VPS13A

Protein-coding gene in the species Homo sapiens
VPS13A
Identifiers
AliasesVPS13A, CHAC, CHOREIN, vacuolar protein sorting 13 homolog A
External IDsOMIM: 605978; MGI: 2444304; HomoloGene: 22068; GeneCards: VPS13A; OMA:VPS13A - orthologs
Gene location (Human)
Chromosome 9 (human)
Chr.Chromosome 9 (human)[1]
Chromosome 9 (human)
Genomic location for VPS13A
Genomic location for VPS13A
Band9q21.2Start77,177,445 bp[1]
End77,421,537 bp[1]
Gene location (Mouse)
Chromosome 19 (mouse)
Chr.Chromosome 19 (mouse)[2]
Chromosome 19 (mouse)
Genomic location for VPS13A
Genomic location for VPS13A
Band19|19 A- BStart16,592,730 bp[2]
End16,758,297 bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • jejunal mucosa

  • biceps brachii

  • Skeletal muscle tissue of biceps brachii

  • Achilles tendon

  • testicle

  • left coronary artery

  • Brodmann area 23

  • hair follicle

  • gastric mucosa

  • rectum
Top expressed in
  • spermatocyte

  • secondary oocyte

  • spermatid

  • zygote

  • renal corpuscle

  • medullary collecting duct

  • primary oocyte

  • dentate gyrus of hippocampal formation granule cell

  • lumbar spinal ganglion

  • lumbar subsegment of spinal cord
More reference expression data
BioGPS


More reference expression data
Gene ontology
Molecular function
  • protein binding
Cellular component
  • dense core granule
  • cytosol
  • intracellular anatomical structure
  • extrinsic component of membrane
Biological process
  • Golgi to endosome transport
  • protein transport
  • social behavior
  • protein localization
  • locomotory behavior
  • nervous system development
  • autophagy
  • protein targeting to vacuole
  • protein retention in Golgi apparatus
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

23230

271564

Ensembl

ENSG00000197969

ENSMUSG00000046230

UniProt

Q96RL7

Q5H8C4

RefSeq (mRNA)

NM_001018037
NM_001018038
NM_015186
NM_033305

NM_173028

RefSeq (protein)

NP_001018047
NP_001018048
NP_056001
NP_150648

NP_766616

Location (UCSC)Chr 9: 77.18 – 77.42 MbChr 19: 16.59 – 16.76 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

VPS13A (Vacuolar protein sorting-associated protein 13A) is a protein that in humans is encoded by the VPS13A gene.[5][6][7]

Function

The protein encoded by this gene may control steps in the cycling of proteins through the trans-Golgi network to endosomes, lysosomes and the plasma membrane. Mutations in this gene cause the autosomal recessive disorder, chorea acanthocytosis. Alternative splicing of this gene results in multiple transcript variants.[7]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000197969 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000046230 – 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.
  5. ^ Rubio JP, Danek A, Stone C, Chalmers R, Wood N, Verellen C, Ferrer X, Malandrini A, Fabrizi GM, Manfredi M, Vance J, Pericak-Vance M, Brown R, Rudolf G, Picard F, Alonso E, Brin M, Németh AH, Farrall M, Monaco AP (Oct 1997). "Chorea-acanthocytosis: genetic linkage to chromosome 9q21". American Journal of Human Genetics. 61 (4): 899–908. doi:10.1086/514876. PMC 1715977. PMID 9382101.
  6. ^ Rampoldi L, Dobson-Stone C, Rubio JP, Danek A, Chalmers RM, Wood NW, Verellen C, Ferrer X, Malandrini A, Fabrizi GM, Brown R, Vance J, Pericak-Vance M, Rudolf G, Carrè S, Alonso E, Manfredi M, Németh AH, Monaco AP (Jun 2001). "A conserved sorting-associated protein is mutant in chorea-acanthocytosis". Nature Genetics. 28 (2): 119–20. doi:10.1038/88821. PMID 11381253. S2CID 2754015.
  7. ^ a b "Entrez Gene: VPS13A vacuolar protein sorting 13 homolog A (S. cerevisiae)".

Further reading

  • Nagase T, Ishikawa K, Suyama M, Kikuno R, Hirosawa M, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O (Feb 1999). "Prediction of the coding sequences of unidentified human genes. XIII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro". DNA Research. 6 (1): 63–70. doi:10.1093/dnares/6.1.63. PMID 10231032.
  • Dias Neto E, Correa RG, Verjovski-Almeida S, Briones MR, Nagai MA, da Silva W, Zago MA, Bordin S, Costa FF, Goldman GH, Carvalho AF, Matsukuma A, Baia GS, Simpson DH, Brunstein A, de Oliveira PS, Bucher P, Jongeneel CV, O'Hare MJ, Soares F, Brentani RR, Reis LF, de Souza SJ, Simpson AJ (Mar 2000). "Shotgun sequencing of the human transcriptome with ORF expressed sequence tags". Proceedings of the National Academy of Sciences of the United States of America. 97 (7): 3491–6. Bibcode:2000PNAS...97.3491D. doi:10.1073/pnas.97.7.3491. PMC 16267. PMID 10737800.
  • Ueno S, Maruki Y, Nakamura M, Tomemori Y, Kamae K, Tanabe H, Yamashita Y, Matsuda S, Kaneko S, Sano A (Jun 2001). "The gene encoding a newly discovered protein, chorein, is mutated in chorea-acanthocytosis". Nature Genetics. 28 (2): 121–2. doi:10.1038/88825. PMID 11381254. S2CID 29708129.
  • Bohlega S, Al-Jishi A, Dobson-Stone C, Rampoldi L, Saha P, Murad H, Kareem A, Roberts G, Monaco AP (Apr 2003). "Chorea-acanthocytosis: clinical and genetic findings in three families from the Arabian peninsula". Movement Disorders. 18 (4): 403–7. doi:10.1002/mds.10361. PMID 12671946. S2CID 34308711.
  • Brandenberger R, Wei H, Zhang S, Lei S, Murage J, Fisk GJ, Li Y, Xu C, Fang R, Guegler K, Rao MS, Mandalam R, Lebkowski J, Stanton LW (Jun 2004). "Transcriptome characterization elucidates signaling networks that control human ES cell growth and differentiation". Nature Biotechnology. 22 (6): 707–16. doi:10.1038/nbt971. PMID 15146197. S2CID 27764390.
  • Velayos-Baeza A, Vettori A, Copley RR, Dobson-Stone C, Monaco AP (Sep 2004). "Analysis of the human VPS13 gene family". Genomics. 84 (3): 536–49. doi:10.1016/j.ygeno.2004.04.012. PMID 15498460.
  • Dobson-Stone C, Velayos-Baeza A, Jansen A, Andermann F, Dubeau F, Robert F, Summers A, Lang AE, Chouinard S, Danek A, Andermann E, Monaco AP (Sep 2005). "Identification of a VPS13A founder mutation in French Canadian families with chorea-acanthocytosis". Neurogenetics. 6 (3): 151–8. doi:10.1007/s10048-005-0220-9. PMID 15918062. S2CID 10875246.

External links

  • GeneReviews/NCBI/NIH/UW entry on Chorea-acanthocytosis


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