这种在性腺发育不良小鼠中的突变是一个大约33.5kb的缺失,它移除了编码大部分蛋白质的两个外显子(来源:J:8515, J:14505, J:94662)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
C3H101H-Rb(1.3)1Bnr
Spontaneous
基因内删除
隐性
1
3
95

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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