这个变异发生在两个密码子上,b等位基因的第650位是CGC(精氨酸),第679位是AGT(丝氨酸)。这两种氨基酸都位于第20外显子,编码C末端具有核酸酶样功能区的一部分。这个等位基因存在于C57BL/6小鼠品系中。(来源:J:78186)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
Not Applicable
Spontaneous
核苷酸替换
--
1
9
1

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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