|  Help  |  About  |  Contact Us

Allele : Tg(LRRK2*R1441G)3IMjff transgene insertion 3I, The Michael J Fox Foundation

Primary Identifier  MGI:5466850 Allele Type  Transgenic
Attribute String  Humanized sequence, Inserted expressed sequence Gene  Tg(LRRK2*R1441G)3IMjff
Strain of Origin  C57BL/6J Is Recombinase  false
Is Wild Type  false
molecularNote  A human bacterial artificial chromosome (BAC) library (CHORI) was used to obtain a 188 kb BAC containing the entire human LRRK2 (leucine-rich repeat kinase 2) gene with 29 kb upstream of the LRRK2 start codon and 42 kb downstream of the LRRK2 stop codon. Bioinformatics analysis predicted that no other genes are present in the BAC. This BAC was modified by targeted mutation of the LRRK2 locus to harbor the LRRK2 R1441G (4321 C>G) mutation associated with autosomal dominant, late-onset Parkinson's disease originally identified in Spanish families originating from the Basque region. Transgene insertion occurred on Chr 1, causing a 39,855 bp deletion.
  • mutations:
  • Nucleotide substitutions,
  • Intergenic deletion,
  • Insertion
  • synonyms:
  • Tg(LRRK2*R1441G)3IGrsr,
  • Tg(LRRK2*R1441G)3IGrsr
Quick Links:
 
Quick Links:
 

1 Feature

Trail: Allele

Genome

1 Expresses

Trail: Allele

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

Trail: Allele

0 Driven By

4 Publication categories

Trail: Allele