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Nucleic Acids Research, 2004, Vol. 32, Database issue D502-D504
© 2004 Oxford University Press

HUGE: a database for human KIAA proteins, a 2004 update integrating HUGEppi and ROUGE

Reiko Kikuno*,1, Takahiro Nagase1, Manabu Nakayama1, Hisashi Koga1,2, Noriko Okazaki1, Daisuke Nakajima1 and Osamu Ohara1,3

1 Kazusa DNA Research Institute, 2-6-7 Kazusa-Kamatari, Kisarazu, Chiba, 292-0818, Japan, 2 Chiba Industry Advancement Center, 2-6 Nakase, Mihama-ku, Chiba, 261-7126, Japan and 3 RIKEN Research Center for Allergy and Immunology, 1-7-22 Suehiro, Tsurumi-ku, Yokohama, Kanagawa, 230-0045, Japan

*To whom correspondence should be addressed. Tel: +81 438 52 3932; Fax: +81 438 52 3931; Email: kikuno{at}kazusa.or.jp

We have been developing a Human Unidentified Gene-Encoded (HUGE) protein database (http://www.kazusa.or.jp/huge) to summarize results from sequence analysis of human novel large (>4 kb) cDNAs identified in the Kazusa cDNA sequencing project. At present, HUGE contains 2031 cDNA entries (KIAA cDNAs), for each of which a gene/protein characteristic table has been prepared. Since we have been shifting our research attention from the identification and cloning of novel cDNAs to the functional analysis of the proteins encoded by these cDNAs (KIAA proteins), we have not substantially increased the number of cDNA entries in HUGE for some time. Instead, we have manually curated 451 KIAA cDNAs in order to prepare a set of genetic resources to facilitate the functional analysis of KIAA proteins. In addition, we have updated the contents of the corresponding gene/protein characteristic tables in HUGE and have constructed two subsidiary databases, HUGEppi (http://www. kazusa.or.jp/huge/ppi) and ROUGE (http://www. kazusa.or.jp/rouge), to make available the results from our study of KIAA protein function. HUGEppi shows detailed information on protein–protein interactions detected between 84 pairs of KIAA proteins by yeast two-hybrid screening. ROUGE summarizes the results of computer-assisted analyses of ~1000 mouse homologues of human large cDNAs that we identified.


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