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Symbol
Name
ID

Lgi4
leucine-rich repeat LGI family, member 4
MGI:2180197

Phenotype annotations related to behavior/neurological

Darker colors indicate more annotations

Human Phenotypes	Decreased fetal movement	Fetal akinesia sequence
Disease(s) Associated with LGI4	Decreased fetal movement	Fetal akinesia sequence
arthrogryposis multiplex congenita-1

Mouse Phenotypes		abnormal behavior	decreased thigmotaxis	impaired righting response	abnormal posture	abnormal locomotor behavior	hyperactivity	abnormal maternal nurturing	abnormal sexual interaction
Availability	Mouse Genotype	abnormal behavior	decreased thigmotaxis	impaired righting response	abnormal posture	abnormal locomotor behavior	hyperactivity	abnormal maternal nurturing	abnormal sexual interaction
	Lgi4^clp/Lgi4^clp
	Lgi4^{tm1.1(KOMP)Vlcg}/Lgi4⁺

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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