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

SYNCRIP Gene

protein-coding   GIFtS: 52
GCID: GC06M086267

synaptotagmin binding, cytoplasmic RNA interacting protein

 Explore 9 diseases affiliated with
SYNCRIP via our new
 Human Malady Compendium 
Biological research products
for SYNCRIP
    

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

Aliases
Synaptotagmin Binding, Cytoplasmic RNA Interacting Protein1 2     DJ3J17.21
GRY-RBP1 2 3     GRYRBP2
NSAP11 2 3     PP682
HNRPQ11 2     Heterogeneous Nuclear Ribonucleoprotein Q2
HnRNP-Q1     HNRPQ3
Glycine- And Tyrosine-Rich RNA-Binding Protein2 3     HnRNP Q3
NS1-Associated Protein 12 3     Synaptotagmin-Binding, Cytoplasmic RNA-Interacting Protein3

External Ids:    HGNC: 169181   Entrez Gene: 104922   Ensembl: ENSG000001353167   UniProtKB: O605063   

Export aliases for SYNCRIP gene to outside databases

Previous GC identifers: GC06M086317 GC06M086318 GC06M086377 GC06M086380 GC06M083541


(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 SYNCRIP:
This gene encodes a member of the cellular heterogeneous nuclear ribonucleoprotein (hnRNP) family. hnRNPs are RNA
binding proteins that complex with heterogeneous nuclear RNA (hnRNA) and regulate alternative splicing,
polyadenylation, and other aspects of mRNA metabolism and transport. The encoded protein plays a role in multiple
aspects of mRNA maturation and is associated with several multiprotein complexes including the apoB RNA
editing-complex and survival of motor neurons (SMN) complex. Alternatively spliced transcript variants encoding
multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the short arm of
chromosome 20. (provided by RefSeq, Dec 2011)

UniProtKB/Swiss-Prot: HNRPQ_HUMAN, O60506
Function: Heterogenous nuclear ribonucleoprotein (hnRNP) implicated in mRNA processing mechanisms. Component of the
CRD-mediated complex that promotes MYC mRNA stability. Isoform 1, isoform 2 and isoform 3 are associated in vitro with
pre-mRNA, splicing intermediates and mature mRNA protein complexes. Isoform 1 binds to apoB mRNA AU-rich sequences.
Isoform 1 is part of the APOB mRNA editosome complex and may modulate the postranscriptional C to U RNA-editing of the
APOB mRNA through either by binding to A1CF (APOBEC1 complementation factor), to APOBEC1 or to RNA itself. May be
involved in translationally coupled mRNA turnover. Implicated with other RNA-binding proteins in the cytoplasmic
deadenylation/translational and decay interplay of the FOS mRNA mediated by the major coding-region determinant of
instability (mCRD) domain. Interacts in vitro preferentially with poly(A) and poly(U) RNA sequences. Isoform 3 may be
involved in cytoplasmic vesicle-based mRNA transport through interaction with synaptotagmins. Component of the GAIT
(gamma interferon-activated inhibitor of translation) complex which mediates interferon-gamma-induced
transcript-selective translation inhibition in inflammation processes. Upon interferon-gamma activation assembles into
the GAIT complex which binds to stem loop-containing GAIT elements in the 3'-UTR of diverse inflammatory mRNAs (such
as ceruplasmin) and suppresses their translation; seems not to be essential for GAIT complex function

Gene Wiki entry for SYNCRIP


(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_000006.11  NC_018917.1  NT_007299.13  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the SYNCRIP gene promoter:
         AhR   SRF   Sp1   Egr-1   SRF (504 AA)   HNF-4alpha2   Nkx2-5   Arnt   HNF-4alpha1   Egr-4   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidSYNCRIP promoter sequence
   Search SABiosciences Chromatin IP Primers for SYNCRIP

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


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

Entrez Gene cytogenetic band: 6q14-q15   Ensembl cytogenetic band:  6q14.3   HGNC cytogenetic band: 6q14-q15

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

GeneLoc information about chromosome 6         GeneLoc Exon Structure

GeneLoc location for GC06M086267:  view genomic region     (about GC identifiers)

