| ID | Sequence | Length | GC content |
|---|---|---|---|
| AGUCAGAGUCACUAUGGCGGCCGGCGCUGGCAAGGUCGGAAAGUUUCCU… | 6240 nt | 0.4223 | |
| CGGCCGCGAUCUCAAACCAAACACAAGAAUUGGCGUGUGACUCAUCUGC… | 5409 nt | 0.3805 | |
| AGUUUGGGCUUGGAUGGUAACGUUUAUUUUCCUUGGCAGAGAAGCUGAU… | 3892 nt | 0.3569 | |
| AGUUUGGGCUUGGAUGGUAACGUUUAUUUUCCUUGGCAGAGAAGCUGAU… | 3694 nt | 0.3549 | |
| AGUUUGGGCUUGGAUGGUAACGUUUAUUUUCCUUGGCAGAGAAGCUGAU… | 3982 nt | 0.3599 | |
| AGUCAGAGUCACUAUGGCGGCCGGCGCUGGCAAGGUCGGAAAGUUUCCU… | 6312 nt | 0.4211 | |
| AGUCAGAGUCACUAUGGCGGCCGGCGCUGGCAAGGUCGGAAAGUUUCCU… | 6291 nt | 0.4217 | |
| AGUCAGAGUCACUAUGGCGGCCGGCGCUGGCAAGGUCGGAAAGUUUCCU… | 6381 nt | 0.4227 | |
| AGUCAGAGUCACUAUGGCGGCCGGCGCUGGCAAGGUCGGAAAGUUUCCU… | 6330 nt | 0.4232 | |
| AGUCAGAGUCACUAUGGCGGCCGGCGCUGGCAAGGUCGGAAAGUUUCCU… | 6330 nt | 0.4227 |
This gene encodes a component of a conserved striatin-interacting phosphatase and kinase complex. Striatin family complexes participate in a variety of cellular processes including signaling, cell cycle control, cell migration, Golgi assembly, and apoptosis. The protein encoded by this gene is a coiled-coil, tail-anchored membrane protein with a single C-terminal transmembrane domain that is posttranslationally inserted into membranes. Mutations in this gene are associated with Brugada syndrome, a cardiac channelopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]
A study in human heart tissue from sudden unexplained death (SUD) cases identified the SLMAP as a differentially expressed cardiac-related gene, with mutations in this gene reported in ion channelopathies or cardiomyopathies [Neubauer et al. DOI:10.1007/S00414-025-03414-4].