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SpastM1Gri
Chemically induced Allele Detail
Nomenclature
Symbol: SpastM1Gri
Name: spastin; mutation 1, Andrew J Grierson
MGI ID: MGI:3813522
Synonyms: SpastdeltaE7
Gene: Spast  Location: Chr17:74338987-74391113 bp, + strand  Genetic Position: Chr17, 45.64 cM, cytoband E3
Mutation
origin
Strain of Origin:  BALB/cAnN
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation details
Inheritance:    Dominant
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 Spast Mutation:  7 strains or lines available
References
Original:  J:148877 Kasher PR, et al., Direct evidence for axonal transport defects in a novel mouse model of mutant spastin-induced hereditary spastic paraplegia (HSP) and human HSP patients. J Neurochem. 2009 Apr 22;
All:  2 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
04/08/2014
MGI 5.17
The Jackson Laboratory