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中文
Exon 16被替换为一个修改过的Exon 16，其中的核苷酸变异导致第639位氨基酸由苯丙氨酸（F639A）替换为Alanine。下游插入了一个敲除的诺卡因抗性基因 cassette（J:209690）。
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：
Show/Hide columns
| Phenotypes |
|---|
References Literature
Title
PMID
Journal
Year
IF
