|
Symbol Name ID |
Mcat
malonyl CoA:ACP acyltransferase (mitochondrial) MGI:2388651 |
| Darker colors indicate more annotations |
| Human Phenotypes | Weakness of facial musculature |
Scapular winging |
Spasticity |
Spastic paraplegia |
Skeletal muscle atrophy |
Myopathy |
| Disease(s) Associated with MCAT | ||||||
| optic atrophy |
| Mouse Phenotypes | increased skeletal muscle glycogen level |
abnormal muscle physiology |
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| Availability | Mouse Genotype | ||
| Mcattm1.1Ssmi/Mcattm1.1Ssmi Tg(CAG-cre/Esr1*)5Amc/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 04/23/2024 MGI 6.23 |
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