Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Xpo1 ENSRNOG00000009935

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Description

exportin 1 [Source:RGD Symbol;Acc:620517]

Gene Synonyms

exp1

Location

Primary_assembly 14: 101,434,517-101,476,714 forward strand.

GRCr8:CM070404.1

About this gene

This gene has 3 transcripts (splice variants), 231 orthologues, 1 paralogue and is associated with 24 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000101915.2	Xpo1-202	4595	1071aa	ENSRNOP00000087052.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A738 A6JQ67 Q80U96	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical,
ENSRNOT00000114310.2	Xpo1-203	4460	1026aa	ENSRNOP00000097648.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AT26	-
ENSRNOT00000014062.6	Xpo1-201	4348	1005aa	ENSRNOP00000014062.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2Q6V5	APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,

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Paralogues

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Personal Data