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Mrpl3dcr
Spontaneous Allele Detail
Nomenclature
Symbol: Mrpl3dcr
Name: mitochondrial ribosomal protein L3; decrepit
MGI ID: MGI:4938306
Synonyms: dcr
Gene: Mrpl3  Location: Chr9:105053268-105077466 bp, + strand  Genetic Position: Chr9, Syntenic
Mutation
origin
Strain of Origin:  B6.Cg-Ptprca H60ac
Mutation
description
Allele Type:    Spontaneous (Hypomorph)
Mutation:    Insertion
 
Mutation detailsThis spontaneous hypomorph has an approximately 133 bp insertion containing an extensive T repeat inserted into the intron between exons 6 and 7. (J:289566)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 4 anatomical structures
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 Mrpl3 Mutation:  1 strain or line available
References
Original:  J:167846 Sproule TJ, et al., A mouse model of heritable cerebrovascular disease. PLoS One. 2010;5(12):e15327
All:  2 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
04/13/2021
MGI 6.16
The Jackson Laboratory