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Allele : Nrxn1<em1Amcr> neurexin I; endonuclease-mediated mutation 1, Ann Craig

Primary Identifier  MGI:7622045 Allele Type  Endonuclease-mediated
Gene  Nrxn1 Strain of Origin  C57BL/6J
Is Recombinase  false Is Wild Type  false
molecularNote  The exon 22 alternative splice donor site was modified by changing sequence GGTGgGtTAGgT to GGTGaGcTAGcT. The mutations abolish the downstream alternative splice site (G-GT), as well as the cryptic splice site (G-GT) 5' from that, at splice site S5, while maintaining the upstream alternative splice site (G-GT). The loss of the alternative splice site causes the loss of a serine residue to which heparan sulfate (HS) can potentially be attached.
  • mutations:
  • Intragenic deletion
  • synonyms:
  • Nrxn1<deltaS5>,
  • Nrxn1<deltaS5>
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

2 Publication categories