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| Nomenclature |
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Symbol:
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Nhlrc1tm1.2Geno
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Name:
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NHL repeat containing 1;
targeted mutation 1.2, Genoway
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MGI ID: |
MGI:5312925 |
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Gene:
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Nhlrc1
Location:
Chr13:47012558-47014850 bp, - strand
Genetic Position: Chr13,
24.5 cM
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Mutation
origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:181559
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Parent Cell Line:
| Not Specified (ES Cell) |
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Strain of Origin:
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129S2/SvPas
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Mutation
description |
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Allele
Type: | |
Targeted (knock-out) |
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Mutations: | |
Insertion, Intragenic deletion |
| |
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Cre-mediated recombination removed the neo cassette and coding exon. (J:181559)
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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 Nhlrc1 Mutation:
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1 strain or line available |
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| References |
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Original: |
J:181559
Criado O et al.,
"Lafora bodies and neurological defects in malin-deficient mice correlate with impaired autophagy."
Hum Mol Genet 2012 Apr 1;21(7):1521-33
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All: |
1 reference(s)
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Analysis Tools
