Ptprv^{tm1b(NCOM)Mfgc}
Targeted Allele Detail

Summary

• Symbol: Ptprv^{tm1b(NCOM)Mfgc}
• Name: protein tyrosine phosphatase receptor type V; targeted mutation 1b, Mammalian Functional Genomics Centre
• MGI ID: MGI:5513815
• Gene: Ptprv Location: Chr1:135036236-135060313 bp, - strand Genetic Position: Chr1, 58.24 cM, cytoband F-G
• Alliance: Ptprv^{tm1b(NCOM)Mfgc} page
• IMPC: Ptprv gene page

Mutation origin

• Mutant Cell Line: M00020_C_362W_C10
• Germline Transmission: Earliest citation of germline transmission: J:200814
• Parent Cell Line: C2 (Tcp) (ES Cell)
• Strain of Origin: C57BL/6N
• Project Collection: NorCOMM

Mutation description

• Allele Type: Targeted (Null/knockout, Reporter)
• Mutations: Insertion, Intragenic deletion Vector: L1L2_MFGC3
• Mutation details: Cre excision of the tm1a allele removes the promoter-driven neo and critical exon(s) leaving behind the lacZ reporter (J:200814)

Expression

In Structures Affected by this Mutation:

1 anatomical structure(s)

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 1 strain available Cell Lines: 0 lines available
• Carrying any Ptprv Mutation: 30 strains or lines available

References

• Original: J:200814 Toronto Centre for Phenogenomics, Strains and alleles submitted by Toronto Centre for Phenogenomics (NorCOMM2, funded by Genome Canada and Ontario Genomics Institute OGI-051). MGI Direct Data Submission. 2013
• All: 3 reference(s)