| Gene Symbol | LCA5 |
| Entrez Gene ID | 167691 |
| Full Name | LCA5, lebercilin |
| Synonyms | C6orf152 |
| General protein information |
|
| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | This gene encodes a protein that is thought to be involved in centrosomal or ciliary functions. Mutations in this gene cause Leber congenital amaurosis type V. Alternatively spliced transcript variants are described. [provided by RefSeq, Oct 2009]. |
| Disorder MIM: | |
| Disorder Html: | Leber congenital amaurosis 5, 604537 (3) |








































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