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中文
在AT丰富交互域(ARID)内一个98bp的外显子被通过同源重组插入了诺卡因选择标记。对从胚胎成纤维细胞提取的RNA进行RT-PCR确认了目标外显子的去除。序列分析发现了一个造成框架移位的突变。(来源：J:70658)
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 |
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References Literature
Title
PMID
Journal
Year
IF
