2. Gene
  3. Kctd7 - potassium channel tetramerisation domain containing 7 Gene

Kctd7 - potassium channel tetramerisation domain containing 7 Gene

  • Gene
  • Protein
  • Agent
  • Ortholog
Mus musculus

Also known as 4932409E18; 9430010P06Rik

Gene ID: 212919 | Gene type: protein coding

About Kctd7

Summary

Predicted to enable identical protein binding activity. Involved in cellular potassium ion homeostasis; membrane hyperpolarization; and positive regulation of transporter activity. Located in plasma membrane. Human ortholog(s) of this gene implicated in progressive myoclonus epilepsy 3. Orthologous to human KCTD7 (Potassium Channel tetramerization domain containing 7). [provided by Alliance of Genome Resources, Apr 2022]

Kctd7 Products(1)

mRNA Protein Name
NM_172509.4 NP_766097.1 BTB/POZ domain-containing protein KCTD7
Gene Ontology
  • Biological Process
  • Cellular Component
Biological Process GO Annotation Evidence Reference Source
involved in intracellular potassium ion homeostasis IMP
IMP: Inferred from mutant phenotype
27742667 MGI
involved in membrane hyperpolarization IMP
IMP: Inferred from mutant phenotype
27742667 MGI
involved in positive regulation of transporter activity IMP
IMP: Inferred from mutant phenotype
27742667 MGI
Cellular Component GO Annotation Evidence Reference Source
located in plasma membrane IDA
IDA: Inferred from direct assay
27742667 MGI
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

BTB/POZ domain-containing protein KCTD7

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS07198 KCTD7 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens Kctd7 NCBI NCBI:154881