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Mcm4Sdla
Spontaneous Allele Detail
Summary
Symbol: Mcm4Sdla
Name: minichromosome maintenance complex component 4; Spontaneous dominant leukemia
MGI ID: MGI:5473704
Synonyms: Mcm4D573H, Sdl
Gene: Mcm4  Location: Chr16:15441761-15455264 bp, - strand  Genetic Position: Chr16, 10.09 cM, cytoband B1
Alliance: Mcm4Sdla page
Mutation
origin
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Spontaneous
Mutation:    Single point mutation
 
Mutation detailsA spontaneous mutation in mice carrying Gt(ROSA)26Sortm1(sb11)Njen produces G-to-C transversion that results in the amino acid substitution of aspartic acid with histidine at position 573 (p.D573H). Western blot analysis confirmed protein expression in mouse embryonic fibroblasts. (J:194117)
Inheritance:    Dominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 1 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation: 3 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 Mcm4 Mutation:  42 strains or lines available
References
Original:  J:194117 Bagley BN, et al., A dominantly acting murine allele of Mcm4 causes chromosomal abnormalities and promotes tumorigenesis. PLoS Genet. 2012;8(11):e1003034
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
04/16/2024
MGI 6.23
The Jackson Laboratory