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Symbol
Name
ID

Stac3
SH3 and cysteine rich domain 3
MGI:3606571

Phenotype annotations related to muscle

Darker colors indicate more annotations

Human Phenotypes

Weakness of facial musculature

Increased intramyocellular lipid droplets

Flexion contracture

Congenital contracture

Arthrogryposis multiplex congenita

Camptodactyly

Hypotonia

Muscle weakness

Proximal muscle weakness

Gowers sign

Abnormality of skeletal muscle fiber size

Muscle fiber atrophy

Skeletal muscle atrophy

Fatty replacement of skeletal muscle

Disease(s) Associated with STAC3

Native American myopathy

Mouse Phenotypes

abnormal tongue muscle morphology

abnormal extensor digitorum longus morphology

abnormal sarcomere morphology

abnormal Z line morphology

abnormal skeletal muscle fiber morphology

increased skeletal muscle fiber diameter

centrally nucleated skeletal muscle fibers

decreased skeletal muscle fiber number

abnormal skeletal muscle morphology

abnormal diaphragm morphology

thin diaphragm muscle

decreased skeletal muscle mass

impaired skeletal muscle contractility

abnormal muscle electrophysiology

Availability

Mouse Genotype

Stac3^{tm1a(KOMP)Wtsi}/Stac3^{tm1a(KOMP)Wtsi}

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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