Identity
HGNC
LOCATION
15q14
LOCUSID
ALIAS
DKCB1,NOLA3,NOP10P
FUSION GENES
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: 55505
MIM: 606471
HGNC: 14378
Ensembl: ENSG00000182117
Variants:
dbSNP: 55505
ClinVar: 55505
TCGA: ENSG00000182117
COSMIC: NOP10
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000182117 | ENST00000328848 | Q9NPE3 |
| ENSG00000182117 | ENST00000557912 | H0YM60 |
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 33161513 | 2021 | Nucleolar protein 10 (NOP10) predicts poor prognosis in invasive breast cancer. | 6 |
| 33288886 | 2021 | NOP10 predicts lung cancer prognosis and its associated small nucleolar RNAs drive proliferation and migration. | 26 |
| 33161513 | 2021 | Nucleolar protein 10 (NOP10) predicts poor prognosis in invasive breast cancer. | 6 |
| 33288886 | 2021 | NOP10 predicts lung cancer prognosis and its associated small nucleolar RNAs drive proliferation and migration. | 26 |
| 32554502 | 2020 | Pseudouridylation defect due to DKC1 and NOP10 mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitis. | 18 |
| 32910990 | 2020 | Acute depletion of telomerase components DKC1 and NOP10 induces oxidative stress and disrupts ribosomal biogenesis via NPM1 and activation of the P53 pathway. | 8 |
| 32554502 | 2020 | Pseudouridylation defect due to DKC1 and NOP10 mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitis. | 18 |
| 32910990 | 2020 | Acute depletion of telomerase components DKC1 and NOP10 induces oxidative stress and disrupts ribosomal biogenesis via NPM1 and activation of the P53 pathway. | 8 |
| 25906515 | 2014 | Detection of mutations in TERT, the genes for telomerase reverse transcriptase, in Indian patients of aplastic anaemia: a pilot study. | 1 |
| 25906515 | 2014 | Detection of mutations in TERT, the genes for telomerase reverse transcriptase, in Indian patients of aplastic anaemia: a pilot study. | 1 |
| 20008900 | 2010 | Effects of dyskeratosis congenita mutations in dyskerin, NHP2 and NOP10 on assembly of H/ACA pre-RNPs. | 29 |
| 20008900 | 2010 | Effects of dyskeratosis congenita mutations in dyskerin, NHP2 and NOP10 on assembly of H/ACA pre-RNPs. | 29 |
| 17507419 | 2007 | Genetic heterogeneity in autosomal recessive dyskeratosis congenita with one subtype due to mutations in the telomerase-associated protein NOP10. | 151 |
| 17507419 | 2007 | Genetic heterogeneity in autosomal recessive dyskeratosis congenita with one subtype due to mutations in the telomerase-associated protein NOP10. | 151 |
| 15814878 | 2005 | Mutations in TERT, the gene for telomerase reverse transcriptase, in aplastic anemia. | 289 |
Citation
Dessen P
NOP10 (NOP10 ribonucleoprotein)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/70904
