Gene: Fbxw2 ENSRNOG00000018687

Description

F-box and WD repeat domain containing 2 [Source:RGD Symbol;Acc:1310460]

Gene Synonyms

LOC311881

Location

mRatBN7.2:CM026976.1

About this gene

This gene has 2 transcripts (splice variants), 213 orthologues and is associated with 1 phenotype.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000109847.1	Fbxw2-202	2241	481aa	ENSRNOP00000090377.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ABP5	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 P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSRNOT00000025399.5	Fbxw2-201	1544	389aa	ENSRNOP00000025399.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QDA1	APPRIS ALT1: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that is conserved in at least three tested species. 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 ALT1,

Summary