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Category   Symbol Source: HGNC EntrezGene Ensembl GeneCards RNA genes CroW21
GIFtS

SYNGR2 Gene

protein-coding   GIFtS: 52
GCID: GC17P076164

synaptogyrin 2

 Explore 1 disease affiliated with
SYNGR2 via our new
 Human Malady Compendium 
Biological research products
for SYNGR2
    

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, and/or 10fRNAdb)
About This Section

Aliases
Synaptogyrin 21 2
Cellugyrin3
Synaptogyrin-21
Cellugyrin3

External Ids:    HGNC: 114991   Entrez Gene: 91442   Ensembl: ENSG000001086397   OMIM: 6039265   UniProtKB: O437603   

Export aliases for SYNGR2 gene to outside databases

Previous GC identifers: GC17P075988 GC17P079151 GC17P076625 GC17P076761 GC17P073676 GC17P071589


(According to Entrez Gene, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
About This Section

Entrez Gene summary for SYNGR2:
This gene encodes an integral membrane protein containing four transmembrane regions and a C-terminal cytoplasmic tail
that is tyrosine phosphorylated. The exact function of this protein is unclear, but studies of a similar rat protein
suggest that it may play a role in regulating membrane traffic in non-neuronal cells. The gene belongs to the
synaptogyrin gene family. (provided by RefSeq, Jul 2008)




(According to GeneLoc and/or HGNC, and/or
Entrez Gene (NCBI build 37),
and/or miRBase,
Genomic Views according to UCSC (hg19) and Ensembl (release 69), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000017.10  NC_018928.1  NT_010783.15  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the SYNGR2 gene promoter:
         Pax-5   Nkx6-1   AML1a   Pax-2b   p53   Pax-2   Pax-2a   GATA-1   
         Other transcription factors

Browse SwitchGear Promoter luciferase reporter plasmids
   Search SABiosciences Chromatin IP Primers for SYNGR2

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat SYNGR2


Genomic Location:
Genomic View: UCSC Golden Path with GeneCards custom track

Entrez Gene cytogenetic band: 17q25.3   Ensembl cytogenetic band:  17q25.3   HGNC cytogenetic band: 17q25.3

SYNGR2 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
SYNGR2 gene location

GeneLoc information about chromosome 17         GeneLoc Exon Structure

GeneLoc location for GC17P076164:  view genomic region     (about GC identifiers)

Start:
76,164,639 bp from pter      End:
76,169,608 bp from pter
Size:
4,970 bases      Orientation:
plus strand

(According to 1UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to 2PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE MOPED and PaxDb, RefSeq according to NCBI, PDB rendering according to OCA and/or Proteopedia, Recombinant Proteins from EMD Millipore, R&D Systems, GenScript, Enzo Life Sciences, OriGene, Novus Biologicals, Sino Biological, ProSpec, and/or Uscn,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Uscn, Ontologies according to Gene Ontology Consortium 01 Mar 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, Abcam, and/or Uscn)
About This Section

UniProtKB/Swiss-Prot: SNG2_HUMAN, O43760 (See protein sequence)
Recommended Name: Synaptogyrin-2  
Size: 224 amino acids; 24810 Da
Subcellular location: Membrane; Multi-pass membrane protein. Cytoplasmic vesicle (By similarity)
Secondary accessions: O43762 Q658S7

Explore the universe of human proteins at neXtProt for SYNGR2: NX_O43760

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_O43760

  • SYNGR2 Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins: NP_004701.1  
    ENSEMBL proteins: 
     ENSP00000225777   ENSP00000465678   ENSP00000466942   ENSP00000466032   ENSP00000467600  
     ENSP00000466204   ENSP00000465005  

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    Uscn Proteins for SYNGR2

    Gene Ontology (GO): 3 cellular component terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005887integral to plasma membrane ----
    GO:0008021synaptic vesicle IEA--
    GO:0016021integral to membrane NAS9760194


    SYNGR2 for ontologies           About GeneDecksing



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    (According to InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section

    SYNGR2 for domains           About GeneDecksing

    3 InterPro domains/families:
     IPR016579 Synaptogyrin
     IPR021128 MARVEL-like_dom
     IPR008253 Marvel

    Graphical View of Domain Structure for InterPro Entry O43760

    ProtoNet protein and cluster: O43760

    1 Blocks protein family: IPB008253 Marvel

    UniProtKB/Swiss-Prot: SNG2_HUMAN, O43760
    Similarity: Belongs to the synaptogyrin family
    Similarity: Contains 1 MARVEL domain


