Rnf216^{tm1d(EUCOMM)Wtsi}
Targeted Allele Detail

Summary

• Symbol: Rnf216^{tm1d(EUCOMM)Wtsi}
• Name: ring finger protein 216; targeted mutation 1d, Wellcome Trust Sanger Institute
• MGI ID: MGI:7705851
• Gene: Rnf216 Location: Chr5:142976648-143098749 bp, - strand Genetic Position: Chr5, 81.86 cM, cytoband G2
• Alliance: Rnf216^{tm1d(EUCOMM)Wtsi} page
• IMPC: Rnf216 gene page

Mutation origin

• Germline Transmission: Earliest citation of germline transmission: J:352248
• Parent Cell Line: JM8A3.N1 (ES Cell)
• Strain of Origin: C57BL/6N-A^tm1Brd
• Project Collection: EUCOMM

Mutation description

• Allele Type: Targeted (Null/knockout)
• Mutation: Intragenic deletion
• Mutation details: The L1L2_Bact_P cassette was inserted at position 143074473 of Chromosome 5 upstream of the critical exon(s) (Build GRCm39). The cassette is composed of an FRT site followed by lacZ sequence and a loxP site. This first loxP site is followed by a neomycin resistance gene under the control of the human beta-actin promoter, SV40 polyA, a second FRT site and a second loxP site. A third loxP site is inserted downstream of the targeted exon(s) at position 143077547. The critical exon(s) is/are thus flanked by loxP sites. A null/knockout allele was created by flp and cre recombinase expression in mice carrying this allele to remove the lacZ sequence, neo selection cassette and the loxP-flanked critical exon(s). Further information on targeting strategies used for this and other IKMC alleles can be found at http://www.informatics.jax.org/mgihome/nomen/IKMC_schematics.shtml (J:352248)

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 Rnf216 Mutation: 54 strains or lines available

References

• Original: J:352248 George AJ, et al., Gordon Holmes Syndrome Model Mice Exhibit Alterations in Microglia, Age, and Sex-Specific Disruptions in Cognitive and Proprioceptive Function. eNeuro. 2024 Jan;11(1):ENEURO.0074-23.2023
• All: 1 reference(s)