This loxP flanked allele from project Loxl1-6513J-101P2M(2R)was generated at The Jackson Laboratory by injecting Cas9 RNA and 2 guide sequences, GAATGGCATGCCACAAGTAA and TCAGATACTTTGCCAGACTC, along with a plasmid containing 2618 bp of Loxl1 sequence comprised of 1 kb 5-prime and 3-prime homology arms with two 60 bp-cassettes flanking exon 2 that contain a loxP site, HindIII cut site, and an additional unique 20 bp sequence as a sequencing primer. This allele shows a complete integration of the Loxl1 2618 bp sequence by homologous recombination beginning in Chromosome 9 negative strand position 58,298,994 bp CATGACTCAAGCACCCCATCTTTAC, and ending after GGACTATCTTAAGTGCCCAGC at 58,296,497 bp (GRCm38), resulting in a loxP flanked exon 2. It is predicted that mating this strain with cre will generate a deletion of exon 2 causing a change of amino acid sequence after amino acid 400 and early truncation 22 amino acids later. (J:188991)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
C57BL/6NJ
Endonuclease-mediated
Insertion
Not Specified
1
1
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Phenotypes

Legend:
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes:
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Phenotypes

References Literature

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PMID
Journal
Year
IF
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