This allele from project C2cd2-8190J-M1399 was generated at The Jackson Laboratory by injecting Cas9 RNA and 4 guide sequences TTTTCACTATATTTCTGCAG, CTAATGGGCTTGGGGTCCAA, AGGATGTGTGAGGTTGGCCA and ACAGAGTCATCACTATTTGC, which resulted in a 353 bp deletion beginning at Chromosome 16 negative strand position 97,883,448 bp CTGGCCAACCTCACACATCC, and ending after GGGCTTGGGGTCCAAAGGCC at 97,883,096 bp (GRCm38/mm10). This mutation deletes exon 6 and 229 bp of flanking intronic sequence including the splice acceptor and donor. In addition there is an 11 bp deletion (ATTTGCAGGTT) 159 bp before the 353 bp deletion that will not effect the results of the exon deletion. This mutation is predicted to cause a change of amino acid sequence after residue 236 and early truncation 9 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

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PMID
Journal
Year
IF
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