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Symbol Name ID |
Tpm3
tropomyosin 3, gamma MGI:1890149 |
| Darker colors indicate more annotations |
| Human Phenotypes | Facial palsy |
Facial diplegia |
Distal lower limb muscle weakness |
Shoulder girdle muscle atrophy |
Flexion contracture |
Limb joint contracture |
Neonatal hypotonia |
EMG: myopathic abnormalities |
Bulbar palsy |
Generalized muscle weakness |
Neck muscle weakness |
Proximal muscle weakness |
Respiratory insufficiency due to muscle weakness |
Type 1 fibers relatively smaller than type 2 fibers |
Centrally nucleated skeletal muscle fibers |
Nemaline bodies |
Distal lower limb amyotrophy |
| Disease(s) Associated with TPM3 | |||||||||||||||||
| congenital myopathy 4A | |||||||||||||||||
| nemaline myopathy 1 |
| Mouse Phenotypes | abnormal muscle morphology |
abnormal muscle contractility |
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| Availability | Mouse Genotype | ||
| Tpm3tm3Pgun/Tpm3tm3Pgun | |||
| Tpm3tm4.1Pgun/Tpm3tm4.1Pgun | |||
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 04/16/2024 MGI 6.23 |
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