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Slitrk5tm2Vlcg
Targeted Allele Detail
Nomenclature
Symbol: Slitrk5tm2Vlcg
Name: SLIT and NTRK-like family, member 5; targeted mutation 2, Velocigene
MGI ID: MGI:4459459
Gene: Slitrk5  Location: Chr14:111675115-111683134 bp, + strand  Genetic Position: Chr14, 57.86 cM, cytoband E3
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:160616
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Targeted (Null/knockout, Reporter)
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 Slitrk5 Mutation:  3 strains or lines available
References
Original:  J:160616 Shmelkov SV, et al., Slitrk5 deficiency impairs corticostriatal circuitry and leads to obsessive-compulsive-like behaviors in mice. Nat Med. 2010 May;16(5):598-602, 1p following 602
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
12/09/2014
MGI 5.20
The Jackson Laboratory