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中文
这种在exon 1a的ATG起始密码子上的自发胸腺嘧啶替换为胞嘧啶，导致exon 3成为下一个内切起始密码子，预测会形成一个起始缺失变异，影响到第一个锌指域。Rorb1转录在大脑和视网膜中的表达显著增加，而Rorb2转录在视网膜中的量显著减少。（来源：J:337403）
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 |
|---|
References Literature
Title
PMID
Journal
Year
IF
