Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: SNRPB ENSPTRG00000013176

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Description

small nuclear ribonucleoprotein polypeptides B and B1 [Source:VGNC Symbol;Acc:VGNC:9994]

Location

Chromosome 20: 2,322,220-2,331,553 reverse strand.

Pan_tro_3.0:CM000334.4

About this gene

This gene has 2 transcripts (splice variants), 219 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000084121.1	SNRPB-201	870	289aa	ENSPTRP00000063658.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RH05	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,
ENSPTRT00000067711.3	SNRPB-202	1153	231aa	ENSPTRP00000059297.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2RDT2	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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