Btbd9^{tm1d(EUCOMM)Wtsi}
Targeted Allele Detail

Summary

• Symbol: Btbd9^{tm1d(EUCOMM)Wtsi}
• Name: BTB domain containing 9; targeted mutation 1d, Wellcome Trust Sanger Institute
• MGI ID: MGI:6488232
• Gene: Btbd9 Location: Chr17:30434498-30795462 bp, - strand Genetic Position: Chr17, 15.62 cM, cytoband B1
• Alliance: Btbd9^{tm1d(EUCOMM)Wtsi} page

Mutation origin

• Mutant Cell Line: EPD0631_3_A09
• Germline Transmission: Earliest citation of germline transmission: J:282582
• Parent Cell Line: JM8A3.N1 (ES Cell)
• Strain of Origin: C57BL/6N-A^tm1Brd

Mutation description

• Allele Type: Targeted (Null/knockout)
• Mutations: Insertion, Intragenic deletion Vector: L1L2_Bact_P
• Mutation details: Cre-mediated excision of the floxed B9d1^{tm1c(EUCOMM)Wtsi} allele removed exon 4. (J:282582)

Disease models

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 Btbd9 Mutation: 51 strains or lines available

References

• Original: J:282582 Lyu S, et al., The role of BTBD9 in the cerebral cortex and the pathogenesis of restless legs syndrome. Exp Neurol. 2020 Jan;323:113111
• All: 4 reference(s)