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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Lgi1
leucine-rich repeat LGI family, member 1
MGI:1861691
27 phenotypes from 3 alleles in 6 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Lgi1tm1.1Ics/Lgi1+
involves: 129S2/SvPas * BALB/c * C57BL/6
audiogenic seizures J:182795
Lgi1tm1.1Ics/Lgi1tm1.1Ics
involves: 129S2/SvPas * BALB/c * C57BL/6
abnormal brain wave pattern J:182795
abnormal cerebellar granule cell morphology J:182795
abnormal cerebellum external granule cell layer morphology J:182795
abnormal hippocampal mossy fiber morphology J:182795
abnormal spike wave discharge J:182795
akinesia J:182795
aphagia J:182795
decreased body size J:182795
decreased body weight J:182795
decreased total body fat amount J:182795
environmentally induced seizures J:182795
gliosis J:182795
neurodegeneration J:182795
postnatal growth retardation J:182795
postnatal lethality, complete penetrance J:182795
seizures J:182795
tonic-clonic seizures J:182795
Lgi1tm1Mafu/Lgi1+
involves: 129S6/SvEvTac * C57BL/6
clonic seizures J:157578
increased susceptibility to pharmacologically induced seizures J:157578
tonic seizures J:157578
Lgi1tm1Mafu/Lgi1tm1Mafu
involves: 129S6/SvEvTac * C57BL/6
abnormal glutamate-mediated receptor currents J:157578
decreased miniature excitatory postsynaptic current amplitude J:157578
normal nervous system phenotype J:157578
postnatal growth retardation J:157578
premature death J:157578
seizures J:157578
tonic-clonic seizures J:157578
Lgi1tm2.1Jkc/Lgi1tm2.1Jkc
Pvalbtm1(cre)Arbr/0
involves: 129/Sv * 129P2/OlaHsd * C57BL/6
normal nervous system phenotype J:269784
Lgi1tm2.1Jkc/Lgi1tm2.1Jkc
Tg(Camk2a-cre)T29-1Stl/0
involves: 129/Sv * BALB/cJ * C57BL/6
normal nervous system phenotype J:269784
Lgi1tm2.1Jkc/Lgi1tm2.1Jkc
Tg(CMV-cre)1Cgn/0
involves: 129/Sv * BALB/cJ * C57BL/6
abnormal cerebral cortex morphology J:269784
abnormal neocortex morphology J:269784
seizures J:269784
Lgi1tm2.1Jkc/Lgi1tm2.1Jkc
Tg(GFAP-cre)25Mes/0
involves: 129/Sv * C57BL/6 * FVB/N
normal nervous system phenotype J:269784
Lgi1tm2.1Jkc/Lgi1tm2.1Jkc
Tg(Nes-cre)1Kln/0
involves: 129/Sv * C57BL/6 * SJL
abnormal cerebral cortex morphology J:269784
abnormal neocortex morphology J:269784
seizures J:269784

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
04/09/2024
MGI 6.23
The Jackson Laboratory