ENTPD6
From Wikipedia, the free encyclopedia
Ectonucleoside triphosphate diphosphohydrolase 6 (putative function)
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Identifiers | |||||||||||
Symbol(s) | ENTPD6; CD39L2; DKFZp781G2277; DKFZp781K21102; FLJ36711; IL-6SAG; IL6ST2; NTPDase-6; dJ738P15.3 | ||||||||||
External IDs | OMIM: 603160 MGI: 1202295 HomoloGene: 68170 | ||||||||||
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RNA expression pattern | |||||||||||
Orthologs | |||||||||||
Human | Mouse | ||||||||||
Entrez | 955 | 12497 | |||||||||
Ensembl | ENSG00000197586 | ENSMUSG00000033068 | |||||||||
Uniprot | O75354 | n/a | |||||||||
Refseq | NM_001247 (mRNA) NP_001238 (protein) |
NM_172117 (mRNA) NP_742115 (protein) |
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Location | Chr 20: 25.12 - 25.16 Mb | Chr 2: 150.44 - 150.46 Mb | |||||||||
Pubmed search | [1] | [2] |
Ectonucleoside triphosphate diphosphohydrolase 6 (putative function), also known as ENTPD6, is a human gene.[1]
ENTPD6 is similar to E-type nucleotidases (NTPases). NTPases, such as CD39, mediate catabolism of extracellular nucleotides. ENTPD6 contains 4 apyrase-conserved regions which is characteristic of NTPases.[1]
[edit] References
[edit] Further reading
- Chadwick BP, Frischauf AM (1997). "Cloning and mapping of a human and mouse gene with homology to ecto-ATPase genes.". Mamm. Genome 8 (9): 668-72. PMID 9271669.
- Chadwick BP, Frischauf AM (1998). "The CD39-like gene family: identification of three new human members (CD39L2, CD39L3, and CD39L4), their murine homologues, and a member of the gene family from Drosophila melanogaster.". Genomics 50 (3): 357-67. doi: . PMID 9676430.
- Hicks-Berger CA, Chadwick BP, Frischauf AM, Kirley TL (2000). "Expression and characterization of soluble and membrane-bound human nucleoside triphosphate diphosphohydrolase 6 (CD39L2).". J. Biol. Chem. 275 (44): 34041-5. doi: . PMID 10948193.
- Yeung G, Mulero JJ, McGowan DW, et al. (2000). "CD39L2, a gene encoding a human nucleoside diphosphatase, predominantly expressed in the heart.". Biochemistry 39 (42): 12916-23. PMID 11041856.
- Hartley JL, Temple GF, Brasch MA (2001). "DNA cloning using in vitro site-specific recombination.". Genome Res. 10 (11): 1788-95. PMID 11076863.
- Wiemann S, Weil B, Wellenreuther R, et al. (2001). "Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs.". Genome Res. 11 (3): 422-35. doi: . PMID 11230166.
- Deloukas P, Matthews LH, Ashurst J, et al. (2002). "The DNA sequence and comparative analysis of human chromosome 20.". Nature 414 (6866): 865-71. doi: . PMID 11780052.
- 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: . PMID 12477932.
- Ivanenkov VV, Murphy-Piedmonte DM, Kirley TL (2004). "Bacterial expression, characterization, and disulfide bond determination of soluble human NTPDase6 (CD39L2) nucleotidase: implications for structure and function.". Biochemistry 42 (40): 11726-35. doi: . PMID 14529283.
- 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: . PMID 14702039.
- 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: . PMID 15489334.
- Wiemann S, Arlt D, Huber W, et al. (2004). "From ORFeome to biology: a functional genomics pipeline.". Genome Res. 14 (10B): 2136-44. doi: . PMID 15489336.
- Otsuki T, Ota T, Nishikawa T, et al. (2007). "Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries.". DNA Res. 12 (2): 117-26. doi: . PMID 16303743.
- Mehrle A, Rosenfelder H, Schupp I, et al. (2006). "The LIFEdb database in 2006.". Nucleic Acids Res. 34 (Database issue): D415-8. doi: . PMID 16381901.
- Lim J, Hao T, Shaw C, et al. (2006). "A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration.". Cell 125 (4): 801-14. doi: . PMID 16713569.