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CRISPR/Cas9 technology generated a 20 bp deletion (5-TCGTCCACCGCGGCTTTTTG-3) in the first exon. The sgRNA sequence used for microinjection was 5'-GAGAAGGCAAAAAGCCGCGG-3' for the first exon. The deletion causes a frameshift mutation leading to a premature termination codon after the 17th amino acid. (J:279308)
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
