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Leucine codon 25 (TTA) and tryptophan codon 26 (TGG) were changed to glutamine (CAA) and serine (TCG) (p.L25Q, p.W26S). This mutation is similar to a known human mutation. The allele also contains a spontaneous or strain specific p.A135V mutation (compared to C57BL/6). (J:64367)
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
