这个等位基因包含至少48.3kb的缺失,包括Pax1以及40kb的周边序列。缺失影响了删除区域内的其他物理连锁基因,特别是在曲折短尾鼠中Nkx2-2被异常激活。(来源:J:85847)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
CC57BR/MvY
Spontaneous
基因间区删除
半显性
1
2
10

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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