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Allele : Ahcy<tm1(NCOM)Cmhd> S-adenosylhomocysteine hydrolase; targeted mutation 1, Centre for Modeling Human Disease

Primary Identifier  MGI:4880030 Allele Type  Targeted
Attribute String  Null/knockout, Reporter Gene  Ahcy
Transmission  Cell Line Strain of Origin  C57BL/6N
Is Recombinase  false Is Wild Type  false
Project Collection  NorCOMM
molecularNote  The insertion of NorCOMM cassette pNTARU created a deletion of size 392bp between positions 154910647-154911039 of Chromosome 2 (Build GRCm39). This deletion results in the removal of functionally critical exon(s). The cassette is composed of an F3 site followed by a universal inverse PCR primer site and a splice acceptor lacZ-neomycin phosphotransferase fusion (beta-geo) sequence. This is followed by a PhiC31 attP site and a puromycin sequence that is not active unless a promoter is inserted by PhiC31 at the attP site. The cassette is finished with an FRT site. Variations of this allele can be made using PhiC31 docking and subsequent cloning (Nagy et al., 2009. Methods Mol. Biol. 530:365-78).
  • mutations:
  • Intragenic deletion,
  • Insertion
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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