mRNA)

NM_001313
NM_001014809
NM_001288661
NM_001288662

NM_001136058
NM_007765

RefSeq (protein)

NP_001014809
NP_001275590
NP_001275591
NP_001304

NP_001129530
NP_031791

Location (UCSC)Chr 4: 5.75 – 5.89 MbChr 5: 37.4 – 37.45 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

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

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]

Interactions

CRMP1 has been shown to

interact with DPYSL2.[9]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000072832Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000029121Ensembl, 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. ^ a b "Entrez Gene: CRMP1 collapsin response mediator protein 1".
  6. PMID 17182786
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External links

Further reading


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