Summary | Mutation origin | Mutation description | Expression | Phenotypes | Find Mice (IMSR) | References

Symbol:	Syn3tm1.1(KOMP)Vlcg
Name:	synapsin III; targeted mutation 1.1, Velocigene
MGI ID:	MGI:5507835
Gene:	Syn3  Location: Chr10:85890989-86334760 bp, - strand  Genetic Position: Chr10, 41.95 cM, cytoband C2
Alliance:	Syn3tm1.1(KOMP)Vlcg page
IMPC:	Syn3 gene page

Mutant Cell Line:	13871A-D1
Germline Transmission:	Earliest citation of germline transmission: J:188991
Parent Cell Line:	VGB6 (ES Cell)
Strain of Origin:	C57BL/6NTac
Project Collection:	KOMP-Regeneron

Allele Type:    Targeted (Null/knockout, Reporter) Mutations:    Insertion, Intragenic deletion     Vector: ZEN-Ub1   Mutation details: The insertion of Velocigene cassette ZEN-Ub1 created a deletion of size 18415bp between positions 85911617-85930031 of Chromosome 10 (Genome Build37), and subsequent Cre-mediated excision deleted the neomycin selection cassette. (J:136110, J:188991)

View phenotypes and curated references for all genotypes (concatenated display).

In Mice Carrying this Mutation:	43 assay results
In Structures Affected by this Mutation:	3 anatomical structure(s)

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Syn3 Mutation:	35 strains or lines available

Original:	J:188991 The Jackson Laboratory, Alleles produced for the KOMP project by The Jackson Laboratory. MGI Direct Data Submission. 2012;
All:	6 reference(s)