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: SLC2A2 ENSSSCG00000020927

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Description

solute carrier family 2 member 2 [Source:NCBI gene (formerly Entrezgene);Acc:397429]

Gene Synonyms

GLUT2

Location

Primary_assembly 13: 109,587,258-109,638,510 reverse strand.

Sscrofa11.1:CM000824.5

About this gene

This gene has 4 transcripts (splice variants), 311 orthologues and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000095571.1	SLC2A2-204	5261	596aa	ENSSSCP00000081133.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8W4FPK7	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 ALT2: 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 appear to be conserved in fewer than 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 ALT2,
ENSSSCT00000083137.2	SLC2A2-203	6818	522aa	ENSSSCP00000074300.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2RNB3	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be 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 P2,
ENSSSCT00000077905.2	SLC2A2-202	5260	490aa	ENSSSCP00000060505.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2Q8G8	-
ENSSSCT00000027703.4	SLC2A2-201	3499	546aa	ENSSSCP00000025763.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D0VIQ4 A0A8D1R206	APPRIS ALT2: 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 appear to be conserved in fewer than 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 ALT2,

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Breeds

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Genomic alignments

Gene tree

Orthologues

Paralogues

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data