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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: P2rx2 ENSRNOG00000037456

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Description

purinergic receptor P2X 2 [Source:RGD Symbol;Acc:620251]

Gene Synonyms

P2X2

Location

Primary_assembly 12: 51,999,372-52,002,627 forward strand.

GRCr8:CM070402.1

About this gene

This gene has 3 transcripts (splice variants), 188 orthologues, 6 paralogues and is associated with 6 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000056694.6	P2rx2-202	1930	497aa	ENSRNOP00000053533.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A140TAH4	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSRNOT00000085661.3	P2rx2-203	1723	428aa	ENSRNOP00000074992.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K9G8	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSRNOT00000056693.5	P2rx2-201	1479	445aa	ENSRNOP00000053532.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	P49653-3	-

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Paralogues

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