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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Pik3r4
phosphoinositide-3-kinase regulatory subunit 4
MGI:1922919
22 phenotypes from 3 alleles in 7 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Neurod6tm1(cre)Kan/Neurod6+
Pik3r4mbe/Pik3r4tm1.1Mpnd
involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C3H/HeH * C57BL/6
abnormal hippocampus pyramidal cell layer J:258027
abnormal hippocampus stratum oriens morphology J:258027
ectopic hippocampus pyramidal cells J:258027
Pik3r4mbe/Pik3r4mbe
involves: C3H/HeH * C57BL/6
abnormal autophagy J:258027
abnormal cell physiology J:258027
abnormal hippocampal pyramidal neuron dendrite morphology J:258027
abnormal hippocampus pyramidal cell layer J:258027
abnormal hippocampus stratum oriens morphology J:258027
abnormal neuronal migration J:258027
abnormal spatial working memory J:258027
ectopic hippocampus pyramidal cells J:258027
Pik3r4mbe/Pik3r4tm1.1Mpnd
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * C3H/HeH * C57BL/6
abnormal hippocampus pyramidal cell layer J:258027
abnormal hippocampus stratum oriens morphology J:258027
ectopic hippocampus pyramidal cells J:258027
Pik3r4tm1.1Mpnd/Pik3r4tm1.1Mpnd
involves: 129S2/SvPas * C57BL/6
abnormal neuronal migration J:258027
Pik3r4tm1.1Mpnd/Pik3r4tm1.1Mpnd
involves: 129S2/SvPas * C57BL/6N
no abnormal phenotype detected J:198770
Pik3r4tm1.1Mpnd/Pik3r4tm1.1Mpnd
involves: 129S2/SvPas * C57BL/6N
abnormal autophagy J:198770
Pik3r4tm1.1Mpnd/Pik3r4tm1.1Mpnd
Emx1tm1(cre)Krj/Emx1+
involves: 129S2/SvPas * C57BL/6
abnormal cerebral cortex morphology J:258027
abnormal hippocampus morphology J:258027
thin cerebral cortex J:258027
Pik3r4tm1.1Mpnd/Pik3r4tm1.1Mpnd
Tg(ACTA1-cre)79Jme/0
involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL
abnormal autophagy J:198770
abnormal sarcolemma morphology J:198770
centrally nucleated skeletal muscle fibers J:198770
increased circulating creatine kinase level J:198770
increased skeletal muscle glycogen level J:198770
muscle weakness J:198770
myopathy J:198770
myositis J:198770
skeletal muscle degeneration J:198770
skeletal muscle fiber necrosis J:198770
Pik3r4tm1.2Mpnd/Pik3r4tm1.2Mpnd
involves: 129S2/SvPas * BALB/cJ * C57BL/6N
embryonic lethality, complete penetrance J:198770

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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
04/09/2024
MGI 6.23
The Jackson Laboratory