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

COG4 Gene

protein-coding   GIFtS: 55
GCID: GC16M070514

component of oligomeric golgi complex 4

 Explore 4 diseases affiliated with
COG4 via our new
 Human Malady Compendium 
Biological research products
for COG4
    

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

Aliases
Component Of Oligomeric Golgi Complex 41 2 3     DKFZP586E15191
COD11 2 5     Complexed With Dor1p2
COG Complex Subunit 42 3     Conserved Oligomeric Golgi Complex Protein 42
CDG2J2 5     Conserved Oligomeric Golgi Complex Subunit 42

External Ids:    HGNC: 186201   Entrez Gene: 258392   Ensembl: ENSG000001030517   OMIM: 6069765   UniProtKB: Q9H9E33   

Export aliases for COG4 gene to outside databases

Previous GC identifers: GC16M061216 GC16M070934 GC16M070249 GC16M070290 GC16M069071 GC16M056346


(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 COG4:
The protein encoded by this gene is a component of an oligomeric protein complex involved in the structure and function
of the Golgi apparatus. Defects in this gene may be a cause of congenital disorder of glycosylation type IIj. Two
transcript variants encoding different isoforms have been found for this gene.(provided by RefSeq, Aug 2010)

UniProtKB/Swiss-Prot: COG4_HUMAN, Q9H9E3
Function: Required for normal Golgi function. Plays a role in SNARE-pin assembly and Golgi-to-ER retrograde transport
via its interaction with SCFD1

Gene Wiki entry for COG4


(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_000016.9  NC_018927.1  NT_010498.15  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the COG4 gene promoter:
         STAT1   FOXF2   NRSF form 1   NCX/Ncx   LCR-F1   NRSF form 2   Tal-1beta   ITF-2   ATF6   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidCOG4 promoter sequence
   Search SABiosciences Chromatin IP Primers for COG4

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat COG4


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

Entrez Gene cytogenetic band: 16q22.1   Ensembl cytogenetic band:  16q22.1   HGNC chromosome: 16

COG4 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
COG4 gene location

GeneLoc information about chromosome 16         GeneLoc Exon Structure

GeneLoc location for GC16M070514:  view genomic region     (about GC identifiers)

Start:
70,514,471 bp from pter      End:
70,557,468 bp from pter
Size:
42,998 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: COG4_HUMAN, Q9H9E3 (See protein sequence)
Recommended Name: Conserved oligomeric Golgi complex subunit 4  
Size: 785 amino acids; 89083 Da
Subunit: Monomer. Component of the conserved oligomeric Golgi (COG) complex which is composed of eight different
subunits and is required for normal Golgi morphology and localization. Mediates interaction of SCFD1 with the COG
complex. Interacts with STX5
Subcellular location: Golgi apparatus membrane; Peripheral membrane protein; Cytoplasmic side (Probable)
Sequence caution: Sequence=BAB15483.1; Type=Erroneous initiation; Note=Translation N-terminally extended;
1 PDB 3D structure from and Proteopedia for COG4:
3HR0 (3D)    
Secondary accessions: B4DMN8 C9JS23 Q96D40 Q9BRF0 Q9BVZ2 Q9H5Y4 Q9Y3W3
Alternative splicing: 3 isoforms:  Q9H9E3-1   Q9H9E3-2   Q9H9E3-3   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for COG4: NX_Q9H9E3

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q9H9E3

  • COG4 Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins (2 alternative transcripts): 
    NP_001182068.1  NP_056201.2  

    ENSEMBL proteins: 
     ENSP00000456653   ENSP00000315775   ENSP00000432802   ENSP00000455693   ENSP00000454573  
     ENSP00000461912   ENSP00000434160   ENSP00000463732   ENSP00000377236  

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    Uscn Proteins for COG4

    Gene Ontology (GO): 2 cellular component terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0000139Golgi membrane IEA--
    GO:0017119Golgi transport complex IDA15047703


    COG4 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

    COG4 for domains           About GeneDecksing

    1 InterPro domain/family:
     IPR013167 COG_su4

    Graphical View of Domain Structure for InterPro Entry Q9H9E3

    ProtoNet protein and cluster: Q9H9E3

    UniProtKB/Swiss-Prot: COG4_HUMAN, Q9H9E3
    Similarity: Belongs to the COG4 family


