NUP35 (nucleoporin 35)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 129401 |
| Gene name | Nucleoporin 35 |
| Gene symbol | NUP35 |
| Synonyms (NCBI Gene) |
MP-44MP44NP44NUP53
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| Chromosome | 2 |
| Chromosome location | 2q32.1 |
| Summary | This gene encodes a member of the nucleoporin family. The encoded protein contains two membrane binding regions, is localized to the nuclear rim, and is part of the nuclear pore complex. All molecules entering or leaving the nucleus either diffuse through |
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miRNA
miRNA information provided by mirtarbase database.
152
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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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Q8NFH5 | ||||||||||
| Protein name | Nucleoporin NUP35 (35 kDa nucleoporin) (Mitotic phosphoprotein 44) (MP-44) (Nuclear pore complex protein Nup53) (Nucleoporin NUP53) | ||||||||||
| Protein function | Functions as a component of the nuclear pore complex (NPC). NPC components, collectively referred to as nucleoporins (NUPs), can play the role of both NPC structural components and of docking or interaction partners for transiently associated nu | ||||||||||
| PDB | 4LIR , 7MW1 , 7R5J , 7R5K , 8OZB | ||||||||||
| Family and domains |
Pfam
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| Sequence |
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| Sequence length | 326 | ||||||||||
| Interactions | View interactions | ||||||||||
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
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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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