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The gene was disrupted by replacement of the end of intron 3 and the first 60 codons of the cytoplasmic catalytic domain containing exon 4 with a PGK-neo cassette via homologous recombination. Homozygous mutant embryos were observed at days E9.5-E11.5 and RT-PCR analysis of embryonic mRNA detected truncated mutant transcripts. (J:63748)
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 |
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References Literature
Title
PMID
Journal
Year
IF
