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: p2rx3b ENSDARG00000029718

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Description

purinergic receptor P2X, ligand-gated ion channel, 3b [Source:NCBI gene (formerly Entrezgene);Acc:387300]

Location

Chromosome 1: 44,746,154-44,758,388 forward strand.

GRCz11:CM002885.2

About this gene

This gene has 2 transcripts (splice variants), 203 orthologues and 8 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000133926.3	p2rx3b-201	2930	412aa	ENSDARP00000118882.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8M9PCJ8	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,
ENSDART00000148758.2	p2rx3b-202	759	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron	-	-

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Summary

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