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Exons 1 and 2 were targeted with respective sgRNAs using CRISPR/Cas9 technology. This resulted in the loss of coding nucleotides 65-297 spanning exons 1 and 2. The deletion causes a frameshift and premature translation stop codon, creating a knockout allele. (J:267641)
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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| Phenotypes |
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References Literature
Title
PMID
Journal
Year
IF
