This allele from project Lgals4-7682J-F3313 was generated at The Jackson Laboratory by injecting Cas9 RNA and 4 guide sequences ACTCTCAGTCCCTTAAGCGG, GACCAGGTGAAGAGCCTCAG, GCACTTCCCCGCTCACCCCA and TCCCTAACTCTGATGCCAGG, which resulted in a 278 bp deletion in exon 2 beginning at Chromosome 7 positive strand position 28,834,332 bp, CTCCTTACCCTAAGTCTCAT, and ending after TTCCCTAACTCTGATGCCAG at 28,834,609 bp (GRCm38/mm10). This mutation deletes exon 2 and 189 bp of flanking intronic sequence including the splice acceptor and donor, and is predicted to cause a change of amino acid sequence after residue 15 and early truncation 10 amino acids later. (J:188991)

Basic Information

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

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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