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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Hipk2
homeodomain interacting protein kinase 2
MGI:1314872
29 phenotypes from 4 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Hipk2tm1Afus/Hipk2tm1Afus
involves: 129X1/SvJ * C57BL/6
abnormal cell cycle J:156574
abnormal motor capabilities/coordination/movement J:156574
decreased birth weight J:156574
decreased body weight J:156574
decreased cell proliferation J:156574
limb grasping J:156574
Hipk2tm1Ejh/Hipk2tm1Ejh
involves: 129X1/SvJ * C57BL/6
abnormal gait J:117465
abnormal response to novelty J:117465
abnormal voluntary movement J:117465
decreased dopamine level J:117465
decreased dopaminergic neuron number J:117465
decreased exploration in new environment J:117465
decreased neuron apoptosis J:117465
decreased substantia nigra size J:117465
decreased tegmentum size J:117465
dystonia J:117465
impaired behavioral response to addictive substance J:117465
impaired coordination J:117465
limb grasping J:117465
short stride length J:117465
Hipk2tm1Ejh/Hipk2tm1Ejh
involves: 129X1/SvJ * C57BL/6J
enlarged trigeminal ganglion J:93311
Hipk2tm1Hko/Hipk2tm1Hko
involves: C57BL/6
abnormal neural tube morphology J:106931
decreased cellular sensitivity to ultraviolet irradiation J:106931
Hipk2tm2b(EUCOMM)Hmgu/Hipk2+
C57BL/6N-Hipk2tm2b(EUCOMM)Hmgu/Cnrm
increased heart weight J:211773
increased kidney weight J:211773
Hipk2tm2b(EUCOMM)Hmgu/Hipk2tm2b(EUCOMM)Hmgu
C57BL/6N-Hipk2tm2b(EUCOMM)Hmgu/Cnrm
abnormal lens morphology J:211773
abnormal maxilla morphology J:211773
abnormal snout morphology J:211773
abnormal tooth morphology J:211773
preweaning lethality, incomplete penetrance J:211773

Contributing Projects:
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