Lgi1 Phenotype Annotations - Multigenic Genotypes

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Lgi1
leucine-rich repeat LGI family, member 1
MGI:1861691

11 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Lgi1^tm1.1Jkc/Lgi1⁺ Tyr^c-Brd/Tyr^c-Brd B6.Cg-Tyr^c-Brd Lgi1^tm1.1Jkc	abnormal eye pigmentation	J:158715
	absent coat pigmentation	J:158715
Lgi1^tm1.1Jkc/Lgi1^tm1.1Jkc Tyr^c-Brd/Tyr^c-Brd B6.Cg-Tyr^c-Brd Lgi1^tm1.1Jkc	abnormal coat/hair pigmentation	J:158715
	abnormal eye pigmentation	J:158715
	clonic seizures	J:158715
	decreased body size	J:158715
	enhanced AMPA-mediated synaptic currents	J:158715
	enhanced NMDA-mediated synaptic currents	J:158715
	increased miniature excitatory postsynaptic current frequency	J:158715
	normal nervous system phenotype	J:158715
	postnatal lethality, complete penetrance	J:158715
	seizures	J:158715

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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