    (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:

         UniProtKB/Swiss-Prot: COG4_HUMAN, Q9H9E3
    Function: Required for normal Golgi function. Plays a role in SNARE-pin assembly and Golgi-to-ER retrograde transport
    via its interaction with SCFD1

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    hsa-miR-142-3p hsa-miR-20b*
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    Inhib. RNA
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    Gene Ontology (GO): 1 molecular function term (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005515protein binding IPI15047703


    COG4 for ontologies           About GeneDecksing


    1 GenomeRNAi human phenotype for COG4:
     Decreased p24 protein expressi 


    (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:

        SABiosciences Gene Network CentralTM Interacting Genes and Proteins Network for COG4

    STRING Interaction Network Preview (showing 5 interactants - click image to see 17)

    5/24 Interacting proteins for COG4 (Q9H9E31, 2, 3 ENSP000003157754) via UniProtKB, MINT, STRING, and/or I2D (see all 24)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    SCFD1Q8WVM82, 3, ENSP000003907834MINT-7296985 MINT-7296900 MINT-7296997 MINT-7296837 MINT-7296817 MINT-7296950 MINT-7296858 MINT-7296787 MINT-7296930 MINT-7296769 MINT-7296883 MINT-7296802 I2D: score=1 STRING: ENSP00000390783
    COG3Q96JB22, 3, ENSP000002586544MINT-7296817 MINT-7296787 MINT-7296769 MINT-7296802 I2D: score=1 STRING: ENSP00000258654
    COG1Q8WTW31, 3, ENSP000002998864EBI-368382,EBI-368371 I2D: score=3 STRING: ENSP00000299886
    COG2Q147461, 3, ENSP000003556294EBI-368382,EBI-389449 I2D: score=3 STRING: ENSP00000355629
    SEPT2Q150192, 3, ENSP000003531574MINT-8270099 I2D: score=2 STRING: ENSP00000353157
    About this table

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0006890retrograde vesicle-mediated transport, Golgi to ER IMP19536132
    GO:0007030Golgi organization IMP19536132
    GO:0015031protein transport IEA--
    GO:0048213Golgi vesicle prefusion complex stabilization IMP19536132


    COG4 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 COG4
    Search CenterWatch for drugs/clinical trials and news about COG4 

    (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,
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    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 COG4 gene (2 alternative transcripts): 
    NM_001195139.1  NM_015386.2  

    Unigene Cluster for COG4:

    Component of oligomeric golgi complex 4
    Hs.208680  [show with all ESTs]
    Unigene Representative Sequence: BX648010
    14 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000564415 ENST00000323786(uc002ezc.3 uc002ezd.3) ENST00000530314(uc002eze.3)
    ENST00000482252(uc010cfu.3) ENST00000526700 ENST00000565715 ENST00000564315
    ENST00000567244 ENST00000562200 ENST00000564653 ENST00000534772 ENST00000530160
    ENST00000524584 ENST00000393612

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    2 QIAGEN miScript miRNA Assays for microRNAs that regulate COG4:
    hsa-miR-142-3p hsa-miR-20b*
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    Additional cDNA sequence: 

    AK022874.1 AK026435.1 AK096557.1 AK293235.1 AK297557.1 AL050101.1 BC000796.1 BC006306.2 
    BC013347.2 BC027726.2 BC072438.1 BC128144.1 BC128145.1 BX648010.1 

    22 DOTS entries:

    DT.100670471  DT.100730780  DT.100816127  DT.316115  DT.100812988  DT.100812987  DT.97851961  DT.100816132 
    DT.92451125  DT.102825854  DT.120690638  DT.91818536  DT.92451123  DT.92451145  DT.100719520  DT.120690734 
    DT.120690755  DT.100801567  DT.100831553  DT.120690635  DT.92451119  DT.120690717 

    24/406 AceView cDNA sequences (see all 406):