Start:
86,267,696 bp from pter      End:
86,353,510 bp from pter
Size:
85,815 bases      Orientation:
minus 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: HNRPQ_HUMAN, O60506 (See protein sequence)
Recommended Name: Heterogeneous nuclear ribonucleoprotein Q  
Size: 623 amino acids; 69603 Da
Subunit: Isoform 1 is a component of the APOB mRNA editosome complex and interacts with APOBEC1 and A1CF (APOBEC1
complementation factor). Part of a complex associated with the FOS mCRD domain and consisting of PABPC1, PAIP1,
CSDE1/UNR, HNRPD and SYNCRIP. Isoform 3 interacts with HNRPR. Interacts with POLR2A hyperphosphorylated C-terminal
domain. Interacts with minute virus of mice (MVM) NS1 protein. Isoform 1, isoform 2 and isoform 3 interact with SMN.
Isoform 3 interacts through its C-terminal domain with SYT7, SYT8 and SYT9 (By similarity). The non-phosphorylated and
phosphorylated forms are colocalized with PAIP1 in polysomes (By similarity). Identified in a histone pre-mRNA
complex, at least composed of ERI1, LSM11, SLBP, SNRPB, SYNCRIP and YBX1 (By similarity). Identified in the
spliceosome C complex. Component of the coding region determinant (CRD)-mediated complex, composed of DHX9, HNRNPU,
IGF2BP1, SYNCRIP and YBX1. Identified in a mRNP complex, at least composed of DHX9, DDX3X, ELAVL1, HNRNPU, IGF2BP1,
ILF3, PABPC1, PCBP2, PTBP2, STAU1, STAU2, SYNCRIP and YBX1. Identified in a mRNP granule complex, at least composed of
ACTB, ACTN4, DHX9, ERG, HNRNPA1, HNRNPA2B1, HNRNPAB, HNRNPD, HNRNPL, HNRNPR, HNRNPU, HSPA1, HSPA8, IGF2BP1, ILF2,
ILF3, NCBP1, NCL, PABPC1, PABPC4, PABPN1, RPLP0, RPS3, RPS3A, RPS4X, RPS8, RPS9, SYNCRIP, TROVE2, YBX1 and
untranslated mRNAs. Interacts with GTPBP1. Component of the GAIT complex; in humans the complex assembly seems to be a
two-step process in which EPRS first associates with SYNCRIP to form a pre-GAIT complex which is deficient in GAIT
element binding
Subcellular location: Cytoplasm. Microsome (By similarity). Endoplasmic reticulum (By similarity). Nucleus (By
similarity). Note=The tyrosine phosphorylated form bound to RNA is found in microsomes (By similarity). Localized in
cytoplasmic mRNP granules containing untranslated mRNAs
Subcellular location: Isoform 1: Nucleus, nucleoplasm (By similarity). Note=Expressed predominantly in the nucleoplasm
(By similarity)
Subcellular location: Isoform 2: Nucleus, nucleoplasm (By similarity). Note=Expressed predominantly in the nucleoplasm
(By similarity)
Subcellular location: Isoform 3: Nucleus, nucleoplasm (By similarity). Note=Expressed predominantly in the nucleoplasm
(By similarity)
Sequence caution: Sequence=AAH15575.1; Type=Miscellaneous discrepancy; Note=Contaminating sequence. Potential poly-A
sequence starting in position 413;
1 PDB 3D structure from and Proteopedia for SYNCRIP:
2DGU (3D)    
Secondary accessions: E1P501 E1P502 Q53H05 Q5TCG2 Q5TCG3 Q8IW78 Q8N599 Q96LC1 Q96LC2 Q9Y583
Alternative splicing: 5 isoforms:  O60506-1   O60506-2   O60506-3   O60506-4   O60506-5   (May be due to a competing donor splice site and to an exon inclusion)

Explore the universe of human proteins at neXtProt for SYNCRIP: NX_O60506

Post-translational modifications:

  • Phosphorylated on tyrosine. The membrane-bound form found in microsomes is phosphorylated in vitro by insulin receptor
  • tyrosine kinase (INSR). Phosphorylation is inhibited upon binding to RNA, whereas the cytoplasmic form is poorly
    phosphorylated (By similarity)1
  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_O60506

