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Gene Gene information from NCBI Gene database.
Entrez ID 9670
Gene name Importin 13
Gene symbol IPO13
Synonyms (NCBI Gene)
IMP13KAP13LGL2RANBP13
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
miRNA miRNA information provided by mirtarbase database.
12 Show/Hide all (12)
miRTarBase ID miRNA Experiments Reference
MIRT050040 hsa-miR-26b-5p CLASH 23622248
MIRT040004 hsa-miR-615-3p CLASH 23622248
MIRT039497 hsa-miR-652-3p CLASH 23622248
MIRT440439 hsa-miR-541-5p HITS-CLIP 24374217
MIRT440437 hsa-miR-412-3p HITS-CLIP 24374217
Transcription factors Transcription factors information provided by TRRUST V2 database.
1
Transcription factor Regulation Reference
CTCF Unknown 23620300
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
10 Show/Hide all (10)
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 16189514, 21139563, 23435562, 24722188, 25416956, 26816005, 29892012, 31515488, 32296183
GO:0005634 Component Nucleus IEA
GO:0005737 Component Cytoplasm IBA
GO:0005737 Component Cytoplasm IEA
GO:0006606 Process Protein import into nucleus IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
610411 16853 ENSG00000117408
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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

Accession ID Position in sequence Description Type
PF03810 IBN_N 45 → 111 Importin-beta N-terminal domain Family
PF08389 Xpo1 116 → 263 Exportin 1-like protein Family
PF18773 Importin_rep 402 → 441 Importin 13 repeat Repeat
PF18786 Importin_rep_2 584 → 627 Importin 13 repeat Repeat
PF18786 Importin_rep_2 631 → 672 Importin 13 repeat Repeat
PF18806 Importin_rep_3 826 → 900 Importin 13 repeat Repeat
Tissue specificity TISSUE SPECIFICITY: Expressed in fetal brain, heart, intestine and kidney. {ECO:0000269|PubMed:10745026}.
Sequence
MERREEQPGAAGAGAAPALDFTVENVEKALHQLYYDPNIENKNLAQKWLMQAQVSPQAWH
FSWQLLQPDKVPEIQYFGASALHIKISRYWSDIPTDQYESLKAQLFTQITR
FASGSKIVL
TRLCVALASLALSMMPDAWPCAVADMVRLFQAEDSPVDGQGRCLALLELLTVLPEEFQTS
RLPQYRKGLVRTSLAVECGAVFPLLEQLLQQPSSPSCVRQKVLKCFSSWVQLEVPLQDCE
ALIQAAFAALQDSELFDSSVEAI
VNAISQPDAQRYVNTLLKLIPLVLGLQEQLRQAVQNG
DMETSHGICRIAVALGENHSRALLDQVEHWQSFLALVNMIMFCTGIPGHYPVNETTSSLT
LTFWYTLQDDILSFEAEKQAVYQQVYRPVYFQLVDVLLHKAQFPSDEEYGFWSSDEKEQF
RIYRVDISDTLMYVYEMLGAE
LLSNLYDKLGRLLTSSEEPYSWQHTEALLYGFQSIAETI
DVNYSDVVPGLIGLIPRISISNVQLADTVMFTIGALSEWLADHPVMINSVLPLVLHALGN
PELSVSSVSTLKKICRECKYDLPPYAANIVAVSQDVLMKQIHKTSQCMWLMQALGFLLSA
LQVEEILKNLHSLISPYIQQLEKLAEE
IPNPSNKLAIVHILGLLSNLFTTLDISHHEDDH
EGPELRKLPVPQ
GPNPVVVVLQQVFQLIQKVLSKWLNDAQVVEAVCAIFEKSVKTLLDDF
APMVPQLCEMLGRMYSTIPQASALDLTRQLVHIFAHEPAHFPPIEALFLLVTSVTLTLFQ
QGPRDHPDIVDSFMQLLAQALKRKPDLFLCERLDVKAVFQCAVLALKFPEAPTVKASCGF
FTELLPRCGEVESVGKVVQEDGRMLLIAVLEAIGGQASRSLMDCFADILFALNKHCFSLL

SMWIKEALQPPGFPSARLSPEQKDTFSQQILRERVNKRRVKEMVKEFTLLCRGLHGTDYT
ADY
Sequence length 963
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
KEGG Pathway
Nucleocytoplasmic transport
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Reference Evidence Score
IPO13-related disorder Likely benign; Uncertain significance ClinVar —
★★★★★
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Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Show/Hide Text Mining Associations (18)
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Asthma Asthma Pubtator 19619331 Associate
★★★★★
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Found in Text Mining only
Asthma Asthma BEFREE 19619331
★★★★★
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Found in Text Mining only
Bronchopulmonary Dysplasia Bronchopulmonary Dysplasia BEFREE 23295978
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★☆☆☆☆
Found in Text Mining only
Bronchopulmonary Dysplasia Bronchopulmonary dysplasia Pubtator 23295978 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Cataract Cataract BEFREE 29700284
★★★★★
★☆☆☆☆
Found in Text Mining only
Childhood asthma Asthma BEFREE 19619331
★★★★★
★☆☆☆☆
Found in Text Mining only
Congenital ocular coloboma (disorder) Congenital ocular coloboma BEFREE 29700284
★★★★★
★☆☆☆☆
Found in Text Mining only
Endometrial Carcinoma Endometrial carcinoma BEFREE 22648251
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★☆☆☆☆
Found in Text Mining only
Endometrial Neoplasms Endometrial neoplasm Pubtator 22648251 Stimulate
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★☆☆☆☆
Found in Text Mining only
Endometriosis Endometriosis BEFREE 22648251
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★☆☆☆☆
Found in Text Mining only