VPS53

VPS53
Identifiers
Aliases	VPS53 , HCCS1, PCH2E, hVps53L, pp13624, GARP complex subunit, VPS53 subunit of GARP complex
External IDs	OMIM: 615850 MGI: 1915549 HomoloGene: 6264 GeneCards: VPS53
Gene location (Human)
Chr.	Chromosome 17 (human)
End	721,717 bp
Gene location (Mouse)
Chr.	Chromosome 11 (mouse)
End	76,070,473 bp
RNA expression pattern
	Top expressed in
	sural nerve; ; bone marrow cells; ; stromal cell of endometrium; ; cerebellum; ; cerebellar cortex; ; cerebellar hemisphere; ; corpus callosum; ; prefrontal cortex; ; thymus; ; superior frontal gyrus;
	Top expressed in
	retinal pigment epithelium; ; Epithelium of stomach; ; facial motor nucleus; ; supraoptic nucleus; ; ankle; ; subiculum; ; Region I of hippocampus proper; ; medial dorsal nucleus; ; temporal lobe; ; ciliary body;
	More reference expression data
	n/a
Gene ontology
Molecular function	protein binding ;
Cellular component	perinuclear region of cytoplasm ; recycling endosome ; EARP complex ; endosome ; Golgi apparatus ; endosome membrane ; GARP complex ; membrane ; trans-Golgi network ; trans-Golgi network membrane ; cytosol ;
Biological process	protein transport ; endocytic recycling ; lysosomal transport ; retrograde transport, endosome to Golgi ;
	Sources:Amigo / QuickGO
Orthologs
	55275
	68299
	ENSG00000283883 ; ENSG00000141252
	ENSMUSG00000017288
	Q5VIR6
	Q8CCB4
	NM_001128159 ; NM_018289 ; NM_001366253 ; NM_001366254
	NM_026664 ; NM_001364738
	NP_001121631 ; NP_060759 ; NP_001353182 ; NP_001353183
	NP_080940 ; NP_001351667
	Wikidata
View/Edit Human	View/Edit Mouse

Last updated March 05, 2023

Vacuolar protein sorting 53 homolog (S. cerevisiae) is a protein that in humans is encoded by the VPS53 gene.^[5]

Function

This gene encodes a protein with sequence similarity to the yeast Vps53p protein. Vps53p is involved in retrograde vesicle trafficking in late Golgi. [provided by RefSeq, Jul 2008].

Mutations in VPS53 cause cerebello-cerebral atrophy type 2.^[6]

Related Research Articles

Retromer is a complex of proteins that has been shown to be important in recycling transmembrane receptors from endosomes to the trans-Golgi network (TGN).

VPS13B, also known as vacuolar protein sorting-associated protein 13B, is a protein that in humans is encoded by the VPS13B gene. It is a giant protein associated with the Golgi apparatus that is believed to be involved in post-Golgi apparatus sorting and trafficking. Mutations in the human VPS13B gene cause Cohen syndrome.

AP-1 complex subunit mu-1 is a protein that in humans is encoded by the AP1M1 gene.

ADP-ribosylation factor-binding protein GGA3 is a protein that in humans is encoded by the GGA3 gene.

ADP-ribosylation factor-binding protein GGA2 is a protein that in humans is encoded by the GGA2 gene.

AP-3 complex subunit delta-1 is a protein that in humans is encoded by the AP3D1 gene.

Vacuolar protein sorting-associated protein 4A is a protein that in humans is encoded by the VPS4A gene.

Sorting nexin-2 is a protein that in humans is encoded by the SNX2 gene.

Vacuolar protein sorting-associated protein 26A is a protein that in humans is encoded by the VPS26A gene.

Vacuolar protein sorting-associated protein 28 homolog is a protein that in humans is encoded by the VPS28 gene.

VPS29 is a human gene coding for the vacuolar protein sorting protein Vps29, a component of the retromer complex.

Rab GTPase-binding effector protein 1 is an enzyme that in humans is encoded by the RABEP1 gene. It belongs to rabaptin protein family.

Vacuolar protein sorting-associated protein 45 is a protein that in humans is encoded by the VPS45 gene.

hVamp6/Vps39-like protein is a protein that in humans is encoded by the VPS39 gene.

Vacuolar protein sorting-associated protein 18 homolog is a protein that in humans is encoded by the VPS18 gene.

Vacuolar protein sorting-associated protein 13D is a protein that in humans is encoded by the VPS13D gene.

Vacuolar protein sorting-associated protein 52 homolog is a protein that in humans is encoded by the VPS52 gene.

Vacuolar protein-sorting-associated protein 25 is a protein that in humans is encoded by the VPS25 gene.

Vacuolar protein sorting 37 homolog A is a protein in humans that is encoded by the VPS37A gene. It is a member of the endosomal sorting complex required for transport (ESCRT) system.

Vacuolar protein sorting 26 homolog B is a protein in humans that is encoded by the VPS26B gene.

