Log In|Sign Up
中文
这个突变是在Jackson实验室通过电穿孔Cas9蛋白和指导序列ACCTGCGGAGGTCTTTCATA和GAAACTAACTATAATGGTCT产生的，导致X染色体106,709,117bp至106,709,745bp之间629bp的缺失。这个变异删除了ENSMUSE00000654025(第4外显子)的629bp，并预测会导致第1位氨基酸序列改变后终止。(来源：J:188991)
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：
Show/Hide columns
| Phenotypes |
|---|
References Literature
Title
PMID
Journal
Year
IF
