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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Hipk2tm1Hko
targeted mutation 1, Haruhiko Koseki
MGI:3624127
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Hipk2tm1Hko/Hipk2tm1Hko involves: C57BL/6 MGI:3624996
cx2
Hipk1tm1Hko/Hipk1tm1Hko
Hipk2tm1Hko/Hipk2tm1Hko
Trp53tm2Mok/Trp53+
involves: 129S/SvEv * C57BL/6 MGI:3625003
cx3
Hipk1tm1Hko/Hipk1tm1Hko
Hipk2tm1Hko/Hipk2tm1Hko
involves: C57BL/6 MGI:3624999
cx4
Hipk1tm1Hko/Hipk1+
Hipk2tm1Hko/Hipk2tm1Hko
involves: C57BL/6 MGI:3625000
cx5
Hipk1tm1Hko/Hipk1tm1Hko
Hipk2tm1Hko/Hipk2+
involves: C57BL/6 MGI:3625001


Genotype
MGI:3624996
hm1
Allelic
Composition
Hipk2tm1Hko/Hipk2tm1Hko
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hipk2tm1Hko mutation (0 available); any Hipk2 mutation (55 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• embryonic fibroblasts from null mice are slightly resistant to UV radiation compared to wild-type
• decreased numbers of apoptotic cells induced by UV irradiation are observed in MEFs compared to wild-type

nervous system
• neural tube defects occur more frequently in female compound mutants

embryo
• neural tube defects occur more frequently in female compound mutants




Genotype
MGI:3625003
cx2
Allelic
Composition
Hipk1tm1Hko/Hipk1tm1Hko
Hipk2tm1Hko/Hipk2tm1Hko
Trp53tm2Mok/Trp53+
Genetic
Background
involves: 129S/SvEv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hipk1tm1Hko mutation (0 available); any Hipk1 mutation (61 available)
Hipk2tm1Hko mutation (0 available); any Hipk2 mutation (55 available)
Trp53tm2Mok mutation (2 available); any Trp53 mutation (240 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• four triple mutants were found to be exencephalic, whereas none were found to be wild-type for Trp53




Genotype
MGI:3624999
cx3
Allelic
Composition
Hipk1tm1Hko/Hipk1tm1Hko
Hipk2tm1Hko/Hipk2tm1Hko
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hipk1tm1Hko mutation (0 available); any Hipk1 mutation (61 available)
Hipk2tm1Hko mutation (0 available); any Hipk2 mutation (55 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

growth/size/body
• at E9.5, 14 of 17 live double homozygotes are smaller and developmentally delayed compared to Hipk1tm1Kho homozygous or Hipk1tm1Kho/Hipk1tm1Kho Hipk2+/+ embryos

cellular
• significantly more apoptotic cells are observed in the condensing trigeminal and facioacoustic neural crest cells, as well as in the sclerotomal compartment, compared to Hipk1-null, Hipk2-wild-type mutants
• at E9.5, the frequency of mitotic cells in the cranial and caudal regions of the neural tube of double homozygotes is reduced to 45% and 29% compared to Hipk1-null, Hipk2 wild-type homozygotes
• proliferation of the cephalic mesoderm is reduced to 43% of that in Hipk1-null, Hipk2-wild-type double mutants

nervous system
• neural tube defects occur more frequently in female compound mutants
• half of the homozygous embryos surviving to beyond E9.5 exhibit exencephaly

vision/eye
• in mutants lens vesicle formation fails with disorientation of the optic cups and fusion of the dorsal root ganglia

embryo
• at E9.5, 14 of 17 live double homozygotes are smaller and developmentally delayed compared to Hipk1tm1Kho homozygous or Hipk1tm1Kho/Hipk1tm1Kho Hipk2+/+ embryos
• neural tube defects occur more frequently in female compound mutants




Genotype
MGI:3625000
cx4
Allelic
Composition
Hipk1tm1Hko/Hipk1+
Hipk2tm1Hko/Hipk2tm1Hko
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hipk1tm1Hko mutation (0 available); any Hipk1 mutation (61 available)
Hipk2tm1Hko mutation (0 available); any Hipk2 mutation (55 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• about half of the mutants are lost during gestation, compared to the predicted number

cellular
• embryonic fibroblasts from mutant mice are more resistant to UV radiation compared to single Hipk1 or Hipk2-null mice
• decreased numbers of apoptotic cells induced by UV irradiation are observed in MEFs compared to wild-type

nervous system
• neural tube defects occur more frequently in female compound mutants

embryo
• neural tube defects occur more frequently in female compound mutants




Genotype
MGI:3625001
cx5
Allelic
Composition
Hipk1tm1Hko/Hipk1tm1Hko
Hipk2tm1Hko/Hipk2+
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hipk1tm1Hko mutation (0 available); any Hipk1 mutation (61 available)
Hipk2tm1Hko mutation (0 available); any Hipk2 mutation (55 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• neural tube defects occur more frequently in female compound mutants
• a small number of these mutants exhibit exencephaly

embryo
• neural tube defects occur more frequently in female compound mutants





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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory