1. Gene
  2. COPS3 - COP9 signalosome subunit 3 Gene

COPS3 - COP9 signalosome subunit 3 Gene

Homo sapiens

Also known as CSN3; SGN3

Gene ID: 8533 | Gene type: protein coding

About COPS3

Cytogenetic location: 17p11.2 Genomic coordinates (GRCh38): 17:17,246,616-17,281,246 (from NCBI)

This gene has 18 transcripts (splice variants), 212 orthologues and 1 paralogue. Ubiquitous expression in testis (RPKM 49.1), bone marrow (RPKM 38.5) and 25 other tissues.

Summary

The protein encoded by this gene possesses kinase activity that phosphorylates regulators involved in signal transduction. It phosphorylates I kappa-Balpha, p105, and c-Jun. It acts as a docking site for complex-mediated phosphorylation. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]

COPS3 Products(7)

mRNA Protein Name
NM_001199125.1 NP_001186054.1 COP9 signalosome complex subunit 3 isoform 2
NM_001316354.2 NP_001303283.1 COP9 signalosome complex subunit 3 isoform 3
NM_001316355.2 NP_001303284.1 COP9 signalosome complex subunit 3 isoform 4
NM_001316356.2 NP_001303285.1 COP9 signalosome complex subunit 3 isoform 5
NM_001316357.2 NP_001303286.1 COP9 signalosome complex subunit 3 isoform 6
NM_001316358.2 NP_001303287.1 COP9 signalosome complex subunit 3 isoform 6
NM_003653.4 NP_003644.2 COP9 signalosome complex subunit 3 isoform 1
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
10777491 GOA
Biological Process GO Annotation Evidence Reference Source
involved in protein deneddylation IDA
IDA: Inferred from direct assay
19141280 GOA
involved in regulation of DNA damage response, signal transduction by p53 class mediator resulting in transcription of p21 class mediator IMP
IMP: Inferred from mutant phenotype
15861129 GOA
Cellular Component GO Annotation Evidence Reference Source
part of COP9 signalosome IDA
IDA: Inferred from direct assay
18850735 GOA
part of COP9 signalosome IPI
IPI: Inferred from physical interaction
25043011 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
24421388 GOA
located in nucleus IDA
IDA: Inferred from direct assay
24421388 GOA
located in perinuclear region of cytoplasm IDA
IDA: Inferred from direct assay
15861129 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

COPS3 Protein Structure

PCI

PCI: PCI domain (259 - 361)

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  • 423 a.a.
Protein Preferred Names Protein Names

