Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: FBXW2 ENSPTRG00000021304

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Description

F-box and WD repeat domain containing 2 [Source:VGNC Symbol;Acc:VGNC:13878]

Location

Chromosome 9: 98,823,321-98,852,688 reverse strand.

Pan_tro_3.0:CM000323.3

About this gene

This gene has 2 transcripts (splice variants) and 215 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000039407.3	FBXW2-202	2248	454aa	ENSPTRP00000036412.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2WZ89 H2QXS8	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,
ENSPTRT00000111070.1	FBXW2-201	2052	389aa	ENSPTRP00000078601.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3SQ07	-

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Summary

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