PEX11B

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PEX11B
Identifiers
Aliases PEX11B, PEX11-BETA, PEX14B, peroxisomal biogenesis factor 11 beta
External IDs MGI: 1338882 HomoloGene: 2852 GeneCards: PEX11B
RNA expression pattern
PBB GE PEX11B 202658 at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001184795
NM_003846

NM_001162387
NM_001162388
NM_011069

RefSeq (protein)

NP_001171724
NP_003837

NP_001155859.1
NP_035199.3
NP_001155859
NP_001155860
NP_035199

Location (UCSC) Chr 1: 145.91 – 145.92 Mb Chr 3: 96.64 – 96.65 Mb
PubMed search [1] [2]
Wikidata
View/Edit Human View/Edit Mouse

Peroxisomal membrane protein 11B is a protein that in humans is encoded by the PEX11B gene.[3][4] It is involved in the regulation of peroxisome abundance. [5]


Interactions[edit]

PEX11B has been shown to interact with PEX19.[6][7]

Related gene problems[edit]

References[edit]

  1. ^ "Human PubMed Reference:". 
  2. ^ "Mouse PubMed Reference:". 
  3. ^ 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. 
  4. ^ "Entrez Gene: PEX11B peroxisomal biogenesis factor 11B". 
  5. ^ 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. 
  6. ^ 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 2174547Freely accessible. PMID 10704444. 
  7. ^ 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 87101Freely accessible. PMID 11390669. 
  8. ^ 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 1785342Freely accessible. PMID 17236129. 

Further reading[edit]