    BM044494 CR601969 BM550673 BU630342 AI382773 AI364170 AB088369 BQ689620 
    T31346 AI685978 BQ066375 BQ185791 BU620219 AU154526 BQ019415 AK096557 
    AL050101 BM818073 BU737929 AU125729 BM910766 BM011683 BG747770 BM563035 

    GeneLoc Exon Structure

    5/7 Alternative Splicing Database (ASD) splice patterns (SP) for COG4 (see all 7)    About this scheme

    ExUns: 1 ^ 2 ^ 3 ^ 4 ^ 5 ^ 6 ^ 7 ^ 8 ^ 9 ^ 10a · 10b ^ 11a · 11b ^ 12 ^ 13 ^ 14 ^ 15 ^ 16 ^ 17a · 17b ^ 18 ^ 19 ^ 20 ^ 21a · 21b · 21c
    SP1:                                                        -                                               -                                                   
    SP2:                                            -           -                                               -                                                   
    SP3:                                            -           -                                   -           -                                                   
    SP4:        -                                               -                                               -                                                   
    SP5:                                                                                                                                                            


    ECgene alternative splicing isoforms for COG4

    (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

    COG4 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: GATGGTCAGT

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

    About this image
    See COG4 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for COG4

    SOURCE GeneReport for Unigene cluster: Hs.208680
        SABiosciences Custom PCR Arrays for COG4
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    In Situ
    Assay Products:
     

     
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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 eukaryotes.

    Orthologs for COG4 gene from 9/30 species (see all 30)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Cog41 , 5 component of oligomeric golgi complex 41, 5 89.68(n)1
    94.39(a)1
      8 (57.76 cM)5
    1023391  NM_133973.21  NP_598734.11 
     1108466005 
    chicken
    (Gallus gallus)
    Aves COG41 component of oligomeric golgi complex 4 80.17(n)
    86.01(a)
      415681  NM_001012775.1  NP_001012793.1 
    lizard
    (Anolis carolinensis)
    Reptilia COG46
    --
    85(a)
    1 ↔ 1
    GL343539.1(65140-79771)
    zebrafish
    (Danio rerio)
    Actinopterygii Dr.2142 Transcribed sequence with moderate similarity to protein more 77.67(n)    57066186 
    fruit fly
    (Drosophila melanogaster)
    Insecta CG74561 , 3 CG74561 38(a)3
    50.8(n)1
    40.79(a)1
      31F13
    344421  NM_135569.31  NP_609413.11 
    worm
    (Caenorhabditis elegans)
    Secernentea Y51H7C.6a3
    cogc-41
    Protein COGC-41 32(a)
    (best of 2)3
    46.53(n)1
    34.21(a)1
      II(1403616-1408976)3
    1735181  NM_061565.31  NP_493966.11 
    baker's yeast
    (Saccharomyces cerevisiae)
    Saccharomycetes COG4(YPR105C)4
    COG41
    Essential component of the conserved oligomeric Golgi more4
    Cog4p1
    37.56(n)1
    22.62(a)1
      16(739569-736984)4
    8562201, 4  NP_015430.11, 4 
    thale cress
    (Arabidopsis thaliana)
    eudicotyledons AT4G014001 hypothetical protein 46.4(n)
    35.23(a)
      827943  NM_001160726.1  NP_001154198.1 
    rice
    (Oryza sativa)
    Liliopsida Os.156102 Transcribed sequence with moderate similarity to protein more 71.67(n)    CB633133.1 


    ENSEMBL Gene Tree for COG4 (if available)
    TreeFam Gene Tree for COG4 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
      --

