RMI1
From Wikipedia, the free encyclopedia
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RMI1, RecQ mediated genome instability 1, homolog (S. cerevisiae)
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| Identifiers | |||||||||||
| Symbol(s) | RMI1; BLAP75; C9orf76; FLJ12888; RP11-346I8.1 | ||||||||||
| External IDs | OMIM: 610404 MGI: 1921636 HomoloGene: 41601 | ||||||||||
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| RNA expression pattern | |||||||||||
| Orthologs | |||||||||||
| Human | Mouse | ||||||||||
| Entrez | 80010 | 74386 | |||||||||
| Ensembl | ENSG00000178966 | ENSMUSG00000035367 | |||||||||
| Uniprot | Q9H9A7 | Q9D4G9 | |||||||||
| Refseq | NM_024945 (mRNA) NP_079221 (protein) |
NM_028904 (mRNA) NP_083180 (protein) |
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| Location | Chr 9: 85.79 - 85.81 Mb | Chr 13: 58.41 - 58.42 Mb | |||||||||
| Pubmed search | [1] | [2] | |||||||||
RMI1, RecQ mediated genome instability 1, homolog (S. cerevisiae), also known as RMI1, is a human gene.[1]
[edit] References
[edit] Further reading
- 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:. PMID 12477932.
- Meetei AR, de Winter JP, Medhurst AL, et al. (2003). "A novel ubiquitin ligase is deficient in Fanconi anemia.". Nat. Genet. 35 (2): 165-70. doi:. PMID 12973351.
- Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs.". Nat. Genet. 36 (1): 40-5. doi:. PMID 14702039.
- Humphray SJ, Oliver K, Hunt AR, et al. (2004). "DNA sequence and analysis of human chromosome 9.". Nature 429 (6990): 369-74. doi:. PMID 15164053.
- Suzuki Y, Yamashita R, Shirota M, et al. (2004). "Sequence comparison of human and mouse genes reveals a homologous block structure in the promoter regions.". Genome Res. 14 (9): 1711-8. doi:. PMID 15342556.
- 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:. PMID 15489334.
- Yin J, Sobeck A, Xu C, et al. (2005). "BLAP75, an essential component of Bloom's syndrome protein complexes that maintain genome integrity.". EMBO J. 24 (7): 1465-76. doi:. PMID 15775963.
- Wu L, Bachrati CZ, Ou J, et al. (2006). "BLAP75/RMI1 promotes the BLM-dependent dissolution of homologous recombination intermediates.". Proc. Natl. Acad. Sci. U.S.A. 103 (11): 4068-73. doi:. PMID 16537486.
- Raynard S, Bussen W, Sung P (2006). "A double Holliday junction dissolvasome comprising BLM, topoisomerase IIIalpha, and BLAP75.". J. Biol. Chem. 281 (20): 13861-4. doi:. PMID 16595695.
- Olsen JV, Blagoev B, Gnad F, et al. (2006). "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks.". Cell 127 (3): 635-48. doi:. PMID 17081983.
- Bussen W, Raynard S, Busygina V, et al. (2007). "Holliday junction processing activity of the BLM-Topo IIIalpha-BLAP75 complex.". J. Biol. Chem. 282 (43): 31484-92. doi:. PMID 17728255.
- Broberg K, Höglund M, Gustafsson C, et al. (2008). "Genetic variant of the human homologous recombination-associated gene RMI1 (S455N) impacts the risk of AML/MDS and malignant melanoma.". Cancer Lett. 258 (1): 38-44. doi:. PMID 17900800.

