Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Biological process
- GO: Cellular component
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: P2ry1 ENSRNOG00000014232

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Description

purinergic receptor P2Y1 [Source:RGD Symbol;Acc:3242]

Gene Synonyms

P2y, P2y1

Location

Primary_assembly 2: 147,390,681-147,398,027 forward strand.

GRCr8:CM070392.1

About this gene

This gene has 1 transcript (splice variant), 192 orthologues, 14 paralogues and is associated with 3 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000019305.6	P2ry1-201	5025	373aa	ENSRNOP00000019304.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6JVM2 P49651	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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