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This allele produced from project TCPR0260 at The Centre for Phenogenomics by injecting Cas9 mRNA and one guide RNA with the spacer sequence CAGGGTCTCCGCGCTTTTCG. This resulted in an indel comprised of an 11-bp deletion of Chr2 from 118926684 to 118926694 bp and a 1-bp insertion of A on the +1 strand (GRCm38). (J:165963)
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
