Ttll3^{tm1b(EUCOMM)Wtsi}
Targeted Allele Detail

Summary

• Symbol: Ttll3^{tm1b(EUCOMM)Wtsi}
• Name: tubulin tyrosine ligase-like family, member 3; targeted mutation 1b, Wellcome Trust Sanger Institute
• MGI ID: MGI:6383655
• Gene: Ttll3 Location: Chr6:113366221-113391548 bp, + strand Genetic Position: Chr6, 52.76 cM
• Alliance: Ttll3^{tm1b(EUCOMM)Wtsi} page
• IMPC: Ttll3 gene page

Mutation origin

• Mutant Cell Line: EPD0058_5_D03
• Germline Transmission: Earliest citation of germline transmission: J:249732
• Parent Cell Line: JM8.F6 (ES Cell)
• Strain of Origin: C57BL/6N
• Project Collection: EUCOMM

Mutation description

• Allele Type: Targeted (Null/knockout, Reporter)
• Mutations: Insertion, Intragenic deletion Vector: L1L2_gt0
• Mutation details: The L1L2_gt0 cassette was inserted at position 113375266 of Chromosome 6 upstream of exon 6 (Build GRCm39). The cassette is composed of an FRT flanked lacZ/neomycin sequence followed by a loxP site. An additional loxP site is inserted downstream of exon 6 at position 113376103. Exon 6 is thus flanked by loxP sites. This reporter knockout allele was created through subsequent cre-mediated recombination. (J:249732)

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 Ttll3 Mutation: 84 strains or lines available

References

• Original: J:249732 Bosch Grau M, et al., Alterations in the balance of tubulin glycylation and glutamylation in photoreceptors leads to retinal degeneration. J Cell Sci. 2017 Mar 01;130(5):938-949
• All: 1 reference(s)