Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: SOGA1 ENSSSCG00000007324

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Description

suppressor of glucose, autophagy associated 1 [Source:VGNC Symbol;Acc:VGNC:95740]

Location

Primary_assembly 17: 40,020,440-40,099,001 reverse strand.

Sscrofa11.1:CM000828.5

About this gene

This gene has 2 transcripts (splice variants), 261 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000008014.5	SOGA1-202	7102	1659aa	ENSSSCP00000007800.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D1GUK3 F1SEM9	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 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,
ENSSSCT00000087589.2	SOGA1-201	5192	1018aa	ENSSSCP00000070013.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QYR1	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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Summary

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