Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: SNRPB2 ENSSSCG00000037602

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Description

small nuclear ribonucleoprotein polypeptide B2 [Source:VGNC Symbol;Acc:VGNC:108738]

Location

Primary_assembly 17: 25,363,167-25,373,281 forward strand.

Sscrofa11.1:CM000828.5

About this gene

This gene has 1 transcript (splice variant), 250 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000047100.2	SNRPB2-201	1139	225aa	ENSSSCP00000041317.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1UXE9 Q06A96	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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