CRISPR/Cas9 genome editing technology was used to generate a 1,233 bp deletion including exon 3, which encodes a large part of the tubulin-binding stathmin-like domain of the encoded protein and parts of the surrounding introns, as confirmed by DNA sequencing. Western blot analysis demonstrated absence of protein expression in brain lysates from adult homozygous mutant mice. (J:337175)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
C57BL/6N
Endonuclease-mediated
Intragenic deletion
--
1
1
1

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

References Literature

Title
PMID
Journal
Year
IF
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