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EN
This ENU induced mutation is a G-to-A transition at chromosome 15:97,984,776 (GRCm38), which causes a premature stop codon at amino acid 645, and an A-to-T transversion at chromosome 15:97,825,743, in intron 12 that could potentially act as a cryptic splice acceptor site, though RT-PCR did not reveal splicing abnormalities. (J:176116, J:222308)
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
