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中文
这个等位基因是在表型基因组学中心通过电穿孔方式，用带有CTGCACAGGGGCCACTCTAC和AGCCACAGGGTATGACACGG的单导RNA同质体，针对染色体10的5'和3'端，对关键区域进行了编辑(ENSMUSE00000305070, ENSMUSE00000305063, ENSMUSE00000304985, ENSMUSE00000305049)。这导致了1,246个碱基的染色体10缺失，位置从80,698,362到80,699,607(GRCh39)。(来源：J:265051)
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
