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
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Fbxw17 ENSRNOG00000030027

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Description

F-box and WD-40 domain protein 17 [Source:RGD Symbol;Acc:1566133]

Gene Synonyms

LOC361219, RGD1566133

Location

Primary_assembly 17: 14,511,194-14,530,275 forward strand.

GRCr8:CM070407.1

About this gene

This gene has 1 transcript (splice variant), 136 orthologues and 15 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000044073.6	Fbxw17-201	3010	466aa	ENSRNOP00000039789.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3Z9G1	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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