Log In|Sign Up
EN
Sequence encoding enhanced GFP was inserted at codon 35 of the endogenous locus via homologous recombination. In addition to the insertion, sequence encoding amino acids 141 through 184 containing the N-terminal part of the homeodomain was deleted, introducing a frameshift mutation. Expression of GFP was similar to that of the endogenous gene. (J:81343)
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
