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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Kcnh3
potassium voltage-gated channel, subfamily H (eag-related), member 3
MGI:1341723
17 phenotypes from 4 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Kcnh3tm1.1(KOMP)Vlcg/Kcnh3+
C57BL/6N-Kcnh3tm1.1(KOMP)Vlcg/J
abnormal retina morphology J:211773
increased circulating free fatty acids level J:211773
Kcnh3tm1.1(KOMP)Vlcg/Kcnh3tm1.1(KOMP)Vlcg
C57BL/6N-Kcnh3tm1.1(KOMP)Vlcg/J
abnormal retina morphology J:211773
hyperactivity J:211773
improved glucose tolerance J:211773
increased fasting circulating glucose level J:211773
increased hemoglobin content J:211773
Kcnh3tm1.1Tije/Kcnh3tm1.1Tije
involves: C57BL/6
abnormal single cell response J:165296
decreased single cell response threshold J:165296
Kcnh3tm1.2Tije/Kcnh3+
involves: C57BL/6
abnormal spike wave discharge J:165296
Kcnh3tm1.2Tije/Kcnh3tm1.2Tije
involves: C57BL/6
abnormal single cell response J:165296
abnormal spike wave discharge J:165296
normal behavior/neurological phenotype J:165296
decreased single cell response threshold J:165296
increased susceptibility to pharmacologically induced seizures J:165296
nonconvulsive seizures J:165296
Kcnh3tm1Akmi/Kcnh3+
involves: 129S4/SvJae * C57BL/6
abnormal long-term object recognition memory J:155749
abnormal spatial reference memory J:155749
Kcnh3tm1Akmi/Kcnh3tm1Akmi
involves: 129S4/SvJae * C57BL/6
abnormal CNS synaptic transmission J:155749
abnormal long-term object recognition memory J:155749
abnormal long-term potentiation J:155749
abnormal spatial reference memory J:155749
abnormal spatial working memory J:155749

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
04/30/2024
MGI 6.23
The Jackson Laboratory