CHMP1B
From Wikipedia, the free encyclopedia
Chromatin modifying protein 1B
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Identifiers | ||||||||
Symbol(s) | CHMP1B; C18orf2; C10orf2; C18-ORF2; CHMP1.5; Vps46-2 | |||||||
External IDs | OMIM: 606486 MGI: 1914314 HomoloGene: 41374 | |||||||
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Orthologs | ||||||||
Human | Mouse | |||||||
Entrez | 57132 | 67064
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Refseq | NM_020412 (mRNA) NP_065145 (protein) |
NM_024190 (mRNA) NP_077152 (protein) |
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Pubmed search | [1] | [2] |
Chromatin modifying protein 1B, also known as CHMP1B, is a human gene.[1]
[edit] References
[edit] Further reading
- Vuoristo JT, Berrettini WH, Ala-Kokko L (2001). "C18orf2, a novel, highly conserved intronless gene within intron 5 of the GNAL gene on chromosome 18p11.". Cytogenet. Cell Genet. 93 (1-2): 19–22. PMID 11474171.
- Stauffer DR, Howard TL, Nyun T, Hollenberg SM (2002). "CHMP1 is a novel nuclear matrix protein affecting chromatin structure and cell-cycle progression.". J. Cell. Sci. 114 (Pt 13): 2383–93. PMID 11559747.
- Howard TL, Stauffer DR, Degnin CR, Hollenberg SM (2002). "CHMP1 functions as a member of a newly defined family of vesicle trafficking proteins.". J. Cell. Sci. 114 (Pt 13): 2395–404. PMID 11559748.
- 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.
- Strack B, Calistri A, Craig S, et al. (2003). "AIP1/ALIX is a binding partner for HIV-1 p6 and EIAV p9 functioning in virus budding.". Cell 114 (6): 689–99. PMID 14505569.
- von Schwedler UK, Stuchell M, Müller B, et al. (2003). "The protein network of HIV budding.". Cell 114 (6): 701–13. PMID 14505570.
- Martin-Serrano J, Yarovoy A, Perez-Caballero D, et al. (2003). "Divergent retroviral late-budding domains recruit vacuolar protein sorting factors by using alternative adaptor proteins.". Proc. Natl. Acad. Sci. U.S.A. 100 (21): 12414–9. doi: . PMID 14519844.
- 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.
- Reid E, Connell J, Edwards TL, et al. (2005). "The hereditary spastic paraplegia protein spastin interacts with the ESCRT-III complex-associated endosomal protein CHMP1B.". Hum. Mol. Genet. 14 (1): 19–38. doi: . PMID 15537668.
- Scott A, Gaspar J, Stuchell-Brereton MD, et al. (2005). "Structure and ESCRT-III protein interactions of the MIT domain of human VPS4A.". Proc. Natl. Acad. Sci. U.S.A. 102 (39): 13813–8. doi: . PMID 16174732.
- Tsang HT, Connell JW, Brown SE, et al. (2006). "A systematic analysis of human CHMP protein interactions: additional MIT domain-containing proteins bind to multiple components of the human ESCRT III complex.". Genomics 88 (3): 333–46. doi: . PMID 16730941.
- Row PE, Liu H, Hayes S, et al. (2007). "The MIT domain of UBPY constitutes a CHMP binding and endosomal localization signal required for efficient epidermal growth factor receptor degradation.". J. Biol. Chem. 282 (42): 30929–37. doi: . PMID 17711858.