Log In|Sign Up
EN
This allele has a C to G point substitution that changes isoleucine to methionine at amino acid 183 in the homeodomain region, equivalent to I184 in human, and a loxP-flanked neomycin cassette in the 3-prime UTR. (J:239808)
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
