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: FBXW9 ENSSSCG00000013725

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Description

F-box and WD repeat domain containing 9 [Source:VGNC Symbol;Acc:VGNC:88057]

Location

Primary_assembly 2: 66,291,172-66,297,213 forward strand.

Sscrofa11.1:CM000813.5

About this gene

This gene has 1 transcript (splice variant), 183 orthologues and 14 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000014999.4	FBXW9-201	1760	458aa	ENSSSCP00000014595.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1UD17 F1SEX6	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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