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Allele : Mycn<tm1(EUCOMM)Wtsi> v-myc avian myelocytomatosis viral related oncogene, neuroblastoma derived; targeted mutation 1, Wellcome Trust Sanger Institute

Primary Identifier  MGI:4888950 Allele Type  Targeted
Attribute String  Null/knockout, Reporter Gene  Mycn
Transmission  Cell Line Strain of Origin  C57BL/6N-A<tm1Brd>
Is Recombinase  false Is Wild Type  false
Project Collection  EUCOMM
molecularNote  The insertion of the L1L2_Bact_P cassette created a deletion of size 3557 starting at position 12986939 and ending at position 12990496 of Chromosome 12 (Genome Build GRCm39). This deletion results in the removal of functionally critical exon(s). The cassette is composed of an FRT site followed by lacZ sequence and a loxP site. This first loxP site is followed by a neomycin resistance gene under the control of the human beta-actin promoter, SV40 polyA, a second FRT site and a second loxP site.
  • mutations:
  • Insertion,
  • Intragenic deletion
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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