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Symbol
Name
ID

Lmod3
leiomodin 3 (fetal)
MGI:2444169

Phenotype annotations related to behavior/neurological

Darker colors indicate more annotations

Human Phenotypes	Decreased fetal movement	Feeding difficulties
Disease(s) Associated with LMOD3	Decreased fetal movement	Feeding difficulties
nemaline myopathy 10

Mouse Phenotypes		abnormal startle reflex	decreased startle reflex	decreased grip strength	decreased locomotor activity	abnormal vocalization
Availability	Mouse Genotype	abnormal startle reflex	decreased startle reflex	decreased grip strength	decreased locomotor activity	abnormal vocalization
	Lmod3^em1(IMPC)Mbp/Lmod3^em1(IMPC)Mbp
	Lmod3^{Tn(pb-Act-RFP)1.1Zhu}/Lmod3^{Tn(pb-Act-RFP)1.1Zhu}

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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