890 bp of coding sequence of the intronless Nap1l2 gene between two HincII restriction endonuclease recognition sites were replaced, in-frame, by a nuclear-localized beta-galactosidase (lacZ) reporter gene and a neomycin resistance gene. The insertion of these cassettes disrupts the reading frame of the remainder of the Nap1l2 gene, so that the resulting fusion protein includes only 5 N-terminal amino acids of the NAP1L2 protein. Beta-galactosidase expression in developing chimeric embryos was first observed by X-gal staining in the tip of the tail at embryonic day (E) 9.5, and by E10.5 throughout the neural tube. By E12.5 the neural tube, ganglia and some upper and lower thoracic muscles were labeled. Histologic brain sections showed strong lacZ expression in the rhombencephalon and spinal cord. (J:63883)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
129S2/SvPas
Targeted
Intragenic deletion
--
1
--
1

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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