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Smarca5MommeD35
Chemically induced Allele Detail
Summary
Symbol: Smarca5MommeD35
Name: SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 5; modifier of murine metastable epialleles, D35
MGI ID: MGI:5515388
Gene: Smarca5  Location: Chr8:81426572-81466088 bp, - strand  Genetic Position: Chr8, 38.41 cM
Alliance: Smarca5MommeD35 page
Mutation
origin
Strain of Origin:  FVB/N
Mutation
description
Allele Type:    Chemically induced (ENU) (Hypomorph)
Mutation:    Single point mutation
 
Mutation detailsA A-to-G single point mutation in exon 9 is predicted to result in a N341S amino acid substitution in the encoded protein. Reduced amounts of encoded protein were detected on Western blot of embryonic tissue, suggesting that this allele is hypomorphic. (J:201508)
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 Smarca5 Mutation:  49 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)
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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory