Log In|Sign Up
EN
ENU-mutagenesis induced a T-to-G mutation (T is base 3203 in NCBI Reference Sequence NM_001080819.1) that results in the amino acid substitution of glycine for valine at position 1068 (V1068G). This allele is hypomorphic. (J:192829)
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
