About   Help   FAQ
Relnrl
Spontaneous Allele Detail
Nomenclature
Symbol: Relnrl
Name: reelin; reeler
MGI ID: MGI:1856398
Synonyms: rl, rl-, rlJ, rlnrl
Gene: Reln  Location: Chr5:21884454-22344702 bp, - strand  Genetic Position: Chr5, 9.98 cM, cytoband A3-B1
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: 176 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:  133 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:  264 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 Notice
Send questions and comments to User Support.
last database update
09/22/2020
MGI 6.16
The Jackson Laboratory