VPS53

VPS53
Identifiers
Aliases VPS53, HCCS1, PCH2E, hVps53L, pp13624, GARP complex subunit
External IDs MGI: 1915549 HomoloGene: 6264 GeneCards: VPS53
Orthologs
Species Human Mouse
Entrez

55275

68299

Ensembl

ENSG00000141252

ENSMUSG00000017288

UniProt

Q5VIR6

Q8CCB4

RefSeq (mRNA)

NM_001128159
NM_018289

NM_026664

RefSeq (protein)

NP_001121631.1
NP_060759.2

NP_080940.2

Location (UCSC) Chr 17: 0.51 – 0.72 Mb Chr 11: 76.05 – 76.18 Mb
PubMed search [1] [2]
Wikidata
View/Edit HumanView/Edit Mouse

Vacuolar protein sorting 53 homolog (S. cerevisiae) is a protein that in humans is encoded by the VPS53 gene. [3]

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 .[4]

References

  1. "Human PubMed Reference:".
  2. "Mouse PubMed Reference:".
  3. "Entrez Gene: Vacuolar protein sorting 53 homolog (S. cerevisiae)". Retrieved 2014-04-30.
  4. 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, O. S. (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.

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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