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This allele represents five point mutations that are found in the PWK strain: chrX:g.67690875G>T (changes codon 95 from arginine to serine (p.R95S)), 67690938C>T (changes codon 74 from valine to isoleucine (p.V74I)), 67693489T>C (changes codon 25 from aspartic acid to glycine (p.D25G)), and 67693536TT>GG (changes codon 9 from lysine to asparagine (p.K9T)) (GRCm38 coordinates). (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：
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References Literature
Title
PMID
Journal
Year
IF
