PEX11B

From Wikipedia, the free encyclopedia
Peroxisomal biogenesis factor 11 beta
Identifiers
SymbolsPEX11B; PEX11-BETA; PEX14B
External IDsOMIM: 603867 MGI: 1338882 HomoloGene: 2852 GeneCards: PEX11B Gene
RNA expression pattern
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez879918632
EnsemblENSG00000131779ENSMUSG00000028102
UniProtO96011Q9Z210
RefSeq (mRNA)NM_001184795NM_001162387
RefSeq (protein)NP_001171724NP_001155859
Location (UCSC)Chr 1:
145.52 – 145.52 Mb
Chr 3:
96.64 – 96.65 Mb
PubMed search

Peroxisomal membrane protein 11B is a protein that in humans is encoded by the PEX11B gene.[1][2] It is involved in the regulation of peroxisome abundance. [3]

Interactions

PEX11B has been shown to interact with PEX19.[4][5]

Related gene problems

References

  1. Schrader M, Reuber BE, Morrell JC, Jimenez-Sanchez G, Obie C, Stroh TA, Valle D, Schroer TA, Gould SJ (December 1998). "Expression of PEX11beta mediates peroxisome proliferation in the absence of extracellular stimuli". J Biol Chem 273 (45): 29607–14. doi:10.1074/jbc.273.45.29607. PMID 9792670. 
  2. "Entrez Gene: PEX11B peroxisomal biogenesis factor 11B". 
  3. Thoms S, Erdmann R (October 2005). "Dynamin-related proteins and Pex11 proteins in peroxisome division and proliferation.". FEBS J 272 (20): 5169–81. doi:10.1111/j.1742-4658.2005.04939.x. PMID 16218949. 
  4. Sacksteder, K A; Jones J M, South S T, Li X, Liu Y, Gould S J (March 2000). "Pex19 Binds Multiple Peroxisomal Membrane Proteins, Is Predominantly Cytoplasmic, and Is Required for Peroxisome Membrane Synthesis". J. Cell Biol. (UNITED STATES) 148 (5): 931–44. doi:10.1083/jcb.148.5.931. ISSN 0021-9525. PMC 2174547. PMID 10704444. 
  5. Fransen, M; Wylin T, Brees C, Mannaerts G P, Van Veldhoven P P (July 2001). "Human Pex19p Binds Peroxisomal Integral Membrane Proteins at Regions Distinct from Their Sorting Sequences". Mol. Cell. Biol. (United States) 21 (13): 4413–24. doi:10.1128/MCB.21.13.4413-4424.2001. ISSN 0270-7306. PMC 87101. PMID 11390669. 
  6. Klopocki E, Schulze H, Strauss G, et al. (February 2007). "Complex Inheritance Pattern Resembling Autosomal Recessive Inheritance Involving a Microdeletion in Thrombocytopenia–Absent Radius Syndrome". Am. J. Hum. Genet. 80 (2): 232–40. doi:10.1086/510919. PMC 1785342. PMID 17236129. 

Further reading

  • Kobayashi S, Tanaka A, Fujiki Y (2007). "Fis1, DLP1, and Pex11p coordinately regulate peroxisome morphogenesis". Exp. Cell Res. 313 (8): 1675–86. doi:10.1016/j.yexcr.2007.02.028. PMID 17408615. 


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