Log In|Sign Up
EN
This allele produced from project TCPR0368 at TCP by injecting Cas9 mRNA and two guide RNAs with the spacer sequences GGAACAGGACATGCACCTAG and AGGGAGTGACCGAAGACTGC. This resulted in a 61 bp deletion from Chr13:21433448 to 21433508 in ENSMUSE00000571630. This mutation is predicted to cause a frameshift with amino acid changes after residue 57 and early truncation 51 amino acids later (p.L57Rfs*53) (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
