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The bm10 mutation consists of six nucleotide substitutions resulting in amino acid changes at codon 163 (threonine to alanine), 165 (valine to methionine), 167 (tryptophan to serine), 173 (lysine to glutamate) and 174 (asparagine to leucine). (J:109273)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
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