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013,
    bound targets from SABiosciences, miRNA Gene Targets from miRTarBase shRNA from OriGene, RNAi from EMD Millipore, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
    About This Section

    Function Summary:
         Genatlas biochemistry entry for SYNGR2:
    synaptogyrin 2,putative vesicle protein,expressed in all tissues except in brain

    miRNA
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    1 GenomeRNAi human phenotype for SYNGR2:
     Metaphase cells 


    (Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Reactome, Tocris Bioscience, GeneGo (Thomson Reuters), QIAGEN, and/or UniProtKB, Sets of similar genes according to GeneDecks, Interaction Networks according to SABiosciences, and/or STRING, Interactions according to 1UniProtKB, 2MINT, 3I2D, and/or 4STRING, with links to IntAct and Ensembl, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene).
    About This Section



    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for SYNGR2

    STRING Interaction Network Preview (showing 1 interactants - click image to see more details)

    2 Interacting proteins for SYNGR2 (O437603 ENSP000002257774) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    FATE1Q969F03I2D: score=1 
    UBCENSP000003448184STRING: ENSP00000344818
    About this table

    Gene Ontology (GO): 1 biological process term (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0006605protein targeting IEA--


    SYNGR2 for ontologies           About GeneDecksing



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB, with drugs/clinical trials/news search links to CenterWatch)
    About This Section
    Browse Small Molecules at EMD Millipore
    Browse drugs & compounds from Enzo Life Sciences

    Browse Tocris compounds for SYNGR2
    Search CenterWatch for drugs/clinical trials and news about SYNGR2 / SNG2 

    (Secondary structures according to fRNAdb,
    GenBank/EMBL/DDBJ Accessions according to
    Unigene (Build 235 Homo sapiens; Mar 10 2013) or GenBank,
    RefSeq according to Entrez Gene,
    DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
    exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
    RNAi Products from EMD Millipore,
    siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN,
    Tagged/untagged cDNA clones from OriGene, SwitchGear Genomics, GenScript, DNA2.0, Vector BioLabs, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section

    REFSEQ mRNAs for SYNGR2 gene: 
    NM_004710.3  

    Unigene Cluster for SYNGR2:

    Synaptogyrin 2
    Hs.464210  [show with all ESTs]
    Unigene Representative Sequence: BC000407
    9 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000225777(uc002jut.3 uc002juu.1) ENST00000585591 ENST00000589183
    ENST00000589711 ENST00000591770 ENST00000588282 ENST00000589168 ENST00000590201
    ENST00000592456

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    8/10 QIAGEN miScript miRNA Assays for microRNAs that regulate SYNGR2 (see all 10):
    hsa-miR-320a hsa-miR-320d hsa-miR-609 hsa-miR-519e* hsa-miR-515-5p hsa-miR-320b hsa-miR-320e hsa-miR-3658
    SwitchGear 3'UTR luciferase reporter plasmidSYNGR2 3' UTR sequence
    Inhib. RNA
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    OriGene 29mer shRNA kits in GFP-retroviral vector in human, mouse, rat for SYNGR2 (see all 7)
    OriGene shRNA RFP: SYNGR2
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    Additional cDNA sequence: 

    AJ002308.1 AY358916.1 BC000407.2 BC029755.1 BC105992.1 

    24/27 DOTS entries (see all 27):

    DT.100818287  DT.452646  DT.95327492  DT.40106689  DT.92455229  DT.95187297  DT.100818291  DT.100818271 
    DT.92455227  DT.100818290  DT.120955048  DT.121075567  DT.95187289  DT.100847467  DT.120955055  DT.121621457 
    DT.86842947  DT.92455222  DT.92455224  DT.95187288  DT.95187308  DT.95310891  DT.97796112  DT.100818269 

    24/752 AceView cDNA sequences (see all 752):

    AI139048 BQ929185 AW117881 BC029755 BM672975 BQ677781 BQ893082 CD365882 
    CR592439 AW473135 BU541667 BG286601 BU541270 BM763368 AI684266 AW512364 
    CR610377 BM310803 AI687780 BQ682050 CR614467 BE744419 AW574792 BM764418 

