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中文
这个基因在编码着homeodomain和NK-2特异性区域的exon 2被替换成诺卡因抗性基因座，导致其功能受损。通过在E9.5胚胎上进行原地杂交实验，用1和2号染色体的探针对 homozygous突变体进行了基因表达缺失的确认(来源：J:61335)。
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 |
|---|
References Literature
Title
PMID
Journal
Year
IF
