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COP9 signalosome complex subunit 3

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Protein-coding gene in the species Homo sapiens

COPS3
Available structures
PDBOrtholog search: PDBe RCSB
List of PDB id codes

4D10, 4D18, 4WSN

Identifiers
AliasesCOPS3, CSN3, SGN3, COP9 signalosome subunit 3
External IDsOMIM: 604665; MGI: 1349409; HomoloGene: 2710; GeneCards: COPS3; OMA:COPS3 - orthologs
Gene location (Human)
Chromosome 17 (human)
Chr.Chromosome 17 (human)
Chromosome 17 (human)Genomic location for COPS3Genomic location for COPS3
Band17p11.2Start17,246,616 bp
End17,281,273 bp
Gene location (Mouse)
Chromosome 11 (mouse)
Chr.Chromosome 11 (mouse)
Chromosome 11 (mouse)Genomic location for COPS3Genomic location for COPS3
Band11|11 B1.3Start59,817,795 bp
End59,839,838 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • gastrocnemius muscle

  • gonad

  • muscle of thigh

  • ganglionic eminence

  • right testis

  • left testis

  • skeletal muscle tissue

  • Skeletal muscle tissue of rectus abdominis

  • vastus lateralis muscle

  • muscle of arm
Top expressed in
  • spermatocyte

  • facial motor nucleus

  • medial ganglionic eminence

  • spermatid

  • abdominal wall

  • mandibular prominence

  • maxillary prominence

  • intercostal muscle

  • primitive streak

  • endocardial cushion
More reference expression data
BioGPS
More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

8533

26572

Ensembl

ENSG00000141030

ENSMUSG00000019373

UniProt

Q9UNS2

O88543

RefSeq (mRNA)
NM_001199125
NM_003653
NM_001316354
NM_001316355
NM_001316356

NM_001316357
NM_001316358

NM_011991

RefSeq (protein)
NP_001186054
NP_001303283
NP_001303284
NP_001303285
NP_001303286

NP_001303287
NP_003644

NP_036121

Location (UCSC)Chr 17: 17.25 – 17.28 MbChr 11: 59.82 – 59.84 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

COP9 signalosome complex subunit 3 is a protein that in humans is encoded by the COPS3 gene. It encodes a subunit of the COP9 signalosome.

The protein encoded by this gene possesses kinase activity that phosphorylates regulators involved in signal transduction. It phosphorylates I-kappa-B-alpha, 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.

See also

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000141030Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000019373Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Seeger M, Kraft R, Ferrell K, Bech-Otschir D, Dumdey R, Schade R, Gordon C, Naumann M, Dubiel W (Apr 1998). "A novel protein complex involved in signal transduction possessing similarities to 26S proteasome subunits". FASEB J. 12 (6): 469–78. doi:10.1096/fasebj.12.6.469. PMID 9535219. S2CID 25424324.
  6. Potocki L, Chen KS, Lupski JR (Jun 1999). "Subunit 3 of the COP9 signal transduction complex is conserved from plants to humans and maps within the smith-magenis syndrome critical region in 17p11.2". Genomics. 57 (1): 180–2. doi:10.1006/geno.1998.5748. PMID 10191102.
  7. ^ "Entrez Gene: COPS3 COP9 constitutive photomorphogenic homolog subunit 3 (Arabidopsis)".

External links

Further reading


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