Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Cellular component
- 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: Fbxl22 ENSRNOG00000017684

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Description

F-box and leucine-rich repeat protein 22 [Source:RGD Symbol;Acc:1311830]

Gene Synonyms

LOC363083, RGD1311830

Location

Primary_assembly 8: 75,965,027-75,971,714 reverse strand.

GRCr8:CM070398.1

About this gene

This gene has 1 transcript (splice variant), 214 orthologues and 18 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000023810.7	Fbxl22-201	4460	236aa	ENSRNOP00000023810.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6J5I2 D3ZS59	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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