这个基因在编码螺旋环域N端的对应区域时,通过插入了lacZ-neo衍生的 cassette,导致了功能受损。通过纯合动物的Northern blot分析确认了基因表达缺失。突变胚胎的X-gal染色显示了在软骨组织中存在lacZ的表达。(来源:J:80666)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
129S7/SvEvBrd-Hprt1+
Targeted
插入
--
1
1
10

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
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