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Gt(ROSA)26Sortm2(SNCA*119)Djmo
Targeted Allele Detail

Nomenclature
Symbol: Gt(ROSA)26Sortm2(SNCA*119)Djmo
Name: gene trap ROSA 26, Philippe Soriano; Targeted mutation 2, Darren Moore
MGI ID: MGI:3840596
Synonyms: ROSA26-a-synuclein C-terminal truncation variant (Syn119), ROSA26-Syn119, ROSA26-SynCT119Tg
Gene: Gt(ROSA)26Sor   Location: unknown     Genetic Position: Chr6, 48.7 cM
Mutation
origin
Germline Transmission: Earliest citation of germline transmission: J:147331
Parent Cell Line: Other (see notes) (ES Cell)
Strain of Origin: 129
Mutation
description
Allele Type: Targeted (knock-in)
Mutation: Insertion
  A targeting vector was designed with an SV40 splice acceptor, a loxP-flanked STOP cassette (PGK-neo and triple SV40 transcriptional termination sequence), a cDNA encoding the 119 amino acid C-terminal truncation of human alpha-synuclein associated with familial Parkinson's disease (Syn119 or SynCT119; encoding amino acids 1-119 of the full length protein), and a bovine polyadenylation signal. (J:147331, J:150777)
Find Mice (IMSR) 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 Gt(ROSA)26Sor Mutation: 90 strains or lines available
Phenotype
summary
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Phenotype Summary by Mammalian Phenotype terms

(show or hide all annotated terms)

Genotypes are listed in the next section.

      Key:  
hm homozygous ht heterozygous
cn conditional genotype  cx complex: > 1 genome feature
tg involves transgenes ot other: hemizygous, indeterminate,...
N normal phenotype expected model not found
Affected SystemsGenotypes:
 
cn1
 
cn2
 
cn3
 
cn4
  
homeostasis/metabolism          
  
  
nervous system          
  
  
normal phenotype          
N  N
 
  
Disease Models          
  
Phenotypic
data by
genotype
Phenotypic Data by Genotype

(show or hide all phenotypic details)

GenotypeAllelic CompositionGenetic Background
  
 cn1   
Gt(ROSA)26Sortm2(SNCA*119)Djmo/Gt(ROSA)26Sortm2(SNCA*119)Djmo involves: 129 * C57BL/6J
  
 cn2   Disease Model  
Gt(ROSA)26Sortm2(SNCA*119)Djmo/Gt(ROSA)26Sortm2(SNCA*119)Djmo
Tg(Th-cre)1Tmd/0
involves: 129 * C57BL/6
  
 cn3   Disease Model  
Gt(ROSA)26Sortm2(SNCA*119)Djmo/Gt(ROSA)26Sortm2(SNCA*119)Djmo
Tg(Th-cre)1Tmd/0
involves: 129 * C57BL/6 * SJL
  
 cn4   
Gt(ROSA)26Sortm2(SNCA*119)Djmo/Gt(ROSA)26Sor+
Tg(Nes-cre)1Kln/0
involves: 129 * C57BL/6 * SJL
Disease
models
Mouse Models
of Human Disease
NoteGenotypeRef(s)
 
Allelic Composition
Genetic Background
Models with phenotypic similarity to human diseases associated with genes lacking mouse orthologs, or diseases of unknown human etiology.
Parkinson Disease; PD
OMIM ID: 168600
1
 
cn3
Gt(ROSA)26Sortm2(SNCA*119)Djmo/Gt(ROSA)26Sortm2(SNCA*119)Djmo
Tg(Th-cre)1Tmd/0
involves: 129 * C57BL/6 * SJLJ:150777
1
 
cn2
Gt(ROSA)26Sortm2(SNCA*119)Djmo/Gt(ROSA)26Sortm2(SNCA*119)Djmo
Tg(Th-cre)1Tmd/0
involves: 129 * C57BL/6J:150777
1Conditionally targeted allele(s).
Notes Authors state that 129/SvJ-derived embryonic stem cells were used.
References
Original: J:147331 Moore D, "Generation of a conditional knockin allele expresing a truncated human alpha-synuclein (SNCA)" MGI Direct Data Submission 2009;():
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
11/20/2009
MGI_4.31
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