COP9 signalosome complex subunit 3

COP9 complex subunit 3

COPS3 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
COPS3 Q9UNS2 NF2 Homo sapiens P35240 32814053
Intra
COPS3 Q9UNS2 NF2 Homo sapiens P35240 32814053
Intra
COPS3 Q9UNS2 NF2 Homo sapiens P35240 32814053
Intra
COPS3 Q9UNS2 YARS1 Homo sapiens P54577 32814053
Intra
COPS3 Q9UNS2 YARS1 Homo sapiens P54577 32814053
Intra
COPS3 Q9UNS2 YARS1 Homo sapiens P54577 32814053
Intra
COPS3 Q9UNS2 COPS2 Homo sapiens P61201 25043011
Intra
COPS3 Q9UNS2 COPS2 Homo sapiens P61201 24421388
Intra
COPS3 Q9UNS2 COPS2 Homo sapiens P61201 24421388
Intra
COPS3 Q9UNS2 COPS2 Homo sapiens P61201 20399188
Intra
COPS3 Q9UNS2 COPS2 Homo sapiens P61201 33961781
Intra
COPS3 Q9UNS2 RAB7A Homo sapiens P51149 32814053
Intra
COPS3 Q9UNS2 RAB7A Homo sapiens P51149 32814053
Intra
COPS3 Q9UNS2 RAB7A Homo sapiens P51149 32814053
Intra
COPS3 Q9UNS2 MECP2 Homo sapiens P51608 32814053
Intra
COPS3 Q9UNS2 MECP2 Homo sapiens P51608 32814053
Intra
COPS3 Q9UNS2 MECP2 Homo sapiens P51608 32814053
Intra
COPS3 Q9UNS2 ERCC8 Homo sapiens Q13216-2 32814053
Intra
COPS3 Q9UNS2 ERCC8 Homo sapiens Q13216-2 32814053
Intra
COPS3 Q9UNS2 ERCC8 Homo sapiens Q13216-2 32814053
Intra
COPS3 Q9UNS2 GLE1 Homo sapiens Q53GS7 32814053
Intra
COPS3 Q9UNS2 GLE1 Homo sapiens Q53GS7 32814053
Intra
COPS3 Q9UNS2 GLE1 Homo sapiens Q53GS7 32814053
Intra
COPS3 Q9UNS2 COPS8 Homo sapiens Q99627 25043011
Intra
COPS3 Q9UNS2 COPS8 Homo sapiens Q99627 20399188
Intra
COPS3 Q9UNS2 DCTN1 Homo sapiens Q14203-5 32814053
Intra
COPS3 Q9UNS2 DCTN1 Homo sapiens Q14203-5 32814053
Intra
COPS3 Q9UNS2 DCTN1 Homo sapiens Q14203-5 32814053
Intra
COPS3 Q9UNS2 PANK2 Homo sapiens Q9BZ23-2 32814053
Intra
COPS3 Q9UNS2 PANK2 Homo sapiens Q9BZ23-2 32814053
Intra
COPS3 Q9UNS2 PANK2 Homo sapiens Q9BZ23-2 32814053
Intra
COPS3 Q9UNS2 TTBK2 Homo sapiens Q6IQ55-3 32814053
Intra
COPS3 Q9UNS2 TTBK2 Homo sapiens Q6IQ55-3 32814053
Intra
COPS3 Q9UNS2 TTBK2 Homo sapiens Q6IQ55-3 32814053
Intra
COPS3 Q9UNS2 SOS1 Homo sapiens Q07889
Y2H
30631038
Intra
COPS3 Q9UNS2 SOS1 Homo sapiens Q07889 30631038
Intra
COPS3 Q9UNS2 DDB1 Homo sapiens Q16531 33961781
Intra
COPS3 Q9UNS2 DDB1 Homo sapiens Q16531
Y2H
10777491
Intra
COPS3 Q9UNS2 LMNA Homo sapiens P02545-2 32814053
Intra
COPS3 Q9UNS2 LMNA Homo sapiens P02545-2 32814053
Intra
COPS3 Q9UNS2 LMNA Homo sapiens P02545-2 32814053
Intra
COPS3 Q9UNS2 HSPB1 Homo sapiens P04792 32814053
Intra
COPS3 Q9UNS2 HSPB1 Homo sapiens P04792 32814053
Intra
COPS3 Q9UNS2 HSPB1 Homo sapiens P04792 32814053
Intra
COPS3 Q9UNS2 CCT5 Homo sapiens P48643 32814053
Intra
COPS3 Q9UNS2 CCT5 Homo sapiens P48643 32814053
Intra
COPS3 Q9UNS2 CCT5 Homo sapiens P48643 32814053
Intra
COPS3 Q9UNS2 RNF11 Homo sapiens Q9Y3C5 32814053
Intra
COPS3 Q9UNS2 RNF11 Homo sapiens Q9Y3C5 32814053
Intra
COPS3 Q9UNS2 RNF11 Homo sapiens Q9Y3C5 32814053
Intra
COPS3 Q9UNS2 COPS6 Homo sapiens Q7L5N1 24421388
Intra
COPS3 Q9UNS2 COPS6 Homo sapiens Q7L5N1 33961781
Intra
COPS3 Q9UNS2 COPS6 Homo sapiens Q7L5N1 25043011
Intra
