HPS6

Protein found in humans
HPS6
Identifiers
AliasesHPS6, BLOC2S3, biogenesis of lysosomal organelles complex 2 subunit 3, HPS6 biogenesis of lysosomal organelles complex 2 subunit 3
External IDsOMIM: 607522; MGI: 2181763; HomoloGene: 11691; GeneCards: HPS6; OMA:HPS6 - orthologs
Gene location (Human)
Chromosome 10 (human)
Chr.Chromosome 10 (human)[1]
Chromosome 10 (human)
Genomic location for HPS6
Genomic location for HPS6
Band10q24.32Start102,065,349 bp[1]
End102,068,036 bp[1]
Gene location (Mouse)
Chromosome 19 (mouse)
Chr.Chromosome 19 (mouse)[2]
Chromosome 19 (mouse)
Genomic location for HPS6
Genomic location for HPS6
Band19 C3|19 38.75 cMStart45,991,947 bp[2]
End45,994,612 bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • stromal cell of endometrium

  • monocyte

  • pancreatic ductal cell

  • right adrenal gland

  • epithelium of esophagus

  • vulva

  • blood

  • prefrontal cortex

  • left adrenal gland

  • body of stomach
Top expressed in
  • secondary oocyte

  • proximal tubule

  • morula

  • yolk sac

  • lip

  • quadriceps femoris muscle

  • facial motor nucleus

  • adrenal gland

  • kidney

  • spleen
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
  • GTP-dependent protein binding
  • protein binding
Cellular component
  • cytoplasm
  • organelle membrane
  • BLOC-2 complex
  • endosome
  • cytosol
  • early endosome membrane
  • endoplasmic reticulum
  • membrane
  • intracellular membrane-bounded organelle
  • lysosome
  • lysosomal membrane
Biological process
  • protein localization to membrane
  • pigmentation
  • blood coagulation
  • lysosome localization
  • organelle organization
  • melanocyte differentiation
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

79803

20170

Ensembl

ENSG00000166189

ENSMUSG00000074811

UniProt

Q86YV9

Q8BLY7

RefSeq (mRNA)

NM_024747

NM_176785

RefSeq (protein)

NP_079023

NP_789742

Location (UCSC)Chr 10: 102.07 – 102.07 MbChr 19: 45.99 – 45.99 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Hermansky–Pudlak syndrome 6 (HPS6), also known as ruby-eye protein homolog (Ru), is a protein that in humans is encoded by the HPS6 gene.[5]

Function

This intronless gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes.[6] HPS6 along with HPS3 and HPS5 form a stable protein complex named Biogenesis of Lysosome-related Organelles Complex-2 (BLOC-2).[7]

Clinical significance

Mutations in this gene are associated with Hermansky–Pudlak syndrome type 6 characterized by albinism and prolonged bleeding.[5][8]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000166189 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000074811 – 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. ^ a b Zhang Q, Zhao B, Li W, Oiso N, Novak EK, Rusiniak ME, Gautam R, Chintala S, O'Brien EP, Zhang Y, Roe BA, Elliott RW, Eicher EM, Liang P, Kratz C, Legius E, Spritz RA, O'Sullivan TN, Copeland NG, Jenkins NA, Swank RT (February 2003). "Ru2 and Ru encode mouse orthologs of the genes mutated in human Hermansky–Pudlak syndrome types 5 and 6". Nat. Genet. 33 (2): 145–53. doi:10.1038/ng1087. PMID 12548288. S2CID 23938527.
  6. ^ "Entrez Gene: HPS6 Hermansky–Pudlak syndrome 6".
  7. ^ Di Pietro SM, Falcón-Pérez JM, Dell'Angelica EC (April 2004). "Characterization of BLOC-2, a complex containing the Hermansky–Pudlak syndrome proteins HPS3, HPS5 and HPS6". Traffic. 5 (4): 276–83. doi:10.1111/j.1600-0854.2004.0171.x. PMID 15030569. S2CID 20584286.
  8. ^ Wei ML (February 2006). "Hermansky–Pudlak syndrome: a disease of protein trafficking and organelle function". Pigment Cell Res. 19 (1): 19–42. doi:10.1111/j.1600-0749.2005.00289.x. PMID 16420244.

Further reading

  • Stelzl U, Worm U, Lalowski M, et al. (2005). "A human protein-protein interaction network: a resource for annotating the proteome". Cell. 122 (6): 957–68. doi:10.1016/j.cell.2005.08.029. hdl:11858/00-001M-0000-0010-8592-0. PMID 16169070. S2CID 8235923.
  • Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
  • Huizing M, Pederson B, Hess RA, et al. (2009). "Clinical and cellular characterisation of Hermansky–Pudlak syndrome type 6". J. Med. Genet. 46 (12): 803–10. doi:10.1136/jmg.2008.065961. PMC 3500784. PMID 19843503.
  • Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
  • Grupe A, Li Y, Rowland C, et al. (2006). "A Scan of Chromosome 10 Identifies a Novel Locus Showing Strong Association with Late-Onset Alzheimer Disease". Am. J. Hum. Genet. 78 (1): 78–88. doi:10.1086/498851. PMC 1380225. PMID 16385451.
  • Strausberg RL, Feingold EA, Grouse LH, et al. (2002). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.

External links

  • GeneReviews/NCBI/NIH/UW entry on Hermansky–Pudlak syndrome


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