RAB34

From Wikipedia, the free encyclopedia

RAB34, member RAS oncogene family

Identifiers

RAB34; RAB39; RAH

External IDs

Gene ontology
Molecular Function:	• nucleotide binding • GTP binding
Cellular Component:	• membrane
Biological Process:	• small GTPase mediated signal transduction • protein transport

Orthologs

Human

Mouse

Refseq

NM_031934 (mRNA)
NP_114140 (protein)

XM_984679 (mRNA)
XP_989773 (protein)

Location

Chr 17: 24.07 - 24.07 Mb

Chr 11: 78 - 78.01 Mb

Pubmed search

[1]

[2]

RAB34, member RAS oncogene family, also known as RAB34, is a human gene.^[1]

[edit] References

^ Entrez Gene: RAB34 RAB34, member RAS oncogene family.

[edit] Further reading

Sun P, Yamamoto H, Suetsugu S, et al. (2003). "Small GTPase Rah/Rab34 is associated with membrane ruffles and macropinosomes and promotes macropinosome formation.". J. Biol. Chem. 278 (6): 4063–71. doi:10.1074/jbc.M208699200. PMID 12446704.
Wang T, Hong W (2003). "Interorganellar regulation of lysosome positioning by the Golgi apparatus through Rab34 interaction with Rab-interacting lysosomal protein.". Mol. Biol. Cell 13 (12): 4317–32. doi:10.1091/mbc.E02-05-0280. PMID 12475955.
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. PMID 12477932.
Chen T, Han Y, Yang M, et al. (2003). "Rab39, a novel Golgi-associated Rab GTPase from human dendritic cells involved in cellular endocytosis.". Biochem. Biophys. Res. Commun. 303 (4): 1114–20. PMID 12684051.
Wang T, Wong KK, Hong W (2004). "A unique region of RILP distinguishes it from its related proteins in its regulation of lysosomal morphology and interaction with Rab7 and Rab34.". Mol. Biol. Cell 15 (2): 815–26. doi:10.1091/mbc.E03-06-0413. PMID 14668488.
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:10.1038/ng1285. PMID 14702039.
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. PMID 15489334.
Barrios-Rodiles M, Brown KR, Ozdamar B, et al. (2005). "High-throughput mapping of a dynamic signaling network in mammalian cells.". Science 307 (5715): 1621–5. doi:10.1126/science.1105776. PMID 15761153.
Colucci AM, Campana MC, Bellopede M, Bucci C (2005). "The Rab-interacting lysosomal protein, a Rab7 and Rab34 effector, is capable of self-interaction.". Biochem. Biophys. Res. Commun. 334 (1): 128–33. doi:10.1016/j.bbrc.2005.06.067. PMID 15996637.
Speight P, Silverman M (2005). "Diacylglycerol-activated Hmunc13 serves as an effector of the GTPase Rab34.". Traffic 6 (10): 858–65. doi:10.1111/j.1600-0854.2005.00321.x. PMID 16138900.
Otsuki T, Ota T, Nishikawa T, et al. (2007). "Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries.". DNA Res. 12 (2): 117–26. doi:10.1093/dnares/12.2.117. PMID 16303743.
Coyne CB, Shen L, Turner JR, Bergelson JM (2007). "Coxsackievirus entry across epithelial tight junctions requires occludin and the small GTPases Rab34 and Rab5.". Cell Host Microbe 2 (3): 181–92. doi:10.1016/j.chom.2007.07.003. PMID 18005733.