Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 5393
MIM: 606180
HGNC: 9137
Ensembl: ENSG00000123737
Variants:
dbSNP: 5393
ClinVar: 5393
TCGA: ENSG00000123737
COSMIC: EXOSC9
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 37887339 | 2023 | Exosc9 Initiates SUMO-Dependent lncRNA TERRA Degradation to Impact Telomeric Integrity in Endocrine Therapy Insensitive Hormone Receptor-Positive Breast Cancer. | 1 |
| 37887339 | 2023 | Exosc9 Initiates SUMO-Dependent lncRNA TERRA Degradation to Impact Telomeric Integrity in Endocrine Therapy Insensitive Hormone Receptor-Positive Breast Cancer. | 1 |
| 33040083 | 2021 | Novel EXOSC9 variants cause pontocerebellar hypoplasia type 1D with spinal motor neuronopathy and cerebellar atrophy. | 7 |
| 33040083 | 2021 | Novel EXOSC9 variants cause pontocerebellar hypoplasia type 1D with spinal motor neuronopathy and cerebellar atrophy. | 7 |
| 30690203 | 2020 | Expanded PCH1D phenotype linked to EXOSC9 mutation. | 7 |
| 32518284 | 2020 | EXOSC9 depletion attenuates P-body formation, stress resistance, and tumorigenicity of cancer cells. | 17 |
| 30690203 | 2020 | Expanded PCH1D phenotype linked to EXOSC9 mutation. | 7 |
| 32518284 | 2020 | EXOSC9 depletion attenuates P-body formation, stress resistance, and tumorigenicity of cancer cells. | 17 |
| 29727687 | 2018 | Variants in EXOSC9 Disrupt the RNA Exosome and Result in Cerebellar Atrophy with Spinal Motor Neuronopathy. | 37 |
| 29727687 | 2018 | Variants in EXOSC9 Disrupt the RNA Exosome and Result in Cerebellar Atrophy with Spinal Motor Neuronopathy. | 37 |
| 17545563 | 2007 | Human cell growth requires a functional cytoplasmic exosome, which is involved in various mRNA decay pathways. | 48 |
| 17545563 | 2007 | Human cell growth requires a functional cytoplasmic exosome, which is involved in various mRNA decay pathways. | 48 |
| 14872500 | 2004 | PM-Scl-75 is the main autoantigen in patients with the polymyositis/scleroderma overlap syndrome. | 14 |
| 14872500 | 2004 | PM-Scl-75 is the main autoantigen in patients with the polymyositis/scleroderma overlap syndrome. | 14 |
| 12788944 | 2003 | The association of the human PM/Scl-75 autoantigen with the exosome is dependent on a newly identified N terminus. | 9 |
Citation
Dessen P
EXOSC9 (exosome component 9)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/62955/exosc9-(exosome-component-9)
