IPO13 (importin 13)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 9670 |
| Gene name | Importin 13 |
| Gene symbol | IPO13 |
| Synonyms (NCBI Gene) |
IMP13KAP13LGL2RANBP13
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| Chromosome | 1 |
| Chromosome location | 1p34.1 |
| Summary | This gene encodes a member of the importin-beta family of nuclear transport proteins. The encoded protein mediates the import of specific cargo proteins from the cytoplasm to the nucleus and is dependent on the Ras-related nuclear protein-GTPase system. T |
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miRNA
miRNA information provided by mirtarbase database.
12
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Transcription factors
Transcription factors information provided by TRRUST V2 database.
1
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
10
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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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O94829 | |||||||||||||||||||||||||||||||||||
| Protein name | Importin-13 (Imp13) (Karyopherin-13) (Kap13) (Ran-binding protein 13) (RanBP13) | |||||||||||||||||||||||||||||||||||
| Protein function | Functions in nuclear protein import as nuclear transport receptor. Serves as receptor for nuclear localization signals (NLS) in cargo substrates. Is thought to mediate docking of the importin/substrate complex to the nuclear pore complex (NPC) t | |||||||||||||||||||||||||||||||||||
| PDB | 2X19 , 2XWU , 3ZJY | |||||||||||||||||||||||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Expressed in fetal brain, heart, intestine and kidney. {ECO:0000269|PubMed:10745026}. | |||||||||||||||||||||||||||||||||||
| Sequence |
MERREEQPGAAGAGAAPALDFTVENVEKALHQLYYDPNIENKNLAQKWLMQAQVSPQAWH |
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| Sequence length | 963 | |||||||||||||||||||||||||||||||||||
| 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.).
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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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Related Genes
Genes most often co-reported with IPO13 across shared curated disease and pathway associations.
0
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to IPO13 (see Related Genes above), that are NOT already directly curated for IPO13 itself -- a lead worth checking, not a confirmed association.
0
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