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中文
这种由TALEN诱发的突变发生在携带retinal degeneration 8（rd8）基因这一特定等位的菌株中，它在exon 9中有5个不连续的碱基对缺失，原始rd8突变的第3481位核苷酸，随后是3486到3489位，这会导致框架移位，并引入11个全新的氨基酸，然后提前终止(来源：J:265859)
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
