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Spg20tm1.1Xen
Targeted Allele Detail
Nomenclature
Symbol: Spg20tm1.1Xen
Name: spastic paraplegia 20, spartin (Troyer syndrome) homolog (human); targeted mutation 1.1, Taconic Biosciences
MGI ID: MGI:5430946
Gene: Spg20  Location: Chr3:55112108-55137322 bp, + strand  Genetic Position: Chr3, 26.53 cM
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:185987
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation details
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 Spg20 Mutation:  6 strains or lines available
References
Original:  J:185987 Renvoise B, et al., Spg20-/- mice reveal multimodal functions for Troyer syndrome protein spartin in lipid droplet maintenance, cytokinesis and BMP signaling. Hum Mol Genet. 2012 Aug 15;21(16):3604-18
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
08/26/2014
MGI 5.19
The Jackson Laboratory