Log In|Sign Up
EN
CRISPR/Cas9 endonuclease-mediated genome editing introduced an indel comprised of a 16 bp (Chr7:29013738 to 29013752) deletion in exon 96 of the gene. Sequencing N1 pups revealed the repair template was not incorporated into this allele, which resulted from non-homologous end-joining repair of the double strand break. (J:275500)
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：
Show/Hide columns
| Phenotypes |
|---|
References Literature
Title
PMID
Journal
Year
IF
