Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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: SLC8A2 ENSPTRG00000011209

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Description

solute carrier family 8 member A2 [Source:VGNC Symbol;Acc:VGNC:12110]

Location

Chromosome 19: 49,555,732-49,600,236 reverse strand.

Pan_tro_3.0:CM000333.3

About this gene

This gene has 2 transcripts (splice variants), 262 orthologues and 7 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000086547.1	SLC8A2-201	5227	921aa	ENSPTRP00000092948.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3TUT9 A0A6D2W3H8	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,
ENSPTRT00000020829.5	SLC8A2-202	3739	915aa	ENSPTRP00000019235.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2QGP5	-

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Summary

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