About   Help   FAQ
Smchd1MommeD1
Chemically induced Allele Detail
Summary
Symbol: Smchd1MommeD1
Name: SMC hinge domain containing 1; modifiers of murine metastable epiallele D1
MGI ID: MGI:3586547
Gene: Smchd1  Location: Chr17:71651484-71782338 bp, - strand  Genetic Position: Chr17, 41.87 cM
Alliance: Smchd1MommeD1 page
Mutation
origin
Strain of Origin:  FVB/N
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsMice carrying Tg(Hba1-Gfp)1Ew were treated with ENU. A cytosine to thymine transition in exon 23 results in a nonsense codon. (J:142334)
Inheritance:    Semidominant
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 72 assay results
6 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation: 1 anatomical structure(s)
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 Smchd1 Mutation:  144 strains or lines available
References
Original:  J:99816 Blewitt ME, et al., An N-ethyl-N-nitrosourea screen for genes involved in variegation in the mouse. Proc Natl Acad Sci U S A. 2005 May 24;102(21):7629-34
All:  15 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
12/10/2024
MGI 6.24
The Jackson Laboratory