CRISPR/Cas9 technology was used to design guide RNAs that disrupt exons 59 and 62 of mouse Itpr1. Three founder mice with a deletion in exon 59 at a high mosaic rate died soon after birth for unknown reasons. Another mouse line with a seven-base pair deletion (c.8238_8244delAGCCGGC) in the last exon of Itpr1 which resulted in a frameshift and readthrough mutation was established and used for the study. (J:308935)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
C57BL/6J
Endonuclease-mediated
Intragenic deletion
--
1
4
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

Title
PMID
Journal
Year
IF
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