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中文
TALEN导向产生了一个位于chr7:142217981(GRCh39)的G到A点突变，这个位置在一个由多个物种共享的保守序列中，这个序列被转录抑制因子ZBED6结合。同时，随机发生了一个插入/复制单个胞嘧啶的变异，从C变为CC，位于chr7:142217984。(来源：J:331260)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
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
