Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
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: Panx2 ENSRNOG00000055530

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Description

pannexin 2 [Source:RGD Symbol;Acc:735191]

Location

Primary_assembly 7: 122,018,937-122,032,004 forward strand.

GRCr8:CM070397.1

About this gene

This gene has 3 transcripts (splice variants), 191 orthologues, 2 paralogues and is associated with 7 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000089707.3	Panx2-201	2466	713aa	ENSRNOP00000069647.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	P60571 R9PXY9	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,
ENSRNOT00000111032.2	Panx2-203	2505	675aa	ENSRNOP00000085314.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A329	-
ENSRNOT00000105173.2	Panx2-202	1947	648aa	ENSRNOP00000076858.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5XVH3	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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