IPO8 importin 8 [Macaca mulatta (Rhesus monkey)] - Gene

Summary

Official Symbol: IPO8provided by VGNC
Official Full Name: importin 8provided by VGNC
Primary source: VGNC:VGNC:73815
Locus tag: EGK_03498
See related: Ensembl:ENSMMUG00000001361
Gene type: protein coding
RefSeq status: PROVISIONAL
Organism: Macaca mulatta
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Cercopithecidae; Cercopithecinae; Macaca
Also known as: Importin-8
Orthologs: human mouse all
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Genomic context

Location:: chromosome: 11

Exon count:: 25

Annotation release	Status	Assembly	Chr	Location
103	current	Mmul_10 (GCF_003339765.1)	11	NC_041764.1 (31973229..32040071, complement)
102	previous assembly	Mmul_8.0.1 (GCF_000772875.2)	11	NC_027903.1 (31861400..31931406, complement)

Chromosome 11 - NC_041764.1 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

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General gene information

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Markers

RH69811 (e-PCR)
- UniSTS:3130

D12F92S2 (e-PCR)
- UniSTS:148552

Cda19e03 (e-PCR)
- UniSTS:86900

SGC31987 (e-PCR)
- UniSTS:78558

Gene Ontology Provided by RefSeq

Function	Evidence Code	Pubs
enables small GTPase binding	IEA Inferred from Electronic Annotation more info	PubMed

Process	Evidence Code	Pubs
involved_in protein import into nucleus	IEA Inferred from Electronic Annotation more info	PubMed

Component	Evidence Code	Pubs
located_in cytosol	IEA Inferred from Electronic Annotation more info	PubMed
located_in nuclear envelope	IEA Inferred from Electronic Annotation more info	PubMed

General protein information

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Preferred Names: importin-8

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.