在exon 3b的位置替换了一段,其中的核苷酸变异导致了 alanine 替换为 serine 或 threonine:T354A(AC到GCC)、S355A(TCC到GCC)、S356A(TCC到GCC);T357A(ACA到GCA)、S363A(TCT到GCC)、T370A(AC到GCC)、S375A(TCC到GCC)、T376A(ACG到GCC)、T379A(ACA到GCA)、T383A(AC到GCC)。通过Cre介导,去除了在修改后的exon 3b下游插入的neo抗药性 cassette。

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
C57BL/6
Targeted
Insertion, Nucleotide substitutions
--
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
No Data Found!
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