Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
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: Faul2 ENSRNOG00000020982

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Description

FAU ubiquitin like and ribosomal protein S30 fusion [Source:RGD Symbol;Acc:61938]

Gene Synonyms

LOC100360647, LOC363650, LOC687780, RGD1565317

Location

Primary_assembly 1: 212,779,473-212,781,026 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 1 transcript (splice variant), 204 orthologues and 5 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000028481.8	Faul2-201	554	133aa	ENSRNOP00000028481.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A9K3Y6P2 Q5BJN7	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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