The endogenous allele was disrupted by the insertion of a vector containing exons 9 through 13, selection genes, and a 300 bp gap in intron 11. Homologous recombination of the vector results in double stranded gap repair, producing an allele in which exon 13 is followed by the selection genes and duplicates of exons 9 through 13. Transcript was undetected in homozygous mutant mice by RT-PCR analysis of gonad and spleen tissue. Expression of Vrk2, the adjacent locus, was unaffected. (J:80424)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
129S7/SvEvBrd-Hprt1+
Targeted
Insertion, Intragenic deletion
--
1
5
3

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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