Log In|Sign Up
EN
CRISPR/cas9 mediated recombination created a 2 bp deletion in exon 1 resulting in a frameshift mutation in the region after the first transmembrane domain. While mRNA was detected immunoblot and immunohistochemical analysis confirmed the absence of protein in reticuloendothelial tissues from homozygous mice. (J:282829)
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
