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

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Gene: SNRPB ENSBTAG00000001038

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Description

small nuclear ribonucleoprotein polypeptides B and B1 [Source:VGNC Symbol;Acc:VGNC:35076]

Location

Primary_assembly 13: 52,666,541-52,675,557 forward strand.

ARS-UCD1.3:CM008180.2

About this gene

This gene has 2 transcripts (splice variants), 213 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000067991.2	SNRPB-202	988	242aa	ENSBTAP00000063047.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M489	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,
ENSBTAT00000001379.6	SNRPB-201	1053	231aa	ENSBTAP00000001379.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G1K134	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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