About   Help   FAQ
Relnrl-od
Spontaneous Allele Detail
Summary
Symbol: Relnrl-od
Name: reelin; reeler odense
MGI ID: MGI:2156492
Gene: Reln  Location: Chr5:22089452-22549700 bp, - strand  Genetic Position: Chr5, 9.98 cM, cytoband A3-B1
Alliance: Relnrl-od page
Mutation
origin
Strain of Origin:  C57BL/6 x DBA/2
Mutation
description
Allele Type:    Spontaneous (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsA spontaneous mutant found to be allelic to Relnrl-Ord by complementation testing. The mutation was identified as a 24 kb deletion that comprises exons 13-20. Northern and western blot analysis confirmed the absence of expression in homozygotes. (J:79979)
Inheritance:    Recessive
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 5 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 Reln Mutation:  209 strains or lines available
References
Original:  J:79979 Andersen TE, et al., A reeler mutant mouse with a new, spontaneous mutation in the reelin gene. Brain Res Mol Brain Res. 2002 Sep 30;105(1-2):153-6
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/23/2024
MGI 6.23
The Jackson Laboratory