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Allele : Del(15Krt7-Krt18)1Tmm deletion, Chr 15, Thomas M Magin 1

Primary Identifier  MGI:4410584 Allele Type  Targeted
Attribute String  Conditional ready, No functional change Gene  Del(15Krt7-Krt18)1Tmm
Transmission  Germline Strain of Origin  129S7/SvEvBrd-Hprt1<b-m2>
Is Recombinase  false Is Wild Type  false
molecularNote  LoxP sites were inserted 5' and 3' of the keratin type II gene cluster, encompassing 0.68 Mb, 26 type II genes and 1 keratin type I gene (Krt18). Cre mediated recombination deleted the entire cluster leaving a single loxP site flanked by 3' and 5' hprt mini-genes and the the tyrosinase (Tyr) and agouti (A) coat color genes. The absence of the transcripts and gene products was confirmed by RT-PCR and immunofluorescence microscopy in homozygous embryos. Due to the absence of all type II keratins, all the type I keratins were sensitive to proteolysis, so homozygous mice lack all 54 keratin proteins. ES cells carrying Krt1ctm1Tmm and Igs11tm1Tmm and were used to create this deletion.
  • mutations:
  • Intragenic deletion,
  • Intergenic deletion,
  • Insertion
  • synonyms:
  • Del(15Krt80-Krt18)1Tmm,
  • KtyII-,
  • KtyII-,
  • Del(15Krt80-Krt18)1Tmm
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1 Feature

Genome

0 Expresses

34 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

10 Publication categories