Tc(HSA17)2Mdk
Targeted Allele Detail

Summary

• Symbol: Tc(HSA17)2Mdk
• Name: transchromosomal, human 17, line 2, Michael Koob; transchromosomal, human 17, line 2, Michael D Koob
• MGI ID: MGI:6705045
• Synonyms: MAPT(H1.0)-GR
• Gene: Tc(HSA17)2Mdk Location: unknown Genetic Position: Chr11, Syntenic
• Alliance: Tc(HSA17)2Mdk page

Mutation origin

• Germline Transmission: Earliest citation of germline transmission: J:101977
• Parent Cell Line: PRX-B6N (ES Cell)
• Strain of Origin: C57BL/6NTac

Mutation description

• Allele Type: Targeted (Humanized sequence, Inserted expressed sequence)
• Mutations: Insertion, Intergenic deletion
• Tc(HSA17)2Mdk expresses 2 genes
  Knock-in expresses:
  

  Organism

  Expressed Gene

  Homolog in Mouse

  Note

  human

  MAPT (4137)

  Mapt	(MGI:97180)

  human

  SPPL2C (162540)

  Sppl2c

  (MGI:3045264)

• Mutation details: A 157 kb deletion on mouse chromosome 11 stretching from, but not including, Crhr1 to Kansl1 is replaced by a syntenic 190 kb region from human chromosome 17 (HSA17). The mouse Sppl2c (signal peptide peptidase 2C) and Mapt (microtubule-associated protein tau) genes are replaced by human SPPL2C and MAPT (H1 haplotype) genes. A loxN-flanked neomycin resistance cassette was removed by transient cre expression. (J:101977)

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 3 strains available Cell Lines: 0 lines available
• Carrying any Tc(HSA17)2Mdk Mutation: 3 strains or lines available

References

• Original: J:101977 The Jackson Laboratory, Information obtained from The Jackson Laboratory, Bar Harbor, ME. Unpublished. 2005-2017
• All: 1 reference(s)