KCTD8

KCTD8
Identifiers
Aliases	KCTD8, potassium channel tetramerization domain containing 8
External IDs	OMIM: 618442 MGI: 2443804 HomoloGene: 18464 GeneCards: KCTD8
Gene location (Human)
Chr.	Chromosome 4 (human)[1]
End	44,448,809 bp[1]
Gene location (Mouse)
Chr.	Chromosome 5 (mouse)[2]
End	69,499,022 bp[2]
RNA expression pattern
	Top expressed in
	cerebellar vermis; ; corpus callosum; ; cerebellar hemisphere; ; prefrontal cortex; ; superior frontal gyrus; ; spinal cord; ; Brodmann area 9; ; nucleus accumbens; ; caudate nucleus; ; putamen;
	Top expressed in
	habenula; ; inferior colliculus; ; cerebellar vermis; ; medial vestibular nucleus; ; globus pallidus; ; nucleus accumbens; ; facial motor nucleus; ; trigeminal ganglion; ; dorsal tegmental nucleus; ; superior colliculus;
	More reference expression data
	n/a
Orthologs
	386617
	243043
	ENSG00000183783
	ENSMUSG00000037653
	Q6ZWB6
	Q50H33
	NM_198353
	NM_175519
	NP_938167
	NP_780728
	Wikidata
View/Edit Human	View/Edit Mouse

Potassium channel tetramerization domain containing 8 is a protein that in humans is encoded by the KCTD8 gene. [5]

References

GRCh38: Ensembl release 89: ENSG00000183783 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000037653 - 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 8". Retrieved 2016-06-21.

Paus T, Bernard M, Chakravarty MM, Davey Smith G, Gillis J, Lourdusamy A, Melka MG, Leonard G, Pavlidis P, Perron M, Pike GB, Richer L, Schumann G, Timpson N, Toro R, Veillette S, Pausova Z (2012). "KCTD8 gene and brain growth in adverse intrauterine environment: a genome-wide association study". Cereb. Cortex. 22 (11): 2634–42. doi:10.1093/cercor/bhr350. PMC 3464418. PMID 22156575.

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