COPS3 Q9UNS2 COPS6 Homo sapiens Q7L5N1 24421388
Intra
COPS3 Q9UNS2 COPS6 Homo sapiens Q7L5N1 20399188
Intra
COPS3 Q9UNS2 TOR1A Homo sapiens O14656 32814053
Intra
COPS3 Q9UNS2 TOR1A Homo sapiens O14656 32814053
Intra
COPS3 Q9UNS2 TOR1A Homo sapiens O14656 32814053
Intra
COPS3 Q9UNS2 COPS5 Homo sapiens Q92905 25043011
Intra
COPS3 Q9UNS2 COPS5 Homo sapiens Q92905 24421388
Intra
COPS3 Q9UNS2 COPS5 Homo sapiens Q92905 24421388
Intra
COPS3 Q9UNS2 COPS5 Homo sapiens Q92905 20399188
Intra
COPS3 Q9UNS2 COPS5 Homo sapiens Q92905 33961781
Intra
COPS3 Q9UNS2 A2M Homo sapiens P01023 32814053
Intra
COPS3 Q9UNS2 A2M Homo sapiens P01023 32814053
Intra
COPS3 Q9UNS2 A2M Homo sapiens P01023 32814053
Intra
COPS3 Q9UNS2 ATXN10 Homo sapiens Q9UBB4 32814053
Intra
COPS3 Q9UNS2 ATXN10 Homo sapiens Q9UBB4 32814053
Intra
COPS3 Q9UNS2 ATXN10 Homo sapiens Q9UBB4 32814053
Intra
COPS3 Q9UNS2 TTR Homo sapiens P02766 32814053
Intra
COPS3 Q9UNS2 TTR Homo sapiens P02766 32814053
Intra
COPS3 Q9UNS2 TTR Homo sapiens P02766 32814053
Intra
COPS3 Q9UNS2 COPS7A Homo sapiens Q9UBW8 24421388
Intra
COPS3 Q9UNS2 COPS7A Homo sapiens Q9UBW8 20399188
Intra
COPS3 Q9UNS2 COPS7A Homo sapiens Q9UBW8 28514442
Intra
COPS3 Q9UNS2 COPS7A Homo sapiens Q9UBW8 33961781
Intra
COPS3 Q9UNS2 COPS7A Homo sapiens Q9UBW8 25043011
Intra
COPS3 Q9UNS2 HEXB Homo sapiens P07686 32814053
Intra
COPS3 Q9UNS2 HEXB Homo sapiens P07686 32814053
Intra
COPS3 Q9UNS2 HEXB Homo sapiens P07686 32814053
Intra
COPS3 Q9UNS2 NDUFV2 Homo sapiens P19404 32814053
Intra
COPS3 Q9UNS2 NDUFV2 Homo sapiens P19404 32814053
Intra
COPS3 Q9UNS2 NDUFV2 Homo sapiens P19404 32814053
Intra
COPS3 Q9UNS2 UCHL1 Homo sapiens P09936 32814053
Intra
COPS3 Q9UNS2 UCHL1 Homo sapiens P09936 32814053
Intra
COPS3 Q9UNS2 UCHL1 Homo sapiens P09936 32814053
Intra
COPS3 Q9UNS2 PHYH Homo sapiens O14832 32814053
Intra
COPS3 Q9UNS2 PHYH Homo sapiens O14832 32814053
Intra
COPS3 Q9UNS2 PHYH Homo sapiens O14832 32814053
Intra
COPS3 Q9UNS2 PHYH Homo sapiens O14832 17353931
Intra
COPS3 Q9UNS2 GARS1 Homo sapiens P41250 32814053
Intra
COPS3 Q9UNS2 GARS1 Homo sapiens P41250 32814053
Intra
COPS3 Q9UNS2 GARS1 Homo sapiens P41250 32814053
Intra
COPS3 Q9UNS2 SNCB Homo sapiens Q16143 32814053
Intra
COPS3 Q9UNS2 SNCB Homo sapiens Q16143 32814053
Intra
COPS3 Q9UNS2 SNCB Homo sapiens Q16143 32814053
Intra
COPS3 Q9UNS2 ASPA Homo sapiens P45381 32814053
Intra
COPS3 Q9UNS2 ASPA Homo sapiens P45381 32814053
Intra
COPS3 Q9UNS2 ASPA Homo sapiens P45381 32814053
Intra
COPS3 Q9UNS2 PRPH Homo sapiens P41219 32814053
Intra
COPS3 Q9UNS2 PRPH Homo sapiens P41219 32814053
Intra
COPS3 Q9UNS2 PRPH Homo sapiens P41219 32814053
Intra
COPS3 Q9UNS2 DBH Homo sapiens P09172 32814053
Intra
COPS3 Q9UNS2 DBH Homo sapiens P09172 32814053
Intra
COPS3 Q9UNS2 DBH Homo sapiens P09172 32814053
Intra
COPS3 Q9UNS2 PEX1 Homo sapiens O43933 32814053
Intra
COPS3 Q9UNS2 PEX1 Homo sapiens O43933 32814053
Intra
COPS3 Q9UNS2 PEX1 Homo sapiens O43933 32814053
Cross: Cross-species interaction Intra: Intraspecies interaction

