This allele was generated at The Jackson Laboratory by electroporating Cas9 protein and 4 guide sequences AGTGCACCTCTCTTTTCAGG, GGGCAAGTTTCACCCTTTGG, CAATGTTGCAAACACAAAGG and GGGTGGAGCTTAGGGCCTTT, which resulted in a 237 bp deletion beginning at Chromosome 10 position 128,380,503 bp and ending after 128,380,739 bp (GRCm38/mm10). This mutation deletes ENSMUSE00001261771 (exon 6) and 149 bp of flanking intronic sequence including the splice acceptor and donor. In addition, there is a 33 bp deletion (TTTGGGGGTGGAGCTTAGGGCCTTTGGGTTTAC) 58 bp after the exon deletion and a 4 bp insertion (GTCC) at the exon deletion site, that will not alter the results of the exon deletion. This mutation is predicted to cause a change of amino acid sequence after residue 154 and early truncation 2 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
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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

Title
PMID
Journal
Year
IF
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