  • SYNCRIP Protein expression data from MOPED and PaxDb:    About this image 
    SYNCRIP Protein Expression
    REFSEQ proteins (7 alternative transcripts): 
    NP_001153145.1  NP_001153146.1  NP_001153147.1  NP_001153148.1  NP_001153149.1  NP_001240700.1  NP_006363.4  

    ENSEMBL proteins: 
     ENSP00000426494   ENSP00000347380   ENSP00000358635   ENSP00000397782  

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    Novus Biologicals SYNCRIP Proteins
    Novus Biologicals SYNCRIP Lysate
    Browse Sino Biological Recombinant Proteins
    Browse ProSpec Recombinant Proteins
    Uscn Proteins for SYNCRIP

    Gene Ontology (GO): 5/9 cellular component terms (GO ID links to tree view) (see all 9):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005634nucleus TAS9847309
    GO:0005654nucleoplasm IEA--
    GO:0005737cytoplasm ----
    GO:0005783endoplasmic reticulum IEA--
    GO:0005792microsome ----

    SYNCRIP for ontologies           About GeneDecksing



    SYNCRIP Antibody Products: 
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    Uscn ELISAs and CLIAs for SYNCRIP


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

    SYNCRIP for domains           About GeneDecksing

    3 InterPro domains/families:
     IPR006535 HnRNP_R/Q_splicing_fac
     IPR000504 RRM_dom
     IPR012677 Nucleotide-bd_a/b_plait

    Graphical View of Domain Structure for InterPro Entry O60506

    ProtoNet protein and cluster: O60506

    UniProtKB/Swiss-Prot: HNRPQ_HUMAN, O60506
    Domain: The domain containing eight Arg-Gly-Gly repeats may be involved in RNA-binding and protein-protein interactions
    Similarity: Contains 3 RRM (RNA recognition motif) domains


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

    Molecular Function:

         UniProtKB/Swiss-Prot Summary: HNRPQ_HUMAN, O60506
    Function: Heterogenous nuclear ribonucleoprotein (hnRNP) implicated in mRNA processing mechanisms. Component of the
    CRD-mediated complex that promotes MYC mRNA stability. Isoform 1, isoform 2 and isoform 3 are associated in vitro with
    pre-mRNA, splicing intermediates and mature mRNA protein complexes. Isoform 1 binds to apoB mRNA AU-rich sequences.
    Isoform 1 is part of the APOB mRNA editosome complex and may modulate the postranscriptional C to U RNA-editing of the
    APOB mRNA through either by binding to A1CF (APOBEC1 complementation factor), to APOBEC1 or to RNA itself. May be
    involved in translationally coupled mRNA turnover. Implicated with other RNA-binding proteins in the cytoplasmic
    deadenylation/translational and decay interplay of the FOS mRNA mediated by the major coding-region determinant of
    instability (mCRD) domain. Interacts in vitro preferentially with poly(A) and poly(U) RNA sequences. Isoform 3 may be
    involved in cytoplasmic vesicle-based mRNA transport through interaction with synaptotagmins. Component of the GAIT
    (gamma interferon-activated inhibitor of translation) complex which mediates interferon-gamma-induced
    transcript-selective translation inhibition in inflammation processes. Upon interferon-gamma activation assembles into
    the GAIT complex which binds to stem loop-containing GAIT elements in the 3'-UTR of diverse inflammatory mRNAs (such
    as ceruplasmin) and suppresses their translation; seems not to be essential for GAIT complex function

         Gene Ontology (GO): 4 molecular function terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0000166nucleotide binding IEA--
    GO:0003723RNA binding TAS9847309
    GO:0005515protein binding IPI12674497
    GO:0008143poly(A) RNA binding IEA--
         
    SYNCRIP for ontologies           About GeneDecksing


    Phenotypes:
         4 GenomeRNAi human phenotypes for SYNCRIP:
     Decreased NANOG protein expres  Decreased OCT4 protein express  Decreased POU5F1-GFP protein e  Decreased viability with pacli 

    Animal Models:
       inGenious Targeting Laboratory - Customizable classic, inducible, and humanized mouse model solutions for SYNCRIP 

    miRNA
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    hsa-miR-361-5p hsa-miR-106a hsa-miR-3622b-3p hsa-miR-508-5p hsa-miR-200b hsa-miR-642b hsa-miR-130b hsa-miR-509-3-5p
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    Gene Editing
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    In Situ Assay
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for SYNCRIP


