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
  - Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: SNF8 ENSBTAG00000018803

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Description

SNF8 subunit of ESCRT-II [Source:VGNC Symbol;Acc:VGNC:35064]

Location

Primary_assembly 19: 37,587,446-37,596,407 forward strand.

ARS-UCD2.0:CM008186.2

About this gene

This gene has 2 transcripts (splice variants) and 213 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000067735.3	SNF8-201	1930	275aa	ENSBTAP00000073037.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MMK5	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,
ENSBTAT00000025031.4	SNF8-202	2384	258aa	ENSBTAP00000025031.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q08DR7	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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