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Symbol Name ID |
Xk
X-linked Kx blood group MGI:103569 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Muscle weakness |
Myopathy |
Rhabdomyolysis |
| Disease(s) Associated with XK | |||
| McLeod syndrome |
| Mouse Phenotypes | muscle phenotype |
abnormal skeletal muscle fiber morphology |
increased variability of skeletal muscle fiber size |
centrally nucleated skeletal muscle fibers |
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| Availability | Mouse Genotype | ||||
| Xktm1Ariv/Xktm1Ariv | * | ||||
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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