    (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

    Unified GeneCards pathways  About this table 
    See pathways by source

    Super-pathwaycontained gene-specific pathways
    1Translational Control
    Translational Control1.00

    Pathway sources
    See GeneCards unified pathways
    Show all pathways


    1 Cell Signaling Technology (CST) Pathway for SYNCRIP
        Translational Control



    SYNCRIP for pathways           About GeneDecksing

    Interactions:

        SABiosciences Gene Network CentralTM Interacting Genes and Proteins Network for SYNCRIP

    STRING Interaction Network Preview (showing 5 interactants - click image to see 25)

    5/765 Interacting proteins for SYNCRIP (O605061, 2, 3 ENSP000003586354) via UniProtKB, MINT, STRING, and/or I2D (see all 765)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    HNRNPDQ14103-41, ENSP000003131994EBI-1024357,EBI-432545 MINT-7945693 I2D: score=2 STRING: ENSP00000313199
    SMN2Q166372, 3, ENSP000003701194MINT-7945693 I2D: score=1 STRING: ENSP00000370119
    HNRNPH1P319432, 3, ENSP000003491684MINT-7945693 I2D: score=1 STRING: ENSP00000349168
    SF3A2Q154282, 3, ENSP000002214944MINT-5205863 I2D: score=1 STRING: ENSP00000221494
    SMN1Q166372, 3MINT-7945693 I2D: score=1 
    About this table

    Gene Ontology (GO): 5/8 biological process terms (GO ID links to tree view) (see all 8):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0000398mRNA splicing, via spliceosome IC11991638
    GO:0006396RNA processing TAS9847309
    GO:0008380RNA splicing TAS9847309
    GO:0017148negative regulation of translation IMP15479637
    GO:0019048virus-host interaction IEA--

    SYNCRIP 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
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    Search CenterWatch for drugs/clinical trials and news about SYNCRIP / HNRPQ 

    (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, Sirion Biotech, 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 SYNCRIP gene (7 alternative transcripts): 
    NM_001159673.1  NM_001159674.1  NM_001159675.1  NM_001159676.1  NM_001159677.1  NM_001253771.1  NM_006372.4  

    Unigene Cluster for SYNCRIP:

    Synaptotagmin binding, cytoplasmic RNA interacting protein
    Hs.571177  [show with all ESTs]
    Unigene Representative Sequence: NM_001159677
    4 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000503906 ENST00000355238(uc003pku.3 uc003pkv.3 uc003pkw.3 uc003pkx.3 uc003pky.3)
    ENST00000369622(uc003pkz.2 uc003pla.2) ENST00000444272

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    hsa-miR-361-5p hsa-miR-106a hsa-miR-3622b-3p hsa-miR-508-5p hsa-miR-200b hsa-miR-642b hsa-miR-130b hsa-miR-509-3-5p
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    Additional cDNA sequence: 

    AB209098.1 AF037448.1 AF155568.1 AK056188.1 AK222776.1 AK294212.1 AK299796.1 AK313572.1 
    AY034481.1 AY034482.1 AY034483.1 BC009176.2 BC015575.2 BC021932.1 BC024283.1 BC032643.1 
    BC040844.1 

    24/30 DOTS entries (see all 30):

    DT.100874783  DT.100046070  DT.455852  DT.91776556  DT.100874784  DT.91950888  DT.95264437  DT.86854256 
    DT.100874788  DT.99982340  DT.100046084  DT.100840959  DT.97860332  DT.121330193  DT.100668409  DT.120798424 
    DT.91776560  DT.121330146  DT.120834968  DT.121330084  DT.100041401  DT.100733770  DT.100874798  DT.121330247 

    24/467 AceView cDNA sequences (see all 467):

    NM_006372 CA447046 CA413299 AK056188 AI581394 CB130920 CR611039 AA032165 
    BC005110 BM455117 BF732338 AA363926 BM751035 BU164891 AI285030 BQ945048 
    BI438839 AA431154 AA625241 CD358572 CF129670 CD652059 AA987698 BE407142 

    GeneLoc Exon Structure

    5/12 Alternative Splicing Database (ASD) splice patterns (SP) for SYNCRIP (see all 12)    About this scheme

