Symbol Name ID |
Myh3
myosin, heavy polypeptide 3, skeletal muscle, embryonic MGI:1339709 |
Darker colors indicate more annotations |
Human Phenotypes | Camptodactyly of finger |
Hip contracture |
Knee flexion contracture |
Elbow flexion contracture |
Aplasia/Hypoplasia of the abdominal wall musculature |
Flexion contracture |
Arthrogryposis multiplex congenita |
Camptodactyly |
Elbow contracture |
Skeletal muscle atrophy |
Disease(s) Associated with MYH3 | ||||||||||
contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A | ||||||||||
contractures, pterygia, and spondylocarpotarsal fusion syndrome 1B | ||||||||||
distal arthrogryposis type 2B3 |
Mouse Phenotypes | increased myoblast apoptosis |
abnormal muscle precursor cell morphology |
decreased skeletal muscle fiber diameter |
increased skeletal muscle fiber number |
decreased skeletal muscle weight |
abnormal skeletal muscle fiber type ratio |
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Availability | Mouse Genotype | ||||||
Myh3tm1.2Sajm/Myh3tm1.2Sajm | |||||||
Myh3tm1.2Sajm/Myh3tm1.1Sajm Pax3tm1(cre)Joe/Pax3+ (conditional) |
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Myh3tm1.2Sajm/Myh3tm1.1Sajm Pax7tm1(cre)Mrc/Pax7+ (conditional) |
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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last database update 03/19/2024 MGI 6.23 |
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