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Symbol Name ID |
Klhl41
kelch-like 41 MGI:2683854 |
| Darker colors indicate more annotations |
| Human Phenotypes | Arthrogryposis multiplex congenita |
Muscle weakness |
Nemaline bodies |
| Disease(s) Associated with KLHL41 | |||
| nemaline myopathy 9 |
| Mouse Phenotypes | abnormal diaphragm morphology |
myopathy |
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| Availability | Mouse Genotype | ||
| Klhl41tm1a(KOMP)Wtsi/Klhl41tm1a(KOMP)Wtsi | |||
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 04/30/2024 MGI 6.23 |
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