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- Publisher Website: 10.1006/geno.1995.9996
- Scopus: eid_2-s2.0-0029102720
- PMID: 8666380
- WOS: WOS:A1995RY05500004
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Article: Cloning and chromosomal mapping of three novel genes, GPR9, GPR10, and GPR14, encoding receptors related to interleukin 8, neuropeptide Y, and somatostatin receptors
Title | Cloning and chromosomal mapping of three novel genes, GPR9, GPR10, and GPR14, encoding receptors related to interleukin 8, neuropeptide Y, and somatostatin receptors |
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Authors | |
Issue Date | 1995 |
Publisher | Academic Press. The Journal's web site is located at http://www.elsevier.com/locate/ygeno |
Citation | Genomics, 1995, v. 29 n. 2, p. 335-344 How to Cite? |
Abstract | We employed the polymerase chain reaction and genomic DNA library screening to clone novel human genes, GPR9 and GPR10, and a rat gene, GPR14. GPR9, GPR10, and GPR14 each encode G protein-coupled receptors. GPR10 and GPR14 are intronless within their coding regions, while GPR9 contains at least one intron. The receptor encoded by GPR9 shares the highest identity with human IL-8 receptor type B (38% overall and 53% in the transmembrane regions), followed by IL-8 receptor type A (36% overall and 51% in the transmembrane domains). GPR10 encodes a receptor that shares highest identity with the neuropeptide Y receptor (31% overall and 46% in the transmembrane domains). The receptor encoded by GPR14 shares highest identity with the somatostatin receptor SSTR 4 (27% overall and 41% in the transmembrane domains). Fluorescence in situ hybridization analysis localized GPR9 to chromosome 8p11.2-p12 and GPR10 to chromosome 10q25.3-q26. |
Persistent Identifier | http://hdl.handle.net/10722/44289 |
ISSN | 2023 Impact Factor: 3.4 2023 SCImago Journal Rankings: 0.850 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Marchese, A | en_HK |
dc.contributor.author | Heiber, M | en_HK |
dc.contributor.author | Nguyen, T | en_HK |
dc.contributor.author | Heng, HHQ | en_HK |
dc.contributor.author | Saldivia, VR | en_HK |
dc.contributor.author | Cheng, R | en_HK |
dc.contributor.author | Murphy, PM | en_HK |
dc.contributor.author | Tsui, LC | en_HK |
dc.contributor.author | Shi, X | en_HK |
dc.contributor.author | Gregor, P | en_HK |
dc.contributor.author | George, SR | en_HK |
dc.contributor.author | O'Dowd, BF | en_HK |
dc.contributor.author | Docherty, JM | en_HK |
dc.date.accessioned | 2007-09-12T03:50:43Z | - |
dc.date.available | 2007-09-12T03:50:43Z | - |
dc.date.issued | 1995 | en_HK |
dc.identifier.citation | Genomics, 1995, v. 29 n. 2, p. 335-344 | en_HK |
dc.identifier.issn | 0888-7543 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/44289 | - |
dc.description.abstract | We employed the polymerase chain reaction and genomic DNA library screening to clone novel human genes, GPR9 and GPR10, and a rat gene, GPR14. GPR9, GPR10, and GPR14 each encode G protein-coupled receptors. GPR10 and GPR14 are intronless within their coding regions, while GPR9 contains at least one intron. The receptor encoded by GPR9 shares the highest identity with human IL-8 receptor type B (38% overall and 53% in the transmembrane regions), followed by IL-8 receptor type A (36% overall and 51% in the transmembrane domains). GPR10 encodes a receptor that shares highest identity with the neuropeptide Y receptor (31% overall and 46% in the transmembrane domains). The receptor encoded by GPR14 shares highest identity with the somatostatin receptor SSTR 4 (27% overall and 41% in the transmembrane domains). Fluorescence in situ hybridization analysis localized GPR9 to chromosome 8p11.2-p12 and GPR10 to chromosome 10q25.3-q26. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Academic Press. The Journal's web site is located at http://www.elsevier.com/locate/ygeno | en_HK |
dc.relation.ispartof | Genomics | en_HK |
dc.subject.mesh | Antigens, cd - biosynthesis - chemistry - genetics | en_HK |
dc.subject.mesh | Interleukin-8 - metabolism | en_HK |
dc.subject.mesh | Lymphocytes - cytology - immunology - metabolism | en_HK |
dc.subject.mesh | Rna, messenger - isolation & purification - metabolism | en_HK |
dc.subject.mesh | Receptors, interleukin - biosynthesis - chemistry - genetics | en_HK |
dc.title | Cloning and chromosomal mapping of three novel genes, GPR9, GPR10, and GPR14, encoding receptors related to interleukin 8, neuropeptide Y, and somatostatin receptors | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0888-7543&volume=29&issue=2&spage=335&epage=344&date=1995&atitle=Cloning+and+chromosomal+mapping+of+three+novel+genes,+GPR9,+GPR10,+and+GPR14,+encoding+receptors+related+to+interleukin+8,+neuropeptide+Y,+and+somatostatin+receptors | en_HK |
dc.identifier.email | Tsui, LC: tsuilc@hkucc.hku.hk | en_HK |
dc.identifier.authority | Tsui, LC=rp00058 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | en_HK |
dc.identifier.doi | 10.1006/geno.1995.9996 | en_HK |
dc.identifier.pmid | 8666380 | - |
dc.identifier.scopus | eid_2-s2.0-0029102720 | en_HK |
dc.identifier.volume | 29 | en_HK |
dc.identifier.issue | 2 | en_HK |
dc.identifier.spage | 335 | en_HK |
dc.identifier.epage | 344 | en_HK |
dc.identifier.isi | WOS:A1995RY05500004 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Marchese, A=7005075855 | en_HK |
dc.identifier.scopusauthorid | Heiber, M=6507950665 | en_HK |
dc.identifier.scopusauthorid | Nguyen, T=26667936100 | en_HK |
dc.identifier.scopusauthorid | Heng, HHQ=7005338076 | en_HK |
dc.identifier.scopusauthorid | Saldivia, VR=6602144935 | en_HK |
dc.identifier.scopusauthorid | Cheng, R=7201955297 | en_HK |
dc.identifier.scopusauthorid | Murphy, PM=7401685174 | en_HK |
dc.identifier.scopusauthorid | Tsui, LC=7102754167 | en_HK |
dc.identifier.scopusauthorid | Shi, X=7402953863 | en_HK |
dc.identifier.scopusauthorid | Gregor, P=7005077731 | en_HK |
dc.identifier.scopusauthorid | George, SR=35429392100 | en_HK |
dc.identifier.scopusauthorid | O'Dowd, BF=7102778005 | en_HK |
dc.identifier.scopusauthorid | Docherty, JM=7102949746 | en_HK |
dc.identifier.issnl | 0888-7543 | - |