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Relnrl
Spontaneous Allele Detail

Nomenclature
Symbol: Relnrl
Name: reelin; reeler
MGI ID: MGI:1856398
Synonyms: rl, rl-, rlJ
Gene: Reln   Location: Chr5:21390272-21850520 bp, - strand    Genetic Position: Chr5, 8.0 cM, cytoband A3-B1
The Relnrl/Relnrl mouse

Show the 2 image(s) involving this allele.

Mutation
origin
Strain of Origin: "snowy-bellied" stock and unspecified inbred strain
Mutation
description
Allele Type: Spontaneous
Mutation: Deletion
  This allele comprises, minimally, a 150 kb deletion between D5Mit61 and D5Mit72. (J:24458)
Inheritance: Recessive
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: 10 strains or lines available
Expression
In Mice Carrying this Mutation: 39 assay results
Phenotype
summary
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Phenotype Summary by Mammalian Phenotype terms

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Genotypes are listed in the next section.

      Key:  
hm homozygous ht heterozygous
cn conditional genotype  cx complex: > 1 genome feature
tg involves transgenes ot other: hemizygous, indeterminate,...
N normal phenotype expected model not found
Affected SystemsGenotypes:
 
hm1
 
hm2
 
hm3
 
hm4
 
ht5
 
cn6
 
cn7
 
cn8
 
cx9
 
cx10
  
behavior/neurological          
       
  
digestive/alimentary system          
         
  
growth/size          
       
  
lethality/postnatal          
         
  
life span/aging          
        
  
nervous system          
 N
  
reproductive system          
        
  
skin/coat/nails          
         
Phenotypic
data by
genotype
Phenotypic Data by Genotype

(show or hide all phenotypic details)

GenotypeAllelic CompositionGenetic Background
  
 hm1   
Relnrl/Relnrl B6.Cg-Relnrl
  
 hm2   
Relnrl/Relnrl C3.Cg-Relnrl
  
 hm3   
Relnrl/Relnrl involves: 129S4/SvJaeSor * C57BL/6J
  
 hm4   
Relnrl/Relnrl Not Specified
  
 ht5   
Relnrl/Reln+ involves: BALB/c
  
 cn6   
Gt(ROSA)26Sortm1(DTA)Riet/Gt(ROSA)26Sor+
Relnrl/Reln+
Trp73tm1(cre)Agof/Trp73+
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ
  
 cn7   
Gt(ROSA)26Sortm1(DTA)Riet/Gt(ROSA)26Sor+
Relnrl/Reln+
Wnt3atm1(cre)Eag/Wnt3a+
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ
  
 cn8   
Gt(ROSA)26Sortm1(DTA)Riet/Gt(ROSA)26Sor+
Relnrl/Reln+
Trp73tm1(cre)Agof/Trp73+
Wnt3atm1(cre)Eag/Wnt3a+
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ
  
 cx9   
Dab1tm1Cpr/Dab1tm4Cpr
Relnrl/Reln+
involves: 129/Sv * C3HeB/Fe * C57BL/6
  
 cx10   
Dab1tm3.1Cpr/Dab1tm3.1Cpr
Relnrl/Reln+
involves: 129S4/SvJaeSor * C57BL/6J
Notes Relnrl, reeler, recessive. The reeler mutation was identified by Falconer (J:13038) as a spontaneous mutation in a mildly inbred stock. Reeler homozygotes are unable to keep their hindquarters upright and frequently fall over on their sides when walking or running. Viability and fertility are much reduced, particularly when the gene is on an inbred genetic background, but viability is greatly improved on a hybrid background, and an occasional female or rarely a male may breed (J:5312). Healthy reeler mice have fairly normal behavior except for difficulties in locomotion (J:5359). The neuropathology of Relnrl/Relnrl mice has been studied very extensively. These studies were summarized and critically reviewed by Goffinet (J:12281). Briefly, the cerebellum is greatly reduced in size, and the typical organization and lamination of the cerebellar cortex, the cerebral cortex, and the hippocampus are altered. Abnormal arrangement of neurons is also seen in other brain structures. Autoradiographic studies of development of the cerebral cortex in reelers have shown that the different classes of neurons take their origin from the ependymal layer at the normal time but migrate abnormally and come to rest in abnormal relations to each other (J:12728). The earliest cortical neurons may be overly adhesive and may block migration of later neurons (J:26896). The abnormal arrangement of neurons in other parts of the brain is the result of a similar abnormal pattern of migration. In spite of abnormal location of the neurons and also their greatly reduced number in the cerebellum, relatively normal cell connections are established. Chimeras produced by fusion between Relnrl/Relnrl and +/+ embryos indicated that factors extrinsic to the abnormally positioned Purkinje cells were defective in reeler (J:15345).
References
Original: J:13038 Falconer DS, "Two new mutants, "trembler" and "reeler," with neurological actions in the house mouse." J Genet 1951;50():192-201
All: 168 reference(s)

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last database update
11/20/2009
MGI_4.31
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