Mmadhc^{em1(IMPC)Wtsi}
Endonuclease-mediated Allele Detail

Summary

• Symbol: Mmadhc^{em1(IMPC)Wtsi}
• Name: methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria; endonuclease-mediated mutation 1, Wellcome Trust Sanger Institute
• MGI ID: MGI:6281099
• Gene: Mmadhc Location: Chr2:50169893-50186813 bp, - strand Genetic Position: Chr2, 28.92 cM
• Alliance: Mmadhc^{em1(IMPC)Wtsi} page
• IMPC: Mmadhc gene page

Mutation origin

• Strain of Origin: C57BL/6N
• Project Collection: IMPC

Mutation description

• Allele Type: Endonuclease-mediated (Null/knockout)
• Mutation: Intragenic deletion
• Mutation details: This allele was generated at Wellcome Sanger Institute using Cas9 and guides with spacer sequences AACAATTCCGCAGTCCTATC, ACTTAAGCATGTAAACCGGA, GAACACGGGTTGGTCATACA, and TCGTGTGCTTTGAGATCACC that targeted exon(s) ENSMUSE00001268787.2. This resulted in deletion(s) of 464 bp (location: Chr2:50181168-50181631; GRCm39). This description was generated automatically. Additional molecular information including FASTA sequence support for this allele can be found here: (IMPC Gene page) and viewed in a genome context here: (IMPC Genome Browser). (J:384794)

• Inheritance: Not Specified

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 Mmadhc Mutation: 19 strains or lines available

References

• Original: J:265051 MGI and IMPC, MGI Load of Endonuclease-Mediated Alleles (CRISPR) from the International Mouse Phenotyping Consortium (IMPC). Database Release. 2018-2023
• All: 2 reference(s)