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Allele : Igh<tm1.1Feil> immunoglobulin heavy chain complex; targeted mutation 1.1, Robert Feil
Primary Identifier  MGI:5751552 Allele Type  Targeted
Gene  Igh Transmission  Germline
Strain of Origin  129S2/SvPas Is Recombinase  false
Is Wild Type  false
molecularNote  The H19 imprinting control region (ICR) with 4 CTCF binding sites was inserted between Igh-J and Emu. Cre-mediated recombination removed the floxed neomycin resistance cassette.
  • mutations:
  • Insertion
  • synonyms:
  • ICR,
  • ICR
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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

3 Publication categories





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