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EN
CRISPR/cas9 genome editing is used to insert a 5' HA tag, a membrane anchored eGFP repair plasmid (eGFPcaax), a STOP sequence, a bGH polyA sequence and a 3' HA tag into the 3' end of the exon2 locus, and a non-targeting PGK-puromycin plasmid. The endogenous promoter drives eGFP expression. (J:332176)
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
