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Sycntm1(KOMP)Vlcg
Targeted Allele Detail
Nomenclature
Symbol: Sycntm1(KOMP)Vlcg
Name: syncollin; targeted mutation 1, Velocigene
MGI ID: MGI:5051060
Gene: Sycn  Location: Chr7:28540885-28542209 bp, + strand  Genetic Position: Chr7, 16.83 cM, cytoband A3
Mutation
origin
Mutant Cell Lines:  16817A-A4, 16817A-A10, 16817A-B1, 16817A-B2, 16817A-B10, 16817A-F12
Germline Transmission:  Unknown
Parent Cell Line:  VGB6 (ES Cell)
Strain of Origin:  C57BL/6NTac
Project Collection: KOMP-Regeneron
Mutation
description
Allele Type:    Targeted (Null/knockout, Reporter)
Mutations:    Insertion, Intragenic deletion     Vector: ZEN-Ub1
 
Mutation detailsThe insertion of Velocigene cassette ZEN-Ub1 created a deletion of size 1212bp between positions 29325932-29327143 of Chromosome 7 (Genome Build37). (J:136110)
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: 1 line available
Carrying any Sycn Mutation:  2 strains or lines available
References
Original:  J:136110 Velocigene, Alleles produced for the KOMP project by Velocigene (Regeneron Pharmaceuticals). MGI Direct Data Submission. 2008;
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
01/14/2020
MGI 6.14
The Jackson Laboratory