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 |
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OMIM ID | | 300708 |
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