REEP5

REEP5
Identifiers
Aliases	REEP5, C5orf18, D5S346, DP1, TB2, YOP1, Yip2e, receptor accessory protein 5
External IDs	MGI: 1270152 HomoloGene: 68479 GeneCards: REEP5
Genetically Related Diseases
attention deficit hyperactivity disorder[1]
Gene ontology Molecular function • molecular function • protein binding Cellular component • integral component of membrane • extracellular exosome • membrane Biological process • biological process Sources:Amigo / QuickGO
RNA expression pattern
More reference expression data
Orthologs
Species	Human	Mouse
Entrez	7905	13476
Ensembl	ENSG00000129625	ENSMUSG00000005873
UniProt	Q00765	Q60870
RefSeq (mRNA)	NM_005669	NM_007874
RefSeq (protein)	NP_005660.4	n/a
Location (UCSC)	Chr 5: 112.88 – 112.92 Mb	Chr 18: 34.34 – 34.37 Mb
PubMed search	[2]	[3]
Wikidata

View/Edit Human

View/Edit Mouse

Receptor expression-enhancing protein 5 is a protein that in humans is encoded by the REEP5 gene.^[4][5][6]

References

1. "Diseases that are genetically associated with REEP5 view/edit references on wikidata".
2. "Human PubMed Reference:".
3. "Mouse PubMed Reference:".
4. 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.
5. 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.
6. "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.