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55505 NOP10

55505

NOP10

NOP10 ribonucleoprotein

protein-coding

Homo sapiens

基因描述

Type Description
Definition NOP10 ribonucleoprotein

研究结论

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

名称对应

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

全选

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研究热度

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