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

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Gene: FBXW8 ENSSSCG00000009860

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Description

F-box and WD repeat domain containing 8 [Source:VGNC Symbol;Acc:VGNC:107391]

Location

Primary_assembly 14: 35,444,281-35,575,705 reverse strand.

Sscrofa11.1:CM000825.5

About this gene

This gene has 2 transcripts (splice variants), 191 orthologues and 14 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000056206.2	FBXW8-201	1791	596aa	ENSSSCP00000048926.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287AYA4 A0A4X1TRX2	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,
ENSSSCT00000010808.5	FBXW8-202	3450	526aa	ENSSSCP00000010525.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1TS23 F1RKE7	-

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Gene tree

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