| Entrez gene ID | | 92002 |
| Official gene symbol | | FAM58A |
| Full name | | family with sequence similarity 58, member A |
| Aliases | | ,MGC29729,STAR, |
| Gene summary | | Mutations in this gene have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly, telecanthus and anogenital and renal malformations. The protein encoded by this gene contains a cyclin-box-fold domain which suggests it may have a role in controlling nuclear cell division cycles. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq] |
| Location | | Chromosome: X Locus: Xq28 |
| Gene position | | 152864632 - 152853383 Map Viewer |
| Gene orientation | | minus |
| Gene size | | 11250 bp |
| Gene sequence |
| |
| OMIM ID | | 300708 |
|