Rragb^{tm1.1(NCOM)Chmd}
Targeted Allele Detail

Summary

• Symbol: Rragb^{tm1.1(NCOM)Chmd}
• Name: Ras-related GTP binding B; targeted mutation 1.1, Centre for Modeling Human Disease
• MGI ID: MGI:5766151
• Gene: Rragb Location: ChrX:151922977-151954939 bp, + strand Genetic Position: ChrX, 68.46 cM
• Alliance: Rragb^{tm1.1(NCOM)Chmd} page
• IMPC: Rragb gene page

Mutation origin

• Mutant Cell Line: N01574P1_C_40T_B8
• Germline Transmission: Earliest citation of germline transmission: J:165964
• Parent Cell Line: C2 (Tcp) (ES Cell)
• Strain of Origin: C57BL/6N
• Project Collection: NorCOMM

Mutation description

• Allele Type: Targeted (Null/knockout)
• Mutations: Insertion, Intragenic deletion Vector: L1L2_GOHANU
• Mutation details: The Rragb allele (MGI:4880104) was FLP excised removing the neo selection cassette and lacZ reporter leaving behind the floxed critical exon(s). See https://www.mousephenotype.org/data/genes/MGI:3038613 for more information. (J:165964)

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 Rragb Mutation: 10 strains or lines available

References

• Original: J:165964 Mammalian Functional Genomics Centre, Alleles produced for the NorCOMM project by the Mammalian Functional Genomics Centre (Mfgc), University of Manitoba. MGI Direct Data Submission. 2010
• All: 1 reference(s)