Log In|Sign Up
中文
这个来自TCPR0434项目的等位基因是在phenogenomics中心通过向细胞注射Cas9 mRNA和四种引导RNA，这些RNA带有ACTACCCTGGTTGGACTGGC和GCAATCATCCCCTATATCTC的 spacer序列，目标是染色体7的5'端，以及CCCTCTTAAGAACTCTTTTC和ATTGACAGTGCCAAGAAAGT针对3'端的ENSMUSE00000531437（也就是基因2的exon 2），产生了772bp的染色体7缺失，位置从48,020,898到48,021,669（GRCm38建库）。(引用：J:237616)
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
