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| Nomenclature |
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Symbol:
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Leprbrta
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Name:
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leptin receptor;
alberta
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MGI ID: |
MGI:3847119 |
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Gene:
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Lepr
Location:
Chr4:101717404-101815352 bp, + strand
Genetic Position: Chr4,
46.96 cM
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Mutation
origin |
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Strain of Origin:
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C57BL/6Apb
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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: The splice donor site at the exon 10/intron 10-11 boundary, following the triplet coding for valine at amino acid position 532, has been mutated to CGTAGGT/CACG. (J:104190)
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Inheritance: | |
Recessive |
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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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| References |
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Original: |
J:104190
The Australian Phenomics Facility at The Australian National University,
"Heritable mouse mutants from the ENU mutagenesis program at the Australian Phenomics Facility at The Australian National University"
MGI Direct Data Submission 2006-2010;():
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All: |
1 reference(s)
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Analysis Tools
