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Relnctrdel
Chemically induced Allele Detail
Summary
Symbol: Relnctrdel
Name: reelin; C-terminal deletion
MGI ID: MGI:5505412
Synonyms: line 13, RelnCTRdel
Gene: Reln  Location: Chr5:22089452-22549700 bp, - strand  Genetic Position: Chr5, 9.98 cM, cytoband A3-B1
Alliance: Relnctrdel page
Mutation
origin
Strain of Origin:  A/J
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsEight week old A/J male mice were treated weekly for three weeks with ENU. After several weeks of recovery, mice were crossed to C57BL/6 females with or without a lacZ reporter. Resulting females were backrossed to their fathers and subjected to phenotype screening. A 42 bp insertion was found after exon 63 due to a T to C mutation at the exon 63 distal splice junction. Five amino acids and a stop codon were added and the 33 terminal amino acids were lost. (J:199782)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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:199782 Ha S, et al., A forward genetic screen in mice identifies mutants with abnormal cortical patterning. Cereb Cortex. 2015 Jan;25(1):167-79
All:  3 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
10/29/2024
MGI 6.24
The Jackson Laboratory