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H-InvDB in 2013: an omics study platform for human functional gene and transcript discovery
H-InvDB (http://www.h-invitational.jp/) is a comprehensive human gene database started in 2004. In the latest version, H-InvDB 8.0, a total of 244 709 human complementary DNA was mapped onto the hg19 reference genome and 43 829 gene loci, including nonprotein-coding ones, were identified. Of these l...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3531145/ https://www.ncbi.nlm.nih.gov/pubmed/23197657 http://dx.doi.org/10.1093/nar/gks1245 |
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author | Takeda, Jun-ichi Yamasaki, Chisato Murakami, Katsuhiko Nagai, Yoko Sera, Miho Hara, Yuichiro Obi, Nobuo Habara, Takuya Gojobori, Takashi Imanishi, Tadashi |
author_facet | Takeda, Jun-ichi Yamasaki, Chisato Murakami, Katsuhiko Nagai, Yoko Sera, Miho Hara, Yuichiro Obi, Nobuo Habara, Takuya Gojobori, Takashi Imanishi, Tadashi |
author_sort | Takeda, Jun-ichi |
collection | PubMed |
description | H-InvDB (http://www.h-invitational.jp/) is a comprehensive human gene database started in 2004. In the latest version, H-InvDB 8.0, a total of 244 709 human complementary DNA was mapped onto the hg19 reference genome and 43 829 gene loci, including nonprotein-coding ones, were identified. Of these loci, 35 631 were identified as potential protein-coding genes, and 22 898 of these were identical to known genes. In our analysis, 19 309 annotated genes were specific to H-InvDB and not found in RefSeq and Ensembl. In fact, 233 genes of the 19 309 turned out to have protein functions in this version of H-InvDB; they were annotated as unknown protein functions in the previous version. Furthermore, 11 genes were identified as known Mendelian disorder genes. It is advantageous that many biologically functional genes are hidden in the H-InvDB unique genes. As large-scale proteomic projects have been conducted to elucidate the functions of all human proteins, we have enhanced the proteomic information with an advanced protein view and new subdatabase of protein complexes (Protein Complex Database with quality index). We propose that H-InvDB is an important resource for finding novel candidate targets for medical care and drug development. |
format | Online Article Text |
id | pubmed-3531145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-35311452013-03-07 H-InvDB in 2013: an omics study platform for human functional gene and transcript discovery Takeda, Jun-ichi Yamasaki, Chisato Murakami, Katsuhiko Nagai, Yoko Sera, Miho Hara, Yuichiro Obi, Nobuo Habara, Takuya Gojobori, Takashi Imanishi, Tadashi Nucleic Acids Res Articles H-InvDB (http://www.h-invitational.jp/) is a comprehensive human gene database started in 2004. In the latest version, H-InvDB 8.0, a total of 244 709 human complementary DNA was mapped onto the hg19 reference genome and 43 829 gene loci, including nonprotein-coding ones, were identified. Of these loci, 35 631 were identified as potential protein-coding genes, and 22 898 of these were identical to known genes. In our analysis, 19 309 annotated genes were specific to H-InvDB and not found in RefSeq and Ensembl. In fact, 233 genes of the 19 309 turned out to have protein functions in this version of H-InvDB; they were annotated as unknown protein functions in the previous version. Furthermore, 11 genes were identified as known Mendelian disorder genes. It is advantageous that many biologically functional genes are hidden in the H-InvDB unique genes. As large-scale proteomic projects have been conducted to elucidate the functions of all human proteins, we have enhanced the proteomic information with an advanced protein view and new subdatabase of protein complexes (Protein Complex Database with quality index). We propose that H-InvDB is an important resource for finding novel candidate targets for medical care and drug development. Oxford University Press 2013-01 2012-11-28 /pmc/articles/PMC3531145/ /pubmed/23197657 http://dx.doi.org/10.1093/nar/gks1245 Text en © The Author(s) 2012. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial reuse, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com. |
spellingShingle | Articles Takeda, Jun-ichi Yamasaki, Chisato Murakami, Katsuhiko Nagai, Yoko Sera, Miho Hara, Yuichiro Obi, Nobuo Habara, Takuya Gojobori, Takashi Imanishi, Tadashi H-InvDB in 2013: an omics study platform for human functional gene and transcript discovery |
title | H-InvDB in 2013: an omics study platform for human functional gene and transcript discovery |
title_full | H-InvDB in 2013: an omics study platform for human functional gene and transcript discovery |
title_fullStr | H-InvDB in 2013: an omics study platform for human functional gene and transcript discovery |
title_full_unstemmed | H-InvDB in 2013: an omics study platform for human functional gene and transcript discovery |
title_short | H-InvDB in 2013: an omics study platform for human functional gene and transcript discovery |
title_sort | h-invdb in 2013: an omics study platform for human functional gene and transcript discovery |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3531145/ https://www.ncbi.nlm.nih.gov/pubmed/23197657 http://dx.doi.org/10.1093/nar/gks1245 |
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