NOP58 (NOP58 ribonucleoprotein)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 51602 |
| Gene name | NOP58 ribonucleoprotein |
| Gene symbol | NOP58 |
| Synonyms (NCBI Gene) |
HSPC120NOP5NOP5/NOP58
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| Chromosome | 2 |
| Chromosome location | 2q33.1 |
| Summary | The protein encoded by this gene is a core component of box C/D small nucleolar ribonucleoproteins. Some box C/D small nucleolar RNAs (snoRNAs), such as U3, U8, and U14, are dependent upon the encoded protein for their synthesis. This protein is SUMOylate |
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miRNA
miRNA information provided by mirtarbase database.
68
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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Q9Y2X3 | |||||||||||||||
| Protein name | Nucleolar protein 58 (Nucleolar protein 5) | |||||||||||||||
| Protein function | Required for the biogenesis of box C/D snoRNAs such as U3, U8 and U14 snoRNAs (PubMed:15574333, PubMed:17636026, PubMed:19620283, PubMed:34516797). Part of the small subunit (SSU) processome, first precursor of the small eukaryotic ribosomal sub | |||||||||||||||
| PDB | 7MQ8 , 7MQ9 , 7MQA | |||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Ubiquitous. | |||||||||||||||
| Sequence |
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| Sequence length | 529 | |||||||||||||||
| Interactions | View interactions | |||||||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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Evidence Score:
★☆☆☆☆ Gene-disease association found in Text Mining only
★★☆☆☆ Found in Text Mining and Unknown/Other Associations
★★★☆☆ Reported in Unknown/Other Associations across ≥2 Sources
★★★★☆ ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
★★★★★ ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
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