About   Help   FAQ
Relnrl
Spontaneous Allele Detail
Summary
Symbol: Relnrl
Name: reelin; reeler
MGI ID: MGI:1856398
Synonyms: rl, rl-, rlJ, rlnrl
Gene: Reln  Location: Chr5:22089452-22549700 bp, - strand  Genetic Position: Chr5, 9.98 cM, cytoband A3-B1
Alliance: Relnrl page
The Relnrl/Relnrl mouse

Show the 2 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  "snowy-bellied" stock or unspecified inbred strain
Mutation
description
Allele Type:    Spontaneous
Mutation:    Intergenic deletion
 
Mutation detailsThis allele comprises an apprxomately 126.7 kb deletion that has a breakpoint in an intron of reelin and removes coding sequence downstream of cDNA nucleotide 3619. No reelin mRNA is detected in homozygotes. (J:24458, J:24459)
Inheritance:    Recessive
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Disease models
Loading...
Expression
In Mice Carrying this Mutation: 181 assay results
In Structures Affected by this Mutation: 13 anatomical structures
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 3 strains available      Cell Lines: 0 lines available
Carrying any Reln Mutation:  136 strains or lines available
Notes
Early studies were summarized and critically reviewed by Goffinet (J:12281).
References
Original:  J:13038 Falconer DS, Two new mutants, "trembler" and "reeler," with neurological actions in the house mouse. J Genet. 1951;50(2):192-201
All:  280 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, Copyright, and Privacy Statement
Send questions and comments to User Support.
last database update
11/22/2022
MGI 6.22
The Jackson Laboratory