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This allele represents three point mutations that are found in the PWK strain: chrX:g.67695723AA>CC (changes codon 9 from lysine to threonine (p.K9T)) and 67695771A>G (changes codon 25 from aspartic acid to glycine (p.D25G)) (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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| Phenotypes |
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References Literature
Title
PMID
Journal
Year
IF
