KCTD8
potassium channel tetramerization domain containing 8
Summary
Predicted to enable G protein-coupled neurotransmitter receptor activity involved in regulation of presynaptic membrane potential. Predicted to be involved in regulation of G protein-coupled receptor signaling pathway. Predicted to be located in cell projection and postsynaptic membrane. Predicted to be part of receptor complex. Predicted to be active in postsynapse and presynaptic active zone membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs765990631 | 4:44,176,848 | G/A | — | uncertain significance |
| rs752969831 | 4:44,176,854 | G/A | — | uncertain significance |
| rs1187555796 | 4:44,176,917 | C/T | — | uncertain significance |
| rs1713163136 | 4:44,177,019 | G/T | — | uncertain significance |
| rs1378248703 | 4:44,177,025 | G/A | — | uncertain significance |
| rs549391615 | 4:44,177,058 | G/A | — | uncertain significance |
| rs2475058210 | 4:44,177,115 | T/C | — | uncertain significance |
| rs576508629 | 4:44,183,941 | C/G | — | — |
| rs17641529 | 4:44,212,165 | A/G | intron variant | — |
| rs563303919 | 4:44,269,505 | G/C | — | — |
| rs73247537 | 4:44,401,580 | G/A | intron variant | — |
| rs6447335 | 4:44,431,494 | G/C | intron variant | — |
| rs556962187 | 4:44,443,904 | G/A | — | — |
| rs776923781 | 4:44,449,648 | G/A | — | uncertain significance |
| rs1450627002 | 4:44,449,757 | G/A | — | uncertain significance |
| rs200013511 | 4:44,449,781 | C/G | — | uncertain significance |
| rs1280175125 | 4:44,449,793 | C/T | — | uncertain significance |
| rs2475246143 | 4:44,449,819 | A/C | — | uncertain significance |
| rs762454343 | 4:44,449,892 | A/G | — | uncertain significance |
| rs1380053110 | 4:44,449,934 | C/A | — | uncertain significance |
| rs778853493 | 4:44,449,966 | G/A | — | likely benign |
| rs1183514235 | 4:44,449,984 | A/G | — | likely benign |
| rs1043076701 | 4:44,450,054 | T/C | — | uncertain significance |
| rs769825135 | 4:44,450,062 | C/A | — | uncertain significance |
| rs138935237 | 4:44,450,131 | A/T | — | uncertain significance |
| rs2475247974 | 4:44,450,154 | C/A | — | likely benign |
| rs778642107 | 4:44,450,177 | C/T | — | uncertain significance |
| rs1016600855 | 4:44,450,210 | C/A | — | uncertain significance |
| rs1722008156 | 4:44,450,323 | A/G | — | uncertain significance |
| rs770265841 | 4:44,450,327 | T/C | — | uncertain significance |
| rs1395811557 | 4:44,450,377 | T/G | — | uncertain significance |
| rs184972342 | 4:44,450,420 | G/A | — | uncertain significance |
| rs1425729397 | 4:44,450,449 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.