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Allele : Nfix<em2H> nuclear factor I/X; endonuclease-mediated mutation 2, Harwell

Primary Identifier  MGI:6307062 Allele Type  Endonuclease-mediated
Attribute String  Modified isoform(s) Gene  Nfix
Strain of Origin  C57BL/6J Is Recombinase  false
Is Wild Type  false
molecularNote  CRISPR/Cas9 technology generated an in-frame 24-bp deletion in exon 7 from position +49,561 to +49,584 relative to the translation start site. This deletion causes skipping of exon 7 and alternative splicing of exon 6 to exon 8 to produce wild-type Nfix isoforms. MEFs express the mutant long isoform (293 bp) and the wild-type short isoform lacking exon 7 (194 bp).
  • mutations:
  • Intragenic deletion
  • synonyms:
  • Nfix<em2Rvt>,
  • Nfix<em2Rvt>
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

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0 Driven By

2 Publication categories

Trail: Allele