    GeneLoc Exon Structure

    2 Alternative Splicing Database (ASD) splice patterns (SP) for SYNGR2    About this scheme

    ExUns: 1a · 1b ^ 2 ^ 3 ^ 4a · 4b
    SP1:                                    
    SP2:                    -               


    ECgene alternative splicing isoforms for SYNGR2

    (RNA expression data according to H-InvDB, NONCODE, miRBase, and RNAdb, Expression images according to data from BioGPS, Illumina Human BodyMap, and CGAP SAGE, Sets of similar genes according to GeneDecks, in vivo and in vitro expression data from LifeMap Discovery™, plus additional links to Genevestigator, and/or SOURCE, and/or BioGPS, and/or UniProtKB,
    PCR Arrays from SABiosciences, Primers from OriGene, SABiosciences, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
    About This Section

    SYNGR2 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: GCTCCCAGAC

    Microarray
    RNAseq (Illumina Body Map)
    (100×FPKM)½
    SAGE (Serial Analysis of Gene Expression)

    About this image
    See SYNGR2 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for SYNGR2

    SOURCE GeneReport for Unigene cluster: Hs.464210

    UniProtKB/Swiss-Prot: SNG2_HUMAN, O43760
    Tissue specificity: Ubiquitous; low expression in brain

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    In Situ
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    (Orthologs according to 1,2HomoloGene (2older version, for species not in 1newer version), 3euGenes, 4SGD , 5MGI Mar 06 2013, with possible further links to Flybase and/or WormBase, and/or 6Ensembl pan taxonomic compara , Gene Trees according to Ensembl and TreeFam)
    About This Section

    This gene was present in the common ancestor of animals.

    Orthologs for SYNGR2 gene from 5/16 species (see all 16)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    chicken
    (Gallus gallus)
    Aves SYNGR21 synaptogyrin 2 75.74(n)
    73.3(a)
      100859110  XM_003642363.1  XP_003642411.1 
    lizard
    (Anolis carolinensis)
    Reptilia SYNGR26
    --
    66(a)
    1 ↔ 1
    2(102305518-102313185)
    zebrafish
    (Danio rerio)
    Actinopterygii LOC1005378071 synaptogyrin-2-like 60.4(n)
    52.29(a)
      100537807  XM_003199534.1  XP_003199582.1 
    fruit fly
    (Drosophila melanogaster)
    Insecta synaptogyrin3 regulation of calcium ion dependent
    exocytosis
    38(a)   50C6   --
    worm
    (Caenorhabditis elegans)
    Secernentea sng-16
    Synaptogyrin homolog 1
    23(a)
    1 → many
    X(7327559-7329631)


    ENSEMBL Gene Tree for SYNGR2 (if available)
    TreeFam Gene Tree for SYNGR2 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for SYNGR2 gene
    SYNGR42  SYNGR12  SYNGR32  
    3 SIMAP similar genes for SYNGR2 using alignment to 6 protein entries:     SNG2_HUMAN (see all proteins):
    SYNGR1    SYNGR3    SYNGR4

    SYNGR2 for paralogs           About GeneDecksing


    2 Pseudogenes.org Pseudogenes for SYNGR2
    PGOHUM00000258932 PGOHUM00000236219


    (SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, UniProtKB, and DNA2.0, Linkage Disequilibrium by HapMap, Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants, Mutations from the Human Gene Mutation Database (HGMD) and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers from QIAGEN, Cancer Mutation PCR Arrays and Assays and Copy Number PCR Arrays from SABiosciences)
    About This Section

    10/171 NCBI SNPs in SYNGR2 are shown (see all 171    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 17 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs620790911,2
    C,F,--76162693(+) TGACTG/CTGAGC 2 -- us2k1 ds50015Minor allele frequency- C:0.10NA CSA WA 244
    rs781800431,2
    C,F,--76162912(+) GAGGCG/AAGAGG 1 -- us2k15Minor allele frequency- A:0.09NA CSA WA 244
    rs1168286791,2
    --76162919(+) GAGGGG/AGCTGA 1 -- us2k11Minor allele frequency- A:0.01WA 118
    rs777486001,2
    C,--76162959(+) CCTGTC/TGCCCT 1 -- us2k12Minor allele frequency- T:0.03NA 122
    rs1860502541,2
    --76162960(+) CTGTCA/GCCCTG 1 -- us2k10--------
    rs1893754181,2
    --76162982(+) TCTGTC/TTGCAT 1 -- us2k10--------
    rs1814243421,2
    --76163045(+) ATGGAG/TTCTCG 1 -- us2k10--------
    rs1865113821,2
    --76163081(+) CTCACC/TGCAAC 1 -- us2k10--------
    rs1410468821,2
    --76163156(+) CGCGCC/TACCAT 1 -- us2k10--------
    rs1448922501,2
    --76163170(+) CAGCTA/CATTTT 1 -- us2k10--------

