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中文
Cas9和引导序列GTACATCTCTGTCGGCTATG针对H2-D1b，ATAATCCGAGATTTGAGCCG针对H2-K1d，被注入到NOD/ShiLtDvs胚胎中，导致了二个exon 2的缺失，一个11bp，另一个3bp，以及单个碱基的H2-K1em1Dvs变异。(来源：J:257229)
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
