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EN
This allele from project TCPR0237 was generated at the Toronto Centre for Phenogenomics by injecting Cas9 D10A mRNA and a single guide RNA with the spacer sequence TCATGTCCCTCAGACGGCAC. This resulted in a 8 bp insertion TCCAGTGT at Chromosome 10 positive strand 84632456 bp (GRCm38) and is predicted to cause a frameshift mutation with early truncation. c.305_306insTCCAGTGT; p.R103Pfs*3. (J:265051)
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
