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The WS4 mouse arose spontaneously at the Saitama Research Center, Saitama, Japan. The mutation was shown to be allelic to Ednrbs-l by a non-complementation test. Analysis of a cDNA derived from mutant mice revealed that a deletion of nucleotides encoding 106 amino acids corresponding to exons 2 and 3 had occurred. (J:76584, J:115266)
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
