|
Symbol Name ID |
Mcat
malonyl CoA:ACP acyltransferase (mitochondrial) MGI:2388651 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Feeding difficulties |
Fatigue |
Myalgia |
| Disease(s) Associated with MCAT | |||
| optic atrophy |
| Mouse Phenotypes | behavior/neurological phenotype |
decreased exploration in new environment |
abnormal eating behavior |
excessive scratching |
tremors |
decreased grip strength |
abnormal gait |
decreased vertical activity |
decreased locomotor activity |
impaired exercise endurance |
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| Availability | Mouse Genotype | ||||||||||
| Mcattm1.1Ssmi/Mcattm1.1Ssmi Tg(CAG-cre/Esr1*)5Amc/0 (conditional) |
* | ||||||||||
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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