Human Gene COPS4 (uc003hoa.3)
  Description: Homo sapiens COP9 signalosome subunit 4 (COPS4), transcript variant 1, mRNA.
RefSeq Summary (NM_016129): This gene encodes one of eight subunits composing COP9 signalosome, a highly conserved protein complex that functions as an important regulator in multiple signaling pathways. The structure and function of COP9 signalosome is similar to that of the 19S regulatory particle of 26S proteasome. COP9 signalosome has been shown to interact with SCF-type E3 ubiquitin ligases and act as a positive regulator of E3 ubiquitin ligases. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012].
Transcript (Including UTRs)
   Position: hg19 chr4:83,956,239-83,996,971 Size: 40,733 Total Exon Count: 10 Strand: +
Coding Region
   Position: hg19 chr4:83,956,378-83,996,583 Size: 40,206 Coding Exon Count: 10 

Page IndexSequence and LinksUniProtKB CommentsPrimersCTDGene Alleles
RNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein StructureOther SpeciesGO Annotations
mRNA DescriptionsPathwaysOther NamesModel InformationMethods
Data last updated at UCSC: 2013-06-14

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr4:83,956,239-83,996,971)mRNA (may differ from genome)Protein (406 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
AlphaFoldBioGPSEnsemblEntrez GeneExonPrimerGeneCards
GeneNetworkH-INVHGNCHPRDLynxMGI
neXtProtOMIMPubMedReactomeTreefamUniProtKB
WikipediaBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: CSN4_HUMAN
DESCRIPTION: RecName: Full=COP9 signalosome complex subunit 4; Short=SGN4; Short=Signalosome subunit 4; AltName: Full=JAB1-containing signalosome subunit 4;
FUNCTION: Component of the COP9 signalosome complex (CSN), a complex involved in various cellular and developmental processes. The CSN complex is an essential regulator of the ubiquitin (Ubl) conjugation pathway by mediating the deneddylation of the cullin subunits of SCF-type E3 ligase complexes, leading to decrease the Ubl ligase activity of SCF-type complexes such as SCF, CSA or DDB2. The complex is also involved in phosphorylation of p53/TP53, c-jun/JUN, IkappaBalpha/NFKBIA, ITPK1 and IRF8/ICSBP, possibly via its association with CK2 and PKD kinases. CSN-dependent phosphorylation of TP53 and JUN promotes and protects degradation by the Ubl system, respectively.
SUBUNIT: Component of the CSN complex, composed of COPS1/GPS1, COPS2, COPS3, COPS4, COPS5, COP6, COPS7 (COPS7A or COPS7B) and COPS8. In the complex, it probably interacts directly with COPS1, COPS2, COPS3, COPS5, COPS6, COPS7 (COPS7A or COPS7B) and COPS8.
INTERACTION: Q0VDD7:C19orf57; NbExp=2; IntAct=EBI-742413, EBI-741210; P01100:FOS; NbExp=2; IntAct=EBI-742413, EBI-852851;
SUBCELLULAR LOCATION: Cytoplasm. Nucleus.
SIMILARITY: Belongs to the CSN4 family.
SIMILARITY: Contains 1 PCI domain.

-  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

+  Common Gene Haplotype Alleles
  Press "+" in the title bar above to open this section.

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 19.53 RPKM in Pituitary
Total median expression: 580.71 RPKM



View in GTEx track of Genome Browser    View at GTEx portal     View GTEx Body Map

+  Microarray Expression Data
  Press "+" in the title bar above to open this section.

-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -48.00139-0.345 Picture PostScript Text
3' UTR -86.98388-0.224 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.

