Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
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: AABR07054614.1 ENSRNOG00000008245

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Description

prostaglandin I2 synthase [Source:RGD Symbol;Acc:3438]

Location

Primary_assembly 3: 155,916,412-155,965,451 reverse strand.

mRatBN7.2:CM026976.1

About this gene

This gene has 5 transcripts (splice variants), 250 orthologues, 1 paralogue and is associated with 18 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000105814.1	AABR07054614.1-204	2703	530aa	ENSRNOP00000077774.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5Y1K4	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,
ENSRNOT00000115486.1	AABR07054614.1-205	1917	501aa	ENSRNOP00000087709.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q62969	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,
ENSRNOT00000103286.1	AABR07054614.1-203	1807	508aa	ENSRNOP00000088713.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ABA7	-
ENSRNOT00000082474.2	AABR07054614.1-202	1723	490aa	ENSRNOP00000074093.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K776	-
ENSRNOT00000010891.7	AABR07054614.1-201	1637	499aa	ENSRNOP00000010891.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LP67	-

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Summary

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