Sequence Detail

ID/Version

Q8BGV7 Q6AXE9 (UniProt | EBI)

Last sequence update: 2003-03-01
Last annotation update: 2026-06-10

Sequence description from provider

RecName: Full=BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 1;AltName: Full=BTB/POZ domain-containing protein KCTD13;AltName: Full=Polymerase delta-interacting protein 1;

Provider

SWISS-PROT

Sequence

Polypeptide 329 aa

Source

Organism mouse

See UniProt | EBI for source

Annotated genes and markers

Follow the symbol links to get more information on the GO terms, expression assays, orthologs, phenotypic alleles, and other information for the genes or markers below.

Type	Symbol	Name	GO Terms	Expression Assays	Orthologs	Phenotypic Alleles
Gene	Kctd13	potassium channel tetramerisation domain containing 13	43	105	2	17

Sequence references in MGI

J:99680 The FANTOM Consortium and RIKEN Genome Exploration Research Group and Genome Science Group (Genome Network Project Core Group), The Transcriptional Landscape of the Mammalian Genome. Science. 2005;309(5740):1559-1563
J:250125 Escamilla CO, et al., Kctd13 deletion reduces synaptic transmission via increased RhoA. Nature. 2017 Nov 9;551(7679):227-231
J:346633 Cheng J, et al., KCTD10 regulates brain development by destabilizing brain disorder-associated protein KCTD13. Proc Natl Acad Sci U S A. 2024 Mar 19;121(12):e2315707121
J:380584 Gu J, et al., KCTD13-mediated ubiquitination and degradation of GluN1 regulates excitatory synaptic transmission and seizure susceptibility. Cell Death Differ. 2023 Jul;30(7):1726-1741