Log In|Sign Up
EN
This allele from project TCPR443 was generated at The Centre for Phenogenomics by injecting Cas9 ribonucleoprotein complexes and single guide RNA(s) with spacer sequences of ATAGTTCAGTACAGTTCACT and GTATGTTTCATCTAGCCACC targeting the 5' side and GAATTAGCTGAGAGCTAGGT and TCCAAGCCTGGCTCCGATCA targeting the 3' side of a critical exon resulting in a 398-bp deletion on Chr6 from 125046790 to 125047187 (GRCm38). (J:200814)
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
