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: Ipo9 ENSRNOG00000007418

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Description

importin 9 [Source:RGD Symbol;Acc:1310537]

Gene Synonyms

LOC304817

Location

Primary_assembly 13: 49,365,716-49,414,477 reverse strand.

GRCr8:CM070403.1

About this gene

This gene has 2 transcripts (splice variants), 202 orthologues, 5 paralogues and is associated with 6 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000011105.7	Ipo9-201	3421	1041aa	ENSRNOP00000011105.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6ICF3 D4A857	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, 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,
ENSRNOT00000145946.1	Ipo9-202	3464	1005aa	ENSRNOP00000100509.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Paralogues

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