| GENE NAME | AKAP9 |
| CHROMOSOME | 7 |
| ENSEMBL ID | ENSG00000127914 |
| ENTREZ ID | 10142 |
| UNIPROT ACCESSION NUMBER | Q99996 |
| GO MOLECULAR FUNCTION | protein binding; DNA binding; signaling receptor binding; transmembrane transporter binding; molecular adaptor activity; protein kinase A regulatory subunit binding; potassium channel regulator activity |
| ESSENTIAL IN MOUSE | None |
| PATHWAYS | R-HSA-6802957; R-HSA-2565942; R-HSA-397014; R-HSA-453274; R-HSA-5663202; R-HSA-1852241; R-HSA-1643685; R-HSA-380320; R-HSA-5617833; R-HSA-68886; R-HSA-380259; R-HSA-5576893; R-HSA-6802952; R-HSA-8854518; R-HSA-380287; R-HSA-5620912; R-HSA-68877; R-HSA-5576890; R-HSA-69278; R-HSA-380270; R-HSA-5576891; R-HSA-1640170; R-HSA-380284; R-HSA-69275 |
| 2 combinations linked to AKAP9 | OLI1066; OLI647 |
| 2 variants linked to AKAP9 | AKAP9:c.4826G>A, p.Arg1609Lys; AKAP9:c.4351A>G, p.Met1451Val |
| 2 diseases linked to AKAP9 | Primary ovarian failure; Sudden infant death syndrome |