    (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

    10/776 NCBI SNPs in COG4 are shown (see all 776    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 16 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1861504091,2
    --70514187(+) GTCCTC/TGTAAA 3 -- ds50010--------
    rs1908664361,2
    --70514248(+) AACTGA/GCCCTG 3 -- ds50010--------
    rs178844791,2
    C,--70514340(+) GCCCCG/AGACAC 3 -- ds50013Minor allele frequency- A:0.02NS WA 212
    rs1834114971,2
    --70514361(+) TGCACC/TGTGTG 3 -- ds50010--------
    rs178812361,2
    C,--70514382(+) CTGAGG/ATCTTG 3 -- ds50015Minor allele frequency- A:0.03NS NA 218
    rs1873018481,2
    --70514428(+) CTGCCC/TTGCCC 3 -- ds50010--------
    rs787260681,2
    C,F,--70514506(+) TCATAA/CACATC 3 -- ut31 ds50011Minor allele frequency- C:0.04EA 120
    rs1999117501,2
    C--70514510(+) AAACAC/TCACAG 3 -- ut31 ds50010--------
    rs1903926281,2
    --70514544(+) CTGCTA/GGGTCC 3 -- ut31 ds50010--------
    rs178837701,2
    C,--70514591(+) AGCTTG/ATTTGC 3 -- ut31 ds50012Minor allele frequency- A:0.01NS 90

    HapMap Linkage Disequilibrium report for COG4 (70514471 - 70557468 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 7 variations for COG4
         1 CNV: 4965
         6 Indels: 102320 61534 45460 25673 42327 45459
    Human Gene Mutation Database (HGMD): COG4

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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

    COG4 for disorders           About GeneDecksing

    OMIM gene information: 606976   
    OMIM disorders: 613489  
    UniProtKB/Swiss-Prot: COG4_HUMAN, Q9H9E3
  • Defects in COG4 are the cause of congenital disorder of glycosylation type 2J (CDG2J) [MIM:613489]. It is a
  • multisystem disorder caused by a defect in glycoprotein biosynthesis and characterized by under-glycosylated serum
    glycoproteins. Congenital disorders of glycosylation result in a wide variety of clinical features, such as defects in
    the nervous system development, psychomotor retardation, dysmorphic features, hypotonia, coagulation disorders, and
    immunodeficiency. The broad spectrum of features reflects the critical role of N-glycoproteins during embryonic
    development, differentiation, and maintenance of cell functions

    4 diseases for COG4:    About MalaCards
    congenital disorder of glycosylation    congenital disorder of glycosylation type ii    oculocerebrorenal syndrome    hypotonia

    1 disease from the University of Copenhagen DISEASES database for COG4:
    Oculocerebrorenal syndrome
    Human Genome Epidemiology (HuGE) Navigator: COG4 (1 document)

    Export disorders for COG4 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 COG4 gene, integrated from 9 sources (see all 25):
    (articles sorted by number of sources associating them with COG4)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Structural basis for a human glycosylation disorder c aused by mutation of the COG4 gene. (PubMed id 19651599)1, 2 Richardson B.C....Hughson F.M. (2009)
    2. Direct interaction between the COG complex and the SM protein, Sly1, is required for Golgi SNARE pairing. (PubMed id 19536132)1, 2 Laufman O....Lev S. (2009)
    3. Golgi function and dysfunction in the first COG4-defi cient CDG type II patient. (PubMed id 19494034)1, 2 Reynders E....Matthijs G. (2009)
    4. 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)
    5. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (2004)
    6. An unappreciated role for RNA surveillance. (PubMed id 14759258)1, 2 Hillman R.T.... Brenner S.E. (2004)
    7. Characterization of a mammalian Golgi-localized protein complex, COG, that is required for normal Golgi morphology and function. (PubMed id 11980916)1, 3 Ungar D....Waters M.G. (2002)
    8. The Sec34/35 Golgi transport complex is related to the exocyst, defining a family of complexes involved in multiple steps of membrane traffic. (PubMed id 11703943)1, 2 Whyte J.R. and Munro S. (2001)
    9. A census of human soluble protein complexes. (PubMed id 22939629)1 Havugimana P.C....Emili A. (2012)
    10. Initial characterization of the human central proteome. (PubMed id 21269460)2 Burkard T.R.... Colinge J. (2011)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     ANDOR
    Aliases
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    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 25839 HGNC: 18620 AceView: COG4 Ensembl:ENSG00000103051 euGenes: HUgn25839
    ECgene: COG4 H-InvDB: COG4

    (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 COG4 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 COG4 gene:
    Search GeneIP for patents involving COG4

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



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    GeneCards Homepage - Last full update: 19 Mar 2013 - Incrementals: 21 Mar 2013 , 15 Apr 2013 , 27 Apr 2013

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