    HapMap Linkage Disequilibrium report for SYNGR2 (76164639 - 76169608 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 1 variation for SYNGR2
         1 CNV: 30027

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    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section

    SYNGR2 for disorders           About GeneDecksing

    OMIM gene information: 603926    OMIM disorders: --

    1 disease for SYNGR2:    About MalaCards
    neuronitis


    Export disorders for SYNGR2 gene to outside databases

    (in PubMed. Associations of this gene to articles via 1Entrez Gene, 2UniProtKB/Swiss-Prot, 3HGNC, 4GAD, 5PharmGKB, 6HMDB, 7DrugBank, 8UniProtKB/TrEMBL, 9 Novoseek, and/or 10fRNAdb)
    About This Section

    PubMed articles for SYNGR2 gene, integrated from 9 sources (see all 12):
    (articles sorted by number of sources associating them with SYNGR2)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Characterization of the human synaptogyrin gene family. (PubMed id 9760194)1, 2, 3, 9 Kedra D....Dumanski J.P. (1998)
    2. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)1, 2 Gerhard D.S....Malek J. (2004)
    3. The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment. (PubMed id 12975309)1, 2 Clark H.F.... Gray A.M. (2003)
    4. Initial characterization of the human central proteome. (PubMed id 21269460)2 Burkard T.R.... Colinge J. (2011)
    5. Mass spectrometric analysis of lysine ubiquitylation r eveals promiscuity at site level. (PubMed id 21139048)1 Danielsen J.M....Nielsen M.L. (2011)
    6. A proteome-wide, quantitative survey of in vivo ubiqui tylation sites reveals widespread regulatory roles. (PubMed id 21890473)1 Wagner S.A....Choudhary C. (2011)
    7. The full-ORF clone resource of the German cDNA consortium. (PubMed id 17974005)2 Bechtel S.... Schupp I. (2007)
    8. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. (PubMed id 12477932)1 Strausberg R.L....Marra M.A. (2002)
    9. Cellugyrin, a novel ubiquitous form of synaptogyrin that is phosphorylated by pp60c-src. (PubMed id 9446595)1 Janz R. and Sudhof T.C. (1998)
    10. Cellugyrin is a marker for a distinct population of intracellular Glut4-containing vesicles. (PubMed id 10967091)9 Kupriyanova T.A. and Kandror K.V. (2000)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     ANDOR
    Aliases
    Free Text  

      Query String
    PubMed
    OMIM
    NCBI Bookshelf
      (Note: In FireFox, select the above section and copy using Ctrl-C)

    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 9144 HGNC: 11499 AceView: SYNGR2 Ensembl:ENSG00000108639 euGenes: HUgn9144
    ECgene: SYNGR2 H-InvDB: SYNGR2

    (According to HUGE)
    About This Section
      --

    (According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL,
    Wikipedia and/or GeneReviews via UniProtKB/Swiss-Prot)
    About This Section
    NameDescription
    PharmGKB entry for SYNGR2 Pharmacogenomics, SNPs, Pathways

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
    Patent Information for SYNGR2 gene:
    Search GeneIP for patents involving SYNGR2

    GeneCards and IP:
    Japan Patent Office Licenses GeneCards     European Patent Office Licenses GeneCards     Improving the IP Search



    (Antibodies, recombinant proteins, and assays from EMD Millipore, R&D Systems, OriGene, QIAGEN, GenScript, Cell Signaling Technology, SABiosciences, Novus Biologicals, Sino Biological, Enzo Life Sciences, Abcam, ProSpec, Uscn, Thermo Fisher Scientific, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Cell lines from GenScript and LifeMap BioReagents, PCR Arrays from SABiosciences, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, and/or Enzo Life Sciences),
    In Situ Hybridization Assays from
    Advanced Cell Diagnostics
    About This Section

     
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    GeneCards Homepage - Last full update: 18 Mar 2013 - Incrementals: 21 Mar 2013 , 15 Apr 2013 , 26 Apr 2013

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    VWF
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    von Willebrand factor
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