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| Nomenclature |
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Symbol:
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Rtn4rrgsc1836
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Name:
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reticulon 4 receptor;
RIKEN Genomic Sciences Center, 1836
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MGI ID: |
MGI:5293442 |
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Synonyms: |
Rtn4r-R189H |
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Gene:
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Rtn4r
Location:
Chr16:18127642-18152408 bp, + strand
Genetic Position: Chr16,
11.23 cM, cytoband B1
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Mutation
origin |
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Strain of Origin:
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C57BL/6JJcl
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Mutation
description |
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Allele
Type: | |
Chemically induced (ENU) |
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Mutation: | |
Single point mutation |
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Mutation details: ENU mutagenesis induced a G to A transition that results in the amino acid substitution of histidine for arginine at position 189 (R189H). (J:176996)
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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Disease models
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available |
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Carrying any Rtn4r Mutation:
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6 strains or lines available |
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| References |
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Original: |
J:176996
Lazar NL et al.,
"Missense mutation of the reticulon-4 receptor alters spatial memory and social interaction in mice."
Behav Brain Res 2011 Oct 10;224(1):73-9
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All: |
1 reference(s)
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Analysis Tools
