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The whitemouse mutation corresponds to a T-to-C transition at nucleotide position 2303, in the 21st of 24 total exons, resulting in replacement of tryptophan by arginine at amino acid position 725 of the protein (W725R), in the tenth transmembrane domain. (J:133622)
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
