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Symbol Name ID |
Smn1
survival motor neuron 1 MGI:109257 |
| Darker colors indicate more annotations |
| Human Phenotypes | Decreased fetal movement |
| Disease(s) Associated with SMN1 | |
| Werdnig-Hoffmann disease |
| Mouse Phenotypes | abnormal motor capabilities/coordination/movement |
impaired righting response |
tremors |
decreased grip strength |
abnormal limb posture |
abnormal locomotor behavior |
abnormal gait |
decreased vertical activity |
decreased locomotor activity |
paralysis |
paraparesis |
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| Availability | Mouse Genotype | |||||||||||
| Smn1tm1.1Dscd/Smn1tm1.1Dscd | ||||||||||||
| Smn1tm1Msd/Smn1tm1.1Dscd | ||||||||||||
| Smn1tm1Msd/Smn1tm1Rako | ||||||||||||
| Smn1tm1Jme/Smn1tm1Jme Tg(Eno2-cre)39Jme/0 (conditional) |
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| Smn1tm1Jme/Smn1tm1.1Jme Tg(Eno2-cre)39Jme/0 (conditional) |
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| Smn1tm1Jme/Smn1tm1.1Jme Tg(ACTA1-cre)79Jme/0 (conditional) |
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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 04/30/2024 MGI 6.23 |
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