KCTD12

KCTD12
Identifiers
Aliases	KCTD12, C13orf2, PFET1, PFETIN, potassium channel tetramerization domain containing 12
External IDs	OMIM: 610521; MGI: 2145823; HomoloGene: 16316; GeneCards: KCTD12; OMA:KCTD12 - orthologs
Gene location (Human)
Chr.	Chromosome 13 (human)
End	76,886,405 bp
Gene location (Mouse)
Chr.	Chromosome 14 (mouse)
End	103,220,073 bp
RNA expression pattern
	Top expressed in
	trigeminal ganglion; ; urethra; ; bronchial epithelial cell; ; lactiferous duct; ; synovial joint; ; mucosa of paranasal sinus; ; superficial temporal artery; ; lower lobe of lung; ; pericardium; ; parietal pleura;
	Top expressed in
	molar; ; vestibular sensory epithelium; ; granulocyte; ; pineal gland; ; dermis; ; body of femur; ; human fetus; ; lobe of cerebellum; ; skin of external ear; ; cerebellar vermis;
	More reference expression data
	; ;
	More reference expression data
Gene ontology
Molecular function	RNA binding; identical protein binding;
Cellular component	cell junction; postsynaptic membrane; plasma membrane; synapse; extracellular exosome; presynaptic membrane; membrane;
Biological process	protein homooligomerization;
	Sources:Amigo / QuickGO
Orthologs
	115207
	239217
	ENSG00000178695
	ENSMUSG00000098557
	Q96CX2
	Q6WVG3
	NM_138444
	NM_177715
	NP_612453
	NP_808383
	Wikidata
View/Edit Human	View/Edit Mouse

BTB/POZ domain-containing protein KCTD12 is a protein that in humans is encoded by the KCTD12 gene.

It may be associated with rumination and Bipolar Disorder.