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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 details: Mice 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
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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)
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Funding Information
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Send questions and comments to User Support. 		last database update
11/19/2024
MGI 6.24 		The Jackson Laboratory