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: SLC6A2 ENSDARG00000016141

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Description

solute carrier family 6 member 2 [Source:HGNC Symbol;Acc:HGNC:11048]

Location

Chromosome 7: 35,348,471-35,380,186 reverse strand.

GRCz11:CM002891.2

About this gene

This gene has 2 transcripts (splice variants), 204 orthologues and 35 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000148430.3	SLC6A2-201	5388	625aa	ENSDARP00000124452.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1R3H6	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,
ENSDART00000183484.1	SLC6A2-202	5367	625aa	ENSDARP00000151551.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1R3H6	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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