Log In|Sign Up
EN
This allele from project TCPR0253, was generated at The Centre for Phenogenomics by injecting Cas9 mRNA and two guide RNAs with spacer sequences GCAGGTTAACTCCACCTCGG and ACAGAGACAGGTGCCACGCT. This resulted in a 38 bp deletion from Chr8:25971576 to 25971613 (GRCm38) in exon 3 (ENSMUSE00000347052). This mutation is predicted to cause a frameshift with amino acid changes after residue 133 and early truncation 24 amino acids later (p.I133Lfs*25). (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
