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: SLC38A2 ENSSSCG00000000808

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Description

solute carrier family 38 member 2 [Source:VGNC Symbol;Acc:VGNC:93094]

Location

Primary_assembly 5: 77,113,494-77,127,650 reverse strand.

Sscrofa11.1:CM000816.5

About this gene

This gene has 1 transcript (splice variant), 267 orthologues and 15 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000000877.5	SLC38A2-201	4687	406aa	ENSSSCP00000000860.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D0R082 A0A8D1GA70	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,

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Summary

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