Human Gene VPS11 (uc001puy.1)
  Description: vacuolar protein sorting 11
RefSeq Summary (NM_021729): Vesicle mediated protein sorting plays an important role in segregation of intracellular molecules into distinct organelles. Genetic studies in yeast have identified more than 40 vacuolar protein sorting (VPS) genes involved in vesicle transport to vacuoles. This gene encodes the human homolog of yeast class C Vps11 protein. The mammalian class C Vps proteins are predominantly associated with late endosomes/lysosomes, and like their yeast counterparts, may mediate vesicle trafficking steps in the endosome/lysosome pathway. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014].
Transcript (Including UTRs)
   Position: hg18 chr11:118,443,703-118,457,898 Size: 14,196 Total Exon Count: 17 Strand: +
Coding Region
   Position: hg18 chr11:118,443,745-118,457,543 Size: 13,799 Coding Exon Count: 17 

Page IndexSequence and LinksPrimersCTDMicroarray ExpressionRNA Structure
Other SpeciesmRNA DescriptionsOther NamesModel InformationMethods
Data last updated at UCSC: 2009-03-03

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr11:118,443,703-118,457,898)mRNA (may differ from genome)Protein (941 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
BioGPSEnsemblEntrez GeneExonPrimerGeneCardsGeneNetwork
H-INVHGNCHPRDMGIOMIMPubMed
TreefamBioGrid CRISPR DB

-  Primer design for this transcript
 

Primer3Plus can design qPCR Primers that straddle exon-exon-junctions, which amplify only cDNA, not genomic DNA.
Click here to load the transcript sequence and exon structure into Primer3Plus

Exonprimer can design one pair of Sanger sequencing primers around every exon, located in non-genic sequence.
Click here to open Exonprimer with this transcript

To design primers for a non-coding sequence, zoom to a region of interest and select from the drop-down menu: View > In External Tools > Primer3


-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene           more ... click here to view the complete list

-  Microarray Expression Data
 
Expression ratio colors:

GNF Expression Atlas 2 Data from U133A and GNF1H Chips

      
      
      
     
    
     
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Affymetrix All Exon Microarrays

           
Ratios

-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -12.9042-0.307 Picture PostScript Text
3' UTR -115.01355-0.324 Picture PostScript Text

The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.

-  Orthologous Genes in Other Species
  Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
MouseRatZebrafishD. melanogasterC. elegansS. cerevisiae
Genome BrowserNo orthologGenome BrowserGenome BrowserGenome BrowserGenome Browser
Gene Details  Gene DetailsGene DetailsGene Details
Gene Sorter  Gene SorterGene SorterGene Sorter
MGI EnsemblFlyBaseWormBaseSGD
Protein Sequence Protein SequenceProtein SequenceProtein SequenceProtein Sequence
Alignment AlignmentAlignmentAlignmentAlignment

-  Descriptions from all associated GenBank mRNAs
  AK023279 - Homo sapiens cDNA FLJ13217 fis, clone NT2RP4001656, weakly similar to VACUOLAR BIOGENESIS PROTEIN END1.
AB027508 - Homo sapiens mRNA for hVPS11, complete cds.
AK056701 - Homo sapiens cDNA FLJ32139 fis, clone PLACE5000037, highly similar to Vacuolar protein sorting 11.
AK223158 - Homo sapiens mRNA for vacuolar protein sorting 11 (yeast homolog) variant, clone: LNG11645.
AL834218 - Homo sapiens mRNA; cDNA DKFZp564P2364 (from clone DKFZp564P2364).
BC065563 - Homo sapiens vacuolar protein sorting 11 homolog (S. cerevisiae), mRNA (cDNA clone MGC:74765 IMAGE:6144541), complete cds.
AK302973 - Homo sapiens cDNA FLJ54956 complete cds, highly similar to Vacuolar protein sorting 11.
AF308800 - Homo sapiens vacuolar protein sorting protein 11 (VPS11) mRNA, complete cds.
AB527816 - Synthetic construct DNA, clone: pF1KB8507, Homo sapiens VPS11 gene for vacuolar protein sorting 11 homolog, without stop codon, in Flexi system.
AF258558 - Homo sapiens PP3476 mRNA, complete cds.
BC012051 - Homo sapiens vacuolar protein sorting 11 homolog (S. cerevisiae), mRNA (cDNA clone IMAGE:4640302), partial cds.
AK026012 - Homo sapiens cDNA: FLJ22359 fis, clone HRC06443.
CU680178 - Synthetic construct Homo sapiens gateway clone IMAGE:100018972 5' read VPS11 mRNA.
JD389159 - Sequence 370183 from Patent EP1572962.
JD515931 - Sequence 496955 from Patent EP1572962.
JD483102 - Sequence 464126 from Patent EP1572962.
JD420051 - Sequence 401075 from Patent EP1572962.
JD539601 - Sequence 520625 from Patent EP1572962.
JD380549 - Sequence 361573 from Patent EP1572962.
JD431822 - Sequence 412846 from Patent EP1572962.
KJ902886 - Synthetic construct Homo sapiens clone ccsbBroadEn_12280 VPS11 gene, encodes complete protein.
JD249484 - Sequence 230508 from Patent EP1572962.
JD168728 - Sequence 149752 from Patent EP1572962.
JD039884 - Sequence 20908 from Patent EP1572962.
JD097040 - Sequence 78064 from Patent EP1572962.
JD211779 - Sequence 192803 from Patent EP1572962.
JD079186 - Sequence 60210 from Patent EP1572962.
JD273836 - Sequence 254860 from Patent EP1572962.
LF384542 - JP 2014500723-A/192045: Polycomb-Associated Non-Coding RNAs.
MA620119 - JP 2018138019-A/192045: Polycomb-Associated Non-Coding RNAs.

-  Other Names for This Gene
  Alternate Gene Symbols: NM_021729, NP_068375
UCSC ID: uc001puy.1
RefSeq Accession: NM_021729

-  Gene Model Information
 
category: coding nonsense-mediated-decay: no RNA accession: NM_021729.4
exon count: 16CDS single in 3' UTR: no RNA size: 3279
ORF size: 2825CDS single in intron: no Alignment % ID: 100.00
txCdsPredict score: 4481.50frame shift in genome: yes % Coverage: 98.20
has start codon: yes stop codon in genome: no # of Alignments: 1
has end codon: yes retained intron: no # AT/AC introns 1
selenocysteine: no end bleed into intron: 0# strange splices: 0
Click here for a detailed description of the fields of the table above.

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.