KCTD12

From Wikipedia, the free encyclopedia

Potassium channel tetramerisation domain containing 12

Identifiers

KCTD12; C13orf2; FLJ33073; KIAA1778; PFET1

External IDs

OMIM: 610521 MGI: 2145823 HomoloGene: 16316

Gene ontology
Molecular Function:	• voltage-gated potassium channel activity • protein binding
Cellular Component:	• voltage-gated potassium channel complex • membrane
Biological Process:	• potassium ion transport

RNA expression pattern

More reference expression data

Orthologs

Human

Mouse

n/a

n/a

Refseq

NM_138444 (mRNA)
NP_612453 (protein)

NM_177715 (mRNA)
NP_808383 (protein)

Location

Chr 13: 76.35 - 76.36 Mb

n/a

Pubmed search

[1]

[2]

Potassium channel tetramerisation domain containing 12, also known as KCTD12, is a human gene.^[1]

[edit] References

^ Entrez Gene: KCTD12 potassium channel tetramerisation domain containing 12.

[edit] Further reading

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Bonaldo MF, Lennon G, Soares MB (1997). "Normalization and subtraction: two approaches to facilitate gene discovery.". Genome Res. 6 (9): 791-806. PMID 8889548.
Yu W, Andersson B, Worley KC, et al. (1997). "Large-scale concatenation cDNA sequencing.". Genome Res. 7 (4): 353-8. 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. 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.
Resendes BL, Kuo SF, Robertson NG, et al. (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. PMID 15357420.
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. 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. 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: 89. doi:10.1038/msb4100134. PMID 17353931.