| Type | Description |
|---|---|
| Definition | NOP10 ribonucleoprotein |
| Date | Results | Publications |
|---|---|---|
| 2021-01-09 13:33:00 | Acute depletion of telomerase components DKC1 and NOP10 induces oxidative stress and disrupts ribosomal biogenesis via NPM1 and activation of the P53 pathway. | 32910990 |
| 2020-10-24 14:10:00 | Pseudouridylation defect due to DKC1 and NOP10 mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitis. | 32554502 |
| 2015-05-30 11:38:00 | Indian aplastic anemia patients did not have NOP10 mutations. | 25906515 |
| 2010-07-05 12:10:00 | Effects of dyskeratosis congenita mutations in NOP10 on assembly of H/ACA pre-RNPs | 20008900 |
| 2010-01-21 00:00:00 | NOP10 has a role in the telomerase complex and telomere maintenance, and in autosomal recessive dyskeratosis congenita | 17507419 |
| Type | IDs |
|---|---|
| Synonymous | DKCB1, NOLA3, NOP10P |
| Gene |
UniProtKB-ID:
NOP10_HUMAN
UniprotKB:
Q9NPE3
UniParc:
UPI0000022AEE
EMBL:
BC063023,
BC008886,
AB043103,
AB043104
Ensembl:
ENSG00000182117
KO:
hsa:55505
|
| Nucleutide sequences |
EMBL-CDS:
AAH08886.1,
BAA96133.1,
AAH63023.1,
BAA96107.1
Ensembl_TRS:
ENST00000328848
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000332198
RefSeq:
NP_061118.1
|
| Others |
UniRef100:
UniRef100_Q9NPE3
UniRef90:
UniRef90_Q9NPE3
UniRef50:
UniRef50_Q9NPE3
UniGene:
Hs.14317
CCDS:
CCDS10037.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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