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This allele from IMPC was generated at Medical Research Council Harwell by injecting CAS9 RNA and 4 guide sequences TGCGAAACACTTCCCTACTCTGG, GCCATATAGATTGGTGGCAGTGG, GCTAGATGCCGGTGTAGGTTTGG, CCACGGCATGAAAGCTAGATGCC, which resulted in a Exon Deletion. Sequencing of F0 animals revealed an individual with a 716 nt deletion encompassing ENSMUSE00000122772 of Spata13 resulting in a frameshift and premature stop codon in the following exon. (J:237616, J:274791)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
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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References Literature
Title
PMID
Journal
Year
IF
