CRISPR技术引入了名为A4V的 missense突变(等同于NM_000454.4(SOD1):c.14CtoT, p.Ala5Val),在Sod1tm1.1(SOD1)Emcf这个模型中(来源:J:90559)。

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
B6.129-Sod1tm1.1(SOD1)Emcf/H
Endonuclease-mediated
插入
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1
4
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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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