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: SLC17A2 ENSBTAG00000002642

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Description

solute carrier family 17 member 2 [Source:VGNC Symbol;Acc:VGNC:34697]

Location

Primary_assembly 23: 31,959,620-31,977,850 forward strand.

ARS-UCD1.3:CM008190.2

About this gene

This gene has 3 transcripts (splice variants), 388 orthologues and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000089606.1	SLC17A2-203	1762	482aa	ENSBTAP00000075857.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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 ALT1: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that is conserved in at least three tested species. 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 ALT1,
ENSBTAT00000120363.1	SLC17A2-201	2556	440aa	ENSBTAP00000093187.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000003426.6	SLC17A2-202	1985	479aa	ENSBTAP00000003426.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q32LF0	APPRIS P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform as the principal variant. 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 P4,

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Summary

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