| Gene Symbol | KLHL41 |
| Entrez Gene ID | 10324 |
| Full Name | kelch like family member 41 |
| Synonyms | KBTBD10,Krp1,SARCOSIN |
| General protein information |
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| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | This gene is a member of the kelch-like family. The encoded protein contains a BACK domain, a BTB/POZ domain, and 5 Kelch repeats. This protein is thought to function in skeletal muscle development and maintenance. Mutations in this gene have been associated with nemaline myopathy (NM), a rare congenital muscle disorder. [provided by RefSeq, Mar 2015]. |
| Disorder MIM: | |
| Disorder Html: | Nemaline myopathy 9, 615731 (3) |
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