Clmn^{tm1c(EUCOMM)Wtsi}
Targeted Allele Detail

Summary

• Symbol: Clmn^{tm1c(EUCOMM)Wtsi}
• Name: calmin; targeted mutation 1c, Wellcome Trust Sanger Institute
• MGI ID: MGI:5513755
• Gene: Clmn Location: Chr12:104729376-104831335 bp, - strand Genetic Position: Chr12, 54.91 cM, cytoband F1
• Alliance: Clmn^{tm1c(EUCOMM)Wtsi} page
• IMPC: Clmn gene page

Mutation origin

• Mutant Cell Line: EPD0330_2_H12
• Germline Transmission: Earliest citation of germline transmission: J:200814
• Parent Cell Line: JM8A1.N3 (ES Cell)
• Strain of Origin: C57BL/6N-A^tm1Brd
• Project Collection: EUCOMM

Mutation description

• Allele Type: Targeted (Conditional ready)
• Mutation: Insertion Vector: L1L2_Bact_P
• Mutation details: Flp excision of MGI:4432753 tm1a allele removes the lacZ/neo cassette leaving behind a loxP-flanked critical exon(s) (J:200814)

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 Clmn Mutation: 38 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: 1 reference(s)