Lrrc7 Phenotype Annotations - Multigenic Genotypes

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Lrrc7
leucine rich repeat containing 7
MGI:2676665

10 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Lrrc7^{Tg(Myl2-TSPYL)1Sich}/Lrrc7⁺ involves: FVB/N	abnormal social investigation	J:293568
Lrrc7^{Tg(Myl2-TSPYL)1Sich}/Lrrc7⁺ involves: FVB/N	increased thigmotaxis	J:293568
Lrrc7^{Tg(Myl2-TSPYL)1Sich}/Lrrc7^{Tg(Myl2-TSPYL)1Sich} involves: FVB/N	abnormal hippocampal pyramidal neuron dendrite morphology	J:293568
	abnormal neurite morphology	J:293568
	abnormal social investigation	J:293568
	abnormal spatial working memory	J:293568
	decreased body size	J:293568
	dehydration	J:293568
	impaired coordination	J:293568
	increased aggression towards mice	J:293568
	increased thigmotaxis	J:293568
	postnatal lethality	J:293568

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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