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

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Gene: slc26a11 ENSDARG00000043021

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Description

solute carrier family 26 member 11 [Source:ZFIN;Acc:ZDB-GENE-030131-5349]

Gene Synonyms

wu:fd14d06, zgc:64158

Location

Chromosome 22: 11,497,366-11,520,405 reverse strand.

GRCz11:CM002906.2

About this gene

This gene has 2 transcripts (splice variants), 210 orthologues and 11 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000063157.5	slc26a11-201	2688	572aa	ENSDARP00000063156.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B0V3V8	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,
ENSDART00000193885.1	slc26a11-202	4854	572aa	ENSDARP00000146354.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B0V3V8	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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