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Symbol
Name
ID

Lmod3
leiomodin 3 (fetal)
MGI:2444169

Phenotype annotations related to muscle

Darker colors indicate more annotations

Human Phenotypes

Facial palsy

Flexion contracture

Congenital contracture

Generalized hypotonia

Severe muscular hypotonia

Muscle weakness

Bulbar palsy

Generalized muscle weakness

Respiratory insufficiency due to muscle weakness

Nemaline bodies

Skeletal muscle atrophy

Fatty replacement of skeletal muscle

Disease(s) Associated with LMOD3

nemaline myopathy 10

Mouse Phenotypes

decreased cardiac muscle contractility

increased skeletal muscle glycogen level

abnormal sarcomere morphology

abnormal Z line morphology

abnormal skeletal muscle fiber morphology

decreased skeletal muscle fiber size

skeletal muscle fiber atrophy

centrally nucleated skeletal muscle fibers

abnormal skeletal muscle morphology

decreased skeletal muscle size

muscle weakness

Availability

Mouse Genotype

Lmod3^em1(IMPC)Mbp/Lmod3^em1(IMPC)Mbp

Lmod3^em1Eno/Lmod3^em1Eno

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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