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Allele : Khdrbs2<Tg(LRRK2*R1441G)135Cjli> KH domain containing, RNA binding, signal transduction associated 2; transgene insertion 135, Chenjian Li

Primary Identifier  MGI:3847811 Allele Type  Transgenic
Attribute String  Humanized sequence, Inserted expressed sequence, Null/knockout Gene  Khdrbs2
Strain of Origin  FVB/NTac 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 (4321C>G) mutation associated with autosomal dominant, late-onset Parkinson's disease originally identified in Spanish families originating from the Basque region. Line 135 inserted into an intron of the gene at 32289302-32289738 (Build GRCm38/mm10) resulting in a 436 bp deletion. The deletion results in a functional knock-out of Khdrbs2 in homozygous mice. Founder line 135 has a copy number of greater than 5.
  • mutations:
  • Insertion,
  • Intragenic deletion
  • synonyms:
  • TG-RP135,
  • TG-RP135,
  • LRRK2<R1441G>,
  • LRRK2<R1441G>
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1 Feature

Trail: Allele

Genome

1 Expresses

Trail: Allele

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

2 Carried By

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0 Driven By

19 Publication categories

Trail: Allele