COPS3 Antibodies

Cat. No. Product Name Application Reactivity
HY-P82446 COPS3 Antibody (YA2191) WB, ICC/IF, IP, FC Human, Mouse, Rat

Related Diseases

Diseases Alias
Smith-Magenis Syndrome

SMS

Chromosome 17p11.2 Deletion Syndrome

17p11.2 Microdeletion Syndrome

17p11.2 Monosomy

Chromosome 17p Deletion Syndrome

Del(17)

P11.2

17p- Syndrome

Deletion 17p Syndrome

Partial Monosomy 17p

Bone Angioendothelial Sarcoma

Osseous Hemangiosarcoma

Bone Angiosarcoma

Xeroderma Pigmentosum, Complementation Group E

Xeroderma Pigmentosum V

Xp5

Xeroderma Pigmentosum, Group E, Ddb-Negative Subtype

Xpe

Xp, Group E

Xeroderma Pigmentosum, Type 5

Xeroderma Pigmentosum Complementation Group E

XP-E

Xp Group E

Parosteal Osteosarcoma

Juxtacortical Osteosarcoma

Parosteal Osteogenic Sarcoma

Osteosarcoma, Juxtacortical

Peripheral Osteosarcoma

Surface Osteosarcoma

Bone Surface Osteosarcoma

Telangiectatic Osteogenic Sarcoma

Telangiectatic Osteosarcoma

Conventional Osteosarcoma

Intracortical Osteosarcoma

Conventional Central Osteosarcoma

Intracortical Osteogenic Sarcoma

Medullary Osteosarcoma

Bone Osteosarcoma

Osteosarcoma Of Bone

Primary Osteosarcoma Of Bone

Potocki-Lupski Syndrome

PTLS

Chromosome 17p11.2 Duplication Syndrome

17p11.2 Microduplication Syndrome

Duplication 17p11.2 Syndrome

Trisomy 17p11.2

Potocki-Lupski Syndrome (Dup(17)(P11.2p11.2))

17p11.2 Duplication Syndrome

Dup(17)(P11.2p11.2)

Pls

Chromosome 17, Trisomy 17p11 2

Cerebral Palsy

Infantile Cerebral Palsy

Mixed Cerebral Palsy

Palsy Cerebral

Palsy, Cerebral

Cerebral Palsy, Mixed

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Felis catus COPS3 VGNC VGNC:61088
Rattus norvegicus COPS3 RGD RGD:1303002
Macaca mulatta COPS3 VGNC VGNC:71316
Mus musculus COPS3 MGD MGI:1349409
Canis familiaris COPS3 VGNC VGNC:39510
Bos taurus COPS3 VGNC VGNC:27600