Log In|Sign Up
EN
This chrX:g.65047953T-to-G mutation (GRCm38 coordinates), which changes codon 90 from valine to glycine (p.V90G), is the minor variant of SNP rs29050889 that is found in the PWD and PWK strains. (J:292550)
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
