Kctd17 - potassium channel tetramerization domain containing 17 Gene
Also Known as RGD1311154
Species: Rattus norvegicus
Summary
Predicted to enable cullin family protein binding activity and identical protein binding activity. Predicted to be involved in endoplasmic reticulum calcium ion homeostasis; positive regulation of cilium assembly; and proteasome-mediated ubiquitin-dependent protein catabolic process. Predicted to be located in endoplasmic reticulum. Predicted to be part of Cul3-RING ubiquitin Ligase complex. Predicted to be active in cytoplasm. Human ortholog(s) of this gene implicated in myoclonic dystonia 26. Orthologous to human KCTD17 (Potassium Channel tetramerization domain containing 17). [provided by Alliance of Genome Resources, Apr 2022]
Kctd17 Products (2)
| mRNA | Protein | Name |
|---|---|---|
| NM_001134529.1 | NP_001128001.1 | BTB/POZ domain-containing protein KCTD17 isoform 2 |
| NM_001395732.1 | NP_001382661.1 | BTB/POZ domain-containing protein KCTD17 isoform 1 |
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
BTB/POZ domain-containing protein KCTD17 |
|
Related Agents
- Pre-clinical Phase
Pre-clinical Phase
| Cat. No. | Product Name |
Effect
|
Purity |
Rare Diseases
|
|---|---|---|---|---|
| HY-RS07194 | KCTD17 Human Pre-designed siRNA Set A | Pre-designed Set | / | Unkown |
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