Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
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Ontologies
Phenotypes
Genetic Variation
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Pathway
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External references
Supporting evidence
ID History
- Gene history

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Gene: SNF8 ENSSSCG00000021461

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Description

SNF8 subunit of ESCRT-II [Source:VGNC Symbol;Acc:VGNC:93288]

Location

Primary_assembly 12: 25,142,813-25,153,016 reverse strand.

Sscrofa11.1:CM000823.5

About this gene

This gene has 2 transcripts (splice variants) and 214 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000030250.4	SNF8-202	1104	258aa	ENSSSCP00000019779.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1UL97 I3L6X7	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,
ENSSSCT00000088577.2	SNF8-201	791	244aa	ENSSSCP00000064785.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QL86 A0A8D1Z6Y5	-

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Summary

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