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Nhlrc1tm1.2Geno
Targeted Allele Detail
Nomenclature
Symbol: Nhlrc1tm1.2Geno
Name: NHL repeat containing 1; targeted mutation 1.2, Genoway
MGI ID: MGI:5312925
Gene: Nhlrc1  Location: Chr13:47012558-47014850 bp, - strand  Genetic Position: Chr13, 24.5 cM
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:181559
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  129S2/SvPas
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
    Cre-mediated recombination removed the neo cassette and coding exon. (J:181559)
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Disease models
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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 Nhlrc1 Mutation:  1 strain or line available
References
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
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/11/2014
MGI 5.20
The Jackson Laboratory