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Allele : Mmab<em1(IMPC)Hmgu> methylmalonic aciduria (cobalamin deficiency) cblB type homolog (human); endonuclease-mediated mutation 1, Helmholtz Zentrum Muenchen GmbH
Primary Identifier  MGI:6435666 Allele Type  Endonuclease-mediated
Attribute String  Null/knockout Gene  Mmab
Inheritance Mode  Not Specified Strain of Origin  C57BL/6NCrl
Is Recombinase  false Is Wild Type  false
Project Collection  IMPC
molecularNote  This allele from IMPC was generated at Helmholtz-Zentrum Muenchen by injecting CAS9 Protein and 4 guide sequences CACAGAGTGACTTGCTGACCTGG, AGGGCGGCCAGCTGGAGCTCAGG, CCACCCCGAGTCAGCTGTTCTTA, GCCCAAGTTAACCCGCTCATGGG, which resulted in a Exon Deletion.
  • mutations:
  • Intragenic deletion
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

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Trail: Allele

0 Driven By

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Trail: Allele




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