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中文
这种变异发生在8号内含子的C端，位置为c.1207-6T>G。它与一个附有floxed neo cassette的基因座一起被敲入，然后在经过Cre介导的重组后，9号外显子被移除。这是人类中报告的Pseudohypoaldosteronism类型II相关的一种基因突变(来源：J:226618)。
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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References Literature
Title
PMID
Journal
Year
IF
