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Smarca5MommeD4
Chemically induced Allele Detail
Summary
Symbol: Smarca5MommeD4
Name: SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 5; modifiers of murine metastable epiallele D4
MGI ID: MGI:3586551
Gene: Smarca5  Location: Chr8:81426572-81466088 bp, - strand  Genetic Position: Chr8, 38.41 cM
Alliance: Smarca5MommeD4 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 single T1921A point mutation in exon 12 results in a W520R amino acid residue change in the helicase domain. (J:122400)
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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 Smarca5 Mutation:  49 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:  3 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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last database update
10/29/2024
MGI 6.24
The Jackson Laboratory