    ExUns: 1a · 1b · 1c ^ 2a · 2b · 2c · 2d · 2e ^ 3a · 3b ^ 4a · 4b ^ 5a · 5b · 5c ^ 6a · 6b · 6c ^ 7 ^ 8a · 8b · 8c ^ 9a · 9b ^ 10 ^ 11 ^
    SP1:                                                                                                                                                            
    SP2:                                                                                                                                            -               
    SP3:                    -     -     -     -     -                                                                                                               
    SP4:                                                  -     -                                               -                                                   
    SP5:                                                  -     -                                                                                                   

    ExUns: 12a · 12b ^ 13a · 13b ^ 14a · 14b
    SP1:                                    
    SP2:                                    
    SP3:                                    
    SP4:                                    
    SP5:                                    


    ECgene alternative splicing isoforms for SYNCRIP

    (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

    SYNCRIP expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: GCAAACAATC
    SYNCRIP Expression
    About this image
    See SYNCRIP Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for SYNCRIP

    SOURCE GeneReport for Unigene cluster: Hs.571177

    UniProtKB/Swiss-Prot: HNRPQ_HUMAN, O60506
    Tissue specificity: Ubiquitously expressed. Detected in heart, brain, pancreas, placenta, spleen, lung, liver, skeletal
    muscle, kidney, thymus, prostate, uterus, small intestine, colon, peripheral blood and testis

        SABiosciences Custom PCR Arrays for SYNCRIP
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for SYNCRIP

    (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 eukaryotes.

    Orthologs for SYNCRIP gene from 8/23 species (see all 23)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    chicken
    (Gallus gallus)
    Aves SYNCRIP6
    synaptotagmin binding, cytoplasmic RNA interacting...
    98(a)
    1 ↔ 1
    3(79601699-79624544)
    lizard
    (Anolis carolinensis)
    Reptilia SYNCRIP6
    --
    97(a)
    1 ↔ 1
    1(176810175-176829871)
    African clawed frog
    (Xenopus laevis)
    Amphibia Xl.252492 Xenopus laevis transcribed sequence with moderate similarity more 87.48(n)    BJ072864.1 
    zebrafish
    (Danio rerio)
    Actinopterygii BC056750.12   -- 81.81(n)    BC056750.1 
    fruit fly
    (Drosophila melanogaster)
    Insecta CG178386
    --
    42(a)
    1 → many
    3R(16582451-16631963)
    worm
    (Caenorhabditis elegans)
    Secernentea hrp-26
    human HnRNP A1 homolog family member (hrp-2)
    37(a)
    1 → many
    I(12060267-12064890)
    thale cress
    (Arabidopsis thaliana)
    eudicotyledons AT4G008306
    AT3G526606
    (see all 4)
    RNA recognition motif-containing protein
    (see all 4)
    21(a)
    20(a)
    (see all 4)
    many ↔ many
    many ↔ many
    (see all 4)
    4(352016-355233)
    3(19521660-19524953)
    rice
    (Oryza sativa)
    Liliopsida --
    --
    (see all 8)
    RNA recognition motif containing protein, expresse...
    RNA recognition motif containing protein, expresse...
    (see all 8)
    23(a)
    22(a)
    (see all 8)
    many ↔ many
    many ↔ many
    (see all 8)
    12(1754561-1758698)
    10(3112799-3117851)


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

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for SYNCRIP gene
    RBM472  DND12  RBM462  A1CF2  HNRNPR2  
    8 SIMAP similar genes for SYNCRIP using alignment to 5 protein entries:     HNRPQ_HUMAN (see all proteins):
    DKFZp686A13234    HNRPR    DKFZp686O0665    HNRNPR    RBM46    A1CF
    RBM47    TIAL1

