|  Help  |  About  |  Contact Us

Allele : Chchd5<tm1(KOMP)Wtsi> coiled-coil-helix-coiled-coil-helix domain containing 5; targeted mutation 1, Wellcome Trust Sanger Institute

Primary Identifier  MGI:4419215 Allele Type  Targeted
Attribute String  Null/knockout, Reporter Gene  Chchd5
Transmission  Cell Line Strain of Origin  C57BL/6N-A<tm1Brd>
Is Recombinase  false Is Wild Type  false
Project Collection  KOMP-CSD
molecularNote  The insertion of the L1L2_Bact_P cassette created a deletion of size 407 starting at position 128972096 and ending at position 128972503 of Chromosome 2 (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
Quick Links:
 
Quick Links:
 

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