REEP5
| Receptor accessory protein 5 | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Identifiers | |||||||||||||
| Symbols | REEP5 ; C5orf18; D5S346; DP1; TB2; YOP1 | ||||||||||||
| External IDs | OMIM: 125265 MGI: 1270152 HomoloGene: 68479 GeneCards: REEP5 Gene | ||||||||||||
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| RNA expression pattern | |||||||||||||
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| More reference expression data | |||||||||||||
| Orthologs | |||||||||||||
| Species | Human | Mouse | |||||||||||
| Entrez | 7905 | 13476 | |||||||||||
| Ensembl | ENSG00000129625 | ENSMUSG00000005873 | |||||||||||
| UniProt | Q00765 | Q9CQG4 | |||||||||||
| RefSeq (mRNA) | NM_005669 | NM_007874 | |||||||||||
| RefSeq (protein) | NP_005660 | NP_031900 | |||||||||||
| Location (UCSC) |
Chr 5: 112.88 – 112.92 Mb |
Chr 18: 34.34 – 34.37 Mb | |||||||||||
| PubMed search | |||||||||||||
Receptor expression-enhancing protein 5 is a protein that in humans is encoded by the REEP5 gene.[1][2][3]
References
- ↑ Clark AJ, Metherell LA, Cheetham ME, Huebner A (Nov 2005). "Inherited ACTH insensitivity illuminates the mechanisms of ACTH action". Trends Endocrinol Metab 16 (10): 451–7. doi:10.1016/j.tem.2005.10.006. PMID 16271481.
- ↑ Saito H, Kubota M, Roberts RW, Chi Q, Matsunami H (Nov 2004). "RTP family members induce functional expression of mammalian odorant receptors". Cell 119 (5): 679–91. doi:10.1016/j.cell.2004.11.021. PMID 15550249.
- ↑ "Entrez Gene: REEP5 receptor accessory protein 5".
Further reading
- Kinzler KW, Nilbert MC, Su LK, et al. (1991). "Identification of FAP locus genes from chromosome 5q21.". Science 253 (5020): 661–5. doi:10.1126/science.1651562. PMID 1651562.
- Nishisho I, Nakamura Y, Miyoshi Y, et al. (1991). "Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients.". Science 253 (5020): 665–9. doi:10.1126/science.1651563. PMID 1651563.
- Spirio L, Joslyn G, Nelson L, et al. (1991). "A CA repeat 30–70 KB downstream from the adenomatous polyposis coli (APC) gene". Nucleic Acids Res. 19 (22): 6348. doi:10.1093/nar/19.22.6348. PMC 329171. PMID 1659692.
- Joslyn G, Carlson M, Thliveris A, et al. (1991). "Identification of deletion mutations and three new genes at the familial polyposis locus". Cell 66 (3): 601–13. doi:10.1016/0092-8674(81)90022-2. PMID 1678319.
- Prieschl EE, Pendl GG, Harrer NE, Baumruker T (1996). "The murine homolog of TB2/DP1, a gene of the familial adenomatous polyposis (FAP) locus". Gene 169 (2): 215–8. doi:10.1016/0378-1119(95)00827-6. PMID 8647449.
- 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. PMC 139241. PMID 12477932.
- 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. PMC 528928. 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. PMC 1356129. PMID 16344560.
- Shin SM, Chung YJ, Oh ST, et al. (2006). "HCCR-1-interacting molecule "deleted in polyposis 1" plays a tumor-suppressor role in colon carcinogenesis". Gastroenterology 130 (7): 2074–86. doi:10.1053/j.gastro.2006.03.055. PMID 16762630.
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