About   Help   FAQ
Smchd1MommeD36
Chemically induced Allele Detail
Summary
Symbol: Smchd1MommeD36
Name: SMC hinge domain containing 1; modifier of murine metastable epialleles, D36
MGI ID: MGI:5515389
Gene: Smchd1  Location: Chr17:71651484-71782338 bp, - strand  Genetic Position: Chr17, 41.87 cM
Alliance: Smchd1MommeD36 page
Mutation
origin
Strain of Origin:  FVB/N
Mutation
description
Allele Type:    Chemically induced (ENU) (Null/knockout)
Mutation:    Single point mutation
 
Mutation detailsA C-to-T single point mutation in exon 42 is predicted to result in a Q1732 to a stop codon in the encoded protein. The encoded protein was not detected on Western blot of embryonic tissue, suggesting that this allele is null. (J:201508)
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 Smchd1 Mutation:  146 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)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
12/30/2025
MGI 6.24
The Jackson Laboratory