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

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Gene: Slc31a2 ENSRNOG00000013631

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Description

solute carrier family 31 member 2 [Source:RGD Symbol;Acc:1307963]

Gene Synonyms

LOC298091, MGC124776

Location

Primary_assembly 5: 80,753,618-80,764,123 forward strand.

GRCr8:CM070395.1

About this gene

This gene has 1 transcript (splice variant), 220 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000019379.9	Slc31a2-201	1763	143aa	ENSRNOP00000019379.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6J7T6 D4AAE7	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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Paralogues

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