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The mutation is a 2 bp deletion in exon 2 (c.792-793delTG) generated by CRISPR/Cas9 genome editing technology. This deletion results in a frameshift mutation, and Western blot analysis confirmed the lack of full length protein in mutant tissue. (J:307534)
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
