Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: slc26a2 ENSDARG00000011618

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Description

solute carrier family 26 member 2 [Source:HGNC Symbol;Acc:HGNC:10994]

Location

Chromosome 14: 25,438,015-25,452,503 reverse strand.

GRCz11:CM002898.2

About this gene

This gene has 2 transcripts (splice variants), 195 orthologues, 11 paralogues and is associated with 16 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000148652.3	slc26a2-201	4920	699aa	ENSDARP00000124111.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7F9I7	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,
ENSDART00000183448.1	slc26a2-202	4690	699aa	ENSDARP00000148044.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7F9I7	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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