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kkt
Transgenic Allele Detail
Summary
Symbol: kkt
Name: kyphoscoliosis kinked tail
MGI ID: MGI:2670329
Gene: kkt  Location: unknown  Genetic Position: Chr2, cytoband G-H
Alliance: kkt page
Transgene
origin
Strain of Origin:  (C57BL/6 x CBA)F1
Transgene
description
Transgene Type:    Transgenic
Mutations:    Deletion, Insertion
  kkt involves 1 genes/genome features (kkt) View all
 
Mutation detailsThe kkt mutant mouse was produced by the random insertion of a fusion transgene in which the myogenin promoter was used to direct expression of a human myf5 cDNA-IRESLacZ bicistronic transcript. Heterozygous animals contain about 15 copies of the transgene as determined by Southern blot analysis. Southern blot analysis suggested that a small deletion of less than 10 kb exists at the transgene integration site. (J:60410)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 13 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any kkt Mutation:  0 strains or lines available
References
Original:  J:60410 Bialek P, et al., Characterization of a novel insertional mouse mutation, kkt: A closely linked modifier of Pax1. Dev Biol. 2000 Feb 15;218(2):354-66
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory