PEX26

PEX26
Identifiers
Aliases	PEX26, PBD7A, PBD7B, PEX26M1T, Pex26pM1T, peroxisomal biogenesis factor 26
External IDs	OMIM: 608666 MGI: 1921293 HomoloGene: 9922 GeneCards: PEX26
Gene location (Human)
Chr.	Chromosome 22 (human)
End	18,105,396 bp
Gene location (Mouse)
Chr.	Chromosome 6 (mouse)
End	121,175,796 bp
RNA expression pattern
	Top expressed in
	islet of Langerhans; ; prefrontal cortex; ; rectum; ; ganglionic eminence; ; stromal cell of endometrium; ; duodenum; ; internal globus pallidus; ; cerebellar vermis; ; left adrenal gland; ; amygdala;
	Top expressed in
	secondary oocyte; ; Paneth cell; ; lacrimal gland; ; left lung lobe; ; medullary collecting duct; ; hair follicle; ; left lobe of liver; ; motor neuron; ; islet of Langerhans; ; prostate;
	More reference expression data
	n/a
Gene ontology
Molecular function	ATPase binding; protein C-terminus binding; protein binding; protein-containing complex binding;
Cellular component	integral component of membrane; peroxisome; membrane; integral component of peroxisomal membrane; peroxisomal membrane;
Biological process	protein transport; protein import into peroxisome matrix; protein import into peroxisome membrane; protein targeting to peroxisome;
	Sources:Amigo / QuickGO
Orthologs
	55670
	74043
	ENSG00000215193
	ENSMUSG00000067825
	Q7Z412
	Q8BGI5
	NM_017929; NM_001127649; NM_001199319
	NM_028730; NM_001304773; NM_001304774
	NP_001121121; NP_001186248; NP_060399; NP_001121121.1; NP_060399.1
	NP_001291702; NP_001291703; NP_083006
	Wikidata
View/Edit Human	View/Edit Mouse

Peroxisome assembly protein 26 is a protein that in humans is encoded by the PEX26 gene.^[5]^[6]^[7]

Interactions[edit]

PEX26 has been shown to interact with PEX1,^[5] PEX6^[5] and SUFU.^[8]

References[edit]

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000215193 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000067825 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ ^a ^b ^c Matsumoto N, Tamura S, Fujiki Y (May 2003). "The pathogenic peroxin Pex26p recruits the Pex1p-Pex6p AAA ATPase complexes to peroxisomes". Nature Cell Biology. 5 (5): 454–60. doi:10.1038/ncb982. PMID 12717447. S2CID 2426040.
^ Matsumoto N, Tamura S, Furuki S, Miyata N, Moser A, Shimozawa N, Moser HW, Suzuki Y, Kondo N, Fujiki Y (Aug 2003). "Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation". American Journal of Human Genetics. 73 (2): 233–46. doi:10.1086/377004. PMC 1180364. PMID 12851857.
^ "Entrez Gene: PEX26 peroxisome biogenesis factor 26".
^ Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, Berriz GF, Gibbons FD, Dreze M, Ayivi-Guedehoussou N, Klitgord N, Simon C, Boxem M, Milstein S, Rosenberg J, Goldberg DS, Zhang LV, Wong SL, Franklin G, Li S, Albala JS, Lim J, Fraughton C, Llamosas E, Cevik S, Bex C, Lamesch P, Sikorski RS, Vandenhaute J, Zoghbi HY, Smolyar A, Bosak S, Sequerra R, Doucette-Stamm L, Cusick ME, Hill DE, Roth FP, Vidal M (Oct 2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. Bibcode:2005Natur.437.1173R. doi:10.1038/nature04209. PMID 16189514. S2CID 4427026.

External links[edit]

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[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000215193 – Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000067825 – Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[pmid12717447-5] Matsumoto N, Tamura S, Fujiki Y (May 2003). "The pathogenic peroxin Pex26p recruits the Pex1p-Pex6p AAA ATPase complexes to peroxisomes". Nature Cell Biology. 5 (5): 454–60. doi:10.1038/ncb982. PMID 12717447. S2CID 2426040.

[pmid12851857-6] Matsumoto N, Tamura S, Furuki S, Miyata N, Moser A, Shimozawa N, Moser HW, Suzuki Y, Kondo N, Fujiki Y (Aug 2003). "Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation". American Journal of Human Genetics. 73 (2): 233–46. doi:10.1086/377004. PMC 1180364. PMID 12851857.

[entrez-7] "Entrez Gene: PEX26 peroxisome biogenesis factor 26".

[pmid16189514-8] Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, Berriz GF, Gibbons FD, Dreze M, Ayivi-Guedehoussou N, Klitgord N, Simon C, Boxem M, Milstein S, Rosenberg J, Goldberg DS, Zhang LV, Wong SL, Franklin G, Li S, Albala JS, Lim J, Fraughton C, Llamosas E, Cevik S, Bex C, Lamesch P, Sikorski RS, Vandenhaute J, Zoghbi HY, Smolyar A, Bosak S, Sequerra R, Doucette-Stamm L, Cusick ME, Hill DE, Roth FP, Vidal M (Oct 2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. Bibcode:2005Natur.437.1173R. doi:10.1038/nature04209. PMID 16189514. S2CID 4427026.

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PEX26

Interactions[edit]

References[edit]

Further reading[edit]

External links[edit]

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