These mice contain a T to A transversion at nucleotide position 1903 in exon 3. This mutation caused a substitution of serine for cysteine at amino acid 95 and the loss of the A6-A11 intrachain disulfide bond. (J:122098, J:137483)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
C3HeB/FeJ
Chemically induced
Single point
Dominant
1
9
3

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

References Literature

Title
PMID
Journal
Year
IF
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