|
Symbol Name ID |
H2-K1
histocompatibility 2, K1, K region MGI:95904 |
| Darker colors indicate more annotations |
| Human Phenotypes | Facial palsy |
Abnormality of the musculature |
Functional motor deficit |
Muscle weakness |
Proximal muscle weakness |
| Disease(s) Associated with HLA-A | |||||
| Moyamoya disease | |||||
| Disease(s) Associated with HLA-B | |||||
| Graves' disease | |||||
| sarcoidosis | |||||
| Mouse Phenotypes | myositis |
skeletal muscle fiber atrophy |
skeletal muscle fiber degeneration |
abnormal skeletal muscle morphology |
muscle weakness |
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| Availability | Mouse Genotype | |||||
| Tg(CKMM-tTA)A3Rhvh/0 Tg(tetO-H2-K1)#Papl/0 |
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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 05/28/2024 MGI 6.13 |
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