    SYNCRIP for paralogs           About GeneDecksing


    1 Pseudogenes.org Pseudogene for SYNCRIP
    PGOHUM00000247585


    (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

    10/613 NCBI SNPs in SYNCRIP are shown (see all 613    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 6 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs10591621,2
    --83541894(-) AACATT/CTATAT 5 -- ut312Minor allele frequency- C:0.02NA 122
    rs784221671,2
    F--83541979(+) TGCTCG/ATCCCG 5 -- ut311Minor allele frequency- A:0.06WA 118
    rs69026381,2
    C,F,A,H--83542892(+) ACTTTT/CAAAAA 5 -- ut31 ese310Minor allele frequency- C:0.14NS EA WA NA 772
    rs93445371,2
    H--83542969(+) AATTAG/ACATCT 5 -- ut314Minor allele frequency- A:0.00NS EA 418
    rs1122023841,2
    --83543204(+) AACTTG/CAGAAG 5 -- ut311Minor allele frequency- C:0.50CSA 2
    rs1134733371,2
    --83543449(+) ATTTCT/CATGTT 5 -- ut312Minor allele frequency- C:0.03CSA WA 120
    rs109441321,2
    C,F,H--83543733(+) AAGTAG/ATCTGC 5 -- ut31 ese36Minor allele frequency- A:0.01NS EA NA 592
    rs2003428141,2
    C--83544607(+) ACAAAA/CCTGTC 5 -- ut310--------
    rs37781431,2
    C--83545159(+) ATACAG/CGCTAT 5 -- ut31 ese33Minor allele frequency- C:0.01NA 142
    rs102233971,2
    C,H--83546007(+) CAAAAG/ATAACA 5 -- ut315Minor allele frequency- A:0.00NS EA 588

    HapMap Linkage Disequilibrium report for SYNCRIP (86267696 - 86353510 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
          Database of Genomic Variants (DGV) variations for SYNCRIP: --
    Human Gene Mutation Database (HGMD): SYNCRIP

    SABiosciences Cancer Mutation PCR Assays
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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

    SYNCRIP for disorders           About GeneDecksing

    9 diseases for SYNCRIP:    About MalaCards
    spinal muscular atrophy    muscular atrophy    neuronitis    hepatitis c
    hepatocellular carcinoma    colon cancer    hepatitis    carcinoma
    prostatitis


    Export disorders for SYNCRIP 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 SYNCRIP gene, integrated from 9 sources (see all 76):
    (articles sorted by number of sources associating them with SYNCRIP)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Two-hybrid cloning identifies an RNA-binding protein, GRY-RBP, as a component of apobec-1 editosome. (PubMed id 11352648)1, 2, 3, 9 Lau P.P.... Chan L. (2001)
    2. A novel heterogeneous nuclear ribonucleoprotein-like protein interacts with NS1 of the minute virus of mice. (PubMed id 9847309)1, 2, 3, 9 Harris C.E.... Astell C.R. (1999)
    3. SMN interacts with a novel family of hnRNP and spliceosomal proteins. (PubMed id 11574476)1, 2, 9 Mourelatos Z.... Dreyfuss G. (2001)
    4. Control of c-myc mRNA stability by IGF2BP1-associated cytoplasmic RNPs. (PubMed id 19029303)1, 2 Weidensdorfer D....HA1ttelmaier S. (2009)
    5. Tryptic digestion of ubiquitin standards reveals an improved strategy for identifying ubiquitinated proteins by mass spectrometry. (PubMed id 17370265)1, 2 Denis N.J.... Figeys D. (2007)
    6. Molecular composition of IMP1 ribonucleoprotein granules. (PubMed id 17289661)1, 2 Joeson L.... Nielsen F.C. (2007)
    7. Noncanonical function of glutamyl-prolyl-tRNA synthetase: gene-specific silencing of translation. (PubMed id 15479637)1, 2 Sampath P....Fox P.L. (2004)
    8. 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)
    9. Signaling initiated by overexpression of the fibroblast growth factor receptor-1 investigated by mass spectrometry. (PubMed id 12601080)1, 2 Hinsby A.M.... Mann M. (2003)
    10. The DNA sequence and analysis of human chromosome 6. (PubMed id 14574404)1, 2 Mungall A.J.... Beck S. (2003)

    (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: 10492 HGNC: 16918 AceView: SYNCRIPandSNX14 Ensembl:ENSG00000135316 euGenes: HUgn10492
    ECgene: SYNCRIP H-InvDB: SYNCRIP

    (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 SYNCRIP 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 SYNCRIP gene:
    Search GeneIP for patents involving SYNCRIP

    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 and Sirion Biotech, Clones from EMD Millipore, OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Cell lines from GenScript, LifeMap BioReagents, and Sirion Biotech, PCR Arrays from SABiosciences, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, and/or Enzo Life Sciences, In Situ Hybridization Assays from
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    About This Section

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