Log In|Sign Up
中文
这个来自项目Pbsn-6978J-F3145的等位基因是由Jackson实验室通过向细胞注射Cas9 RNA和4个指导序列产生的：TTAAGGTCGTGCATTCATTC, ACATTGGAATGTAGATATCA, TCGTATTGTATATTACTCCA, 和TTTATGTGGAATCAGGACCC。这个操作导致了X染色体负链77,845,123bp位置到77,844,912bp的212bp内含子3的缺失。缺失部分的序列是CCCTGGAGTAATATACAATACG。这个变异删除了exon 3，预测会导致在第72个氨基酸后产生早期截断。(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
