Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Xpo7 ENSRNOG00000013288

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Description

exportin 7 [Source:RGD Symbol;Acc:1310928]

Gene Synonyms

LOC361070

Location

Primary_assembly 15: 45,742,053-45,828,050 reverse strand.

mRatBN7.2:CM026988.1

About this gene

This gene has 3 transcripts (splice variants), 204 orthologues, 2 paralogues and is associated with 2 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000018440.8	Xpo7-201	5025	1088aa	ENSRNOP00000018441.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LQM9	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,
ENSRNOT00000107622.1	Xpo7-203	5447	1052aa	ENSRNOP00000092146.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AH01	-
ENSRNOT00000087450.2	Xpo7-202	4827	1088aa	ENSRNOP00000069802.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JWA3	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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