|
Symbol Name ID |
Polrmt
polymerase (RNA) mitochondrial (DNA directed) MGI:1915843 |
| Darker colors indicate more annotations |
| Human Phenotypes | Hypotonia |
Muscle weakness |
Proximal muscle weakness |
Type 2 muscle fiber predominance |
Skeletal muscle atrophy |
Myopathy |
| Disease(s) Associated with POLRMT | ||||||
| combined oxidative phosphorylation deficiency 55 |
| Mouse Phenotypes | dilated cardiomyopathy |
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| Availability | Mouse Genotype | |
| Polrmttm1.1Arte/Polrmttm1.1Arte Tg(Ckmm-cre)5Khn/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 04/16/2024 MGI 6.23 |
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