References

1 2 3 ENSG00000141252 GRCh38: Ensembl release 89: ENSG00000283883, ENSG00000141252 - Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000017288 - 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.
↑ "Entrez Gene: Vacuolar protein sorting 53 homolog (S. cerevisiae)".
↑ Feinstein M, Flusser H, Lerman-Sagie T, Ben-Zeev B, Lev D, Agamy O, Cohen I, Kadir R, Sivan S, Leshinsky-Silver E, Markus B, Birk OS (May 2014). "VPS53 mutations cause progressive cerebello-cerebral atrophy type 2 (PCCA2)". Journal of Medical Genetics. 51 (5): 303–8. doi:10.1136/jmedgenet-2013-101823. PMID 24577744. S2CID 8752023.

Cardoso C, Leventer RJ, Ward HL, Toyo-Oka K, Chung J, Gross A, Martin CL, Allanson J, Pilz DT, Olney AH, Mutchinick OM, Hirotsune S, Wynshaw-Boris A, Dobyns WB, Ledbetter DH (April 2003). "Refinement of a 400-kb critical region allows genotypic differentiation between isolated lissencephaly, Miller-Dieker syndrome, and other phenotypes secondary to deletions of 17p13.3". American Journal of Human Genetics. 72 (4): 918–30. doi:10.1086/374320. PMC 1180354 . PMID 12621583.
Pérez-Victoria FJ, Schindler C, Magadán JG, Mardones GA, Delevoye C, Romao M, Raposo G, Bonifacino JS (October 2010). "Ang2/fat-free is a conserved subunit of the Golgi-associated retrograde protein complex". Molecular Biology of the Cell. 21 (19): 3386–95. doi:10.1091/mbc.E10-05-0392. PMC 2947474 . PMID 20685960.
Zhu JD, Fei Q, Wang P, Lan F, Mao DQ, Zhang HY, Yao XB (September 2006). "Transcription of the putative tumor suppressor gene HCCS1 requires binding of ETS-2 to its consensus near the transcription start site". Cell Research. 16 (9): 780–96. doi: 10.1038/sj.cr.7310092 . PMID 16953216.
Pérez-Victoria FJ, Bonifacino JS (October 2009). "Dual roles of the mammalian GARP complex in tethering and SNARE complex assembly at the trans-golgi network". Molecular and Cellular Biology. 29 (19): 5251–63. doi:10.1128/MCB.00495-09. PMC 2747979 . PMID 19620288.
Ko JK, Choi KH, Pan Z, Lin P, Weisleder N, Kim CW, Ma J (August 2007). "The tail-anchoring domain of Bfl1 and HCCS1 targets mitochondrial membrane permeability to induce apoptosis" (PDF). Journal of Cell Science. 120 (Pt 16): 2912–23. doi: 10.1242/jcs.006197 . PMID 17666431. S2CID 14635274.
Liewen H, Meinhold-Heerlein I, Oliveira V, Schwarzenbacher R, Luo G, Wadle A, Jung M, Pfreundschuh M, Stenner-Liewen F (May 2005). "Characterization of the human GARP (Golgi associated retrograde protein) complex". Experimental Cell Research. 306 (1): 24–34. doi:10.1016/j.yexcr.2005.01.022. PMID 15878329.
Zhao X, He M, Wan D, Ye Y, He Y, Han L, Guo M, Huang Y, Qin W, Wang MW, Chong W, Chen J, Zhang L, Yang N, Xu B, Wu M, Zuo L, Gu J (February 2003). "The minimum LOH region defined on chromosome 17p13.3 in human hepatocellular carcinoma with gene content analysis". Cancer Letters. 190 (2): 221–32. doi:10.1016/s0304-3835(02)00622-5. PMID 12565177.
Pérez-Victoria FJ, Mardones GA, Bonifacino JS (June 2008). "Requirement of the human GARP complex for mannose 6-phosphate-receptor-dependent sorting of cathepsin D to lysosomes". Molecular Biology of the Cell. 19 (6): 2350–62. doi:10.1091/mbc.E07-11-1189. PMC 2397299 . PMID 18367545.

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[refGRCh38Ensembl-1] 1 2 3 ENSG00000141252 GRCh38: Ensembl release 89: ENSG00000283883, ENSG00000141252 - Ensembl, May 2017

[refGRCm38Ensembl-2] 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000017288 - 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.

[entrez-5] "Entrez Gene: Vacuolar protein sorting 53 homolog (S. cerevisiae)".

[6] Feinstein M, Flusser H, Lerman-Sagie T, Ben-Zeev B, Lev D, Agamy O, Cohen I, Kadir R, Sivan S, Leshinsky-Silver E, Markus B, Birk OS (May 2014). "VPS53 mutations cause progressive cerebello-cerebral atrophy type 2 (PCCA2)". Journal of Medical Genetics. 51 (5): 303–8. doi:10.1136/jmedgenet-2013-101823. PMID 24577744. S2CID 8752023.

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VPS53

Contents

Function

Related Research Articles

References

Further reading