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
External references
Supporting evidence
ID History
- Gene history

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Gene: Xpo4 ENSRNOG00000010137

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Description

exportin 4 [Source:RGD Symbol;Acc:1312015]

Gene Synonyms

LOC290280

Location

Primary_assembly 15: 35,832,567-35,923,670 reverse strand.

GRCr8:CM070405.1

About this gene

This gene has 2 transcripts (splice variants), 213 orthologues, 2 paralogues and is associated with 6 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000137138.1	Xpo4-202	9290	1276aa	ENSRNOP00000104034.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000013901.8	Xpo4-201	8688	1113aa	ENSRNOP00000013902.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZQI6	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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Summary

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