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中文
功能性cDNA编码序列来自RARA/PML融合基因的bcr-3亚型转录本，该基因由特征性的t(15;17)(q22;q11.2-q12)染色体易位引起，大约90%的人类急性早幼粒细胞白血病（APML）病例与此相关。bcr-3亚型的异源基因在RARA基因的exon 2和PML基因的exons 4-8之间成框连接。表达通过人酸性激肽G基因的启动子和5'调控元件特异性针对早期粒细胞谱系细胞。构建了两条克隆（2544和2683）并进行了合并。（来源：J:59080）
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
