KCTD7 information

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; ; middle frontal gyrus; ; stromal cell of endometrium; ; substantia nigra; ; Brodmann area 10; ; nucleus accumbens; ; inferior ganglion of vagus nerve; ; frontal pole; ; amygdala; ; cingulate gyrus;
	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.^[4] Alternative splicing results in multiple transcript variants.

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000243335 – 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 tetramerisation domain containing 7". Retrieved 2012-07-24.

[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000243335 – Ensembl, May 2017

[2] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[3] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[entrez-4] "Entrez Gene: Potassium channel tetramerisation domain containing 7". Retrieved 2012-07-24.

KCTD7 information

and 4 Related for: KCTD7 information

KCTD7

Williams syndrome

Potassium channel tetramerisation domain

List of OMIM disorder codes