-  Protein Domain and Structure Information
  InterPro Domains: Graphical view of domain structure
IPR000717 - PCI_dom
IPR011990 - TPR-like_helical
IPR011991 - WHTH_trsnscrt_rep_DNA-bd

Pfam Domains:
PF01399 - PCI domain

SCOP Domains:
46785 - "Winged helix" DNA-binding domain

ModBase Predicted Comparative 3D Structure on Q9BT78
FrontTopSide
The pictures above may be empty if there is no ModBase structure for the protein. The ModBase structure frequently covers just a fragment of the protein. You may be asked to log onto ModBase the first time you click on the pictures. It is simplest after logging in to just click on the picture again to get to the specific info on that model.

-  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
No orthologNo orthologGenome BrowserGenome BrowserGenome BrowserNo ortholog
Gene Details  Gene DetailsGene Details 
Gene Sorter  Gene SorterGene Sorter 
  EnsemblFlyBaseWormBase 
  Protein SequenceProtein SequenceProtein Sequence 
  AlignmentAlignmentAlignment 

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0005515 protein binding
GO:0019784 NEDD8-specific protease activity

Biological Process:
GO:0000338 protein deneddylation
GO:0000715 nucleotide-excision repair, DNA damage recognition
GO:0006283 transcription-coupled nucleotide-excision repair
GO:0043687 post-translational protein modification

Cellular Component:
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0008021 synaptic vesicle
GO:0008180 COP9 signalosome
GO:0016607 nuclear speck
GO:0030054 cell junction
GO:0031410 cytoplasmic vesicle
GO:0045202 synapse


-  Descriptions from all associated GenBank mRNAs
  AK094238 - Homo sapiens cDNA FLJ36919 fis, clone BRACE2003987, highly similar to COP9 signalosome complex subunit 4.
HM005665 - Homo sapiens clone HTL-T-42a testis tissue sperm-binding protein Li 42a mRNA, complete cds.
LF383986 - JP 2014500723-A/191489: Polycomb-Associated Non-Coding RNAs.
AK001148 - Homo sapiens cDNA FLJ10286 fis, clone HEMBB1001384, highly similar to COP9 signalosome complex subunit 4.
AK024005 - Homo sapiens cDNA FLJ13943 fis, clone Y79AA1000966, highly similar to COP9 signalosome complex subunit 4.
BC093007 - Homo sapiens COP9 constitutive photomorphogenic homolog subunit 4 (Arabidopsis), mRNA (cDNA clone MGC:110860 IMAGE:30340740), complete cds.
AK223178 - Homo sapiens mRNA for COP9 signalosome subunit 4 variant, clone: PNC00767.
BC004302 - Homo sapiens COP9 constitutive photomorphogenic homolog subunit 4 (Arabidopsis), mRNA (cDNA clone MGC:10899 IMAGE:3623514), complete cds.
BC009292 - Homo sapiens COP9 constitutive photomorphogenic homolog subunit 4 (Arabidopsis), mRNA (cDNA clone MGC:15160 IMAGE:4111685), complete cds.
AB587420 - Synthetic construct DNA, clone: pF1KB6592, Homo sapiens COPS4 gene for COP9 constitutive photomorphogenic homolog subunit 4, without stop codon, in Flexi system.
KU178633 - Homo sapiens COP9 constitutive photomorphogenic-like protein subunit 4 isoform 1 (COPS4) mRNA, partial cds.
KU178634 - Homo sapiens COP9 constitutive photomorphogenic-like protein subunit 4 isoform 2 (COPS4) mRNA, complete cds, alternatively spliced.
JF432698 - Synthetic construct Homo sapiens clone IMAGE:100073937 COP9 constitutive photomorphogenic homolog subunit 4 (Arabidopsis) (COPS4) gene, encodes complete protein.
KJ904743 - Synthetic construct Homo sapiens clone ccsbBroadEn_14137 COPS4 gene, encodes complete protein.
AF100757 - Homo sapiens COP9 complex subunit 4 mRNA, complete cds.
AK001210 - Homo sapiens cDNA FLJ10348 fis, clone NT2RM2001065.
LF359087 - JP 2014500723-A/166590: Polycomb-Associated Non-Coding RNAs.
LF359088 - JP 2014500723-A/166591: Polycomb-Associated Non-Coding RNAs.
DQ593955 - Homo sapiens piRNA piR-60067, complete sequence.
LF359091 - JP 2014500723-A/166594: Polycomb-Associated Non-Coding RNAs.
LF359094 - JP 2014500723-A/166597: Polycomb-Associated Non-Coding RNAs.
JD382821 - Sequence 363845 from Patent EP1572962.
JD267562 - Sequence 248586 from Patent EP1572962.
JD521695 - Sequence 502719 from Patent EP1572962.
JD109722 - Sequence 90746 from Patent EP1572962.
JD148667 - Sequence 129691 from Patent EP1572962.
JD553203 - Sequence 534227 from Patent EP1572962.
JD554653 - Sequence 535677 from Patent EP1572962.
JD046873 - Sequence 27897 from Patent EP1572962.
JD410062 - Sequence 391086 from Patent EP1572962.
MA619563 - JP 2018138019-A/191489: Polycomb-Associated Non-Coding RNAs.
MA594664 - JP 2018138019-A/166590: Polycomb-Associated Non-Coding RNAs.
MA594665 - JP 2018138019-A/166591: Polycomb-Associated Non-Coding RNAs.
MA594668 - JP 2018138019-A/166594: Polycomb-Associated Non-Coding RNAs.
MA594671 - JP 2018138019-A/166597: Polycomb-Associated Non-Coding RNAs.

