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: 4849
MIM: 604910
HGNC: 7879
Ensembl: ENSG00000088038
Variants:
dbSNP: 4849
ClinVar: 4849
TCGA: ENSG00000088038
COSMIC: CNOT3
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38491013 | 2024 | Translation efficiency driven by CNOT3 subunit of the CCR4-NOT complex promotes leukemogenesis. | 0 |
| 38491013 | 2024 | Translation efficiency driven by CNOT3 subunit of the CCR4-NOT complex promotes leukemogenesis. | 0 |
| 36802310 | 2023 | Clinical features of CNOT3-associated neurodevelopmental disorder in three Chinese patients. | 0 |
| 37846490 | 2023 | CCR4-NOT differentially controls host versus virus poly(a)-tail length and regulates HCMV infection. | 3 |
| 36802310 | 2023 | Clinical features of CNOT3-associated neurodevelopmental disorder in three Chinese patients. | 0 |
| 37846490 | 2023 | CCR4-NOT differentially controls host versus virus poly(a)-tail length and regulates HCMV infection. | 3 |
| 34073619 | 2021 | A Genetic Study of Cerebral Atherosclerosis Reveals Novel Associations with NTNG1 and CNOT3. | 2 |
| 34613789 | 2021 | CNOT3 interacts with the Aurora B and MAPK/ERK kinases to promote survival of differentiating mesendodermal progenitor cells. | 0 |
| 34680937 | 2021 | Determinants of Disease Penetrance in PRPF31-Associated Retinopathy. | 6 |
| 34073619 | 2021 | A Genetic Study of Cerebral Atherosclerosis Reveals Novel Associations with NTNG1 and CNOT3. | 2 |
| 34613789 | 2021 | CNOT3 interacts with the Aurora B and MAPK/ERK kinases to promote survival of differentiating mesendodermal progenitor cells. | 0 |
| 34680937 | 2021 | Determinants of Disease Penetrance in PRPF31-Associated Retinopathy. | 6 |
| 31474762 | 2020 | The pleiotropy associated with de novo variants in CHD4, CNOT3, and SETD5 extends to moyamoya angiopathy. | 25 |
| 32720325 | 2020 | Inherited cases of CNOT3-associated intellectual developmental disorder with speech delay, autism, and dysmorphic facies. | 6 |
| 31474762 | 2020 | The pleiotropy associated with de novo variants in CHD4, CNOT3, and SETD5 extends to moyamoya angiopathy. | 25 |
Citation
Dessen P
CNOT3 (CCR4-NOT transcription complex subunit 3)
Atlas Genet Cytogenet Oncol Haematol. 2013-04-01
Online version: http://atlasgeneticsoncology.org/gene/53235/cnot3
