Symbol Name ID |
Slc18a3
solute carrier family 18 (vesicular monoamine), member 3 MGI:1101061 |
Darker colors indicate more annotations |
Human Phenotypes | Weakness of facial musculature |
Knee flexion contracture |
Hypotonia |
Difficulty walking |
Easy fatigability |
Fatigable weakness of skeletal muscles |
Disease(s) Associated with SLC18A3 | ||||||
congenital myasthenic syndrome 21 |
Mouse Phenotypes | skeletal muscle fiber atrophy |
abnormal skeletal muscle morphology |
skeletal muscle atrophy |
hypotonia |
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Availability | Mouse Genotype | ||||
Chat/Slc18a3tm1.1Vpra/Chat/Slc18a3tm1.1Vpra |
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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