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EN
ENU treatment caused an T>C mutation in the coding region (c.71T>C) that leads to to the change of valine codon 24 to alanine (p.Val24Ala). This mutation is linked to H3c14 and the two mutations are found in mice with a dominant small-eye phenotype (microphthalmia without a lens but with retinal hyperproliferation). (J:277247)
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
