Smarcc1^MommeD19
Chemically induced Allele Detail

Summary

• Symbol: Smarcc1^MommeD19
• Name: SWI/SNF related BAF chromatin remodeling complex subunit C1; modifier of murine metastable epialleles, D19
• MGI ID: MGI:5515368
• Gene: Smarcc1 Location: Chr9:109961129-110069773 bp, + strand Genetic Position: Chr9, 59.87 cM
• Alliance: Smarcc1^MommeD19 page

Mutation origin

• Strain of Origin: FVB/N

Mutation description

• Allele Type: Chemically induced (ENU) (Null/knockout)
• Mutation: Single point mutation
• Mutation details: A T-to-G single point mutation in the exon 10 splice acceptor site is predicted to result in a splicing defect in the mRNA. The encoded protein was not detected on Western blot of embryonic tissue, suggesting that this allele is null. (J:201508)
• Inheritance: Dominant

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 Smarcc1 Mutation: 71 strains or lines available

References

• Original: J:201508 Daxinger L, et al., An ENU mutagenesis screen identifies novel and known genes involved in epigenetic processes in the mouse. Genome Biol. 2013 Sep 11;14(9):R96
• All: 1 reference(s)