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: SNRPB ENSSSCG00000040857

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Description

small nuclear ribonucleoprotein polypeptides B and B1 [Source:UniProtKB Gene Name;Acc:A0A287AG39]

Location

Primary_assembly 17: 33,080,407-33,094,602 forward strand.

Sscrofa11.1:CM000828.5

About this gene

This gene has 1 transcript (splice variant), 180 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000056681.3	SNRPB-201	1403	231aa	ENSSSCP00000042994.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287AG39 A0A4X1SHZ4	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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