KCTD9

KCTD9
Available structures
PDB	Ortholog search: PDBe RCSB
List of PDB id codes
	5BXH
Identifiers
Aliases	KCTD9, BTBD27, potassium channel tetramerization domain containing 9
External IDs	OMIM: 617265 MGI: 2145579 HomoloGene: 9754 GeneCards: KCTD9
Gene location (Human)
Chr.	Chromosome 8 (human)[1]
End	25,458,476 bp[1]
Gene location (Mouse)
Chr.	Chromosome 14 (mouse)[2]
End	67,742,310 bp[2]
Gene ontology
Molecular function	• GO:0001948 protein binding; • identical protein binding; • protein self-association; • cullin family protein binding;
Cellular component	• intracellular;
Biological process	• protein homooligomerization; • GO:0007243 intracellular signal transduction; • protein ubiquitination;
	Sources:Amigo / QuickGO
Orthologs
	54793
	105440
	ENSG00000104756
	ENSMUSG00000034327
	Q7L273
	Q80UN1
	NM_017634
	NM_001111028; NM_001285933; NM_134073
	NP_060104
	NP_001104498; NP_001272862; NP_598834
	Wikidata
View/Edit Human	View/Edit Mouse

Potassium channel tetramerization domain containing 9 is a protein that in humans is encoded by the KCTD9 gene. [5]

References

GRCh38: Ensembl release 89: ENSG00000104756 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000034327 - Ensembl, May 2017
"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Entrez Gene: Potassium channel tetramerization domain containing 9". Retrieved 2018-04-02.

PDBe-KB provides an overview of all the structure information available in the PDB for Human BTB/POZ domain-containing protein KCTD9

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