Symbol Name ID |
Capn1
calpain 1 MGI:88263 |
Darker colors indicate more annotations |
Human Phenotypes | Lower limb muscle weakness |
Lower limb spasticity |
Spastic paraplegia |
Difficulty walking |
Skeletal muscle atrophy |
Disease(s) Associated with CAPN1 | |||||
hereditary spastic paraplegia 76 |
Mouse Phenotypes | decreased ventricle muscle contractility |
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Availability | Mouse Genotype | |
Tg(Myh6*/tetO-Capn1)L2Gwd/0 |
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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