A neomycin selection cassette was inserted such that the exon encoding the second LIM domain was deleted and that splicing from the exon encoding the first LIM domain to the exon encoding the homeodomain would result in a frameshift mutation. In situ hybridization did not detect transcript produced from this allele in the neural tube of homzygous mutant mice, but message was detected in the mesoderm ventral to the neural tube. Immunohistochemical analysis of homozygous mutant embryonic sections showed a lack of protein in all analyzed tissues. (J:31131)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
129S1/Sv-Oca2+ Tyr+ Kitl+
Targeted
Insertion, Intragenic deletion
--
1
1
13

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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