Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: SNRPN ENSBTAG00000008251

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Description

small nuclear ribonucleoprotein polypeptide N [Source:VGNC Symbol;Acc:VGNC:35082]

Location

Primary_assembly 21: 1,954,825-2,049,761 forward strand.

ARS-UCD1.3:CM008188.2

About this gene

This gene has 2 transcripts (splice variants), 71 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000072712.2	SNRPN-202	1390	302aa	ENSBTAP00000073157.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MFZ6	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,
ENSBTAT00000010856.7	SNRPN-201	1000	240aa	ENSBTAP00000010856.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q17QN3	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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