-  Biochemical and Signaling Pathways
  Reactome (by CSHL, EBI, and GO)

Protein Q9BT78 (Reactome details) participates in the following event(s):

R-HSA-8863721 NEDD8-STON binds TOR1 hexamer and COP9 complex
R-HSA-5691006 XPC:RAD23:CETN2 and UV-DDB bind distorted dsDNA site
R-HSA-6781833 ERCC8 (CSA) binds stalled RNA Pol II
R-HSA-8956040 COP9 signalosome deneddylates cytosolic CRL E3 ubiquitin ligase complexes
R-HSA-8956045 COP9 signalosome deneddylates nuclear CRL4 E3 ubiquitin ligase complex
R-HSA-8856825 Cargo recognition for clathrin-mediated endocytosis
R-HSA-5696394 DNA Damage Recognition in GG-NER
R-HSA-6781823 Formation of TC-NER Pre-Incision Complex
R-HSA-8856828 Clathrin-mediated endocytosis
R-HSA-8951664 Neddylation
R-HSA-5696399 Global Genome Nucleotide Excision Repair (GG-NER)
R-HSA-6781827 Transcription-Coupled Nucleotide Excision Repair (TC-NER)
R-HSA-199991 Membrane Trafficking
R-HSA-597592 Post-translational protein modification
R-HSA-5696398 Nucleotide Excision Repair
R-HSA-5653656 Vesicle-mediated transport
R-HSA-392499 Metabolism of proteins
R-HSA-73894 DNA Repair

-  Other Names for This Gene
  Alternate Gene Symbols: B3KN88, CSN4, CSN4_HUMAN, NM_016129, NP_057213, Q561W7, Q9BT78, Q9NW31, Q9Y677
UCSC ID: uc003hoa.3
RefSeq Accession: NM_016129
Protein: Q9BT78 (aka CSN4_HUMAN)
CCDS: CCDS3600.1

-  Gene Model Information
 
category: coding nonsense-mediated-decay: no RNA accession: NM_016129.2
exon count: 10CDS single in 3' UTR: no RNA size: 1765
ORF size: 1221CDS single in intron: no Alignment % ID: 100.00
txCdsPredict score: 2642.00frame shift in genome: no % Coverage: 99.04
has start codon: yes stop codon in genome: no # of Alignments: 1
has end codon: yes retained intron: no # AT/AC introns 0
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.