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中文
在13号染色体的v38位点(101,702,776基对)，由ENU诱导的T到A的转换，或者在GenBank的NC_000079基因组区域的65,442号位置，这个变异对应于NM_001077495 mRNA序列中的第1,188位氨基酸。这个突变导致p85alpha蛋白中酪氨酸189被替换为一个早停密码子(Y189*)；p55alpha和p50alpha不受影响。(来源：J:254890)
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
