KCTD7

KCTD7
Identifiers
Aliases	KCTD7, CLN14, EPM3, potassium channel tetramerization domain containing 7
External IDs	OMIM: 611725; MGI: 2442265; HomoloGene: 17687; GeneCards: KCTD7; OMA:KCTD7 - orthologs
Gene location (Human)
Chr.	Chromosome 7 (human)
End	66,649,067 bp
RNA expression pattern
	Top expressed in
	ganglionic eminence; ; C1 segment; ; middle frontal gyrus; ; ventricular zone; ; stromal cell of endometrium; ; buccal mucosa cell; ; substantia nigra; ; Brodmann area 10; ; tendon of biceps brachii; ; nucleus accumbens;
	n/a
	More reference expression data
	n/a
Gene ontology
Molecular function	protein binding;
Cellular component	membrane; cytosol; cytoplasm; plasma membrane;
Biological process	protein homooligomerization; post-translational protein modification; cellular potassium ion homeostasis; positive regulation of transporter activity; membrane hyperpolarization; glutamate homeostasis;
	Sources:Amigo / QuickGO
Orthologs
	154881
	212919
	ENSG00000243335
	n/a
	Q96MP8
	Q8BJK1
	NM_153033; NM_001167961
	NM_172509
	NP_001161433; NP_694578; NP_694578.1
	NP_766097
	Wikidata
View/Edit Human	View/Edit Mouse

Potassium channel tetramerisation domain containing 7 is a protein in humans that is encoded by the KCTD7 gene. Alternative splicing results in multiple transcript variants.