KCTD12

BTB/POZ domain-containing protein KCTD12 is a protein that in humans is encoded by the KCTD12 gene.[5][6]

KCTD12
Identifiers
Aliases	KCTD12, C13orf2, PFET1, PFETIN, potassium channel tetramerization domain containing 12
External IDs	OMIM: 610521 MGI: 2145823 HomoloGene: 16316 GeneCards: KCTD12
Gene location (Human) Chr. Chromosome 13 (human)[1] Band 13q22.3 Start 76,880,175 bp[1] End 76,886,405 bp[1]
Gene location (Mouse) Chr. Chromosome 14 (mouse)[2] Band 14|14 E2.3 Start 102,976,581 bp[2] End 102,982,637 bp[2]
RNA expression pattern More reference expression data
Gene ontology Molecular function • RNA binding • identical protein binding Cellular component • cell junction • postsynaptic membrane • cell membrane • synapse • extracellular exosome • presynaptic membrane • membrane Biological process • protein homooligomerization Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	115207	239217
Ensembl	ENSG00000178695	ENSMUSG00000098557
UniProt	Q96CX2	Q6WVG3
RefSeq (mRNA)	NM_138444	NM_177715
RefSeq (protein)	NP_612453	NP_808383
Location (UCSC)	Chr 13: 76.88 – 76.89 Mb	Chr 14: 102.98 – 102.98 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

References

1. GRCh38: Ensembl release 89: ENSG00000178695 - Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000098557 - Ensembl, May 2017
3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
5. Resendes BL, Kuo SF, Robertson NG, Giersch AB, Honrubia D, Ohara O, Adams JC, Morton CC (Sep 2004). "Isolation from cochlea of a novel human intronless gene with predominant fetal expression". J Assoc Res Otolaryngol. 5 (2): 185–202. doi:10.1007/s10162-003-4042-x. PMC 2538407. PMID 15357420.
6. "Entrez Gene: KCTD12 potassium channel tetramerisation domain containing 12".

Further reading

• Andersson B, Wentland MA, Ricafrente JY, et al. (1996). "A "double adaptor" method for improved shotgun library construction". Anal. Biochem. 236 (1): 107–13. doi:10.1006/abio.1996.0138. PMID 8619474.
• Bonaldo MF, Lennon G, Soares MB (1997). "Normalization and subtraction: two approaches to facilitate gene discovery". Genome Res. 6 (9): 791–806. doi:10.1101/gr.6.9.791. PMID 8889548.
• Yu W, Andersson B, Worley KC, et al. (1997). "Large-scale concatenation cDNA sequencing". Genome Res. 7 (4): 353–8. doi:10.1101/gr.7.4.353. PMC 139146. PMID 9110174.
• Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
• Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
• Bouwmeester T, Bauch A, Ruffner H, et al. (2004). "A physical and functional map of the human TNF-alpha/NF-kappa B signal transduction pathway". Nat. Cell Biol. 6 (2): 97–105. doi:10.1038/ncb1086. PMID 14743216.
• Ballif BA, Villén J, Beausoleil SA, et al. (2005). "Phosphoproteomic analysis of the developing mouse brain". Mol. Cell. Proteomics. 3 (11): 1093–101. doi:10.1074/mcp.M400085-MCP200. PMID 15345747.
• Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
• Kimura K, Wakamatsu A, Suzuki Y, et al. (2006). "Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes". Genome Res. 16 (1): 55–65. doi:10.1101/gr.4039406. PMC 1356129. PMID 16344560.
• Ewing RM, Chu P, Elisma F, et al. (2007). "Large-scale mapping of human protein-protein interactions by mass spectrometry". Mol. Syst. Biol. 3 (1): 89. doi:10.1038/msb4100134. PMC 1847948. PMID 17353931.