Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
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Ontologies
Phenotypes
Genetic Variation
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- Structural variants
Gene expression
Pathway
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External references
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ID History
- Gene history

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Gene: Snupn ENSRNOG00000005426

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Description

snurportin 1 [Source:RGD Symbol;Acc:1303191]

Gene Synonyms

MGC95000, Rnut1

Location

Primary_assembly 8: 57,348,130-57,380,912 forward strand.

mRatBN7.2:CM026981.1

About this gene

This gene has 1 transcript (splice variant), 195 orthologues and is associated with 6 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000007261.5	Snupn-201	1369	358aa	ENSRNOP00000007261.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q68FP5	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,

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Summary

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