Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
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  - Gene tree
  - Orthologues
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Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
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External references
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ID History
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Gene: SMG6 ENSSSCG00000017826

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Description

SMG6 nonsense mediated mRNA decay factor [Source:VGNC Symbol;Acc:VGNC:93249]

Location

Primary_assembly 12: 48,172,707-48,386,884 reverse strand.

Sscrofa11.1:CM000823.5

About this gene

This gene has 1 transcript (splice variant) and 198 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000019401.5	SMG6-201	5982	1412aa	ENSSSCP00000018886.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1UAW8 F1RHH0	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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