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
- 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: Snupn ENSRNOG00000005426

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Description

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

Gene Synonyms

MGC95000, Rnut1

Location

Primary_assembly 8: 66,235,828-66,286,835 forward strand.

GRCr8:CM070398.1

About this gene

This gene has 5 transcripts (splice variants), 200 orthologues and is associated with 7 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000132077.1	Snupn-203	2341	395aa	ENSRNOP00000099920.1	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,
ENSRNOT00000170389.1	Snupn-205	3016	358aa	ENSRNOP00000110228.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6J4S2	-
ENSRNOT00000144713.1	Snupn-204	2986	381aa	ENSRNOP00000108717.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000129195.1	Snupn-202	2971	376aa	ENSRNOP00000103426.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000007261.6	Snupn-201	1340	337aa	ENSRNOP00000007261.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q68FP5	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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