Log In|Sign Up
EN
This allele produced from project TCPR0367 at The Centre for Phenogenomics by injecting Cas9 mRNA and two guide RNAs with the spacer sequences GTTTACCTAGGCAGCTTCCG and ATGCAGTCCGACCATGGTAT. This resulted in a 71-bp deletion from Chr8:36102633 to 36102703 insT (GRCm38). (J:165963)
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
