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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Hk2
hexokinase 2
MGI:1315197
8 phenotypes from 2 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Hk2tm1.1Uku/Hk2tm1.1Uku
B6.129P2-Hk2tm1.1Uku/Kctt
no abnormal phenotype detected J:82809
Hk2tm1.1Uku/Hk2tm1.1Uku
Tg(GFAP-cre)25Mes/0
B6.Cg-Hk2tm1.1Uku Tg(GFAP-cre)25Mes
abnormal cerebellar granule cell migration J:210113
abnormal cerebellum external granule cell layer morphology J:210113
abnormal neuronal precursor proliferation J:210113
irregular external granule cell layer thickness J:210113
Hk2tm1Laak/Hk2+
involves: 129P2/OlaHsd * BALB/c * DBA/2
decreased body weight J:56644
Hk2tm1Laak/Hk2tm1Laak
involves: 129P2/OlaHsd * BALB/c * DBA/2
embryonic growth retardation J:56644
embryonic lethality between somite formation and embryo turning, complete penetrance J:56644

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
12/10/2024
MGI 6.24
The Jackson Laboratory