Log In|Sign Up
EN
This allele from project TCPR1078 was generated at The Centre for Phenogenomics by electroporating Cas9 ribonucleoprotein complexes with single guide RNAs having spacer sequences of AGTCTAATTCCTATTTAGTG and GCAGGCCAGTGTTTTTGTCC targeting the 5' side and GCTCATTCCCACATAGTATG targeting the 3' side of a critical exon. This resulted in a 578-bp deletion Chr14:59388910 to 59389487;1-bp deletion at Chr14:59389528 (GRCm38). (J:265051)
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
